Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5728 |
|---|---|
| ensemblid | ENSG00000171862.15 |
| hgncid | 9588 |
| symbol | PTEN |
| name | phosphatase and tensin homolog |
| refseq_nuc | NM_000314.8 |
| refseq_prot | NP_000305.3 |
| ensembl_nuc | ENST00000371953.8 |
| ensembl_prot | ENSP00000361021.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 87863625 |
| end | 87971930 |
| strand | + |
| ver | v1.2 |
| region | chr10:87863625-87971930 |
| region5000 | chr10:87858625-87976930 |
| regionname0 | PTEN_chr10_87863625_87971930 |
| regionname5000 | PTEN_chr10_87858625_87976930 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 403 | 322 | 78 | 60 | 152 | 8 | 22 | 116 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 7301 | 59 | 1 | 14 | 43 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0002 | 0/0 | 7303 | 28 | 0 | 3 | 24 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0003 | 0/0 | 7301 | 20 | 17 | 3 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0004 | 0/0 | 7304 | 16 | 1 | 1 | 9 | 1 | 4 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0005 | 0/0 | 7302 | 13 | 2 | 4 | 5 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0006 | 0/1 | 7302 | 13 | 2 | 4 | 4 | 1 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0007 | 0/0 | 7298 | 9 | 0 | 1 | 7 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0008 | 0/0 | 7302 | 7 | 0 | 0 | 7 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0009 | 0/0 | 7303 | 5 | 3 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0010 | 0/0 | 7303 | 5 | 0 | 3 | 1 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0011 | 0/0 | 7306 | 4 | 0 | 3 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0012 | 0/0 | 7299 | 4 | 2 | 1 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0013 | 0/0 | 7301 | 4 | 0 | 0 | 4 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0014 | 0/0 | 7301 | 4 | 0 | 3 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0015 | 0/0 | 7302 | 4 | 4 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0016 | 0/0 | 7290 | 3 | 0 | 0 | 3 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0017 | 0/0 | 7302 | 3 | 0 | 1 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0018 | 0/0 | 7305 | 3 | 0 | 2 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0019 | 0/0 | 7303 | 3 | 0 | 0 | 3 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0020 | 0/0 | 7298 | 3 | 0 | 0 | 0 | 1 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0021 | 0/0 | 7300 | 3 | 3 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0022 | 0/0 | 7302 | 3 | 0 | 2 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0023 | 0/0 | 7303 | 3 | 3 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0024 | 0/0 | 7302 | 3 | 0 | 1 | 1 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0025 | 0/0 | 7304 | 3 | 0 | 2 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0026 | 0/0 | 7298 | 3 | 3 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0027 | 0/0 | 7302 | 2 | 0 | 0 | 0 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0028 | 0/0 | 7302 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0029 | 0/0 | 7301 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0030 | 0/0 | 7303 | 2 | 1 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0031 | 0/0 | 7302 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0032 | 0/0 | 7303 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0033 | 0/0 | 7302 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0034 | 0/0 | 7304 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0035 | 0/0 | 7299 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0036 | 0/0 | 7301 | 2 | 0 | 0 | 0 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0037 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0038 | 0/0 | 7303 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0039 | 0/0 | 7306 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0040 | 0/0 | 7298 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0041 | 0/0 | 7299 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0042 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0043 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0044 | 0/0 | 7304 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0045 | 0/0 | 7303 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0046 | 0/0 | 7303 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0047 | 0/0 | 7305 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0048 | 0/0 | 7304 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0049 | 0/0 | 7303 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0050 | 0/0 | 7304 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0051 | 0/0 | 7306 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0052 | 0/0 | 7305 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0053 | 0/0 | 7307 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0054 | 0/0 | 7306 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0055 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0056 | 0/0 | 7305 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0057 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0058 | 0/0 | 7303 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0059 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0060 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0061 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0062 | 0/0 | 7302 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0063 | 0/0 | 7302 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0064 | 0/0 | 7300 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0065 | 0/0 | 7300 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0066 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0067 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0068 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0069 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0070 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0071 | 0/0 | 7301 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0072 | 0/0 | 7300 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0073 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0074 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0075 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0076 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0077 | 0/0 | 7303 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0078 | 0/0 | 7303 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0079 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0080 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0081 | 0/0 | 7301 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0082 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0083 | 0/0 | 7302 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0084 | 0/0 | 7304 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0085 | 0/0 | 7302 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0086 | 0/0 | 7304 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0087 | 0/0 | 7303 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0088 | 0/0 | 7303 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0089 | 0/0 | 7304 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0090 | 0/0 | 7302 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0091 | 0/0 | 7304 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0092 | 0/0 | 7304 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0093 | 0/0 | 7301 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0094 | 0/0 | 7303 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0095 | 0/0 | 7302 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0096 | 0/0 | 7304 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0097 | 0/0 | 7305 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0098 | 0/0 | 7304 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0099 | 0/0 | 7303 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0100 | 0/0 | 7303 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0101 | 0/0 | 7304 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0102 | 0/0 | 7305 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0103 | 0/0 | 7305 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0104 | 0/0 | 7301 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0105 | 0/0 | 7303 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0106 | 0/0 | 7305 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0107 | 0/0 | 7306 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0108 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0109 | 1/0 | 7304 | 1 | 0 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| t0110 | 0/0 | 7302 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1212 | 321 | 78 | 59 | 152 | 8 | 22 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0002 | 0/0 | 1212 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8512 | 59 | 1 | 14 | 43 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0002 | 0/0 | 8514 | 28 | 0 | 3 | 24 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0003 | 0/0 | 8512 | 20 | 17 | 3 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0004 | 0/0 | 8515 | 16 | 1 | 1 | 9 | 1 | 4 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0005 | 0/0 | 8513 | 13 | 2 | 4 | 5 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0006 | 0/1 | 8513 | 13 | 2 | 4 | 4 | 1 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0007 | 0/0 | 8509 | 9 | 0 | 1 | 7 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0008 | 0/0 | 8513 | 7 | 0 | 0 | 7 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0009 | 0/0 | 8514 | 5 | 3 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0010 | 0/0 | 8514 | 5 | 0 | 3 | 1 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0011 | 0/0 | 8517 | 4 | 0 | 3 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0012 | 0/0 | 8510 | 4 | 2 | 1 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0013 | 0/0 | 8512 | 4 | 0 | 0 | 4 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0014 | 0/0 | 8512 | 4 | 0 | 3 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0015 | 0/0 | 8513 | 4 | 4 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0016 | 0/0 | 8501 | 3 | 0 | 0 | 3 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0017 | 0/0 | 8513 | 3 | 0 | 1 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0018 | 0/0 | 8516 | 3 | 0 | 2 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0019 | 0/0 | 8514 | 3 | 0 | 0 | 3 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0020 | 0/0 | 8509 | 3 | 0 | 0 | 0 | 1 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0021 | 0/0 | 8511 | 3 | 3 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0022 | 0/0 | 8513 | 3 | 0 | 2 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0023 | 0/0 | 8514 | 3 | 3 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0024 | 0/0 | 8513 | 3 | 0 | 1 | 1 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0025 | 0/0 | 8515 | 3 | 0 | 2 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0026 | 0/0 | 8509 | 3 | 3 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0027 | 0/0 | 8513 | 2 | 0 | 0 | 0 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0028 | 0/0 | 8513 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0029 | 0/0 | 8512 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0030 | 0/0 | 8514 | 2 | 1 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0031 | 0/0 | 8513 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0032 | 0/0 | 8514 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0033 | 0/0 | 8513 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0034 | 0/0 | 8515 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0035 | 0/0 | 8510 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0036 | 0/0 | 8512 | 2 | 0 | 0 | 0 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0037 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0038 | 0/0 | 8514 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0039 | 0/0 | 8517 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0040 | 0/0 | 8509 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0041 | 0/0 | 8510 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0042 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0043 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0044 | 0/0 | 8515 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0045 | 0/0 | 8514 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0046 | 0/0 | 8514 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0047 | 0/0 | 8516 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0048 | 0/0 | 8515 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0049 | 0/0 | 8514 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0050 | 0/0 | 8515 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0051 | 0/0 | 8517 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0052 | 0/0 | 8516 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0053 | 0/0 | 8518 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0054 | 0/0 | 8517 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0055 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0056 | 0/0 | 8516 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0057 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0058 | 0/0 | 8514 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0059 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0060 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0061 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0062 | 0/0 | 8513 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0063 | 0/0 | 8513 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0064 | 0/0 | 8511 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0065 | 0/0 | 8511 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0066 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0067 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0068 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0069 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0070 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0071 | 0/0 | 8512 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0072 | 0/0 | 8511 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0073 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0074 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0075 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0076 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0077 | 0/0 | 8514 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0078 | 0/0 | 8514 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0079 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0080 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0081 | 0/0 | 8512 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0082 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0083 | 0/0 | 8513 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0084 | 0/0 | 8515 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0085 | 0/0 | 8513 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0086 | 0/0 | 8515 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0087 | 0/0 | 8514 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0088 | 0/0 | 8514 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0089 | 0/0 | 8515 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0090 | 0/0 | 8513 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0091 | 0/0 | 8515 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0092 | 0/0 | 8515 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0093 | 0/0 | 8512 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0094 | 0/0 | 8514 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0095 | 0/0 | 8513 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0096 | 0/0 | 8515 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0098 | 0/0 | 8515 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0099 | 0/0 | 8514 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0100 | 0/0 | 8514 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0101 | 0/0 | 8515 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0102 | 0/0 | 8516 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0103 | 0/0 | 8516 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0104 | 0/0 | 8512 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0105 | 0/0 | 8514 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0106 | 0/0 | 8516 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0107 | 0/0 | 8517 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0108 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0109 | 1/0 | 8515 | 1 | 0 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0001t0110 | 0/0 | 8513 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| a0001c0002t0097 | 0/0 | 8516 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | copy fasta | chr10 | 87858625 | 87976930 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0010g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0010g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0010g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0011g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0011g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0011g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0011g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0012g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0013g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0013g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0014g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0014g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0015g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0015g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0016g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0016g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0016g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0017g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0017g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0017g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0018g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0018g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0018g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0019g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0019g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0019g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0020g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0020g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0020g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0021g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0021g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0022g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0022g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0022g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0023g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0023g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0023g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0024g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0024g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0024g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0025g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0025g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0025g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0026g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0026g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0026g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0027g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0027g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0028g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0028g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0029g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0029g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0030g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0030g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0031g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0031g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0032g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0032g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0033g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0033g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0034g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0034g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0035g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0035g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0036g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0037g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0038g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0039g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0040g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0041g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0042g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0043g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0044g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0045g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0046g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0047g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0048g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0049g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0050g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0051g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0052g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0053g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0054g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0055g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0056g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0057g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0058g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0059g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0060g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0061g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0062g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0063g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0064g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0065g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0066g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0067g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0068g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0069g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0070g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0071g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0072g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0073g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0074g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0075g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0076g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0077g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0078g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0079g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0080g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0081g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0082g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0083g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0084g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0085g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0086g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0087g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0088g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0089g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0090g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0091g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0092g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0093g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0094g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0095g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0096g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0098g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0099g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0100g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0101g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0102g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0103g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0104g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0105g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0106g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0107g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0108g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0109g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0001t0110g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| a0001c0002t0097g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0247 | EUR | GBR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00099 | hp2 | a0001 | c0001 | t0085 | g0084 | EUR | GBR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0083 | EUR | GBR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00323 | hp2 | a0001 | c0001 | t0094 | g0189 | EUR | FIN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00408 | hp2 | a0001 | c0001 | t0018 | g0263 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00438 | hp1 | a0001 | c0001 | t0069 | g0152 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00597 | hp1 | a0001 | c0001 | t0039 | g0265 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00609 | hp2 | a0001 | c0001 | t0016 | g0289 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00621 | hp1 | a0001 | c0001 | t0057 | g0127 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00639 | hp1 | a0001 | c0001 | t0017 | g0255 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0304 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00673 | hp2 | a0001 | c0001 | t0013 | g0073 | EAS | CHS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0013 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00738 | hp2 | a0001 | c0001 | t0052 | g0236 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01070 | hp1 | a0001 | c0001 | t0100 | g0191 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01081 | hp1 | a0001 | c0001 | t0095 | g0103 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0133 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0116 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01109 | hp1 | a0001 | c0002 | t0097 | g0272 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01109 | hp2 | a0001 | c0001 | t0090 | g0015 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01175 | hp2 | a0001 | c0001 | t0071 | g0275 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01255 | hp1 | a0001 | c0001 | t0022 | g0080 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01257 | hp1 | a0001 | c0001 | t0014 | g0002 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01258 | hp1 | a0001 | c0001 | t0098 | g0090 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01258 | hp2 | a0001 | c0001 | t0014 | g0002 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01261 | hp1 | a0001 | c0001 | t0022 | g0082 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01261 | hp2 | a0001 | c0001 | t0096 | g0297 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01346 | hp1 | a0001 | c0001 | t0088 | g0081 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01346 | hp2 | a0001 | c0001 | t0011 | g0268 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01361 | hp1 | a0001 | c0001 | t0025 | g0296 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0087 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01433 | hp2 | a0001 | c0001 | t0081 | g0079 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01517 | hp1 | a0001 | c0001 | t0020 | g0143 | EUR | IBS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0295 | EUR | IBS | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01928 | hp2 | a0001 | c0001 | t0018 | g0259 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01934 | hp2 | a0001 | c0001 | t0018 | g0262 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01952 | hp2 | a0001 | c0001 | t0025 | g0122 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01975 | hp1 | a0001 | c0001 | t0010 | g0124 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01975 | hp2 | a0001 | c0001 | t0050 | g0245 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01993 | hp2 | a0001 | c0001 | t0010 | g0123 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02004 | hp2 | a0001 | c0001 | t0011 | g0267 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02027 | hp1 | a0001 | c0001 | t0045 | g0283 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0179 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0119 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02071 | hp2 | a0001 | c0001 | t0042 | g0256 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02074 | hp1 | a0001 | c0001 | t0058 | g0132 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0276 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0129 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02145 | hp1 | a0001 | c0001 | t0030 | g0074 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02145 | hp2 | a0001 | c0001 | t0032 | g0070 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02148 | hp1 | a0001 | c0001 | t0011 | g0235 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0131 | EAS | CDX | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CDX | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02165 | hp2 | a0001 | c0001 | t0013 | g0039 | EAS | CDX | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02258 | hp1 | a0001 | c0001 | t0023 | g0111 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02300 | hp1 | a0001 | c0001 | t0054 | g0216 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0086 | AMR | PEL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02572 | hp1 | a0001 | c0001 | t0037 | g0099 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0091 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0254 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02622 | hp1 | a0001 | c0001 | t0029 | g0301 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02622 | hp2 | a0001 | c0001 | t0102 | g0208 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02647 | hp2 | a0001 | c0001 | t0083 | g0068 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02717 | hp1 | a0001 | c0001 | t0086 | g0093 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02717 | hp2 | a0001 | c0001 | t0061 | g0302 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02723 | hp1 | a0001 | c0001 | t0082 | g0290 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02723 | hp2 | a0001 | c0001 | t0106 | g0288 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02735 | hp2 | a0001 | c0001 | t0036 | g0008 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0197 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02818 | hp1 | a0001 | c0001 | t0065 | g0077 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02818 | hp2 | a0001 | c0001 | t0015 | g0112 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02886 | hp1 | a0001 | c0001 | t0034 | g0206 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0198 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02896 | hp1 | a0001 | c0001 | t0031 | g0298 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0134 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02897 | hp1 | a0001 | c0001 | t0073 | g0075 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0135 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02965 | hp1 | a0001 | c0001 | t0026 | g0115 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0109 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02970 | hp2 | a0001 | c0001 | t0031 | g0300 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0205 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02976 | hp2 | a0001 | c0001 | t0076 | g0293 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03017 | hp1 | a0001 | c0001 | t0014 | g0014 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03017 | hp2 | a0001 | c0001 | t0027 | g0049 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03041 | hp1 | a0001 | c0001 | t0029 | g0299 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03041 | hp2 | a0001 | c0001 | t0107 | g0287 | AFR | GWD | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03130 | hp2 | a0001 | c0001 | t0035 | g0107 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03139 | hp1 | a0001 | c0001 | t0026 | g0106 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03195 | hp1 | a0001 | c0001 | t0035 | g0105 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03195 | hp2 | a0001 | c0001 | t0078 | g0031 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03209 | hp2 | a0001 | c0001 | t0026 | g0193 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03225 | hp1 | a0001 | c0001 | t0028 | g0063 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0096 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03453 | hp2 | a0001 | c0001 | t0077 | g0137 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03486 | hp1 | a0001 | c0001 | t0051 | g0294 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03516 | hp1 | a0001 | c0001 | t0063 | g0162 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03579 | hp1 | a0001 | c0001 | t0028 | g0185 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03579 | hp2 | a0001 | c0001 | t0089 | g0178 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03654 | hp1 | a0001 | c0001 | t0020 | g0305 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0028 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0213 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03704 | hp2 | a0001 | c0001 | t0020 | g0154 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03710 | hp1 | a0001 | c0001 | t0012 | g0023 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0061 | SAS | PJL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03942 | hp1 | a0001 | c0001 | t0105 | g0292 | SAS | BEB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03942 | hp2 | a0001 | c0001 | t0027 | g0163 | SAS | BEB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0223 | SAS | STU | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0098 | SAS | STU | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG04199 | hp1 | a0001 | c0001 | t0024 | g0192 | SAS | STU | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG04199 | hp2 | a0001 | c0001 | t0022 | g0303 | SAS | STU | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG04204 | hp1 | a0001 | c0001 | t0036 | g0008 | SAS | STU | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG04204 | hp2 | a0001 | c0001 | t0025 | g0117 | SAS | STU | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18522 | hp1 | a0001 | c0001 | t0074 | g0067 | AFR | YRI | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18522 | hp2 | a0001 | c0001 | t0015 | g0108 | AFR | YRI | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18747 | hp1 | a0001 | c0001 | t0046 | g0237 | EAS | CHB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18747 | hp2 | a0001 | c0001 | t0070 | g0047 | EAS | CHB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | YRI | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18906 | hp2 | a0001 | c0001 | t0084 | g0194 | AFR | YRI | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18939 | hp2 | a0001 | c0001 | t0044 | g0253 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18940 | hp2 | a0001 | c0001 | t0033 | g0174 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18948 | hp1 | a0001 | c0001 | t0093 | g0022 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18948 | hp2 | a0001 | c0001 | t0008 | g0118 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18952 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18953 | hp1 | a0001 | c0001 | t0040 | g0240 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18953 | hp2 | a0001 | c0001 | t0009 | g0102 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18959 | hp1 | a0001 | c0001 | t0049 | g0264 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18959 | hp2 | a0001 | c0001 | t0080 | g0121 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18960 | hp2 | a0001 | c0001 | t0017 | g0239 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18963 | hp2 | a0001 | c0001 | t0068 | g0138 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18965 | hp1 | a0001 | c0001 | t0048 | g0221 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18968 | hp1 | a0001 | c0001 | t0017 | g0229 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18969 | hp2 | a0001 | c0001 | t0033 | g0175 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18972 | hp2 | a0001 | c0001 | t0016 | g0215 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18973 | hp1 | a0001 | c0001 | t0019 | g0284 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18975 | hp2 | a0001 | c0001 | t0055 | g0285 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18978 | hp1 | a0001 | c0001 | t0047 | g0241 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18978 | hp2 | a0001 | c0001 | t0091 | g0291 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18981 | hp2 | a0001 | c0001 | t0030 | g0037 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18983 | hp1 | a0001 | c0001 | t0079 | g0171 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18985 | hp2 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18987 | hp2 | a0001 | c0001 | t0024 | g0190 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18988 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18990 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18993 | hp1 | a0001 | c0001 | t0010 | g0120 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18997 | hp2 | a0001 | c0001 | t0056 | g0269 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19000 | hp2 | a0001 | c0001 | t0087 | g0195 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0100 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19003 | hp1 | a0001 | c0001 | t0019 | g0260 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19004 | hp2 | a0001 | c0001 | t0067 | g0151 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19011 | hp1 | a0001 | c0001 | t0072 | g0146 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19011 | hp2 | a0001 | c0001 | t0110 | g0187 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | LWK | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19030 | hp2 | a0001 | c0001 | t0021 | g0196 | AFR | LWK | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19043 | hp1 | a0001 | c0001 | t0062 | g0011 | AFR | LWK | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19043 | hp2 | a0001 | c0001 | t0075 | g0076 | AFR | LWK | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19059 | hp1 | a0001 | c0001 | t0059 | g0126 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19059 | hp2 | a0001 | c0001 | t0099 | g0209 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19060 | hp2 | a0001 | c0001 | t0066 | g0128 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19068 | hp1 | a0001 | c0001 | t0060 | g0166 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19068 | hp2 | a0001 | c0001 | t0013 | g0032 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19075 | hp1 | a0001 | c0001 | t0043 | g0270 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19075 | hp2 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19076 | hp1 | a0001 | c0001 | t0011 | g0222 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19080 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19080 | hp2 | a0001 | c0001 | t0041 | g0251 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19084 | hp2 | a0001 | c0001 | t0108 | g0136 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19086 | hp1 | a0001 | c0001 | t0013 | g0071 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19090 | hp1 | a0001 | c0001 | t0019 | g0261 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0110 | AFR | ASW | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ASW | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA20905 | hp1 | a0001 | c0001 | t0092 | g0141 | SAS | GIH | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA20905 | hp2 | a0001 | c0001 | t0064 | g0156 | SAS | GIH | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01123 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG01123 | hp2 | a0001 | c0001 | t0024 | g0188 | AMR | CLM | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0114 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02559 | hp1 | a0001 | c0001 | t0104 | g0104 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03471 | hp1 | a0001 | c0001 | t0103 | g0204 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG03471 | hp2 | a0001 | c0001 | t0032 | g0035 | AFR | MSL | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG06807 | hp1 | a0001 | c0001 | t0023 | g0113 | AFR | USA | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | USA | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18955 | hp1 | a0001 | c0001 | t0053 | g0274 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA20300 | hp1 | a0001 | c0001 | t0038 | g0246 | AFR | USA | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | LWK | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| NA21309 | hp2 | a0001 | c0001 | t0101 | g0207 | AFR | LWK | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0085 | REF | REF | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0109 | g0089 | REF | REF | PTEN_chr10_87858625_87976930 | PTEN | chr10 | 87858625 | 87976930 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:87965364
|
T | C | 1 | a0001c0002 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1104T>C | p.Asp368Asp | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1949/8515 | 1104/1212 | 368/403 | chr10 | 87965364 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:87863879
|
G | A | 1 | a0001c0001t0037 | 1 | HG02572.hp1 | 5_prime_UTR_variant | MODIFIER | c.-591G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 591 | chr10 | 87863879 | |||||
| chr10:87863937
|
G | T | 1 | a0001c0001t0036 | 2 | HG02735.hp2 HG04204.hp1 |
5_prime_UTR_variant | MODIFIER | c.-533G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 533 | chr10 | 87863937 | |||||
| chr10:87863938
|
C | T | 1 | a0001c0001t0036 | 2 | HG02735.hp2 HG04204.hp1 |
5_prime_UTR_variant | MODIFIER | c.-532C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 532 | chr10 | 87863938 | |||||
| chr10:87863956
|
C | G | 1 | a0001c0001t0110 | 1 | NA19011.hp2 | 5_prime_UTR_variant | MODIFIER | c.-514C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 514 | chr10 | 87863956 | |||||
| chr10:87863959
|
G | A | 26 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(23): Show | 79 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-511G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 511 | chr10 | 87863959 | |||||
| chr10:87864103
|
CT | C | 109 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(106): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
5_prime_UTR_variant | MODIFIER | c.-366delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 366 | chr10 | 87864103 | |||||
| chr10:87864121
|
C | T | 1 | a0001c0001t0108 | 1 | NA19084.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-349C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | chr10 | 87864121 | ||||||
| chr10:87864144
|
G | C | 109 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(106): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
5_prime_UTR_variant | MODIFIER | c.-326G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 326 | chr10 | 87864144 | |||||
| chr10:87864305
|
C | G | 2 | a0001c0001t0106a0001c0001t0107 | 2 | HG02723.hp2 HG03041.hp2 |
5_prime_UTR_variant | MODIFIER | c.-165C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 165 | chr10 | 87864305 | |||||
| chr10:87864461
|
C | G | 3 | a0001c0001t0019a0001c0001t0055a0001c0001t0056 | 5 | NA18973.hp1 NA18975.hp2 NA18997.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-9C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/9 | 9 | chr10 | 87864461 | |||||
| chr10:87965825
|
C | T | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 353 | chr10 | 87965825 | |||||
| chr10:87966062
|
T | A | 1 | a0001c0001t0038 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 590 | chr10 | 87966062 | |||||
| chr10:87966236
|
G | A | 1 | a0001c0001t0057 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 764 | chr10 | 87966236 | |||||
| chr10:87966260
|
T | C | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 788 | chr10 | 87966260 | |||||
| chr10:87966322
|
T | C | 1 | a0001c0001t0058 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 850 | chr10 | 87966322 | |||||
| chr10:87966614
|
T | G | 1 | a0001c0001t0059 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1142T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1142 | chr10 | 87966614 | |||||
| chr10:87966674
|
T | C | 1 | a0001c0001t0039 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1202T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1202 | chr10 | 87966674 | |||||
| chr10:87966902
|
G | GT | 13 | a0001c0001t0004a0001c0001t0025a0001c0001t0026others(10): Show | 33 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1459dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1460 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966902
|
G | GTT | 7 | a0001c0001t0018a0001c0001t0035a0001c0001t0051others(4): Show | 10 | HG00408.hp2 HG00738.hp2 HG01928.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1458_*1459dupTT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1460 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966902
|
G | GTTT | 7 | a0001c0001t0011a0001c0001t0039a0001c0001t0053others(4): Show | 10 | HG00597.hp1 HG01346.hp2 HG02004.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1457_*1459dupTTT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1460 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966902
|
GT | G | 26 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(23): Show | 70 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1459delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1459 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966902
|
GTT | G | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(27): Show | 123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1458_*1459delTT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1458 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966902
|
GTTT | G | 5 | a0001c0001t0007a0001c0001t0040a0001c0001t0063others(2): Show | 13 | HG01243.hp2 HG02818.hp1 HG03516.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1457_*1459delTTT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1457 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966902
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0016 | 3 | HG00609.hp2 HG02074.hp2 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1447_*1459delTTTT others(9): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1447 | INFO_REALIGN_3_PRIME | chr10 | 87966902 | ||||
| chr10:87966914
|
T | G | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1442T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1442 | chr10 | 87966914 | |||||
| chr10:87966915
|
T | G | 3 | a0001c0001t0060a0001c0001t0061a0001c0001t0062 | 3 | HG02717.hp2 NA19043.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1443T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1443 | chr10 | 87966915 | |||||
| chr10:87966921
|
T | G | 2 | a0001c0001t0062a0001c0001t0105 | 2 | HG03942.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1449T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1449 | chr10 | 87966921 | |||||
| chr10:87966931
|
T | A | 1 | a0001c0001t0066 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1459T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1459 | chr10 | 87966931 | |||||
| chr10:87966932
|
A | T | 3 | a0001c0001t0026a0001c0001t0035a0001c0001t0104 | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1460A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1460 | chr10 | 87966932 | |||||
| chr10:87966988
|
T | C | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(13): Show | 91 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1516T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1516 | chr10 | 87966988 | |||||
| chr10:87967037
|
C | A | 1 | a0001c0001t0031 | 2 | HG02896.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1565C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1565 | chr10 | 87967037 | |||||
| chr10:87967167
|
C | A | 1 | a0001c0001t0043 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1695C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1695 | chr10 | 87967167 | |||||
| chr10:87967174
|
G | A | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1702G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1702 | chr10 | 87967174 | |||||
| chr10:87967217
|
G | A | 1 | a0001c0001t0083 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1745G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1745 | chr10 | 87967217 | |||||
| chr10:87967417
|
G | A | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1945G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1945 | chr10 | 87967417 | |||||
| chr10:87967426
|
A | T | 2 | a0001c0001t0029a0001c0001t0061 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1954A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 1954 | chr10 | 87967426 | |||||
| chr10:87967522
|
A | T | 1 | a0001c0001t0062 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2050A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 2050 | chr10 | 87967522 | |||||
| chr10:87967634
|
A | G | 2 | a0001c0001t0081a0001c0001t0089 | 2 | HG01433.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2162A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 2162 | chr10 | 87967634 | |||||
| chr10:87967657
|
C | T | 20 | a0001c0001t0008a0001c0001t0010a0001c0001t0022others(17): Show | 34 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2185C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 2185 | chr10 | 87967657 | |||||
| chr10:87967887
|
C | G | 2 | a0001c0001t0022a0001c0001t0088 | 4 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2415C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 2415 | chr10 | 87967887 | |||||
| chr10:87968288
|
A | G | 1 | a0001c0001t0046 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2816A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 2816 | chr10 | 87968288 | |||||
| chr10:87968442
|
G | T | 1 | a0001c0001t0052 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2970G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 2970 | chr10 | 87968442 | |||||
| chr10:87968622
|
A | G | 1 | a0001c0001t0076 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3150A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3150 | chr10 | 87968622 | |||||
| chr10:87968876
|
GT | G | 3 | a0001c0001t0014a0001c0001t0082a0001c0001t0090 | 6 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3415delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3415 | INFO_REALIGN_3_PRIME | chr10 | 87968876 | ||||
| chr10:87968914
|
T | TA | 17 | a0001c0001t0022a0001c0001t0023a0001c0001t0027others(14): Show | 25 | HG01109.hp1 HG01255.hp1 HG01261.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3463dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3464 | INFO_REALIGN_3_PRIME | chr10 | 87968914 | ||||
| chr10:87968914
|
T | TAA | 6 | a0001c0001t0063a0001c0001t0077a0001c0001t0078others(3): Show | 6 | HG02717.hp1 HG03195.hp2 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3462_*3463dupAA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3464 | INFO_REALIGN_3_PRIME | chr10 | 87968914 | ||||
| chr10:87968914
|
TA | T | 12 | a0001c0001t0021a0001c0001t0024a0001c0001t0026others(9): Show | 19 | HG01070.hp1 HG01081.hp1 HG01123.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3463delA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3463 | INFO_REALIGN_3_PRIME | chr10 | 87968914 | ||||
| chr10:87968925
|
A | C | 1 | a0001c0001t0050 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3453A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3453 | chr10 | 87968925 | |||||
| chr10:87968933
|
A | C | 5 | a0001c0001t0034a0001c0001t0101a0001c0001t0102others(2): Show | 6 | HG02622.hp2 HG02886.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3461A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3461 | chr10 | 87968933 | |||||
| chr10:87968935
|
A | G | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3463A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3463 | chr10 | 87968935 | |||||
| chr10:87969248
|
C | T | 1 | a0001c0001t0071 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3776C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3776 | chr10 | 87969248 | |||||
| chr10:87969322
|
A | G | 1 | a0001c0001t0095 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3850A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3850 | chr10 | 87969322 | |||||
| chr10:87969357
|
TAAG | T | 1 | a0001c0001t0020 | 3 | HG01517.hp1 HG03654.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3888_*3890delGAA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3888 | INFO_REALIGN_3_PRIME | chr10 | 87969357 | ||||
| chr10:87969456
|
A | T | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3984A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 3984 | chr10 | 87969456 | |||||
| chr10:87969485
|
G | T | 1 | a0001c0001t0108 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4013G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4013 | chr10 | 87969485 | |||||
| chr10:87969554
|
CTA | C | 5 | a0001c0001t0007a0001c0001t0012a0001c0001t0040others(2): Show | 16 | HG01081.hp2 HG01243.hp2 HG02896.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4085_*4086delTA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4085 | INFO_REALIGN_3_PRIME | chr10 | 87969554 | ||||
| chr10:87969563
|
A | C | 1 | a0001c0001t0075 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4091A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4091 | chr10 | 87969563 | |||||
| chr10:87969572
|
GTATTC | G | 3 | a0001c0001t0026a0001c0001t0035a0001c0001t0104 | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4103_*4107delTTCT others(1): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4103 | INFO_REALIGN_3_PRIME | chr10 | 87969572 | ||||
| chr10:87969593
|
C | T | 1 | a0001c0001t0105 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4121C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4121 | chr10 | 87969593 | |||||
| chr10:87969800
|
A | T | 2 | a0001c0001t0013a0001c0001t0033 | 6 | HG00673.hp2 HG02165.hp2 NA18940.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4328A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4328 | chr10 | 87969800 | |||||
| chr10:87969992
|
G | A | 1 | a0001c0001t0073 | 1 | HG02897.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4520 | chr10 | 87969992 | |||||
| chr10:87970015
|
A | G | 9 | a0001c0001t0015a0001c0001t0023a0001c0001t0024others(6): Show | 16 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4543A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4543 | chr10 | 87970015 | |||||
| chr10:87970036
|
T | C | 1 | a0001c0001t0067 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4564T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4564 | chr10 | 87970036 | |||||
| chr10:87970159
|
T | C | 1 | a0001c0001t0074 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4687T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4687 | chr10 | 87970159 | |||||
| chr10:87970403
|
C | T | 1 | a0001c0001t0070 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4931C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 4931 | chr10 | 87970403 | |||||
| chr10:87970584
|
C | T | 2 | a0001c0001t0045a0001c0001t0048 | 2 | HG02027.hp1 NA18965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5112C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 5112 | chr10 | 87970584 | |||||
| chr10:87970759
|
G | A | 1 | a0001c0001t0077 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5287G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 5287 | chr10 | 87970759 | |||||
| chr10:87970855
|
T | A | 2 | a0001c0001t0034a0001c0001t0102 | 3 | HG02622.hp2 HG02886.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5383T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 5383 | chr10 | 87970855 | |||||
| chr10:87971151
|
A | G | 1 | a0001c0001t0069 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5679A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 5679 | chr10 | 87971151 | |||||
| chr10:87971189
|
T | G | 1 | a0001c0001t0054 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5717T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 5717 | chr10 | 87971189 | |||||
| chr10:87971509
|
A | G | 1 | a0001c0001t0085 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6037A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 6037 | chr10 | 87971509 | |||||
| chr10:87971605
|
T | G | 1 | a0001c0001t0068 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6133T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 9/9 | 6133 | chr10 | 87971605 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:87864583
|
C | T | 1 | a0001c0001t0020g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.79+35C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87864583 | ||||||
| chr10:87864879
|
A | G | 1 | a0001c0001t0006g0304 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.79+331A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87864879 | ||||||
| chr10:87864910
|
A | G | 1 | a0001c0001t0022g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79+362A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87864910 | ||||||
| chr10:87864984
|
C | T | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+436C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87864984 | ||||||
| chr10:87865000
|
C | T | 3 | a0001c0001t0010g0295a0001c0001t0025g0296a0001c0001t0096g0297 | 3 | HG01261.hp2 HG01361.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.79+452C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865000 | ||||||
| chr10:87865006
|
C | T | 1 | a0001c0001t0051g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79+458C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865006 | ||||||
| chr10:87865214
|
A | G | 1 | a0001c0001t0076g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.79+666A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865214 | ||||||
| chr10:87865247
|
G | C | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+699G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865247 | ||||||
| chr10:87865368
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+820C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865368 | ||||||
| chr10:87865477
|
A | G | 2 | a0001c0001t0006g0010a0001c0001t0091g0291 | 3 | NA18951.hp1 NA18952.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.79+929A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865477 | ||||||
| chr10:87865584
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+1036T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865584 | ||||||
| chr10:87865790
|
T | C | 1 | a0001c0001t0009g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+1242T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865790 | ||||||
| chr10:87865845
|
A | G | 1 | a0001c0001t0082g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.79+1297A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87865845 | ||||||
| chr10:87865965
|
T | TAA | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+1420_79+1421dup others(2): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87865965 | |||||
| chr10:87866039
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+1491A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87866039 | ||||||
| chr10:87866618
|
T | TC | 95 | a0001c0001t0001g0271a0001c0001t0002g0009a0001c0001t0002g0211others(92): Show | 96 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.79+2073dupC | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87866618 | |||||
| chr10:87866989
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+2441A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87866989 | ||||||
| chr10:87867280
|
T | C | 5 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(2): Show | 5 | HG02622.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+2732T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87867280 | ||||||
| chr10:87867336
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+2788G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87867336 | ||||||
| chr10:87867381
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+2833G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87867381 | ||||||
| chr10:87867485
|
A | G | 1 | a0001c0001t0008g0203 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.79+2937A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87867485 | ||||||
| chr10:87867537
|
A | G | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+2989A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87867537 | ||||||
| chr10:87867708
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+3160T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87867708 | ||||||
| chr10:87868097
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.79+3549C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868097 | ||||||
| chr10:87868236
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | NA18942.hp1 NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.79+3688C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868236 | ||||||
| chr10:87868263
|
T | C | 1 | a0001c0001t0008g0016 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.79+3715T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868263 | ||||||
| chr10:87868307
|
A | G | 1 | a0001c0001t0016g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.79+3759A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868307 | ||||||
| chr10:87868405
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+3857C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868405 | ||||||
| chr10:87868439
|
C | T | 2 | a0001c0001t0006g0010a0001c0001t0091g0291 | 3 | NA18951.hp1 NA18952.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.79+3891C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868439 | ||||||
| chr10:87868495
|
A | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+3947A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868495 | ||||||
| chr10:87868694
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+4146T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868694 | ||||||
| chr10:87868786
|
T | C | 3 | a0001c0001t0002g0211a0001c0001t0004g0210a0001c0001t0099g0209 | 3 | NA18984.hp1 NA19004.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.79+4238T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868786 | ||||||
| chr10:87868887
|
A | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+4339A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868887 | ||||||
| chr10:87868981
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+4433T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87868981 | ||||||
| chr10:87869031
|
A | G | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.79+4483A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869031 | ||||||
| chr10:87869095
|
G | A | 2 | a0001c0001t0003g0003a0001c0001t0003g0017 | 3 | HG02109.hp2 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.79+4547G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869095 | ||||||
| chr10:87869189
|
C | T | 2 | a0001c0001t0106g0288a0001c0001t0107g0287 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.79+4641C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869189 | ||||||
| chr10:87869218
|
A | AT | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 96 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.79+4695dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87869218 | |||||
| chr10:87869218
|
AT | A | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0002g0009others(12): Show | 15 | HG00323.hp1 HG01070.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.79+4695delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87869218 | |||||
| chr10:87869264
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+4716C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869264 | ||||||
| chr10:87869328
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+4780C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869328 | ||||||
| chr10:87869456
|
C | T | 1 | a0001c0001t0068g0138 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.79+4908C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869456 | ||||||
| chr10:87869467
|
C | T | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.79+4919C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869467 | ||||||
| chr10:87869506
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+4958G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869506 | ||||||
| chr10:87869609
|
G | C | 1 | a0001c0001t0051g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79+5061G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869609 | ||||||
| chr10:87869692
|
C | T | 1 | a0001c0001t0077g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.79+5144C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869692 | ||||||
| chr10:87869728
|
A | G | 1 | a0001c0001t0108g0136 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.79+5180A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869728 | ||||||
| chr10:87869823
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+5275G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87869823 | ||||||
| chr10:87870162
|
C | G | 3 | a0001c0001t0012g0133a0001c0001t0012g0134a0001c0001t0012g0135 | 3 | HG01081.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.79+5614C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870162 | ||||||
| chr10:87870385
|
A | T | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+5837A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870385 | ||||||
| chr10:87870497
|
T | C | 1 | a0001c0001t0016g0215 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.79+5949T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870497 | ||||||
| chr10:87870580
|
C | G | 1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+6032C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870580 | ||||||
| chr10:87870581
|
C | A | 1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+6033C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870581 | ||||||
| chr10:87870662
|
T | G | 1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+6114T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870662 | ||||||
| chr10:87870667
|
C | T | 22 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(19): Show | 22 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.79+6119C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870667 | ||||||
| chr10:87870778
|
GTC | G | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.79+6234_79+6235del others(2): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87870778 | |||||
| chr10:87870793
|
A | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+6245A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870793 | ||||||
| chr10:87870793
|
A | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+6245A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870793 | ||||||
| chr10:87870893
|
T | A | 2 | a0001c0001t0003g0139a0001c0001t0003g0140 | 2 | HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.79+6345T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87870893 | ||||||
| chr10:87871106
|
T | G | 1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+6558T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871106 | ||||||
| chr10:87871166
|
T | G | 1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+6618T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871166 | ||||||
| chr10:87871246
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+6698C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871246 | ||||||
| chr10:87871300
|
A | G | 1 | a0001c0001t0009g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+6752A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871300 | ||||||
| chr10:87871413
|
C | T | 1 | a0001c0001t0026g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.79+6865C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871413 | ||||||
| chr10:87871580
|
C | T | 5 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18953.hp2 NA18960.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+7032C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871580 | ||||||
| chr10:87871644
|
G | A | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+7096G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871644 | ||||||
| chr10:87871670
|
T | A | 13 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(10): Show | 13 | HG01243.hp2 HG03654.hp2 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+7122T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871670 | ||||||
| chr10:87871717
|
G | T | 1 | a0001c0001t0036g0008 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.79+7169G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871717 | ||||||
| chr10:87871791
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+7243T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871791 | ||||||
| chr10:87871799
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.79+7251G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871799 | ||||||
| chr10:87871909
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+7361T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87871909 | ||||||
| chr10:87872052
|
A | G | 16 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(13): Show | 16 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+7504A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87872052 | ||||||
| chr10:87872090
|
G | GT | 23 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(20): Show | 23 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.79+7552dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87872090 | |||||
| chr10:87872132
|
G | GTCAGCGA others(43): Show |
1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+7586_79+7635dup others(50): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87872132 | |||||
| chr10:87872153
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+7605C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87872153 | ||||||
| chr10:87872365
|
A | T | 1 | a0001c0001t0026g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.79+7817A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87872365 | ||||||
| chr10:87872422
|
T | A | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+7874T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87872422 | ||||||
| chr10:87872424
|
T | TTTTA | 3 | a0001c0001t0001g0142a0001c0001t0054g0216a0001c0001t0078g0031 | 3 | HG02155.hp2 HG02300.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.79+7900_79+7903dup others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87872424 | |||||
| chr10:87872454
|
T | G | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.79+7906T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87872454 | ||||||
| chr10:87872900
|
T | C | 1 | a0001c0001t0013g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.79+8352T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87872900 | ||||||
| chr10:87873074
|
C | T | 1 | a0001c0001t0056g0269 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.79+8526C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873074 | ||||||
| chr10:87873078
|
A | G | 3 | a0001c0001t0024g0192a0001c0001t0092g0141a0001c0001t0095g0103 | 3 | HG01081.hp1 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.79+8530A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873078 | ||||||
| chr10:87873098
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+8550C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873098 | ||||||
| chr10:87873162
|
C | G | 1 | a0001c0001t0058g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79+8614C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873162 | ||||||
| chr10:87873360
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79+8812G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873360 | ||||||
| chr10:87873473
|
C | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+8925C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873473 | ||||||
| chr10:87873474
|
C | T | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+8926C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873474 | ||||||
| chr10:87873542
|
G | C | 1 | a0001c0001t0029g0299 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+8994G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873542 | ||||||
| chr10:87873550
|
T | C | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+9002T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873550 | ||||||
| chr10:87873615
|
C | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+9067C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873615 | ||||||
| chr10:87873769
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+9221G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873769 | ||||||
| chr10:87873865
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+9317A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873865 | ||||||
| chr10:87873975
|
A | T | 1 | a0001c0001t0100g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.79+9427A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87873975 | ||||||
| chr10:87874122
|
A | G | 5 | a0001c0001t0002g0266a0001c0001t0011g0267a0001c0001t0011g0268others(2): Show | 5 | HG00597.hp1 HG01346.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+9574A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87874122 | ||||||
| chr10:87874140
|
T | C | 1 | a0001c0001t0005g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.79+9592T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87874140 | ||||||
| chr10:87874420
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+9872A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87874420 | ||||||
| chr10:87874601
|
T | A | 2 | a0001c0001t0012g0133a0001c0001t0020g0143 | 2 | HG01081.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.79+10053T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87874601 | ||||||
| chr10:87874687
|
G | A | 2 | a0001c0001t0031g0298a0001c0001t0031g0300 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.79+10139G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87874687 | ||||||
| chr10:87875088
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+10540G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875088 | ||||||
| chr10:87875159
|
A | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+10611A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875159 | ||||||
| chr10:87875169
|
C | T | 1 | a0001c0001t0031g0298 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+10621C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875169 | ||||||
| chr10:87875498
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.79+10950G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875498 | ||||||
| chr10:87875528
|
G | A | 1 | a0001c0001t0032g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79+10980G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875528 | ||||||
| chr10:87875623
|
T | C | 1 | a0001c0001t0002g0144 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.79+11075T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875623 | ||||||
| chr10:87875820
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+11272A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87875820 | ||||||
| chr10:87876114
|
A | C | 5 | a0001c0001t0015g0112a0001c0001t0023g0111a0001c0001t0023g0113others(2): Show | 5 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+11566A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876114 | ||||||
| chr10:87876151
|
C | G | 1 | a0001c0001t0006g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.79+11603C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876151 | ||||||
| chr10:87876302
|
A | G | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+11754A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876302 | ||||||
| chr10:87876390
|
G | GT | 29 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0002g0286others(26): Show | 29 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.79+11852dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87876390 | |||||
| chr10:87876400
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+11852T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876400 | ||||||
| chr10:87876473
|
A | ATTTTAAA others(10): Show |
1 | a0001c0001t0018g0263 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.79+11927_79+11943d others(19): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87876473 | |||||
| chr10:87876672
|
G | A | 3 | a0001c0001t0002g0211a0001c0001t0004g0210a0001c0001t0099g0209 | 3 | NA18984.hp1 NA19004.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.79+12124G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876672 | ||||||
| chr10:87876704
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+12156T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876704 | ||||||
| chr10:87876875
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79+12327T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87876875 | ||||||
| chr10:87876919
|
C | CT | 93 | a0001c0001t0001g0019a0001c0001t0001g0097a0001c0001t0001g0181others(90): Show | 95 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.79+12391dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87876919 | |||||
| chr10:87876919
|
CT | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0036a0001c0001t0007g0020others(10): Show | 13 | HG01070.hp2 HG01517.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+12391delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87876919 | |||||
| chr10:87877256
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+12708G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877256 | ||||||
| chr10:87877284
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.79+12736A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877284 | ||||||
| chr10:87877472
|
T | C | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.79+12924T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877472 | ||||||
| chr10:87877482
|
A | G | 3 | a0001c0001t0077g0137a0001c0001t0078g0031a0001c0001t0086g0093 | 3 | HG02717.hp1 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.79+12934A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877482 | ||||||
| chr10:87877698
|
A | G | 13 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(10): Show | 13 | HG01243.hp2 HG03654.hp2 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+13150A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877698 | ||||||
| chr10:87877769
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+13221C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877769 | ||||||
| chr10:87877925
|
T | C | 2 | a0001c0001t0014g0002a0001c0001t0014g0013 | 3 | HG00738.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.79+13377T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877925 | ||||||
| chr10:87877947
|
T | G | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+13399T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87877947 | ||||||
| chr10:87878096
|
G | A | 3 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0061g0302 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.79+13548G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878096 | ||||||
| chr10:87878379
|
AT | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 21 | HG00423.hp1 HG00438.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.79+13832delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878379 | ||||||
| chr10:87878437
|
C | T | 1 | a0001c0001t0003g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.79+13889C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878437 | ||||||
| chr10:87878557
|
T | G | 1 | a0001c0001t0009g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79+14009T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878557 | ||||||
| chr10:87878577
|
G | A | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | NA18942.hp1 NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.79+14029G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878577 | ||||||
| chr10:87878705
|
C | A | 1 | a0001c0001t0004g0273 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+14157C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878705 | ||||||
| chr10:87878707
|
G | A | 1 | a0001c0001t0004g0273 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+14159G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878707 | ||||||
| chr10:87878712
|
A | G | 1 | a0001c0001t0004g0273 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+14164A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878712 | ||||||
| chr10:87878715
|
A | G | 1 | a0001c0001t0004g0273 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+14167A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878715 | ||||||
| chr10:87878717
|
A | T | 1 | a0001c0001t0004g0273 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.79+14169A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878717 | ||||||
| chr10:87878806
|
G | A | 1 | a0001c0001t0013g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.79+14258G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878806 | ||||||
| chr10:87878859
|
C | T | 16 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(13): Show | 16 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.79+14311C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878859 | ||||||
| chr10:87878871
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+14323T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878871 | ||||||
| chr10:87878898
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.79+14350A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87878898 | ||||||
| chr10:87879064
|
G | A | 11 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0266others(8): Show | 11 | HG00408.hp1 HG00597.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+14516G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879064 | ||||||
| chr10:87879123
|
A | ATG | 27 | a0001c0001t0004g0273a0001c0001t0008g0203a0001c0001t0015g0108others(24): Show | 27 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+14593_79+14594d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87879123 | |||||
| chr10:87879194
|
TCCAGAGA | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 22 | HG00423.hp1 HG00438.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.79+14649_79+14655d others(9): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87879194 | |||||
| chr10:87879230
|
C | T | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+14682C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879230 | ||||||
| chr10:87879299
|
AG | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.80-14725delG | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879299 | ||||||
| chr10:87879322
|
C | G | 1 | a0001c0001t0015g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.80-14703C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879322 | ||||||
| chr10:87879333
|
C | CT | 10 | a0001c0001t0001g0007a0001c0001t0001g0145a0001c0001t0001g0169others(7): Show | 11 | HG00609.hp1 NA18943.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-14682dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87879333 | |||||
| chr10:87879335
|
T | C | 1 | a0001c0001t0015g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.80-14690T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879335 | ||||||
| chr10:87879355
|
T | A | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-14670T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879355 | ||||||
| chr10:87879356
|
C | T | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-14669C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879356 | ||||||
| chr10:87879357
|
T | C | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-14668T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879357 | ||||||
| chr10:87879389
|
G | T | 1 | a0001c0001t0024g0190 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.80-14636G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879389 | ||||||
| chr10:87879429
|
G | A | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-14596G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879429 | ||||||
| chr10:87879450
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-14575T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879450 | ||||||
| chr10:87879586
|
A | T | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-14439A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879586 | ||||||
| chr10:87879737
|
T | A | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-14288T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879737 | ||||||
| chr10:87879805
|
T | G | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-14220T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879805 | ||||||
| chr10:87879852
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-14173G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879852 | ||||||
| chr10:87879925
|
A | T | 2 | a0001c0001t0031g0298a0001c0001t0031g0300 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.80-14100A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879925 | ||||||
| chr10:87879967
|
G | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-14058G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87879967 | ||||||
| chr10:87880067
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-13958G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880067 | ||||||
| chr10:87880205
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 311 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.80-13820G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880205 | ||||||
| chr10:87880264
|
T | G | 3 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0085g0084 | 3 | HG00099.hp2 HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80-13761T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880264 | ||||||
| chr10:87880278
|
G | GT | 16 | a0001c0001t0002g0286a0001c0001t0014g0002a0001c0001t0014g0013others(13): Show | 17 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-13731dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87880278 | |||||
| chr10:87880324
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-13701G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880324 | ||||||
| chr10:87880377
|
CT | C | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.80-13644delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87880377 | |||||
| chr10:87880413
|
T | C | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.80-13612T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880413 | ||||||
| chr10:87880656
|
C | T | 1 | a0001c0001t0003g0062 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.80-13369C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880656 | ||||||
| chr10:87880667
|
A | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0153 | 3 | NA18972.hp1 NA18975.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.80-13358A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880667 | ||||||
| chr10:87880754
|
TAAC | T | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-13267_80-13265d others(5): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87880754 | |||||
| chr10:87880977
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-13048A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87880977 | ||||||
| chr10:87881208
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-12817C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881208 | ||||||
| chr10:87881269
|
A | G | 5 | a0001c0001t0019g0260a0001c0001t0019g0261a0001c0001t0019g0284others(2): Show | 5 | NA18973.hp1 NA18975.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-12756A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881269 | ||||||
| chr10:87881290
|
A | C | 1 | a0001c0001t0005g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.80-12735A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881290 | ||||||
| chr10:87881290
|
A | G | 1 | a0001c0001t0035g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.80-12735A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881290 | ||||||
| chr10:87881369
|
C | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-12656C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881369 | ||||||
| chr10:87881465
|
G | A | 81 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.80-12560G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881465 | ||||||
| chr10:87881537
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-12488C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881537 | ||||||
| chr10:87881848
|
T | C | 2 | a0001c0001t0003g0041a0001c0001t0003g0062 | 2 | HG00639.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.80-12177T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881848 | ||||||
| chr10:87881918
|
T | C | 1 | a0001c0001t0091g0291 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.80-12107T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881918 | ||||||
| chr10:87881981
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-12044A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87881981 | ||||||
| chr10:87882095
|
T | C | 1 | a0001c0001t0006g0083 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.80-11930T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882095 | ||||||
| chr10:87882107
|
A | G | 4 | a0001c0001t0008g0129a0001c0001t0008g0130a0001c0001t0008g0131others(1): Show | 4 | HG00438.hp2 HG02129.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-11918A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882107 | ||||||
| chr10:87882114
|
C | A | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-11911C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882114 | ||||||
| chr10:87882116
|
T | G | 2 | a0001c0001t0003g0041a0001c0001t0003g0062 | 2 | HG00639.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.80-11909T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882116 | ||||||
| chr10:87882135
|
T | C | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-11890T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882135 | ||||||
| chr10:87882137
|
A | G | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-11888A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882137 | ||||||
| chr10:87882140
|
G | A | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-11885G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882140 | ||||||
| chr10:87882147
|
C | T | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-11878C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882147 | ||||||
| chr10:87882264
|
A | G | 1 | a0001c0001t0086g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.80-11761A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882264 | ||||||
| chr10:87882266
|
G | A | 4 | a0001c0001t0010g0116a0001c0001t0010g0295a0001c0001t0025g0296others(1): Show | 4 | HG01106.hp1 HG01261.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-11759G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882266 | ||||||
| chr10:87882611
|
T | C | 4 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-11414T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882611 | ||||||
| chr10:87882644
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-11381C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882644 | ||||||
| chr10:87882788
|
CTT | C | 3 | a0001c0001t0016g0215a0001c0001t0016g0276a0001c0001t0016g0289 | 3 | HG00609.hp2 HG02074.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.80-11235_80-11234d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87882788 | |||||
| chr10:87882852
|
A | G | 13 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(10): Show | 13 | HG01243.hp2 HG03654.hp2 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-11173A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87882852 | ||||||
| chr10:87883143
|
A | G | 6 | a0001c0001t0002g0257a0001c0001t0004g0258a0001c0001t0017g0255others(3): Show | 6 | HG00639.hp1 HG01928.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-10882A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883143 | ||||||
| chr10:87883176
|
G | A | 1 | a0001c0001t0060g0166 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.80-10849G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883176 | ||||||
| chr10:87883205
|
A | G | 1 | a0001c0001t0104g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-10820A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883205 | ||||||
| chr10:87883236
|
G | A | 1 | a0001c0001t0003g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80-10789G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883236 | ||||||
| chr10:87883448
|
A | G | 1 | a0001c0001t0057g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.80-10577A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883448 | ||||||
| chr10:87883469
|
G | A | 1 | a0001c0001t0028g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.80-10556G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883469 | ||||||
| chr10:87883614
|
A | G | 1 | a0001c0001t0011g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.80-10411A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883614 | ||||||
| chr10:87883779
|
A | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-10246A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87883779 | ||||||
| chr10:87884012
|
A | G | 5 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-10013A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87884012 | ||||||
| chr10:87884274
|
C | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-9751C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87884274 | ||||||
| chr10:87884469
|
C | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 34 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.80-9556C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87884469 | ||||||
| chr10:87884529
|
A | C | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-9496A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87884529 | ||||||
| chr10:87884679
|
T | C | 1 | a0001c0001t0011g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.80-9346T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87884679 | ||||||
| chr10:87884989
|
G | A | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0105g0292 | 3 | HG00544.hp1 HG03942.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.80-9036G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87884989 | ||||||
| chr10:87885055
|
C | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-8970C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885055 | ||||||
| chr10:87885086
|
T | C | 2 | a0001c0001t0031g0298a0001c0001t0031g0300 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.80-8939T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885086 | ||||||
| chr10:87885152
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-8873T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885152 | ||||||
| chr10:87885174
|
C | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-8851C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885174 | ||||||
| chr10:87885212
|
G | A | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.80-8813G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885212 | ||||||
| chr10:87885625
|
G | A | 2 | a0001c0001t0003g0172a0001c0001t0006g0304 | 2 | HG00642.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.80-8400G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885625 | ||||||
| chr10:87885670
|
A | G | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-8355A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885670 | ||||||
| chr10:87885716
|
A | G | 51 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(48): Show | 51 | HG00438.hp2 HG00621.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.80-8309A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885716 | ||||||
| chr10:87885861
|
A | G | 1 | a0001c0001t0007g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-8164A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885861 | ||||||
| chr10:87885974
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-8051G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87885974 | ||||||
| chr10:87886066
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-7959C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87886066 | ||||||
| chr10:87886577
|
G | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-7448G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87886577 | ||||||
| chr10:87886673
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-7352T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87886673 | ||||||
| chr10:87886898
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-7127G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87886898 | ||||||
| chr10:87887016
|
C | T | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.80-7009C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887016 | ||||||
| chr10:87887202
|
A | G | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-6823A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887202 | ||||||
| chr10:87887218
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-6807T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887218 | ||||||
| chr10:87887397
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0071g0275 | 2 | HG01175.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.80-6628G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887397 | ||||||
| chr10:87887416
|
G | A | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.80-6609G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887416 | ||||||
| chr10:87887459
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.80-6566T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887459 | ||||||
| chr10:87887849
|
CTACTGCT others(3): Show |
C | 1 | a0001c0001t0103g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-6171_80-6162del others(10): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87887849 | |||||
| chr10:87887912
|
C | T | 8 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.80-6113C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87887912 | ||||||
| chr10:87888075
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.80-5950A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87888075 | ||||||
| chr10:87888186
|
G | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0048a0001c0001t0001g0164 | 3 | HG01070.hp2 HG01071.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.80-5839G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87888186 | ||||||
| chr10:87888589
|
C | T | 3 | a0001c0001t0077g0137a0001c0001t0078g0031a0001c0001t0086g0093 | 3 | HG02717.hp1 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.80-5436C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87888589 | ||||||
| chr10:87888997
|
A | G | 1 | a0001c0001t0015g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.80-5028A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87888997 | ||||||
| chr10:87889085
|
G | T | 1 | a0001c0001t0104g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.80-4940G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889085 | ||||||
| chr10:87889094
|
A | G | 1 | a0001c0001t0070g0047 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.80-4931A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889094 | ||||||
| chr10:87889099
|
G | A | 1 | a0001c0001t0057g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.80-4926G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889099 | ||||||
| chr10:87889411
|
A | C | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-4614A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889411 | ||||||
| chr10:87889733
|
T | C | 1 | a0001c0001t0020g0143 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.80-4292T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889733 | ||||||
| chr10:87889740
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.80-4285A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889740 | ||||||
| chr10:87889820
|
A | G | 30 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(27): Show | 30 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.80-4205A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87889820 | ||||||
| chr10:87890033
|
A | C | 1 | a0001c0001t0001g0180 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.80-3992A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890033 | ||||||
| chr10:87890081
|
G | A | 7 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(4): Show | 7 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-3944G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890081 | ||||||
| chr10:87890116
|
C | T | 1 | a0001c0001t0009g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.80-3909C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890116 | ||||||
| chr10:87890123
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-3902G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890123 | ||||||
| chr10:87890299
|
A | G | 1 | a0001c0001t0044g0253 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.80-3726A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890299 | ||||||
| chr10:87890355
|
G | A | 2 | a0001c0001t0002g0228a0001c0001t0025g0117 | 2 | HG04204.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.80-3670G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890355 | ||||||
| chr10:87890414
|
T | C | 4 | a0001c0001t0009g0012a0001c0001t0012g0133a0001c0001t0012g0134others(1): Show | 4 | HG01081.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-3611T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890414 | ||||||
| chr10:87890570
|
CTATT | C | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.80-3453_80-3450del others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87890570 | |||||
| chr10:87890751
|
G | A | 1 | a0001c0001t0076g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.80-3274G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890751 | ||||||
| chr10:87890896
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.80-3129G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890896 | ||||||
| chr10:87890955
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-3070T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87890955 | ||||||
| chr10:87891002
|
C | T | 5 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0022g0303others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-3023C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891002 | ||||||
| chr10:87891044
|
G | A | 3 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0085g0084 | 3 | HG00099.hp2 HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.80-2981G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891044 | ||||||
| chr10:87891142
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.80-2883G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891142 | ||||||
| chr10:87891540
|
T | G | 1 | a0001c0001t0072g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.80-2485T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891540 | ||||||
| chr10:87891554
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-2471C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891554 | ||||||
| chr10:87891584
|
C | T | 1 | a0001c0001t0077g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.80-2441C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891584 | ||||||
| chr10:87891605
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-2420G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891605 | ||||||
| chr10:87891947
|
T | C | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.80-2078T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87891947 | ||||||
| chr10:87892164
|
T | G | 1 | a0001c0001t0017g0255 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.80-1861T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892164 | ||||||
| chr10:87892199
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-1826T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892199 | ||||||
| chr10:87892246
|
A | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-1779A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892246 | ||||||
| chr10:87892270
|
T | C | 4 | a0001c0001t0002g0218a0001c0001t0002g0230a0001c0001t0004g0277others(1): Show | 4 | NA18964.hp2 NA18968.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-1755T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892270 | ||||||
| chr10:87892271
|
G | A | 1 | a0001c0001t0006g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.80-1754G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892271 | ||||||
| chr10:87892420
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-1605T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892420 | ||||||
| chr10:87892563
|
A | G | 1 | a0001c0001t0093g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.80-1462A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892563 | ||||||
| chr10:87892691
|
T | C | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.80-1334T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892691 | ||||||
| chr10:87892726
|
T | C | 10 | a0001c0001t0003g0033a0001c0001t0003g0040a0001c0001t0003g0064others(7): Show | 10 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-1299T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892726 | ||||||
| chr10:87892845
|
G | A | 3 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0061g0302 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.80-1180G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87892845 | ||||||
| chr10:87893007
|
C | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0065 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.80-1018C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893007 | ||||||
| chr10:87893066
|
CTTTTGAC others(892): Show |
C | 3 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0088g0081 | 3 | HG01255.hp1 HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.80-956_80-58del | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 87893066 | |||||
| chr10:87893123
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-902G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893123 | ||||||
| chr10:87893401
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-624T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893401 | ||||||
| chr10:87893443
|
A | T | 1 | a0001c0001t0011g0267 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.80-582A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893443 | ||||||
| chr10:87893605
|
A | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.80-420A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893605 | ||||||
| chr10:87893787
|
T | A | 1 | a0001c0001t0005g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80-238T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893787 | ||||||
| chr10:87893929
|
A | G | 177 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(174): Show | 179 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.80-96A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893929 | ||||||
| chr10:87893962
|
A | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.80-63A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 1/8 | chr10 | 87893962 | ||||||
| chr10:87894131
|
A | G | 1 | a0001c0001t0006g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.164+22A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87894131 | ||||||
| chr10:87894325
|
G | A | 1 | a0001c0001t0008g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.164+216G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87894325 | ||||||
| chr10:87894364
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+255T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87894364 | ||||||
| chr10:87894426
|
G | A | 1 | a0001c0001t0028g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.164+317G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87894426 | ||||||
| chr10:87894433
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+324G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87894433 | ||||||
| chr10:87894603
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+494C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87894603 | ||||||
| chr10:87895179
|
A | T | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+1070A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87895179 | ||||||
| chr10:87895231
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+1122C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87895231 | ||||||
| chr10:87895280
|
T | C | 1 | a0001c0001t0002g0231 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.164+1171T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87895280 | ||||||
| chr10:87895479
|
A | G | 80 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(77): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.164+1370A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87895479 | ||||||
| chr10:87895485
|
C | CA | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 93 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.164+1382dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87895485 | |||||
| chr10:87895567
|
G | A | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164+1458G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87895567 | ||||||
| chr10:87895656
|
T | C | 1 | a0001c0001t0009g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.164+1547T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87895656 | ||||||
| chr10:87896203
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.164+2094A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87896203 | ||||||
| chr10:87896321
|
A | T | 9 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+2212A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87896321 | ||||||
| chr10:87896399
|
A | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(21): Show | 27 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.164+2290A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87896399 | ||||||
| chr10:87896825
|
A | T | 1 | a0001c0001t0028g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.164+2716A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87896825 | ||||||
| chr10:87896857
|
C | T | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164+2748C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87896857 | ||||||
| chr10:87897047
|
A | AT | 23 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0002g0220others(20): Show | 24 | HG01175.hp1 HG01433.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.164+2959dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87897047 | |||||
| chr10:87897047
|
AT | A | 13 | a0001c0001t0004g0232a0001c0001t0004g0233a0001c0001t0008g0016others(10): Show | 13 | HG01069.hp1 HG02622.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.164+2959delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87897047 | |||||
| chr10:87897090
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.164+2981C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897090 | ||||||
| chr10:87897152
|
A | G | 4 | a0001c0001t0008g0016a0001c0001t0008g0203a0001c0001t0059g0126others(1): Show | 4 | NA18986.hp2 NA18990.hp2 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+3043A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897152 | ||||||
| chr10:87897172
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+3063C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897172 | ||||||
| chr10:87897209
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164+3100G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897209 | ||||||
| chr10:87897217
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+3108G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897217 | ||||||
| chr10:87897329
|
C | T | 1 | a0001c0001t0023g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.164+3220C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897329 | ||||||
| chr10:87897393
|
C | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 34 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.164+3284C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897393 | ||||||
| chr10:87897393
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+3284C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897393 | ||||||
| chr10:87897422
|
C | A | 1 | a0001c0001t0003g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.164+3313C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897422 | ||||||
| chr10:87897837
|
A | G | 1 | a0001c0001t0002g0250 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.164+3728A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897837 | ||||||
| chr10:87897971
|
C | T | 3 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0088g0081 | 3 | HG01255.hp1 HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.164+3862C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897971 | ||||||
| chr10:87897996
|
G | A | 5 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+3887G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87897996 | ||||||
| chr10:87898043
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.164+3934C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898043 | ||||||
| chr10:87898194
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+4085G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898194 | ||||||
| chr10:87898299
|
T | A | 25 | a0001c0001t0003g0033a0001c0001t0003g0040a0001c0001t0003g0064others(22): Show | 25 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.164+4190T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898299 | ||||||
| chr10:87898379
|
C | A | 1 | a0001c0001t0006g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.164+4270C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898379 | ||||||
| chr10:87898485
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.164+4376G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898485 | ||||||
| chr10:87898498
|
G | A | 1 | a0001c0001t0053g0274 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.164+4389G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898498 | ||||||
| chr10:87898724
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164+4615G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898724 | ||||||
| chr10:87898754
|
A | G | 1 | a0001c0001t0045g0283 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.164+4645A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898754 | ||||||
| chr10:87898763
|
C | G | 1 | a0001c0001t0008g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.164+4654C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87898763 | ||||||
| chr10:87899007
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+4898T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899007 | ||||||
| chr10:87899180
|
C | T | 3 | a0001c0001t0077g0137a0001c0001t0078g0031a0001c0001t0086g0093 | 3 | HG02717.hp1 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.164+5071C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899180 | ||||||
| chr10:87899190
|
G | C | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+5081G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899190 | ||||||
| chr10:87899376
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+5267C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899376 | ||||||
| chr10:87899395
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+5286T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899395 | ||||||
| chr10:87899396
|
T | A | 180 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(177): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.164+5287T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899396 | ||||||
| chr10:87899479
|
T | A | 2 | a0001c0001t0005g0155a0001c0001t0032g0070 | 2 | HG01243.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.164+5370T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899479 | ||||||
| chr10:87899526
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+5417C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899526 | ||||||
| chr10:87899651
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.164+5542G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899651 | ||||||
| chr10:87899822
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.164+5713C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899822 | ||||||
| chr10:87899947
|
C | T | 3 | a0001c0001t0002g0248a0001c0001t0002g0282a0001c0001t0002g0286 | 3 | HG00423.hp2 NA18952.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.164+5838C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87899947 | ||||||
| chr10:87900034
|
G | C | 1 | a0001c0001t0039g0265 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.164+5925G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900034 | ||||||
| chr10:87900036
|
C | T | 5 | a0001c0001t0010g0116a0001c0001t0010g0295a0001c0001t0024g0192others(2): Show | 5 | HG01106.hp1 HG01261.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+5927C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900036 | ||||||
| chr10:87900149
|
C | G | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.164+6040C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900149 | ||||||
| chr10:87900219
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.164+6110G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900219 | ||||||
| chr10:87900252
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+6143T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900252 | ||||||
| chr10:87900269
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+6160G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900269 | ||||||
| chr10:87900312
|
T | A | 1 | a0001c0001t0028g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.164+6203T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900312 | ||||||
| chr10:87900343
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164+6234T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900343 | ||||||
| chr10:87900677
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+6568T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900677 | ||||||
| chr10:87900784
|
T | C | 3 | a0001c0001t0002g0234a0001c0001t0002g0278a0001c0001t0004g0232 | 3 | NA19006.hp2 NA19012.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.164+6675T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900784 | ||||||
| chr10:87900790
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.164+6681T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900790 | ||||||
| chr10:87900837
|
G | A | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+6728G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900837 | ||||||
| chr10:87900946
|
C | T | 1 | a0001c0001t0035g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.164+6837C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87900946 | ||||||
| chr10:87901101
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.164+6992C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901101 | ||||||
| chr10:87901466
|
G | T | 3 | a0001c0001t0002g0250a0001c0001t0004g0247a0001c0001t0004g0254 | 3 | HG00099.hp1 HG01175.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.164+7357G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901466 | ||||||
| chr10:87901589
|
T | G | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+7480T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901589 | ||||||
| chr10:87901656
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.164+7547G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901656 | ||||||
| chr10:87901819
|
C | G | 1 | a0001c0001t0003g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.164+7710C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901819 | ||||||
| chr10:87901823
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.164+7714A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901823 | ||||||
| chr10:87901849
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+7740T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901849 | ||||||
| chr10:87901927
|
A | T | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.164+7818A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87901927 | ||||||
| chr10:87902160
|
C | G | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+8051C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902160 | ||||||
| chr10:87902189
|
G | T | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+8080G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902189 | ||||||
| chr10:87902245
|
C | G | 34 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(31): Show | 34 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.164+8136C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902245 | ||||||
| chr10:87902298
|
A | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+8189A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902298 | ||||||
| chr10:87902536
|
C | A | 1 | a0001c0001t0027g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.164+8427C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902536 | ||||||
| chr10:87902586
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+8477G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902586 | ||||||
| chr10:87902623
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+8514G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902623 | ||||||
| chr10:87902645
|
G | A | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.164+8536G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902645 | ||||||
| chr10:87902708
|
GTTTA | G | 5 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0022g0303others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+8602_164+8605d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87902708 | |||||
| chr10:87902747
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 277 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.164+8638A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902747 | ||||||
| chr10:87902758
|
C | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+8649C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902758 | ||||||
| chr10:87902861
|
G | C | 15 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0266others(12): Show | 15 | HG00408.hp1 HG00597.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.164+8752G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87902861 | ||||||
| chr10:87903162
|
CTGCAGAA others(10): Show |
C | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+9074_164+9090d others(19): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87903162 | |||||
| chr10:87903260
|
C | G | 1 | a0001c0001t0049g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.164+9151C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903260 | ||||||
| chr10:87903320
|
G | A | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164+9211G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903320 | ||||||
| chr10:87903333
|
C | T | 5 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0022g0303others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+9224C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903333 | ||||||
| chr10:87903334
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+9225G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903334 | ||||||
| chr10:87903526
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+9417A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903526 | ||||||
| chr10:87903631
|
G | C | 1 | a0001c0001t0002g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.164+9522G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903631 | ||||||
| chr10:87903661
|
G | T | 1 | a0001c0001t0038g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.164+9552G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903661 | ||||||
| chr10:87903673
|
C | T | 1 | a0001c0001t0008g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.164+9564C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903673 | ||||||
| chr10:87903688
|
C | T | 4 | a0001c0001t0003g0078a0001c0001t0006g0176a0001c0001t0028g0063others(1): Show | 4 | HG02055.hp1 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+9579C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903688 | ||||||
| chr10:87903707
|
G | A | 19 | a0001c0001t0002g0220a0001c0001t0006g0101a0001c0001t0007g0020others(16): Show | 19 | HG01081.hp2 HG01243.hp2 HG02896.hp2 others(16): Show |
intron_variant | MODIFIER | c.164+9598G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903707 | ||||||
| chr10:87903796
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+9687T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903796 | ||||||
| chr10:87903812
|
C | T | 1 | a0001c0001t0010g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.164+9703C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903812 | ||||||
| chr10:87903814
|
A | G | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+9705A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903814 | ||||||
| chr10:87903831
|
A | G | 1 | a0001c0001t0008g0125 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.164+9722A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903831 | ||||||
| chr10:87903843
|
G | A | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164+9734G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903843 | ||||||
| chr10:87903856
|
A | G | 2 | a0001c0001t0106g0288a0001c0001t0107g0287 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.164+9747A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903856 | ||||||
| chr10:87903988
|
C | CT | 24 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0002g0257others(21): Show | 24 | HG00639.hp1 HG00642.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.164+9902dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87903988 | |||||
| chr10:87903988
|
CT | C | 19 | a0001c0001t0001g0199a0001c0001t0003g0003a0001c0001t0003g0139others(16): Show | 20 | HG00099.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.164+9902delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87903988 | |||||
| chr10:87903989
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164+9880T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87903989 | ||||||
| chr10:87904017
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.164+9908A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904017 | ||||||
| chr10:87904137
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+10028C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904137 | ||||||
| chr10:87904140
|
C | G | 3 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0025g0122 | 3 | HG01952.hp2 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.164+10031C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904140 | ||||||
| chr10:87904224
|
G | A | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+10115G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904224 | ||||||
| chr10:87904290
|
G | A | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+10181G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904290 | ||||||
| chr10:87904452
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+10343G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904452 | ||||||
| chr10:87904464
|
T | A | 1 | a0001c0001t0004g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164+10355T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904464 | ||||||
| chr10:87904652
|
T | G | 1 | a0001c0001t0004g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.164+10543T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904652 | ||||||
| chr10:87904713
|
T | C | 7 | a0001c0001t0008g0118a0001c0001t0008g0125a0001c0001t0009g0119others(4): Show | 7 | HG00621.hp1 HG02071.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+10604T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904713 | ||||||
| chr10:87904796
|
C | T | 1 | a0001c0001t0041g0251 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.164+10687C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904796 | ||||||
| chr10:87904949
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.164+10840G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87904949 | ||||||
| chr10:87905240
|
C | G | 1 | a0001c0001t0011g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.164+11131C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87905240 | ||||||
| chr10:87905433
|
A | T | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.164+11324A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87905433 | ||||||
| chr10:87905466
|
C | CT | 44 | a0001c0001t0001g0060a0001c0001t0001g0170a0001c0001t0003g0064others(41): Show | 44 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.164+11379dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87905466 | |||||
| chr10:87905466
|
CT | C | 18 | a0001c0001t0001g0147a0001c0001t0001g0202a0001c0001t0002g0266others(15): Show | 18 | HG01069.hp2 HG01081.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.164+11379delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87905466 | |||||
| chr10:87905755
|
G | A | 81 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(78): Show | 81 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.164+11646G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87905755 | ||||||
| chr10:87906163
|
A | T | 3 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0061g0302 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.164+12054A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87906163 | ||||||
| chr10:87906400
|
G | C | 1 | a0001c0001t0022g0080 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.164+12291G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87906400 | ||||||
| chr10:87906704
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+12595G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87906704 | ||||||
| chr10:87906853
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG00423.hp1 HG02129.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+12744G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87906853 | ||||||
| chr10:87907191
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+13082G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907191 | ||||||
| chr10:87907248
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.164+13139A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907248 | ||||||
| chr10:87907487
|
A | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | NA18942.hp1 NA18961.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.164+13378A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907487 | ||||||
| chr10:87907505
|
G | A | 20 | a0001c0001t0003g0033a0001c0001t0003g0064a0001c0001t0003g0065others(17): Show | 20 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.164+13396G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907505 | ||||||
| chr10:87907511
|
A | G | 3 | a0001c0001t0003g0078a0001c0001t0006g0176a0001c0001t0030g0074 | 3 | HG02055.hp1 HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.164+13402A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907511 | ||||||
| chr10:87907514
|
T | TATATATA others(13): Show |
1 | a0001c0001t0006g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.164+13423_164+1344 others(24): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87907514 | |||||
| chr10:87907514
|
TATATATA others(13): Show |
T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.164+13423_164+1344 others(24): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87907514 | |||||
| chr10:87907552
|
A | C | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+13443A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907552 | ||||||
| chr10:87907554
|
G | C | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+13445G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907554 | ||||||
| chr10:87907574
|
GATAT | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+13475_164+1347 others(8): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87907574 | |||||
| chr10:87907763
|
A | C | 2 | a0001c0001t0081g0079a0001c0001t0089g0178 | 2 | HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.164+13654A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907763 | ||||||
| chr10:87907847
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+13738A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907847 | ||||||
| chr10:87907913
|
A | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.164+13804A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87907913 | ||||||
| chr10:87908010
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+13901G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908010 | ||||||
| chr10:87908199
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+14090C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908199 | ||||||
| chr10:87908249
|
T | C | 1 | a0001c0001t0014g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.164+14140T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908249 | ||||||
| chr10:87908419
|
A | G | 1 | a0001c0001t0007g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.164+14310A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908419 | ||||||
| chr10:87908445
|
C | T | 1 | a0001c0001t0013g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.164+14336C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908445 | ||||||
| chr10:87908469
|
C | T | 1 | a0001c0001t0052g0236 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.164+14360C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908469 | ||||||
| chr10:87908477
|
G | A | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+14368G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908477 | ||||||
| chr10:87908485
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+14376C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908485 | ||||||
| chr10:87908519
|
T | C | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+14410T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908519 | ||||||
| chr10:87908994
|
A | C | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+14885A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908994 | ||||||
| chr10:87908999
|
G | A | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.164+14890G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87908999 | ||||||
| chr10:87909101
|
T | C | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164+14992T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909101 | ||||||
| chr10:87909163
|
A | G | 1 | a0001c0001t0003g0092 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164+15054A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909163 | ||||||
| chr10:87909168
|
T | C | 1 | a0001c0001t0058g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.164+15059T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909168 | ||||||
| chr10:87909554
|
C | T | 1 | a0001c0001t0014g0013 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.164+15445C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909554 | ||||||
| chr10:87909649
|
G | T | 1 | a0001c0001t0077g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.164+15540G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909649 | ||||||
| chr10:87909731
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.164+15622A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909731 | ||||||
| chr10:87909744
|
G | T | 1 | a0001c0001t0006g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.164+15635G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909744 | ||||||
| chr10:87909810
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164+15701T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909810 | ||||||
| chr10:87909973
|
C | G | 2 | a0001c0001t0005g0161a0001c0001t0027g0163 | 2 | HG00642.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.165-15540C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87909973 | ||||||
| chr10:87910304
|
G | A | 1 | a0001c0001t0009g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165-15209G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910304 | ||||||
| chr10:87910410
|
T | G | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-15103T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910410 | ||||||
| chr10:87910436
|
T | C | 2 | a0001c0001t0031g0298a0001c0001t0031g0300 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-15077T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910436 | ||||||
| chr10:87910454
|
C | T | 1 | a0001c0001t0107g0287 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165-15059C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910454 | ||||||
| chr10:87910455
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-15058G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910455 | ||||||
| chr10:87910462
|
C | T | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.165-15051C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910462 | ||||||
| chr10:87910487
|
G | A | 1 | a0001c0001t0037g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165-15026G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910487 | ||||||
| chr10:87910495
|
T | G | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-15018T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910495 | ||||||
| chr10:87910574
|
C | T | 1 | a0001c0001t0094g0189 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.165-14939C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910574 | ||||||
| chr10:87910599
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165-14914G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910599 | ||||||
| chr10:87910675
|
C | A | 1 | a0001c0001t0006g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.165-14838C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910675 | ||||||
| chr10:87910699
|
T | C | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-14814T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910699 | ||||||
| chr10:87910706
|
C | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-14807C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910706 | ||||||
| chr10:87910842
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-14671T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910842 | ||||||
| chr10:87910850
|
A | G | 2 | a0001c0001t0003g0033a0001c0001t0003g0040 | 2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.165-14663A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910850 | ||||||
| chr10:87910861
|
A | T | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.165-14652A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910861 | ||||||
| chr10:87910992
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-14521G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87910992 | ||||||
| chr10:87911089
|
C | A | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.165-14424C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87911089 | ||||||
| chr10:87911340
|
A | G | 1 | a0001c0001t0007g0027 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.165-14173A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87911340 | ||||||
| chr10:87911841
|
G | A | 3 | a0001c0001t0012g0133a0001c0001t0012g0134a0001c0001t0012g0135 | 3 | HG01081.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.165-13672G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87911841 | ||||||
| chr10:87911888
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-13625G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87911888 | ||||||
| chr10:87911940
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-13573A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87911940 | ||||||
| chr10:87911958
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-13555C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87911958 | ||||||
| chr10:87912489
|
C | T | 3 | a0001c0001t0003g0072a0001c0001t0065g0077a0001c0001t0073g0075 | 3 | HG02818.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.165-13024C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87912489 | ||||||
| chr10:87912502
|
C | T | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.165-13011C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87912502 | ||||||
| chr10:87912722
|
A | G | 1 | a0001c0001t0019g0261 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.165-12791A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87912722 | ||||||
| chr10:87912830
|
A | G | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165-12683A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87912830 | ||||||
| chr10:87912890
|
C | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-12623C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87912890 | ||||||
| chr10:87913108
|
A | G | 5 | a0001c0001t0007g0029a0001c0001t0009g0012a0001c0001t0012g0133others(2): Show | 5 | HG01081.hp2 HG01243.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-12405A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913108 | ||||||
| chr10:87913308
|
C | T | 1 | a0001c0001t0028g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165-12205C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913308 | ||||||
| chr10:87913339
|
A | G | 1 | a0001c0001t0003g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165-12174A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913339 | ||||||
| chr10:87913366
|
A | G | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-12147A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913366 | ||||||
| chr10:87913661
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-11852T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913661 | ||||||
| chr10:87913699
|
A | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-11814A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913699 | ||||||
| chr10:87913755
|
G | C | 1 | a0001c0001t0023g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.165-11758G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913755 | ||||||
| chr10:87913760
|
C | G | 1 | a0001c0001t0006g0085 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.165-11753C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913760 | ||||||
| chr10:87913812
|
C | T | 182 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(179): Show | 184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.165-11701C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913812 | ||||||
| chr10:87913855
|
T | C | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.165-11658T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913855 | ||||||
| chr10:87913918
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-11595T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913918 | ||||||
| chr10:87913934
|
T | A | 1 | a0001c0001t0022g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.165-11579T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913934 | ||||||
| chr10:87913960
|
A | G | 1 | a0001c0001t0006g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.165-11553A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87913960 | ||||||
| chr10:87914029
|
T | A | 2 | a0001c0001t0031g0298a0001c0001t0031g0300 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-11484T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914029 | ||||||
| chr10:87914197
|
A | C | 5 | a0001c0001t0019g0260a0001c0001t0019g0261a0001c0001t0019g0284others(2): Show | 5 | NA18973.hp1 NA18975.hp2 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-11316A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914197 | ||||||
| chr10:87914290
|
G | T | 1 | a0001c0001t0076g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.165-11223G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914290 | ||||||
| chr10:87914308
|
C | T | 1 | a0001c0001t0008g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.165-11205C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914308 | ||||||
| chr10:87914387
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-11126C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914387 | ||||||
| chr10:87914400
|
T | G | 80 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(77): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.165-11113T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914400 | ||||||
| chr10:87914455
|
TAAATC | T | 6 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(3): Show | 6 | HG02809.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-11054_165-1105 others(9): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87914455 | |||||
| chr10:87914527
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-10986T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914527 | ||||||
| chr10:87914711
|
G | A | 2 | a0001c0001t0101g0207a0001c0001t0105g0292 | 2 | HG03942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.165-10802G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914711 | ||||||
| chr10:87914755
|
A | G | 1 | a0001c0001t0082g0290 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.165-10758A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914755 | ||||||
| chr10:87914770
|
T | TAGAAACT others(317): Show |
1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-10727_165-1072 others(328): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87914770 | |||||
| chr10:87914944
|
T | A | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-10569T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914944 | ||||||
| chr10:87914961
|
G | A | 1 | a0001c0001t0006g0304 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.165-10552G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914961 | ||||||
| chr10:87914965
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-10548C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87914965 | ||||||
| chr10:87915206
|
T | C | 1 | a0001c0001t0026g0193 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.165-10307T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915206 | ||||||
| chr10:87915240
|
A | G | 1 | a0001c0001t0037g0099 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.165-10273A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915240 | ||||||
| chr10:87915272
|
T | C | 1 | a0001c0001t0006g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.165-10241T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915272 | ||||||
| chr10:87915277
|
A | G | 1 | a0001c0001t0034g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.165-10236A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915277 | ||||||
| chr10:87915376
|
T | G | 1 | a0001c0001t0027g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.165-10137T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915376 | ||||||
| chr10:87915539
|
A | G | 175 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(172): Show | 177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.165-9974A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915539 | ||||||
| chr10:87915551
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.165-9962C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915551 | ||||||
| chr10:87915653
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-9860A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915653 | ||||||
| chr10:87915793
|
G | A | 2 | a0001c0001t0005g0044a0001c0001t0005g0157 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.165-9720G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915793 | ||||||
| chr10:87915833
|
G | C | 51 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(48): Show | 51 | HG00438.hp2 HG00621.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.165-9680G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915833 | ||||||
| chr10:87915834
|
A | T | 1 | a0001c0001t0001g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165-9679A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87915834 | ||||||
| chr10:87915901
|
C | CA | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-9601dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87915901 | |||||
| chr10:87916061
|
C | G | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-9452C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87916061 | ||||||
| chr10:87916301
|
A | C | 1 | a0001c0001t0075g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165-9212A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87916301 | ||||||
| chr10:87916307
|
T | G | 1 | a0001c0001t0075g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165-9206T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87916307 | ||||||
| chr10:87916471
|
A | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-9042A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87916471 | ||||||
| chr10:87916540
|
A | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-8973A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87916540 | ||||||
| chr10:87916553
|
GTAGGTCA others(25): Show |
G | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 93 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.165-8954_165-8923d others(34): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87916553 | |||||
| chr10:87917230
|
G | GT | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-8273dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87917230 | |||||
| chr10:87917350
|
A | T | 23 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(20): Show | 23 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.165-8163A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87917350 | ||||||
| chr10:87917630
|
T | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | NA18942.hp1 NA18961.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-7883T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87917630 | ||||||
| chr10:87917678
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-7835G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87917678 | ||||||
| chr10:87917823
|
A | G | 1 | a0001c0001t0054g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.165-7690A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87917823 | ||||||
| chr10:87917855
|
A | G | 2 | a0001c0001t0017g0255a0001c0001t0018g0259 | 2 | HG00639.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.165-7658A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87917855 | ||||||
| chr10:87918010
|
ACAAAGTC others(30): Show |
A | 2 | a0001c0001t0031g0298a0001c0001t0031g0300 | 2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.165-7502_165-7466d others(39): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918010 | ||||||
| chr10:87918081
|
C | T | 8 | a0001c0001t0003g0033a0001c0001t0003g0064a0001c0001t0003g0065others(5): Show | 8 | HG02258.hp2 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-7432C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918081 | ||||||
| chr10:87918259
|
G | T | 1 | a0001c0001t0015g0110 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.165-7254G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918259 | ||||||
| chr10:87918410
|
C | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-7103C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918410 | ||||||
| chr10:87918425
|
TTATAA | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-7083_165-7079d others(7): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87918425 | |||||
| chr10:87918443
|
C | T | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-7070C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918443 | ||||||
| chr10:87918785
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-6728A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918785 | ||||||
| chr10:87918849
|
A | G | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.165-6664A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87918849 | ||||||
| chr10:87919113
|
TAAATA | T | 3 | a0001c0001t0007g0025a0001c0001t0007g0026a0001c0001t0007g0027 | 3 | NA18969.hp1 NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.165-6387_165-6383d others(7): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87919113 | |||||
| chr10:87919155
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.165-6358A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919155 | ||||||
| chr10:87919263
|
T | C | 1 | a0001c0001t0070g0047 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.165-6250T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919263 | ||||||
| chr10:87919312
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-6201T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919312 | ||||||
| chr10:87919528
|
T | TAC | 17 | a0001c0001t0001g0042a0001c0001t0004g0280a0001c0001t0006g0101others(14): Show | 17 | HG00438.hp2 HG00609.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.165-5958_165-5957d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87919528 | |||||
| chr10:87919528
|
T | TACAC | 8 | a0001c0001t0006g0088a0001c0001t0009g0012a0001c0001t0014g0002others(5): Show | 9 | HG00738.hp1 HG01109.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-5960_165-5957d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87919528 | |||||
| chr10:87919528
|
T | TACACACA others(3): Show |
1 | a0001c0001t0003g0172 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.165-5966_165-5957d others(12): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87919528 | |||||
| chr10:87919555
|
A | C | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-5958A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919555 | ||||||
| chr10:87919611
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.165-5902C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919611 | ||||||
| chr10:87919732
|
T | C | 16 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(13): Show | 16 | HG00438.hp2 HG00621.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-5781T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919732 | ||||||
| chr10:87919756
|
C | T | 7 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(4): Show | 7 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-5757C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87919756 | ||||||
| chr10:87920304
|
AG | A | 13 | a0001c0001t0006g0101a0001c0001t0007g0020a0001c0001t0007g0021others(10): Show | 13 | HG01243.hp2 HG03654.hp2 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.165-5208delG | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920304 | ||||||
| chr10:87920366
|
A | C | 4 | a0001c0001t0005g0044a0001c0001t0005g0155a0001c0001t0005g0157others(1): Show | 4 | HG01243.hp1 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-5147A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920366 | ||||||
| chr10:87920461
|
A | G | 3 | a0001c0001t0008g0016a0001c0001t0008g0203a0001c0001t0108g0136 | 3 | NA18986.hp2 NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.165-5052A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920461 | ||||||
| chr10:87920673
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-4840G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920673 | ||||||
| chr10:87920814
|
AAAAC | A | 4 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(1): Show | 5 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-4687_165-4684d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87920814 | |||||
| chr10:87920830
|
A | C | 4 | a0001c0001t0031g0298a0001c0001t0031g0300a0001c0001t0048g0221others(1): Show | 4 | HG01975.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.165-4683A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920830 | ||||||
| chr10:87920831
|
A | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-4682A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920831 | ||||||
| chr10:87920874
|
T | C | 4 | a0001c0001t0002g0009a0001c0001t0004g0009a0001c0001t0004g0212others(1): Show | 4 | HG00323.hp1 HG02735.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-4639T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87920874 | ||||||
| chr10:87921153
|
TTTTC | T | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.165-4343_165-4340d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87921153 | |||||
| chr10:87921219
|
T | TTGCCTTG others(2): Show |
3 | a0001c0001t0003g0078a0001c0001t0006g0176a0001c0001t0030g0074 | 3 | HG02055.hp1 HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.165-4283_165-4275d others(11): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 87921219 | |||||
| chr10:87921330
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.165-4183C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921330 | ||||||
| chr10:87921392
|
C | T | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-4121C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921392 | ||||||
| chr10:87921441
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-4072T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921441 | ||||||
| chr10:87921486
|
C | T | 1 | a0001c0001t0057g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.165-4027C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921486 | ||||||
| chr10:87921561
|
G | C | 1 | a0001c0001t0003g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165-3952G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921561 | ||||||
| chr10:87921701
|
A | G | 16 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(13): Show | 16 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-3812A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921701 | ||||||
| chr10:87921931
|
G | T | 5 | a0001c0001t0002g0244a0001c0001t0002g0250a0001c0001t0004g0247others(2): Show | 5 | HG00099.hp1 HG00741.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-3582G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921931 | ||||||
| chr10:87921948
|
G | C | 1 | a0001c0001t0003g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.165-3565G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87921948 | ||||||
| chr10:87922108
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-3405G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922108 | ||||||
| chr10:87922133
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-3380C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922133 | ||||||
| chr10:87922247
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-3266T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922247 | ||||||
| chr10:87922316
|
G | A | 1 | a0001c0001t0051g0294 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165-3197G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922316 | ||||||
| chr10:87922392
|
A | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-3121A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922392 | ||||||
| chr10:87922452
|
G | A | 9 | a0001c0001t0005g0161a0001c0001t0027g0163a0001c0001t0034g0205others(6): Show | 9 | HG00642.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.165-3061G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922452 | ||||||
| chr10:87922704
|
TC | T | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-2808delC | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922704 | ||||||
| chr10:87922713
|
A | G | 1 | a0001c0001t0057g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.165-2800A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922713 | ||||||
| chr10:87922719
|
C | T | 1 | a0001c0001t0004g0258 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.165-2794C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922719 | ||||||
| chr10:87922820
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-2693T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87922820 | ||||||
| chr10:87923076
|
G | C | 34 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(31): Show | 34 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.165-2437G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923076 | ||||||
| chr10:87923127
|
C | G | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-2386C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923127 | ||||||
| chr10:87923142
|
A | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-2371A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923142 | ||||||
| chr10:87923166
|
C | T | 5 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.165-2347C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923166 | ||||||
| chr10:87923272
|
C | T | 1 | a0001c0001t0041g0251 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.165-2241C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923272 | ||||||
| chr10:87923513
|
A | C | 1 | a0001c0001t0046g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.165-2000A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923513 | ||||||
| chr10:87923714
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-1799T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923714 | ||||||
| chr10:87923875
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-1638T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923875 | ||||||
| chr10:87923876
|
T | A | 8 | a0001c0001t0001g0059a0001c0001t0005g0044a0001c0001t0005g0157others(5): Show | 8 | HG01106.hp1 HG02145.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.165-1637T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87923876 | ||||||
| chr10:87924218
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-1295C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924218 | ||||||
| chr10:87924297
|
A | G | 2 | a0001c0001t0002g0220a0001c0001t0017g0239 | 2 | NA18960.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.165-1216A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924297 | ||||||
| chr10:87924434
|
G | C | 1 | a0001c0001t0009g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165-1079G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924434 | ||||||
| chr10:87924457
|
C | A | 174 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(171): Show | 176 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.165-1056C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924457 | ||||||
| chr10:87924521
|
T | C | 3 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0085g0084 | 3 | HG00099.hp2 HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.165-992T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924521 | ||||||
| chr10:87924579
|
C | T | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165-934C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924579 | ||||||
| chr10:87924721
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-792T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924721 | ||||||
| chr10:87924803
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-710G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924803 | ||||||
| chr10:87924938
|
C | T | 1 | a0001c0001t0032g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.165-575C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924938 | ||||||
| chr10:87924940
|
C | T | 1 | a0001c0001t0009g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165-573C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924940 | ||||||
| chr10:87924952
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-561G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87924952 | ||||||
| chr10:87925047
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-466A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87925047 | ||||||
| chr10:87925076
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165-437C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 2/8 | chr10 | 87925076 | ||||||
| chr10:87925641
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.209+84G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87925641 | ||||||
| chr10:87925774
|
G | T | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.209+217G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87925774 | ||||||
| chr10:87925886
|
T | C | 89 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(86): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.209+329T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87925886 | ||||||
| chr10:87926193
|
C | G | 2 | a0001c0001t0006g0010a0001c0001t0091g0291 | 3 | NA18951.hp1 NA18952.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.209+636C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926193 | ||||||
| chr10:87926291
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.209+734A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926291 | ||||||
| chr10:87926315
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.209+758T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926315 | ||||||
| chr10:87926326
|
T | C | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.209+769T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926326 | ||||||
| chr10:87926338
|
A | G | 1 | a0001c0001t0036g0008 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.209+781A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926338 | ||||||
| chr10:87926409
|
TCA | T | 80 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(77): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.209+853_209+854del others(2): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926409 | ||||||
| chr10:87926474
|
T | TG | 15 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(12): Show | 15 | HG00438.hp2 HG00621.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.209+924dupG | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 87926474 | |||||
| chr10:87926481
|
G | T | 1 | a0001c0001t0006g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.209+924G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926481 | ||||||
| chr10:87926497
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.209+940G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926497 | ||||||
| chr10:87926513
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.209+956A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926513 | ||||||
| chr10:87926576
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.209+1019G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926576 | ||||||
| chr10:87926683
|
G | A | 1 | a0001c0001t0003g0078 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.209+1126G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926683 | ||||||
| chr10:87926752
|
G | T | 24 | a0001c0001t0003g0033a0001c0001t0003g0064a0001c0001t0003g0065others(21): Show | 24 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.209+1195G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87926752 | ||||||
| chr10:87927185
|
G | A | 1 | a0001c0001t0028g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209+1628G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927185 | ||||||
| chr10:87927198
|
A | G | 1 | a0001c0001t0004g0258 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.209+1641A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927198 | ||||||
| chr10:87927250
|
C | T | 7 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(4): Show | 7 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.209+1693C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927250 | ||||||
| chr10:87927274
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.209+1717T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927274 | ||||||
| chr10:87927390
|
C | G | 2 | a0001c0001t0003g0173a0001c0001t0006g0186 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.209+1833C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927390 | ||||||
| chr10:87927596
|
A | C | 1 | a0001c0001t0024g0190 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.209+2039A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927596 | ||||||
| chr10:87927636
|
A | G | 2 | a0001c0001t0021g0196a0001c0001t0021g0198 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.209+2079A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927636 | ||||||
| chr10:87927731
|
T | C | 7 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(4): Show | 7 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.209+2174T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927731 | ||||||
| chr10:87927740
|
A | C | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.209+2183A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927740 | ||||||
| chr10:87927748
|
T | C | 1 | a0001c0001t0038g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.209+2191T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87927748 | ||||||
| chr10:87928298
|
G | A | 3 | a0001c0001t0077g0137a0001c0001t0078g0031a0001c0001t0086g0093 | 3 | HG02717.hp1 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.209+2741G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87928298 | ||||||
| chr10:87928677
|
A | G | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.210-2369A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87928677 | ||||||
| chr10:87928684
|
G | T | 4 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(1): Show | 4 | NA18969.hp1 NA18973.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.210-2362G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87928684 | ||||||
| chr10:87928753
|
T | C | 1 | a0001c0001t0101g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.210-2293T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87928753 | ||||||
| chr10:87929362
|
A | G | 1 | a0001c0001t0055g0285 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.210-1684A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87929362 | ||||||
| chr10:87929564
|
G | A | 175 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(172): Show | 177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.210-1482G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87929564 | ||||||
| chr10:87929926
|
G | C | 6 | a0001c0001t0013g0032a0001c0001t0013g0039a0001c0001t0013g0071others(3): Show | 6 | HG00673.hp2 HG02165.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-1120G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87929926 | ||||||
| chr10:87930006
|
C | T | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-1040C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87930006 | ||||||
| chr10:87930075
|
G | A | 1 | a0001c0001t0003g0072 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210-971G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87930075 | ||||||
| chr10:87930112
|
C | T | 8 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.210-934C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87930112 | ||||||
| chr10:87930518
|
A | G | 1 | a0001c0001t0012g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.210-528A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 3/8 | chr10 | 87930518 | ||||||
| chr10:87931158
|
A | G | 1 | a0001c0001t0031g0298 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.253+69A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87931158 | ||||||
| chr10:87931195
|
T | TTTATC | 181 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(178): Show | 183 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.253+109_253+110ins others(5): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 87931195 | |||||
| chr10:87931272
|
T | C | 1 | a0001c0001t0038g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.253+183T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87931272 | ||||||
| chr10:87931489
|
A | G | 8 | a0001c0001t0009g0012a0001c0001t0034g0205a0001c0001t0034g0206others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+400A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87931489 | ||||||
| chr10:87931555
|
C | T | 3 | a0001c0001t0021g0196a0001c0001t0021g0197a0001c0001t0021g0198 | 3 | HG02809.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.253+466C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87931555 | ||||||
| chr10:87931796
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.253+707G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87931796 | ||||||
| chr10:87931872
|
T | C | 1 | a0001c0001t0036g0008 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.253+783T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87931872 | ||||||
| chr10:87932180
|
G | C | 1 | a0001c0001t0058g0132 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.254-833G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87932180 | ||||||
| chr10:87932697
|
T | C | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-316T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87932697 | ||||||
| chr10:87932812
|
A | T | 1 | a0001c0001t0043g0270 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.254-201A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87932812 | ||||||
| chr10:87932914
|
C | T | 1 | a0001c0001t0005g0165 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.254-99C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87932914 | ||||||
| chr10:87932974
|
G | T | 1 | a0001c0001t0004g0249 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.254-39G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 4/8 | chr10 | 87932974 | ||||||
| chr10:87933468
|
C | T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+217C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87933468 | ||||||
| chr10:87933480
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.492+229T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87933480 | ||||||
| chr10:87933543
|
T | C | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+292T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87933543 | ||||||
| chr10:87934030
|
A | G | 1 | a0001c0001t0070g0047 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.492+779A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934030 | ||||||
| chr10:87934296
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+1045G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934296 | ||||||
| chr10:87934403
|
A | T | 1 | a0001c0001t0001g0153 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.492+1152A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934403 | ||||||
| chr10:87934442
|
T | G | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.492+1191T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934442 | ||||||
| chr10:87934682
|
C | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+1431C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934682 | ||||||
| chr10:87934812
|
C | T | 2 | a0001c0001t0106g0288a0001c0001t0107g0287 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.492+1561C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934812 | ||||||
| chr10:87934813
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.492+1562G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934813 | ||||||
| chr10:87934859
|
G | A | 5 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0022g0303others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+1608G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934859 | ||||||
| chr10:87934898
|
T | G | 1 | a0001c0001t0002g0217 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.492+1647T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87934898 | ||||||
| chr10:87934942
|
C | CA | 8 | a0001c0001t0001g0043a0001c0001t0001g0158a0001c0001t0015g0110others(5): Show | 8 | HG00621.hp1 HG02622.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+1706dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87934942 | |||||
| chr10:87934942
|
CA | C | 8 | a0001c0001t0002g0250a0001c0001t0024g0188a0001c0001t0024g0190others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+1706delA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87934942 | |||||
| chr10:87935009
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+1758T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935009 | ||||||
| chr10:87935018
|
G | T | 2 | a0001c0001t0106g0288a0001c0001t0107g0287 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.492+1767G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935018 | ||||||
| chr10:87935041
|
T | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+1790T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935041 | ||||||
| chr10:87935081
|
G | A | 9 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(6): Show | 9 | HG01928.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.492+1830G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935081 | ||||||
| chr10:87935121
|
T | C | 3 | a0001c0001t0001g0059a0001c0001t0001g0097a0001c0001t0005g0098 | 3 | HG02148.hp2 HG04115.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.492+1870T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935121 | ||||||
| chr10:87935428
|
C | T | 1 | a0001c0001t0018g0262 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.492+2177C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935428 | ||||||
| chr10:87935613
|
T | G | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+2362T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935613 | ||||||
| chr10:87935737
|
G | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+2486G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935737 | ||||||
| chr10:87935906
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+2655G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87935906 | ||||||
| chr10:87936143
|
C | T | 1 | a0001c0001t0059g0126 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.492+2892C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87936143 | ||||||
| chr10:87936717
|
T | C | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+3466T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87936717 | ||||||
| chr10:87936831
|
C | T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+3580C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87936831 | ||||||
| chr10:87937103
|
T | G | 1 | a0001c0001t0101g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.492+3852T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937103 | ||||||
| chr10:87937350
|
G | A | 1 | a0001c0001t0003g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.492+4099G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937350 | ||||||
| chr10:87937427
|
C | T | 5 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+4176C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937427 | ||||||
| chr10:87937431
|
T | G | 1 | a0001c0001t0029g0299 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492+4180T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937431 | ||||||
| chr10:87937475
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+4224T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937475 | ||||||
| chr10:87937519
|
A | G | 1 | a0001c0001t0100g0191 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.492+4268A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937519 | ||||||
| chr10:87937596
|
C | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+4345C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937596 | ||||||
| chr10:87937616
|
G | GT | 8 | a0001c0001t0002g0279a0001c0001t0013g0032a0001c0001t0029g0299others(5): Show | 8 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+4380dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87937616 | |||||
| chr10:87937920
|
A | T | 3 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0025g0122 | 3 | HG01952.hp2 HG01975.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.492+4669A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87937920 | ||||||
| chr10:87938018
|
G | C | 1 | a0001c0001t0009g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.492+4767G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87938018 | ||||||
| chr10:87938433
|
C | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 93 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.492+5182C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87938433 | ||||||
| chr10:87938717
|
T | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+5466T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87938717 | ||||||
| chr10:87939008
|
C | T | 1 | a0001c0001t0104g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.492+5757C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939008 | ||||||
| chr10:87939083
|
A | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+5832A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939083 | ||||||
| chr10:87939115
|
T | C | 1 | a0001c0001t0004g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.492+5864T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939115 | ||||||
| chr10:87939170
|
G | C | 1 | a0001c0001t0006g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.492+5919G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939170 | ||||||
| chr10:87939286
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0149 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.492+6043_492+6056d others(16): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939286 | |||||
| chr10:87939294
|
G | GT | 9 | a0001c0001t0003g0078a0001c0001t0003g0095a0001c0001t0003g0172others(6): Show | 9 | HG01071.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.492+6067dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939294
|
GTT | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0169a0001c0001t0005g0155others(7): Show | 10 | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.492+6066_492+6067d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939294
|
GTTT | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 93 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.492+6065_492+6067d others(5): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939294
|
GTTTT | G | 104 | a0001c0001t0001g0181a0001c0001t0002g0009a0001c0001t0002g0144others(101): Show | 105 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.492+6064_492+6067d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939294
|
GTTTTT | G | 35 | a0001c0001t0002g0218a0001c0001t0003g0003a0001c0001t0003g0017others(32): Show | 36 | HG00438.hp2 HG01081.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.492+6063_492+6067d others(7): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939294
|
GTTTTTT | G | 29 | a0001c0001t0008g0016a0001c0001t0008g0125a0001c0001t0008g0129others(26): Show | 29 | HG00621.hp1 HG01106.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.492+6062_492+6067d others(8): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939294
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.492+6054_492+6067d others(16): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939294 | |||||
| chr10:87939299
|
T | G | 1 | a0001c0001t0011g0267 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.492+6048T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939299 | ||||||
| chr10:87939301
|
T | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.492+6050T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939301 | ||||||
| chr10:87939302
|
T | G | 10 | a0001c0001t0003g0072a0001c0001t0024g0188a0001c0001t0024g0190others(7): Show | 10 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.492+6051T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939302 | ||||||
| chr10:87939303
|
T | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+6052T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939303 | ||||||
| chr10:87939304
|
T | G | 14 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.492+6053T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939304 | ||||||
| chr10:87939358
|
C | G | 1 | a0001c0001t0045g0283 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.492+6107C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939358 | ||||||
| chr10:87939416
|
T | C | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+6165T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939416 | ||||||
| chr10:87939452
|
C | T | 180 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(177): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.492+6201C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939452 | ||||||
| chr10:87939480
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.492+6229C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939480 | ||||||
| chr10:87939498
|
A | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+6247A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939498 | ||||||
| chr10:87939507
|
A | G | 1 | a0001c0001t0083g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.492+6256A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939507 | ||||||
| chr10:87939520
|
C | T | 2 | a0001c0001t0025g0296a0001c0001t0096g0297 | 2 | HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.492+6269C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939520 | ||||||
| chr10:87939535
|
A | T | 77 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(74): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.492+6284A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939535 | ||||||
| chr10:87939536
|
CTGGTCTT others(7): Show |
C | 77 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(74): Show | 77 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.492+6288_492+6301d others(16): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87939536 | |||||
| chr10:87939592
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.492+6341G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939592 | ||||||
| chr10:87939699
|
A | T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+6448A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939699 | ||||||
| chr10:87939794
|
T | A | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+6543T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87939794 | ||||||
| chr10:87940469
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.492+7218C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940469 | ||||||
| chr10:87940478
|
G | A | 1 | a0001c0001t0060g0166 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.492+7227G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940478 | ||||||
| chr10:87940528
|
A | T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+7277A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940528 | ||||||
| chr10:87940578
|
A | G | 3 | a0001c0001t0075g0076a0001c0001t0106g0288a0001c0001t0107g0287 | 3 | HG02723.hp2 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.492+7327A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940578 | ||||||
| chr10:87940590
|
G | A | 1 | a0001c0001t0048g0221 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.492+7339G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940590 | ||||||
| chr10:87940835
|
C | T | 3 | a0001c0001t0077g0137a0001c0001t0078g0031a0001c0001t0086g0093 | 3 | HG02717.hp1 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.492+7584C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940835 | ||||||
| chr10:87940914
|
G | C | 2 | a0001c0001t0001g0042a0001c0001t0071g0275 | 2 | HG01175.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.492+7663G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87940914 | ||||||
| chr10:87941041
|
A | G | 2 | a0001c0001t0034g0206a0001c0001t0102g0208 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.492+7790A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941041 | ||||||
| chr10:87941513
|
T | C | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+8262T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941513 | ||||||
| chr10:87941681
|
A | G | 1 | a0001c0001t0015g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.492+8430A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941681 | ||||||
| chr10:87941719
|
A | G | 1 | a0001c0001t0002g0214 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.492+8468A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941719 | ||||||
| chr10:87941846
|
A | G | 1 | a0001c0001t0002g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.492+8595A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941846 | ||||||
| chr10:87941858
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.492+8607G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941858 | ||||||
| chr10:87941890
|
A | G | 1 | a0001c0001t0004g0258 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.492+8639A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87941890 | ||||||
| chr10:87942034
|
A | G | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.492+8783A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942034 | ||||||
| chr10:87942139
|
A | G | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.492+8888A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942139 | ||||||
| chr10:87942190
|
A | G | 4 | a0001c0001t0009g0012a0001c0001t0012g0133a0001c0001t0012g0134others(1): Show | 4 | HG01081.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.492+8939A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942190 | ||||||
| chr10:87942249
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0069g0152 | 2 | HG00438.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.492+8998A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942249 | ||||||
| chr10:87942282
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.492+9031A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942282 | ||||||
| chr10:87942292
|
C | T | 1 | a0001c0001t0006g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.492+9041C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942292 | ||||||
| chr10:87942303
|
G | A | 1 | a0001c0001t0101g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.492+9052G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942303 | ||||||
| chr10:87942330
|
C | T | 1 | a0001c0001t0090g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.492+9079C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942330 | ||||||
| chr10:87942419
|
A | G | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+9168A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942419 | ||||||
| chr10:87942427
|
G | GGTAAT | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+9178_492+9182d others(7): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87942427 | |||||
| chr10:87942807
|
TA | T | 7 | a0001c0001t0002g0214a0001c0001t0029g0299a0001c0001t0029g0301others(4): Show | 7 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-9299delA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87942807 | |||||
| chr10:87942816
|
A | T | 3 | a0001c0001t0002g0244a0001c0001t0081g0079a0001c0001t0089g0178 | 3 | HG00741.hp2 HG01433.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493-9302A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942816 | ||||||
| chr10:87942820
|
T | A | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-9298T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942820 | ||||||
| chr10:87942976
|
T | C | 1 | a0001c0001t0028g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.493-9142T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87942976 | ||||||
| chr10:87943132
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.493-8986C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943132 | ||||||
| chr10:87943191
|
A | C | 2 | a0001c0001t0014g0002a0001c0001t0014g0013 | 3 | HG00738.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.493-8927A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943191 | ||||||
| chr10:87943222
|
A | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.493-8896A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943222 | ||||||
| chr10:87943323
|
C | G | 1 | a0001c0001t0059g0126 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.493-8795C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943323 | ||||||
| chr10:87943376
|
A | G | 2 | a0001c0001t0008g0130a0001c0001t0008g0131 | 2 | HG00438.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.493-8742A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943376 | ||||||
| chr10:87943403
|
G | GTA | 9 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(6): Show | 9 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.493-8700_493-8699d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87943403 | |||||
| chr10:87943454
|
CT | C | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-8657delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87943454 | |||||
| chr10:87943572
|
A | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-8546A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943572 | ||||||
| chr10:87943695
|
G | A | 1 | a0001c0001t0103g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.493-8423G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943695 | ||||||
| chr10:87943729
|
C | T | 1 | a0001c0001t0008g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.493-8389C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943729 | ||||||
| chr10:87943918
|
A | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-8200A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87943918 | ||||||
| chr10:87944019
|
G | A | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.493-8099G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944019 | ||||||
| chr10:87944274
|
G | A | 6 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(3): Show | 6 | HG02809.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-7844G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944274 | ||||||
| chr10:87944301
|
C | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-7817C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944301 | ||||||
| chr10:87944544
|
C | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-7574C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944544 | ||||||
| chr10:87944595
|
A | G | 3 | a0001c0001t0003g0033a0001c0001t0003g0040a0001c0001t0003g0069 | 3 | HG01884.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.493-7523A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944595 | ||||||
| chr10:87944629
|
A | G | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-7489A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944629 | ||||||
| chr10:87944637
|
A | G | 9 | a0001c0001t0003g0033a0001c0001t0003g0040a0001c0001t0003g0064others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.493-7481A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944637 | ||||||
| chr10:87944766
|
G | A | 1 | a0001c0001t0104g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.493-7352G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944766 | ||||||
| chr10:87944885
|
G | C | 1 | a0001c0001t0027g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.493-7233G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944885 | ||||||
| chr10:87944962
|
A | G | 63 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(60): Show | 63 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.493-7156A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87944962 | ||||||
| chr10:87945416
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-6702G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945416 | ||||||
| chr10:87945462
|
G | A | 1 | a0001c0001t0028g0185 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.493-6656G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945462 | ||||||
| chr10:87945464
|
A | C | 7 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0101g0207others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-6654A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945464 | ||||||
| chr10:87945480
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.493-6638C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945480 | ||||||
| chr10:87945609
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.493-6509A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945609 | ||||||
| chr10:87945614
|
C | G | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-6504C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945614 | ||||||
| chr10:87945672
|
G | C | 180 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(177): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.493-6446G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945672 | ||||||
| chr10:87945709
|
G | C | 2 | a0001c0001t0015g0108a0001c0001t0015g0109 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.493-6409G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945709 | ||||||
| chr10:87945818
|
T | G | 1 | a0001c0001t0072g0146 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.493-6300T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945818 | ||||||
| chr10:87945831
|
C | T | 1 | a0001c0001t0009g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.493-6287C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945831 | ||||||
| chr10:87945889
|
A | G | 1 | a0001c0001t0048g0221 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.493-6229A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945889 | ||||||
| chr10:87945907
|
C | T | 1 | a0001c0001t0028g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.493-6211C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87945907 | ||||||
| chr10:87946162
|
A | G | 1 | a0001c0001t0009g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.493-5956A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87946162 | ||||||
| chr10:87946334
|
A | G | 2 | a0001c0001t0005g0167a0001c0001t0005g0168 | 2 | NA18955.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.493-5784A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87946334 | ||||||
| chr10:87946391
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.493-5727A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87946391 | ||||||
| chr10:87946845
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.493-5273C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87946845 | ||||||
| chr10:87946879
|
A | T | 1 | a0001c0001t0042g0256 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.493-5239A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87946879 | ||||||
| chr10:87947068
|
G | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-5050G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947068 | ||||||
| chr10:87947100
|
T | C | 5 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0022g0303others(2): Show | 5 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-5018T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947100 | ||||||
| chr10:87947144
|
A | G | 1 | a0001c0001t0027g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.493-4974A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947144 | ||||||
| chr10:87947189
|
G | T | 1 | a0001c0001t0004g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.493-4929G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947189 | ||||||
| chr10:87947313
|
A | G | 24 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(21): Show | 24 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.493-4805A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947313 | ||||||
| chr10:87947508
|
T | C | 180 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(177): Show | 182 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.493-4610T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947508 | ||||||
| chr10:87947535
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-4583G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947535 | ||||||
| chr10:87947578
|
T | C | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-4540T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947578 | ||||||
| chr10:87947587
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-4531A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947587 | ||||||
| chr10:87947667
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-4451G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947667 | ||||||
| chr10:87947737
|
A | C | 3 | a0001c0001t0077g0137a0001c0001t0078g0031a0001c0001t0086g0093 | 3 | HG02717.hp1 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.493-4381A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947737 | ||||||
| chr10:87947739
|
A | T | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-4379A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947739 | ||||||
| chr10:87947876
|
G | A | 8 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0062g0011others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-4242G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87947876 | ||||||
| chr10:87947904
|
GAAAA | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0097a0001c0001t0005g0098 | 3 | HG02148.hp2 HG04115.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.493-4212_493-4209d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87947904 | |||||
| chr10:87948240
|
T | C | 1 | a0001c0001t0048g0221 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.493-3878T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87948240 | ||||||
| chr10:87948274
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-3844A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87948274 | ||||||
| chr10:87948550
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-3568A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87948550 | ||||||
| chr10:87948607
|
TA | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(304): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.493-3506delA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87948607 | |||||
| chr10:87948803
|
A | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-3315A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87948803 | ||||||
| chr10:87948937
|
CA | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0019others(262): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.493-3159delA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87948937 | |||||
| chr10:87948937
|
CAA | C | 10 | a0001c0001t0001g0018a0001c0001t0008g0125a0001c0001t0008g0131others(7): Show | 10 | HG00323.hp2 HG01070.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.493-3160_493-3159d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87948937 | |||||
| chr10:87949097
|
A | G | 1 | a0001c0001t0101g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493-3021A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949097 | ||||||
| chr10:87949216
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-2902G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949216 | ||||||
| chr10:87949237
|
C | T | 7 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(4): Show | 7 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-2881C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949237 | ||||||
| chr10:87949560
|
T | C | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.493-2558T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949560 | ||||||
| chr10:87949659
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 34 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.493-2459T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949659 | ||||||
| chr10:87949661
|
T | A | 3 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0102g0208 | 3 | HG02622.hp2 HG02886.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493-2457T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949661 | ||||||
| chr10:87949662
|
A | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-2456A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949662 | ||||||
| chr10:87949904
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.493-2214G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87949904 | ||||||
| chr10:87950077
|
C | T | 1 | a0001c0001t0057g0127 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.493-2041C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950077 | ||||||
| chr10:87950130
|
C | T | 1 | a0001c0001t0049g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.493-1988C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950130 | ||||||
| chr10:87950144
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0159a0001c0001t0020g0143others(4): Show | 7 | HG01175.hp2 HG01257.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-1974C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950144 | ||||||
| chr10:87950192
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-1926A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950192 | ||||||
| chr10:87950259
|
C | CA | 12 | a0001c0001t0001g0057a0001c0001t0001g0170a0001c0001t0005g0168others(9): Show | 12 | HG01109.hp2 HG01361.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.493-1839dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr10 | 87950259 | |||||
| chr10:87950276
|
A | G | 1 | a0001c0001t0086g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.493-1842A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950276 | ||||||
| chr10:87950404
|
C | T | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.493-1714C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950404 | ||||||
| chr10:87950532
|
A | C | 1 | a0001c0001t0014g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.493-1586A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950532 | ||||||
| chr10:87950840
|
T | C | 7 | a0001c0001t0008g0118a0001c0001t0008g0125a0001c0001t0010g0120others(4): Show | 7 | HG00621.hp1 HG02071.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-1278T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950840 | ||||||
| chr10:87950841
|
C | T | 7 | a0001c0001t0008g0118a0001c0001t0008g0125a0001c0001t0010g0120others(4): Show | 7 | HG00621.hp1 HG02071.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.493-1277C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87950841 | ||||||
| chr10:87951007
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.493-1111G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951007 | ||||||
| chr10:87951102
|
A | T | 1 | a0001c0001t0028g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.493-1016A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951102 | ||||||
| chr10:87951249
|
C | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02723.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.493-869C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951249 | ||||||
| chr10:87951279
|
A | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.493-839A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951279 | ||||||
| chr10:87951318
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-800G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951318 | ||||||
| chr10:87951324
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-794G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951324 | ||||||
| chr10:87951686
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0048 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.493-432C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951686 | ||||||
| chr10:87951819
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.493-299C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87951819 | ||||||
| chr10:87952050
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.493-68A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 5/8 | chr10 | 87952050 | ||||||
| chr10:87952716
|
G | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.634+457G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87952716 | ||||||
| chr10:87952904
|
G | A | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.634+645G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87952904 | ||||||
| chr10:87953139
|
A | G | 1 | a0001c0001t0081g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.634+880A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953139 | ||||||
| chr10:87953244
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.634+985A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953244 | ||||||
| chr10:87953365
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.634+1106G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953365 | ||||||
| chr10:87953401
|
C | G | 1 | a0001c0001t0067g0151 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.634+1142C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953401 | ||||||
| chr10:87953428
|
T | C | 1 | a0001c0001t0004g0258 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.634+1169T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953428 | ||||||
| chr10:87953690
|
G | C | 1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.634+1431G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953690 | ||||||
| chr10:87953934
|
C | CAGACGCA others(5): Show |
4 | a0001c0001t0012g0133a0001c0001t0012g0134a0001c0001t0012g0135others(1): Show | 4 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1688_634+1699d others(14): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 87953934 | |||||
| chr10:87953934
|
CAGACGCA others(5): Show |
C | 1 | a0001c0001t0001g0159 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.634+1688_634+1699d others(14): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 87953934 | |||||
| chr10:87953951
|
G | A | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+1692G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87953951 | ||||||
| chr10:87954034
|
G | T | 1 | a0001c0001t0001g0045 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.634+1775G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954034 | ||||||
| chr10:87954184
|
A | G | 1 | a0001c0001t0103g0204 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.634+1925A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954184 | ||||||
| chr10:87954202
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.634+1943C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954202 | ||||||
| chr10:87954231
|
A | AT | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+1972_634+1973i others(3): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954231 | ||||||
| chr10:87954489
|
G | A | 4 | a0001c0001t0002g0218a0001c0001t0002g0230a0001c0001t0004g0277others(1): Show | 4 | NA18964.hp2 NA18968.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+2230G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954489 | ||||||
| chr10:87954598
|
A | G | 1 | a0001c0001t0010g0295 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.634+2339A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954598 | ||||||
| chr10:87954773
|
A | G | 5 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(2): Show | 5 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+2514A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954773 | ||||||
| chr10:87954774
|
T | C | 1 | a0001c0001t0005g0161 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.634+2515T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954774 | ||||||
| chr10:87954856
|
C | A | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.634+2597C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87954856 | ||||||
| chr10:87955293
|
A | G | 1 | a0001c0001t0005g0054 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.635-2560A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955293 | ||||||
| chr10:87955336
|
C | A | 1 | a0001c0001t0033g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.635-2517C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955336 | ||||||
| chr10:87955339
|
T | C | 1 | a0001c0001t0033g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.635-2514T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955339 | ||||||
| chr10:87955340
|
T | A | 1 | a0001c0001t0033g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.635-2513T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955340 | ||||||
| chr10:87955344
|
C | G | 1 | a0001c0001t0033g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.635-2509C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955344 | ||||||
| chr10:87955400
|
A | T | 1 | a0001c0001t0002g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.635-2453A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955400 | ||||||
| chr10:87955800
|
C | T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-2053C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955800 | ||||||
| chr10:87955904
|
T | A | 1 | a0001c0001t0028g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.635-1949T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955904 | ||||||
| chr10:87955953
|
T | C | 2 | a0001c0001t0034g0206a0001c0001t0102g0208 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.635-1900T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87955953 | ||||||
| chr10:87956148
|
A | T | 1 | a0001c0002t0097g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.635-1705A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956148 | ||||||
| chr10:87956262
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.635-1591C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956262 | ||||||
| chr10:87956350
|
T | C | 80 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(77): Show | 80 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.635-1503T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956350 | ||||||
| chr10:87956429
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.635-1424T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956429 | ||||||
| chr10:87956504
|
G | C | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-1349G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956504 | ||||||
| chr10:87956586
|
TTTTATAT others(1): Show |
T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-1265_635-1258d others(10): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 87956586 | |||||
| chr10:87956588
|
T | TTA | 25 | a0001c0001t0001g0043a0001c0001t0002g0217a0001c0001t0002g0244others(22): Show | 25 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.635-1246_635-1245d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 87956588 | |||||
| chr10:87956588
|
T | TTATA | 5 | a0001c0001t0034g0205a0001c0001t0034g0206a0001c0001t0062g0011others(2): Show | 5 | HG02622.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-1248_635-1245d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 87956588 | |||||
| chr10:87956588
|
TTA | T | 24 | a0001c0001t0003g0033a0001c0001t0003g0064a0001c0001t0003g0065others(21): Show | 25 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.635-1246_635-1245d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 87956588 | |||||
| chr10:87956590
|
A | T | 3 | a0001c0001t0012g0133a0001c0001t0012g0134a0001c0001t0012g0135 | 3 | HG01081.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.635-1263A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956590 | ||||||
| chr10:87956743
|
A | C | 1 | a0001c0001t0048g0221 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.635-1110A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956743 | ||||||
| chr10:87956810
|
A | G | 1 | a0001c0001t0046g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.635-1043A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956810 | ||||||
| chr10:87956821
|
T | G | 1 | a0001c0001t0076g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.635-1032T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87956821 | ||||||
| chr10:87957306
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.635-547C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87957306 | ||||||
| chr10:87957355
|
G | T | 8 | a0001c0001t0024g0188a0001c0001t0024g0190a0001c0001t0024g0192others(5): Show | 8 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-498G>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87957355 | ||||||
| chr10:87957489
|
T | A | 6 | a0001c0001t0002g0257a0001c0001t0004g0258a0001c0001t0009g0119others(3): Show | 6 | HG00639.hp1 HG01928.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-364T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87957489 | ||||||
| chr10:87957747
|
A | G | 1 | a0001c0001t0050g0245 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.635-106A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 6/8 | chr10 | 87957747 | ||||||
| chr10:87958300
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.801+281A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958300 | ||||||
| chr10:87958371
|
T | G | 1 | a0001c0001t0002g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.801+352T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958371 | ||||||
| chr10:87958381
|
C | CT | 7 | a0001c0001t0013g0071a0001c0001t0029g0299a0001c0001t0029g0301others(4): Show | 7 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+376dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 87958381 | |||||
| chr10:87958510
|
G | A | 2 | a0001c0001t0003g0173a0001c0001t0006g0186 | 2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.801+491G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958510 | ||||||
| chr10:87958518
|
A | G | 1 | a0001c0001t0005g0167 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.801+499A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958518 | ||||||
| chr10:87958577
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.801+558C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958577 | ||||||
| chr10:87958626
|
T | C | 1 | a0001c0001t0026g0193 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.801+607T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958626 | ||||||
| chr10:87958636
|
T | TA | 3 | a0001c0001t0006g0083a0001c0001t0006g0085a0001c0001t0085g0084 | 3 | HG00099.hp2 HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.801+617_801+618ins others(1): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958636 | ||||||
| chr10:87958839
|
C | T | 1 | a0001c0001t0026g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.801+820C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958839 | ||||||
| chr10:87958848
|
A | C | 1 | a0001c0001t0099g0209 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.801+829A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958848 | ||||||
| chr10:87958903
|
G | C | 1 | a0001c0001t0065g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.801+884G>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958903 | ||||||
| chr10:87958970
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.801+951C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958970 | ||||||
| chr10:87958971
|
G | A | 2 | a0001c0001t0002g0211a0001c0001t0065g0077 | 2 | HG02818.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.801+952G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87958971 | ||||||
| chr10:87959378
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0057 | 3 | HG01106.hp2 HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.801+1359A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959378 | ||||||
| chr10:87959380
|
G | A | 19 | a0001c0001t0003g0033a0001c0001t0003g0064a0001c0001t0003g0065others(16): Show | 19 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.801+1361G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959380 | ||||||
| chr10:87959388
|
G | A | 1 | a0001c0001t0107g0287 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.801+1369G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959388 | ||||||
| chr10:87959611
|
A | T | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.802-1283A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959611 | ||||||
| chr10:87959641
|
T | A | 1 | a0001c0001t0007g0028 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.802-1253T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959641 | ||||||
| chr10:87959664
|
C | A | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.802-1230C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959664 | ||||||
| chr10:87959690
|
A | G | 6 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0031g0298others(3): Show | 6 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.802-1204A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87959690 | ||||||
| chr10:87959817
|
C | CA | 5 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-1071dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 87959817 | |||||
| chr10:87959953
|
AC | A | 13 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(10): Show | 13 | HG02559.hp1 HG02622.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.802-939delC | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 87959953 | |||||
| chr10:87960494
|
T | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 34 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.802-400T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87960494 | ||||||
| chr10:87960535
|
T | A | 30 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0125others(27): Show | 30 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.802-359T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87960535 | ||||||
| chr10:87960681
|
A | G | 1 | a0001c0001t0007g0029 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.802-213A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87960681 | ||||||
| chr10:87960687
|
T | C | 7 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(4): Show | 7 | HG02559.hp1 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-207T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87960687 | ||||||
| chr10:87960729
|
A | C | 1 | a0001c0001t0049g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.802-165A>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87960729 | ||||||
| chr10:87960791
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.802-103A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | chr10 | 87960791 | ||||||
| chr10:87960840
|
ATTAATTA others(31): Show |
A | 7 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(4): Show | 7 | HG02559.hp1 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-51_802-14delAA others(36): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 87960840 | |||||
| chr10:87960876
|
C | CT | 87 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(84): Show | 87 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(84): Show |
splice_acceptor_variant&intron_variant | HIGH | c.802-3dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr10 | 87960876 | |||||
| chr10:87961150
|
T | G | 182 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(179): Show | 184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1026+32T>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961150 | ||||||
| chr10:87961337
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(299): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1026+219C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961337 | ||||||
| chr10:87961506
|
T | C | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1026+388T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961506 | ||||||
| chr10:87961532
|
CTTGA | C | 4 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0227others(1): Show | 4 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+418_1026+421d others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87961532 | |||||
| chr10:87961574
|
G | GT | 10 | a0001c0001t0001g0059a0001c0001t0001g0097a0001c0001t0004g0258others(7): Show | 10 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026+467dupT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87961574 | |||||
| chr10:87961637
|
C | G | 4 | a0001c0001t0014g0002a0001c0001t0014g0013a0001c0001t0014g0014others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+519C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961637 | ||||||
| chr10:87961640
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1026+522C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961640 | ||||||
| chr10:87961655
|
C | T | 88 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(85): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1026+537C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961655 | ||||||
| chr10:87961704
|
A | G | 2 | a0001c0001t0006g0010a0001c0001t0091g0291 | 3 | NA18951.hp1 NA18952.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1026+586A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961704 | ||||||
| chr10:87961770
|
C | G | 1 | a0001c0001t0001g0056 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1026+652C>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961770 | ||||||
| chr10:87961779
|
C | T | 1 | a0001c0001t0026g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1026+661C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961779 | ||||||
| chr10:87961931
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1026+813C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87961931 | ||||||
| chr10:87962186
|
T | A | 8 | a0001c0001t0003g0003a0001c0001t0003g0017a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1026+1068T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962186 | ||||||
| chr10:87962295
|
C | T | 15 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0015g0110others(12): Show | 15 | HG00323.hp2 HG01070.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1026+1177C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962295 | ||||||
| chr10:87962460
|
A | G | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1026+1342A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962460 | ||||||
| chr10:87962480
|
T | TA | 36 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0002g0009others(33): Show | 36 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1026+1384dupA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962480 | |||||
| chr10:87962480
|
T | TAA | 6 | a0001c0001t0002g0217a0001c0001t0002g0234a0001c0001t0002g0257others(3): Show | 6 | HG01928.hp2 HG02165.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+1383_1026+138 others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962480 | |||||
| chr10:87962480
|
TA | T | 39 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0003g0139others(36): Show | 39 | HG00738.hp1 HG01081.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1026+1384delA | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962480 | |||||
| chr10:87962497
|
A | T | 4 | a0001c0001t0010g0295a0001c0001t0025g0296a0001c0001t0042g0256others(1): Show | 4 | HG01261.hp2 HG01361.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1379A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962497 | ||||||
| chr10:87962499
|
A | ATAT | 6 | a0001c0001t0003g0017a0001c0001t0003g0140a0001c0001t0022g0303others(3): Show | 6 | HG02572.hp2 HG03516.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+1381_1026+138 others(7): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962499 | ||||||
| chr10:87962499
|
A | T | 25 | a0001c0001t0008g0016a0001c0001t0008g0118a0001c0001t0008g0129others(22): Show | 25 | HG00438.hp2 HG01106.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1026+1381A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962499 | ||||||
| chr10:87962499
|
AAAAT | A | 15 | a0001c0001t0002g0224a0001c0001t0002g0266a0001c0001t0004g0223others(12): Show | 15 | HG00408.hp2 HG00597.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026+1383_1026+138 others(8): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962499 | |||||
| chr10:87962501
|
A | AAAT | 14 | a0001c0001t0002g0211a0001c0001t0002g0225a0001c0001t0002g0226others(11): Show | 14 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026+1384_1026+138 others(7): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962501 | |||||
| chr10:87962501
|
A | AT | 3 | a0001c0001t0006g0010a0001c0001t0006g0177a0001c0001t0091g0291 | 4 | NA18951.hp1 NA18952.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1383_1026+138 others(5): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962501 | ||||||
| chr10:87962501
|
A | ATATACAC others(8): Show |
1 | a0001c0001t0012g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1026+1383_1026+138 others(19): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962501 | ||||||
| chr10:87962501
|
A | ATATACAC others(10): Show |
2 | a0001c0001t0012g0134a0001c0001t0012g0135 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1026+1383_1026+138 others(21): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962501 | ||||||
| chr10:87962501
|
A | T | 37 | a0001c0001t0001g0056a0001c0001t0003g0003a0001c0001t0003g0017others(34): Show | 38 | HG00438.hp2 HG00544.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1026+1383A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962501 | ||||||
| chr10:87962502
|
AT | A | 3 | a0001c0001t0004g0213a0001c0001t0004g0249a0001c0001t0038g0246 | 3 | HG02083.hp1 HG03704.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1026+1385delT | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962502 | ||||||
| chr10:87962503
|
T | A | 8 | a0001c0001t0004g0280a0001c0001t0006g0101a0001c0001t0034g0205others(5): Show | 8 | HG02723.hp2 HG02886.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+1385T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962503 | ||||||
| chr10:87962503
|
T | C | 17 | a0001c0001t0002g0211a0001c0001t0002g0225a0001c0001t0002g0226others(14): Show | 17 | HG00408.hp1 HG00544.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1026+1385T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962503 | ||||||
| chr10:87962505
|
T | C | 64 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(61): Show | 64 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.1026+1387T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962505 | ||||||
| chr10:87962505
|
T | TACAC | 4 | a0001c0001t0006g0083a0001c0001t0008g0016a0001c0001t0077g0137others(1): Show | 4 | HG00140.hp1 HG03453.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1388_1026+138 others(8): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962505 | |||||
| chr10:87962505
|
T | TACACAC | 12 | a0001c0001t0003g0003a0001c0001t0008g0118a0001c0001t0008g0129others(9): Show | 13 | HG00438.hp2 HG02071.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1026+1388_1026+138 others(10): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962505 | |||||
| chr10:87962505
|
T | TACACACA others(1): Show |
10 | a0001c0001t0010g0123a0001c0001t0010g0124a0001c0001t0010g0295others(7): Show | 10 | HG01109.hp1 HG01261.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026+1388_1026+138 others(12): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962505 | |||||
| chr10:87962505
|
T | TACACACA others(3): Show |
2 | a0001c0001t0009g0012a0001c0001t0010g0116 | 2 | HG01106.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1026+1388_1026+138 others(14): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962505 | |||||
| chr10:87962507
|
T | C | 103 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0002g0009others(100): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.1026+1389T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962507 | ||||||
| chr10:87962507
|
T | TAC | 26 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0045others(23): Show | 26 | HG00642.hp2 HG01070.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1026+1424_1026+142 others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
T | TACAC | 22 | a0001c0001t0001g0050a0001c0001t0001g0059a0001c0001t0005g0157others(19): Show | 23 | HG00323.hp2 HG01109.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1026+1422_1026+142 others(8): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
T | TACACAC | 12 | a0001c0001t0007g0021a0001c0001t0007g0025a0001c0001t0007g0027others(9): Show | 12 | HG00738.hp1 HG01243.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1026+1420_1026+142 others(10): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
T | TACACACA others(1): Show |
4 | a0001c0001t0003g0072a0001c0001t0008g0203a0001c0001t0065g0077others(1): Show | 4 | HG02818.hp1 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1418_1026+142 others(12): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
T | TACACACA others(3): Show |
6 | a0001c0001t0034g0206a0001c0001t0057g0127a0001c0001t0073g0075others(3): Show | 6 | HG00621.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026+1416_1026+142 others(14): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
T | TACACACA others(7): Show |
1 | a0001c0001t0081g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1026+1412_1026+142 others(18): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
T | TACACACA others(9): Show |
1 | a0001c0001t0062g0011 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1026+1410_1026+142 others(20): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
TAC | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0182a0001c0001t0003g0078others(2): Show | 5 | HG00642.hp1 HG02055.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+1424_1026+142 others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
TACAC | T | 5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0032g0070others(2): Show | 5 | HG00438.hp1 HG02145.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+1422_1026+142 others(8): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962507
|
TACACAC | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02717.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+1420_1026+142 others(10): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87962507 | |||||
| chr10:87962509
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0003g0139a0001c0001t0008g0125others(1): Show | 4 | HG01884.hp2 HG02523.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+1391C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962509 | ||||||
| chr10:87962511
|
C | T | 1 | a0001c0001t0008g0125 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1026+1393C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962511 | ||||||
| chr10:87962515
|
C | T | 5 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(2): Show | 5 | HG02965.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+1397C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962515 | ||||||
| chr10:87962527
|
C | T | 1 | a0001c0001t0046g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1026+1409C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962527 | ||||||
| chr10:87962544
|
T | A | 1 | a0001c0001t0006g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1026+1426T>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962544 | ||||||
| chr10:87962944
|
A | G | 3 | a0001c0001t0007g0025a0001c0001t0007g0026a0001c0001t0007g0027 | 3 | NA18969.hp1 NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1026+1826A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962944 | ||||||
| chr10:87962974
|
T | C | 63 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(60): Show | 63 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1026+1856T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87962974 | ||||||
| chr10:87963026
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1026+1908T>C | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963026 | ||||||
| chr10:87963109
|
C | A | 1 | a0001c0001t0079g0171 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1026+1991C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963109 | ||||||
| chr10:87963132
|
A | G | 3 | a0001c0001t0029g0299a0001c0001t0029g0301a0001c0001t0061g0302 | 3 | HG02622.hp1 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1026+2014A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963132 | ||||||
| chr10:87963187
|
CTT | C | 3 | a0001c0001t0012g0133a0001c0001t0012g0134a0001c0001t0012g0135 | 3 | HG01081.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1026+2072_1026+207 others(6): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87963187 | |||||
| chr10:87963392
|
G | A | 8 | a0001c0001t0015g0108a0001c0001t0015g0109a0001c0001t0026g0106others(5): Show | 8 | HG02559.hp1 HG02965.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-1895G>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963392 | ||||||
| chr10:87963442
|
A | T | 6 | a0001c0001t0026g0106a0001c0001t0026g0115a0001c0001t0026g0193others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-1845A>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963442 | ||||||
| chr10:87963585
|
C | T | 182 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(179): Show | 184 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1027-1702C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963585 | ||||||
| chr10:87963640
|
C | T | 1 | a0001c0001t0003g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1027-1647C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963640 | ||||||
| chr10:87963664
|
C | T | 1 | a0001c0001t0105g0292 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1027-1623C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87963664 | ||||||
| chr10:87964003
|
A | G | 6 | a0001c0001t0022g0080a0001c0001t0022g0082a0001c0001t0022g0303others(3): Show | 6 | HG01255.hp1 HG01261.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027-1284A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87964003 | ||||||
| chr10:87964129
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1027-1158C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87964129 | ||||||
| chr10:87964523
|
C | T | 1 | a0001c0001t0024g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1027-764C>T | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87964523 | ||||||
| chr10:87964535
|
A | AAC | 3 | a0001c0001t0001g0097a0001c0001t0007g0028a0001c0001t0067g0151 | 3 | HG02148.hp2 HG03654.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1027-726_1027-725d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87964535 | |||||
| chr10:87964535
|
A | AACACACA others(3): Show |
1 | a0001c0001t0001g0055 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1027-734_1027-725d others(12): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87964535 | |||||
| chr10:87964535
|
AAC | A | 160 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(157): Show | 162 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1027-726_1027-725d others(4): Show |
PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 87964535 | |||||
| chr10:87964537
|
C | A | 6 | a0001c0001t0016g0215a0001c0001t0016g0276a0001c0001t0016g0289others(3): Show | 6 | HG00609.hp2 HG01433.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-750C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87964537 | ||||||
| chr10:87964539
|
C | A | 147 | a0001c0001t0002g0009a0001c0001t0002g0144a0001c0001t0002g0211others(144): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1027-748C>A | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87964539 | ||||||
| chr10:87964699
|
A | G | 1 | a0001c0001t0006g0304 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1027-588A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87964699 | ||||||
| chr10:87965152
|
A | G | 1 | a0001c0001t0007g0024 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1027-135A>G | PTEN | ENSG00000171862.15 | transcript | ENST00000371953.8 | protein_coding | 8/8 | chr10 | 87965152 |