Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 338440 |
|---|---|
| ensemblid | ENSG00000185101.13 |
| hgncid | 20679 |
| symbol | ANO9 |
| name | anoctamin 9 |
| refseq_nuc | NM_001012302.3 |
| refseq_prot | NP_001012302.2 |
| ensembl_nuc | ENST00000332826.7 |
| ensembl_prot | ENSP00000332788.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 417938 |
| end | 442011 |
| strand | - |
| ver | v1.2 |
| region | chr11:417938-442011 |
| region5000 | chr11:412938-447011 |
| regionname0 | ANO9_chr11_417938_442011 |
| regionname5000 | ANO9_chr11_412938_447011 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 782 | 174 | 52 | 34 | 59 | 8 | 21 | 36 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0002 | 0/0 | 782 | 55 | 24 | 5 | 20 | 1 | 5 | 12 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003 | 1/1 | 782 | 18 | 0 | 14 | 0 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0004 | 0/0 | 782 | 7 | 0 | 4 | 0 | 3 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0005 | 0/0 | 782 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0006 | 0/0 | 313 | 5 | 0 | 3 | 2 | 0 | 0 | 2 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0007 | 0/0 | 782 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0008 | 0/0 | 782 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0009 | 0/0 | 782 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0010 | 0/0 | 313 | 3 | 1 | 1 | 1 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0011 | 0/0 | 782 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0012 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0013 | 0/0 | 782 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0014 | 0/0 | 313 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2349 | 163 | 42 | 33 | 59 | 8 | 21 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0002 | 0/0 | 2349 | 55 | 24 | 5 | 20 | 1 | 5 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0003 | 1/1 | 2349 | 8 | 0 | 5 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0004 | 0/0 | 2349 | 7 | 0 | 4 | 0 | 3 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0005 | 0/0 | 2349 | 6 | 0 | 5 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0006 | 0/0 | 2349 | 6 | 6 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0007 | 0/0 | 2349 | 5 | 0 | 0 | 5 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0008 | 0/0 | 2349 | 5 | 0 | 3 | 0 | 2 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0009 | 0/0 | 2350 | 4 | 0 | 2 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0010 | 0/0 | 2349 | 4 | 0 | 4 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0011 | 0/0 | 2349 | 4 | 0 | 3 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0012 | 0/0 | 2349 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0013 | 0/0 | 2349 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0014 | 0/0 | 2350 | 3 | 1 | 1 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0015 | 0/0 | 2349 | 2 | 1 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0016 | 0/0 | 2349 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0017 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0018 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0019 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0020 | 0/0 | 2349 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0021 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| c0022 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 519 | 255 | 69 | 65 | 82 | 17 | 20 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0002 | 0/0 | 519 | 16 | 0 | 4 | 5 | 1 | 6 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0003 | 0/0 | 519 | 5 | 4 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0004 | 0/0 | 519 | 4 | 4 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0005 | 0/0 | 519 | 2 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0006 | 0/0 | 519 | 2 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0007 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| t0008 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2349 | 163 | 42 | 33 | 59 | 8 | 21 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0006 | 0/0 | 2349 | 6 | 6 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0013 | 0/0 | 2349 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0020 | 0/0 | 2349 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0021 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0002c0002 | 0/0 | 2349 | 55 | 24 | 5 | 20 | 1 | 5 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003c0003 | 1/1 | 2349 | 8 | 0 | 5 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003c0005 | 0/0 | 2349 | 6 | 0 | 5 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003c0010 | 0/0 | 2349 | 4 | 0 | 4 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0004c0004 | 0/0 | 2349 | 7 | 0 | 4 | 0 | 3 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0005c0007 | 0/0 | 2349 | 5 | 0 | 0 | 5 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0006c0009 | 0/0 | 2350 | 4 | 0 | 2 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0006c0019 | 0/0 | 2350 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0007c0008 | 0/0 | 2349 | 5 | 0 | 3 | 0 | 2 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0008c0012 | 0/0 | 2349 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0008c0015 | 0/0 | 2349 | 2 | 1 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0009c0011 | 0/0 | 2349 | 4 | 0 | 3 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0010c0014 | 0/0 | 2350 | 3 | 1 | 1 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0011c0016 | 0/0 | 2349 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0012c0017 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0013c0018 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0014c0022 | 0/0 | 2350 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2867 | 150 | 39 | 28 | 59 | 8 | 16 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0001t0002 | 0/0 | 2867 | 9 | 0 | 4 | 0 | 0 | 5 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0001t0003 | 0/0 | 2867 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0001t0004 | 0/0 | 2867 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0006t0003 | 0/0 | 2867 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0006t0004 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0006t0006 | 0/0 | 2867 | 2 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0013t0005 | 0/0 | 2867 | 2 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0013t0008 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0020t0001 | 0/0 | 2867 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0001c0021t0001 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0002c0002t0001 | 0/0 | 2867 | 47 | 24 | 5 | 14 | 0 | 4 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0002c0002t0002 | 0/0 | 2867 | 7 | 0 | 0 | 5 | 1 | 1 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0002c0002t0007 | 0/0 | 2867 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003c0003t0001 | 1/1 | 2867 | 8 | 0 | 5 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003c0005t0001 | 0/0 | 2867 | 6 | 0 | 5 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0003c0010t0001 | 0/0 | 2867 | 4 | 0 | 4 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0004c0004t0001 | 0/0 | 2867 | 7 | 0 | 4 | 0 | 3 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0005c0007t0001 | 0/0 | 2867 | 5 | 0 | 0 | 5 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0006c0009t0001 | 0/0 | 2868 | 4 | 0 | 2 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0006c0019t0001 | 0/0 | 2868 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0007c0008t0001 | 0/0 | 2867 | 5 | 0 | 3 | 0 | 2 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0008c0012t0001 | 0/0 | 2867 | 3 | 3 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0008c0015t0001 | 0/0 | 2867 | 2 | 1 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0009c0011t0001 | 0/0 | 2867 | 4 | 0 | 3 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0010c0014t0001 | 0/0 | 2868 | 3 | 1 | 1 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0011c0016t0001 | 0/0 | 2867 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0012c0017t0003 | 0/0 | 2867 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0013c0018t0001 | 0/0 | 2867 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| a0014c0022t0001 | 0/0 | 2868 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | copy fasta | chr11 | 412938 | 447011 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0006t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0006t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0006t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0006t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0006t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0006t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0013t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0013t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0020t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0001c0021t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0002c0002t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0005t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0005t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0010t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0010t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0003c0010t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0004c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0005c0007t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0005c0007t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0005c0007t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0005c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0005c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0006c0009t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0006c0009t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0006c0009t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0006c0009t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0006c0019t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0007c0008t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0007c0008t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0007c0008t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0007c0008t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0007c0008t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0008c0012t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0008c0012t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0008c0012t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0008c0015t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0008c0015t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0009c0011t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0009c0011t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0009c0011t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0010c0014t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0010c0014t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0010c0014t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0011c0016t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0011c0016t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0012c0017t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0013c0018t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| a0014c0022t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0005 | t0001 | g0086 | EUR | GBR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0083 | EUR | GBR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0047 | EUR | FIN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0040 | EUR | FIN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00323 | hp1 | a0007 | c0008 | t0001 | g0161 | EUR | FIN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00323 | hp2 | a0014 | c0022 | t0001 | g0051 | EUR | FIN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00609 | hp2 | a0013 | c0018 | t0001 | g0176 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00733 | hp2 | a0009 | c0011 | t0001 | g0096 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00735 | hp1 | a0001 | c0020 | t0001 | g0169 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00735 | hp2 | a0011 | c0016 | t0001 | g0171 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0089 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00738 | hp2 | a0007 | c0008 | t0001 | g0144 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00741 | hp1 | a0006 | c0009 | t0001 | g0209 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0085 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0094 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01081 | hp2 | a0009 | c0011 | t0001 | g0005 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01109 | hp2 | a0004 | c0004 | t0001 | g0044 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01169 | hp1 | a0010 | c0014 | t0001 | g0064 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01175 | hp1 | a0003 | c0005 | t0001 | g0087 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01255 | hp1 | a0004 | c0004 | t0001 | g0035 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01255 | hp2 | a0006 | c0019 | t0001 | g0142 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01257 | hp1 | a0004 | c0004 | t0001 | g0053 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01257 | hp2 | a0003 | c0005 | t0001 | g0001 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01258 | hp2 | a0003 | c0005 | t0001 | g0001 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01346 | hp2 | a0003 | c0010 | t0001 | g0004 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01358 | hp1 | a0011 | c0016 | t0001 | g0170 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01515 | hp1 | a0009 | c0011 | t0001 | g0005 | EUR | IBS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01516 | hp2 | a0004 | c0004 | t0001 | g0034 | EUR | IBS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01517 | hp1 | a0004 | c0004 | t0001 | g0030 | EUR | IBS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01928 | hp1 | a0003 | c0010 | t0001 | g0088 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01928 | hp2 | a0007 | c0008 | t0001 | g0158 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01934 | hp1 | a0003 | c0003 | t0001 | g0090 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01943 | hp1 | a0008 | c0015 | t0001 | g0261 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01952 | hp1 | a0007 | c0008 | t0001 | g0162 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01952 | hp2 | a0006 | c0009 | t0001 | g0124 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01975 | hp1 | a0003 | c0010 | t0001 | g0004 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01993 | hp1 | a0009 | c0011 | t0001 | g0095 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02071 | hp2 | a0005 | c0007 | t0001 | g0201 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02135 | hp2 | a0005 | c0007 | t0001 | g0217 | EAS | KHV | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02145 | hp2 | a0001 | c0006 | t0003 | g0014 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02280 | hp2 | a0001 | c0013 | t0005 | g0003 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02293 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02300 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02300 | hp2 | a0003 | c0010 | t0001 | g0092 | AMR | PEL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02451 | hp2 | a0001 | c0006 | t0003 | g0011 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02630 | hp2 | a0001 | c0006 | t0003 | g0013 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02809 | hp1 | a0010 | c0014 | t0001 | g0061 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02818 | hp2 | a0001 | c0021 | t0001 | g0258 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02886 | hp1 | a0008 | c0015 | t0001 | g0260 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02970 | hp2 | a0008 | c0012 | t0001 | g0190 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03130 | hp2 | a0008 | c0012 | t0001 | g0192 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03486 | hp1 | a0012 | c0017 | t0003 | g0010 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03579 | hp2 | a0008 | c0012 | t0001 | g0191 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | STU | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18522 | hp1 | a0001 | c0006 | t0006 | g0015 | AFR | YRI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | YRI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | CHB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18906 | hp1 | a0001 | c0006 | t0004 | g0140 | AFR | YRI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | YRI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18941 | hp1 | a0006 | c0009 | t0001 | g0180 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18951 | hp1 | a0005 | c0007 | t0001 | g0198 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18966 | hp1 | a0006 | c0009 | t0001 | g0179 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18994 | hp1 | a0010 | c0014 | t0001 | g0026 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18995 | hp1 | a0005 | c0007 | t0001 | g0199 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19004 | hp1 | a0002 | c0002 | t0007 | g0067 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19005 | hp1 | a0005 | c0007 | t0001 | g0242 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | LWK | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | YRI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA19240 | hp2 | a0001 | c0013 | t0008 | g0275 | AFR | YRI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | ASW | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | ASW | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20752 | hp2 | a0007 | c0008 | t0001 | g0163 | EUR | TSI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | TSI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | GIH | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | GIH | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01123 | hp1 | a0004 | c0004 | t0001 | g0039 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03471 | hp1 | a0001 | c0006 | t0006 | g0012 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | MSL | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | USA | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | USA | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA20300 | hp2 | a0001 | c0013 | t0005 | g0003 | AFR | USA | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | LWK | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | LWK | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0093 | REF | REF | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0091 | REF | REF | ANO9_chr11_412938_447011 | ANO9 | chr11 | 412938 | 447011 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:419706
|
T | C | 1 | a0007 | 5 | HG00323.hp1 HG00738.hp2 HG01928.hp2 others(2): Show |
missense_variant | MODERATE | c.1810A>G | p.Thr604Ala | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/23 | 1895/2867 | 1810/2349 | 604/782 | chr11 | 419706 | ||
| chr11:428385
|
A | G | 12 | a0001a0002a0004others(9): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
missense_variant | MODERATE | c.1195T>C | p.Cys399Arg | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 14/23 | 1280/2867 | 1195/2349 | 399/782 | chr11 | 428385 | ||
| chr11:428489
|
T | C | 12 | a0001a0002a0004others(9): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
missense_variant | MODERATE | c.1171A>G | p.Ile391Val | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 13/23 | 1256/2867 | 1171/2349 | 391/782 | chr11 | 428489 | ||
| chr11:429587
|
C | T | 1 | a0013 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.898G>A | p.Val300Met | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/23 | 983/2867 | 898/2349 | 300/782 | chr11 | 429587 | ||
| chr11:429613
|
C | CG | 3 | a0006a0010a0014 | 9 | HG00323.hp2 HG00741.hp1 HG01169.hp1 others(6): Show |
frameshift_variant | HIGH | c.871dupC | p.Arg291fs | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/23 | 956/2867 | 871/2349 | 291/782 | chr11 | 429613 | ||
| chr11:430339
|
C | G | 2 | a0004a0014 | 8 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(5): Show |
missense_variant | MODERATE | c.604G>C | p.Val202Leu | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 8/23 | 689/2867 | 604/2349 | 202/782 | chr11 | 430339 | ||
| chr11:431757
|
C | T | 2 | a0005a0013 | 6 | HG00609.hp2 HG02071.hp2 HG02135.hp2 others(3): Show |
missense_variant | MODERATE | c.476G>A | p.Arg159His | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/23 | 561/2867 | 476/2349 | 159/782 | chr11 | 431757 | ||
| chr11:433357
|
G | T | 1 | a0008 | 5 | HG01943.hp1 HG02886.hp1 HG02970.hp2 others(2): Show |
missense_variant | MODERATE | c.307C>A | p.His103Asn | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/23 | 392/2867 | 307/2349 | 103/782 | chr11 | 433357 | ||
| chr11:433867
|
G | A | 4 | a0002a0004a0010others(1): Show | 66 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
missense_variant | MODERATE | c.152C>T | p.Ala51Val | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/23 | 237/2867 | 152/2349 | 51/782 | chr11 | 433867 | ||
| chr11:434082
|
C | T | 1 | a0012 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.23G>A | p.Arg8Gln | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 2/23 | 108/2867 | 23/2349 | 8/782 | chr11 | 434082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:418735
|
G | A | 1 | a0003c0005 | 6 | HG00099.hp1 HG01175.hp1 HG01257.hp2 others(3): Show |
synonymous_variant | LOW | c.2115C>T | p.Phe705Phe | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 22/23 | 2200/2867 | 2115/2349 | 705/782 | chr11 | 418735 | ||
| chr11:419650
|
C | T | 1 | a0001c0013 | 3 | HG02280.hp2 NA19240.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.1866G>A | p.Glu622Glu | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/23 | 1951/2867 | 1866/2349 | 622/782 | chr11 | 419650 | ||
| chr11:420983
|
C | G | 1 | a0003c0010 | 4 | HG01346.hp2 HG01928.hp1 HG01975.hp1 others(1): Show |
synonymous_variant | LOW | c.1452G>C | p.Leu484Leu | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 17/23 | 1537/2867 | 1452/2349 | 484/782 | chr11 | 420983 | ||
| chr11:428514
|
C | A | 1 | a0001c0006 | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
synonymous_variant | LOW | c.1146G>T | p.Gly382Gly | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 13/23 | 1231/2867 | 1146/2349 | 382/782 | chr11 | 428514 | ||
| chr11:428565
|
C | A | 1 | a0001c0020 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1095G>T | p.Ser365Ser | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 13/23 | 1180/2867 | 1095/2349 | 365/782 | chr11 | 428565 | ||
| chr11:428749
|
G | A | 1 | a0006c0019 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.993C>T | p.Thr331Thr | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 12/23 | 1078/2867 | 993/2349 | 331/782 | chr11 | 428749 | ||
| chr11:431878
|
C | A | 1 | a0008c0012 | 3 | HG02970.hp2 HG03130.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.435G>T | p.Gly145Gly | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 6/23 | 520/2867 | 435/2349 | 145/782 | chr11 | 431878 | ||
| chr11:432039
|
G | A | 2 | a0001c0021a0008c0015 | 3 | HG01943.hp1 HG02818.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.366C>T | p.Ile122Ile | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 5/23 | 451/2867 | 366/2349 | 122/782 | chr11 | 432039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:418072
|
A | C | 1 | a0001c0013t0005 | 2 | HG02280.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 23/23 | 299 | chr11 | 418072 | |||||
| chr11:418079
|
G | A | 3 | a0001c0001t0004a0001c0006t0004a0001c0006t0006 | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*292C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 23/23 | 292 | chr11 | 418079 | |||||
| chr11:418179
|
A | C | 2 | a0001c0001t0002a0002c0002t0002 | 16 | HG00280.hp1 HG01081.hp1 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*192T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 23/23 | 192 | chr11 | 418179 | |||||
| chr11:418349
|
G | A | 1 | a0002c0002t0007 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 23/23 | 22 | chr11 | 418349 | |||||
| chr11:441948
|
A | G | 6 | a0001c0001t0003a0001c0006t0003a0001c0006t0006others(3): Show | 10 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-22T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/23 | 22 | chr11 | 441948 | |||||
| chr11:441968
|
G | C | 1 | a0001c0013t0008 | 1 | NA19240.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/23 | chr11 | 441968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:418601
|
A | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252 | 3 | HG01243.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2131-12T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 22/22 | chr11 | 418601 | ||||||
| chr11:418652
|
G | A | 31 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0122others(28): Show | 31 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.2131-63C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 22/22 | chr11 | 418652 | ||||||
| chr11:418653
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2131-64G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 22/22 | chr11 | 418653 | ||||||
| chr11:418654
|
C | T | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.2131-65G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 22/22 | chr11 | 418654 | ||||||
| chr11:419022
|
T | TGGGCTTC others(3): Show |
1 | a0001c0001t0001g0250 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1935-43_1935-34dup others(10): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419022 | ||||||
| chr11:419167
|
T | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(257): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1935-178A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419167 | ||||||
| chr11:419255
|
C | T | 1 | a0003c0003t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1935-266G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419255 | ||||||
| chr11:419263
|
G | C | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1935-274C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419263 | ||||||
| chr11:419321
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1934+261A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419321 | ||||||
| chr11:419323
|
G | C | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1934+259C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419323 | ||||||
| chr11:419324
|
C | A | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1934+258G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419324 | ||||||
| chr11:419325
|
A | G | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1934+257T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419325 | ||||||
| chr11:419390
|
C | T | 3 | a0009c0011t0001g0005a0009c0011t0001g0095a0009c0011t0001g0096 | 4 | HG00733.hp2 HG01081.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1934+192G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419390 | ||||||
| chr11:419557
|
G | A | 3 | a0009c0011t0001g0005a0009c0011t0001g0095a0009c0011t0001g0096 | 4 | HG00733.hp2 HG01081.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1934+25C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 20/22 | chr11 | 419557 | ||||||
| chr11:419794
|
C | CACCCCCG others(64): Show |
11 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252others(8): Show | 12 | HG01243.hp1 HG02280.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1787-66_1787-65ins others(71): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419794 | ||||||
| chr11:419801
|
G | C | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1787-72C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419801 | ||||||
| chr11:419802
|
G | C | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1787-73C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419802 | ||||||
| chr11:419803
|
C | G | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1787-74G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419803 | ||||||
| chr11:419805
|
A | C | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1787-76T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419805 | ||||||
| chr11:419906
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(235): Show | 246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1787-177G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419906 | ||||||
| chr11:419994
|
C | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(234): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1787-265G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 419994 | ||||||
| chr11:420011
|
G | A | 17 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0028others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.1787-282C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 420011 | ||||||
| chr11:420180
|
C | G | 1 | a0002c0002t0001g0056 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1786+283G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 420180 | ||||||
| chr11:420445
|
G | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252 | 3 | HG01243.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1786+18C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 19/22 | chr11 | 420445 | ||||||
| chr11:420643
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1634-28G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 18/22 | chr11 | 420643 | ||||||
| chr11:420681
|
C | A | 2 | a0001c0001t0001g0173a0006c0009t0001g0180 | 2 | NA18941.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1633+37G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 18/22 | chr11 | 420681 | ||||||
| chr11:421046
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.1393-4G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 16/22 | chr11 | 421046 | ||||||
| chr11:421376
|
ACACACAC others(137): Show |
A | 8 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0249others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335-322_1335-179d others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421376 | ||||||
| chr11:421378
|
ACACACAC others(135): Show |
A | 3 | a0001c0001t0001g0121a0002c0002t0001g0070a0002c0002t0001g0071 | 3 | HG01168.hp2 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1335-322_1335-181d others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421378 | ||||||
| chr11:421380
|
ACACACAC others(133): Show |
A | 256 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(253): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1335-322_1335-183d others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421380 | ||||||
| chr11:421382
|
ACACACAC others(131): Show |
A | 1 | a0008c0015t0001g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1335-322_1335-185d others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421382 | ||||||
| chr11:421456
|
CCCCCACA others(132): Show |
C | 2 | a0001c0001t0001g0149a0001c0001t0001g0173 | 2 | HG01099.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1335-397_1335-259d others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421456 | ||||||
| chr11:421565
|
C | A | 1 | a0001c0001t0001g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1335-367G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421565 | ||||||
| chr11:421583
|
A | G | 21 | a0001c0001t0001g0077a0002c0002t0001g0023a0002c0002t0001g0024others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1335-385T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421583 | ||||||
| chr11:421595
|
A | C | 7 | a0004c0004t0001g0030a0004c0004t0001g0034a0004c0004t0001g0035others(4): Show | 7 | HG00280.hp2 HG00323.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335-397T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421595 | ||||||
| chr11:421596
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1335-398G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421596 | ||||||
| chr11:421638
|
C | T | 8 | a0001c0001t0001g0108a0001c0001t0001g0111a0001c0001t0001g0131others(5): Show | 8 | HG02027.hp2 HG02040.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335-440G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421638 | ||||||
| chr11:421798
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1335-600G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 421798 | ||||||
| chr11:422096
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1335-898G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422096 | ||||||
| chr11:422171
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG01884.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1335-973C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422171 | ||||||
| chr11:422303
|
G | A | 7 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(4): Show | 7 | HG02886.hp1 HG03471.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335-1105C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422303 | ||||||
| chr11:422328
|
C | A | 2 | a0001c0013t0005g0003a0001c0013t0008g0275 | 3 | HG02280.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1335-1130G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422328 | ||||||
| chr11:422438
|
T | C | 3 | a0009c0011t0001g0005a0009c0011t0001g0095a0009c0011t0001g0096 | 4 | HG00733.hp2 HG01081.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335-1240A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422438 | ||||||
| chr11:422525
|
ATCAGAAG others(14): Show |
A | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1335-1348_1335-132 others(25): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422525 | ||||||
| chr11:422556
|
C | T | 8 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0249others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335-1358G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422556 | ||||||
| chr11:422725
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1335-1527T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422725 | ||||||
| chr11:422831
|
A | AT | 28 | a0001c0001t0001g0022a0001c0001t0001g0077a0001c0001t0001g0250others(25): Show | 29 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1335-1634dupA | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422831 | ||||||
| chr11:422831
|
AT | A | 15 | a0001c0001t0001g0108a0001c0001t0001g0149a0001c0001t0001g0164others(12): Show | 15 | HG01099.hp2 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1335-1634delA | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422831 | ||||||
| chr11:422987
|
G | A | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(235): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1335-1789C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 422987 | ||||||
| chr11:423027
|
A | G | 2 | a0001c0013t0005g0003a0001c0013t0008g0275 | 3 | HG02280.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1335-1829T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423027 | ||||||
| chr11:423077
|
C | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG01433.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1335-1879G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423077 | ||||||
| chr11:423167
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1335-1969C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423167 | ||||||
| chr11:423413
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335-2215T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423413 | ||||||
| chr11:423432
|
G | A | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0002c0002t0001g0058others(5): Show | 8 | HG01074.hp1 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1335-2234C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423432 | ||||||
| chr11:423610
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1335-2412G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423610 | ||||||
| chr11:423617
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0120others(90): Show | 97 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1335-2419G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423617 | ||||||
| chr11:423634
|
A | C | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335-2436T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423634 | ||||||
| chr11:423664
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1335-2466G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423664 | ||||||
| chr11:423699
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(237): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1335-2501G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423699 | ||||||
| chr11:423712
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1335-2514C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423712 | ||||||
| chr11:423736
|
G | A | 1 | a0002c0002t0001g0139 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1335-2538C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423736 | ||||||
| chr11:423790
|
C | G | 2 | a0001c0001t0002g0141a0001c0001t0002g0143 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1335-2592G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423790 | ||||||
| chr11:423878
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1335-2680A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423878 | ||||||
| chr11:423885
|
T | TCA | 26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0079others(23): Show | 26 | HG01169.hp2 HG02015.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1335-2689_1335-268 others(6): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
T | TCACA | 72 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0102others(69): Show | 74 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1335-2691_1335-268 others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
T | TCACACA | 68 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0105others(65): Show | 71 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1335-2693_1335-268 others(10): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
T | TCACACAC others(1): Show |
48 | a0001c0001t0001g0008a0001c0001t0001g0106a0001c0001t0001g0115others(45): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1335-2695_1335-268 others(12): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
T | TCACACAC others(3): Show |
18 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0197others(15): Show | 18 | HG00733.hp1 HG00741.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1335-2697_1335-268 others(14): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
T | TCACACAC others(5): Show |
6 | a0001c0001t0001g0077a0001c0001t0001g0107a0002c0002t0001g0070others(3): Show | 6 | HG02922.hp1 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335-2699_1335-268 others(16): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
T | TCACACAC others(7): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1335-2701_1335-268 others(18): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
TCACA | T | 4 | a0001c0001t0001g0249a0001c0013t0005g0003a0001c0013t0008g0275others(1): Show | 5 | HG02280.hp2 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335-2691_1335-268 others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
TCACACA | T | 10 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0252others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1335-2693_1335-268 others(10): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:423885
|
TCACACAC others(3): Show |
T | 1 | a0005c0007t0001g0217 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1335-2697_1335-268 others(14): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 423885 | ||||||
| chr11:424127
|
C | G | 3 | a0003c0010t0001g0004a0003c0010t0001g0088a0003c0010t0001g0092 | 4 | HG01346.hp2 HG01928.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335-2929G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424127 | ||||||
| chr11:424289
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1335-3091A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424289 | ||||||
| chr11:424291
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(256): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1335-3093T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424291 | ||||||
| chr11:424314
|
C | T | 2 | a0008c0012t0001g0191a0008c0012t0001g0192 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1335-3116G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424314 | ||||||
| chr11:424546
|
G | A | 1 | a0002c0002t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1335-3348C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424546 | ||||||
| chr11:424598
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335-3400T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424598 | ||||||
| chr11:424750
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1334+3338A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424750 | ||||||
| chr11:424966
|
A | T | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1334+3122T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424966 | ||||||
| chr11:424972
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1334+3116G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424972 | ||||||
| chr11:424982
|
G | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(240): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1334+3106C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424982 | ||||||
| chr11:424995
|
G | GGAGACGG others(28): Show |
1 | a0003c0010t0001g0092 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1334+3058_1334+309 others(39): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 424995 | ||||||
| chr11:425015
|
G | C | 16 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0249others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1334+3073C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425015 | ||||||
| chr11:425023
|
GGCGTGGA others(167): Show |
G | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1334+2891_1334+306 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425023 | ||||||
| chr11:425050
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1334+3038C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425050 | ||||||
| chr11:425060
|
CGTGGAGA others(207): Show |
C | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1334+2814_1334+302 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425060 | ||||||
| chr11:425080
|
GGGAGGAA others(167): Show |
G | 1 | a0001c0001t0001g0203 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1334+2834_1334+300 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425080 | ||||||
| chr11:425083
|
A | G | 1 | a0006c0009t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1334+3005T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425083 | ||||||
| chr11:425084
|
G | A | 1 | a0006c0009t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1334+3004C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425084 | ||||||
| chr11:425085
|
G | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(242): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1334+3003C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425085 | ||||||
| chr11:425086
|
A | C | 1 | a0006c0009t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1334+3002T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425086 | ||||||
| chr11:425094
|
G | C | 1 | a0002c0002t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1334+2994C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425094 | ||||||
| chr11:425095
|
CGTGGAGA others(172): Show |
C | 233 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(230): Show | 238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1334+2814_1334+299 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425095 | ||||||
| chr11:425098
|
G | A | 2 | a0001c0001t0001g0167a0002c0002t0001g0069 | 2 | HG00140.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1334+2990C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425098 | ||||||
| chr11:425099
|
G | C | 2 | a0001c0001t0001g0167a0002c0002t0001g0069 | 2 | HG00140.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1334+2989C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425099 | ||||||
| chr11:425100
|
A | AGAGACGG others(59): Show |
4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334+2987_1334+298 others(70): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425100 | ||||||
| chr11:425100
|
A | C | 2 | a0001c0001t0001g0167a0002c0002t0001g0069 | 2 | HG00140.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1334+2988T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425100 | ||||||
| chr11:425102
|
AGACGGGA others(98): Show |
A | 5 | a0001c0001t0001g0272a0001c0001t0003g0009a0008c0012t0001g0190others(2): Show | 5 | HG01109.hp1 HG02257.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334+2881_1334+298 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425102 | ||||||
| chr11:425120
|
G | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0193a0001c0001t0001g0249others(3): Show | 6 | HG01071.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1334+2968C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425120 | ||||||
| chr11:425121
|
AAAAGGCG others(167): Show |
A | 1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1334+2793_1334+296 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425121 | ||||||
| chr11:425128
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2960C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425128 | ||||||
| chr11:425129
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2959C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425129 | ||||||
| chr11:425130
|
CGTGGAGA others(137): Show |
C | 2 | a0001c0001t0001g0152a0006c0019t0001g0142 | 2 | HG01071.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1334+2814_1334+295 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425130 | ||||||
| chr11:425131
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2957C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425131 | ||||||
| chr11:425132
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2956A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425132 | ||||||
| chr11:425132
|
T | C | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334+2956A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425132 | ||||||
| chr11:425133
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2955C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425133 | ||||||
| chr11:425133
|
GGA | G | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334+2953_1334+295 others(6): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425133 | ||||||
| chr11:425135
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2953T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425135 | ||||||
| chr11:425136
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2952C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425136 | ||||||
| chr11:425146
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2942C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425146 | ||||||
| chr11:425148
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2940C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425148 | ||||||
| chr11:425150
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2938C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425150 | ||||||
| chr11:425154
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2934C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425154 | ||||||
| chr11:425155
|
GAAAAGGC others(98): Show |
G | 4 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+2828_1334+293 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425155 | ||||||
| chr11:425157
|
AAAGGCGG others(142): Show |
A | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1334+2782_1334+293 others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425157 | ||||||
| chr11:425190
|
G | GAAAAGGC others(26): Show |
6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334+2897_1334+289 others(37): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425190 | ||||||
| chr11:425207
|
C | A | 11 | a0001c0001t0001g0238a0001c0001t0004g0113a0001c0001t0004g0118others(8): Show | 12 | HG02280.hp2 HG03471.hp1 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.1334+2881G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425207 | ||||||
| chr11:425273
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0238 | 2 | HG03669.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1334+2815C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425273 | ||||||
| chr11:425274
|
G | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0238 | 2 | HG03669.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1334+2814C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425274 | ||||||
| chr11:425275
|
A | ACC | 236 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(233): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1334+2812_1334+281 others(6): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425275 | ||||||
| chr11:425275
|
A | C | 2 | a0001c0001t0001g0203a0001c0001t0001g0238 | 2 | HG03669.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1334+2813T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425275 | ||||||
| chr11:425496
|
A | G | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334+2592T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425496 | ||||||
| chr11:425553
|
T | TA | 8 | a0001c0001t0001g0183a0001c0001t0001g0231a0001c0001t0001g0268others(5): Show | 9 | HG00673.hp2 HG02280.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1334+2534dupT | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425553 | ||||||
| chr11:425553
|
TA | T | 8 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0230others(5): Show | 8 | HG00323.hp1 HG00733.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.1334+2534delT | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425553 | ||||||
| chr11:425573
|
C | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+2515G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425573 | ||||||
| chr11:425646
|
AG | A | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+2441delC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425646 | ||||||
| chr11:425694
|
TCAC | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(235): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1334+2391_1334+239 others(7): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425694 | ||||||
| chr11:425716
|
T | G | 1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1334+2372A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425716 | ||||||
| chr11:425717
|
G | GT | 10 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0121others(7): Show | 10 | HG00323.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1334+2370dupA | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425717 | ||||||
| chr11:425717
|
G | T | 1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1334+2371C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425717 | ||||||
| chr11:425720
|
TTTTG | T | 9 | a0001c0001t0001g0082a0001c0001t0001g0272a0001c0001t0003g0009others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1334+2364_1334+236 others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425720 | ||||||
| chr11:425723
|
TG | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0002g0141 | 3 | HG01168.hp1 HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1334+2364delC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425723 | ||||||
| chr11:425724
|
G | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(230): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1334+2364C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425724 | ||||||
| chr11:425740
|
T | G | 1 | a0002c0002t0001g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1334+2348A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425740 | ||||||
| chr11:425741
|
G | T | 1 | a0002c0002t0001g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1334+2347C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425741 | ||||||
| chr11:425742
|
T | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG01346.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1334+2346A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425742 | ||||||
| chr11:425792
|
C | T | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1334+2296G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425792 | ||||||
| chr11:425794
|
C | T | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+2294G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425794 | ||||||
| chr11:425801
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(246): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1334+2287T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425801 | ||||||
| chr11:425858
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0249a0001c0001t0001g0252others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+2230T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425858 | ||||||
| chr11:425922
|
TG | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(235): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1334+2165delC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425922 | ||||||
| chr11:425955
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1334+2133T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 425955 | ||||||
| chr11:426024
|
G | A | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1334+2064C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426024 | ||||||
| chr11:426046
|
T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0231 | 2 | NA18953.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1334+2042A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426046 | ||||||
| chr11:426061
|
TA | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0238a0006c0009t0001g0209 | 3 | HG00741.hp1 HG01433.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1334+2026delT | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426061 | ||||||
| chr11:426145
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1334+1943G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426145 | ||||||
| chr11:426296
|
GCGGTAGC others(6): Show |
G | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1334+1779_1334+179 others(17): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426296 | ||||||
| chr11:426334
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1334+1754C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426334 | ||||||
| chr11:426648
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1334+1440T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426648 | ||||||
| chr11:426809
|
C | T | 1 | a0003c0005t0001g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1334+1279G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426809 | ||||||
| chr11:426902
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1334+1186G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426902 | ||||||
| chr11:426995
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1334+1093C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 426995 | ||||||
| chr11:427093
|
C | T | 6 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(3): Show | 6 | HG03471.hp1 HG03471.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1334+995G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427093 | ||||||
| chr11:427320
|
A | G | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1334+768T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427320 | ||||||
| chr11:427426
|
AT | A | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334+661delA | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427426 | ||||||
| chr11:427495
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1334+593T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427495 | ||||||
| chr11:427509
|
A | C | 1 | a0001c0001t0001g0229 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1334+579T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427509 | ||||||
| chr11:427529
|
C | T | 9 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0111others(6): Show | 9 | HG01168.hp2 HG02040.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1334+559G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427529 | ||||||
| chr11:427532
|
A | G | 7 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119others(4): Show | 8 | HG02280.hp2 HG03471.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1334+556T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427532 | ||||||
| chr11:427707
|
G | GTCTC | 3 | a0001c0001t0001g0082a0001c0001t0001g0202a0001c0001t0003g0009 | 3 | HG01109.hp1 HG02027.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1334+377_1334+380d others(6): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427707 | ||||||
| chr11:427707
|
GTC | G | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+379_1334+380d others(4): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427707 | ||||||
| chr11:427726
|
T | A | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+362A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427726 | ||||||
| chr11:427727
|
C | T | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1334+361G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427727 | ||||||
| chr11:427851
|
C | T | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.1334+237G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 427851 | ||||||
| chr11:428014
|
G | GGACATTG others(315): Show |
1 | a0001c0001t0001g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(322): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(315): Show |
1 | a0001c0001t0001g0134 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(322): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(316): Show |
3 | a0001c0001t0001g0183a0001c0001t0001g0251a0001c0001t0001g0254 | 3 | HG02895.hp1 HG02976.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(316): Show |
1 | a0001c0001t0001g0186 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(316): Show |
1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(316): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0248 | 2 | HG02723.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(316): Show |
11 | a0001c0001t0001g0021a0001c0001t0001g0121a0001c0001t0001g0133others(8): Show | 11 | HG00280.hp1 HG01168.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(316): Show |
1 | a0001c0001t0001g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0187 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
3 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0001t0001g0215 | 3 | HG02486.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0244 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0002c0002t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0236 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
29 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0177others(26): Show | 31 | HG00408.hp2 HG01074.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
4 | a0001c0001t0001g0135a0001c0001t0001g0189a0001c0001t0001g0245others(1): Show | 4 | HG02027.hp1 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0132 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
46 | a0001c0001t0001g0022a0001c0001t0001g0105a0001c0001t0001g0109others(43): Show | 46 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
2 | a0002c0002t0001g0027a0002c0002t0001g0049 | 2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
2 | a0001c0001t0002g0156a0001c0001t0002g0160 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0002g0007 | 2 | HG01081.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0225 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0001t0001g0226 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0145 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0002c0002t0001g0020 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
4 | a0001c0001t0001g0210a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG01358.hp2 HG02809.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
1 | a0001c0001t0001g0268 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0005c0007t0001g0201 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0235 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
21 | a0001c0001t0001g0008a0001c0001t0001g0112a0001c0001t0001g0137others(18): Show | 22 | HG00609.hp2 HG00733.hp1 HG02004.hp1 others(19): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
25 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0115others(22): Show | 25 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0002c0002t0001g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0002g0159 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0002c0002t0002g0025 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0002g0196 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0150 | 3 | HG01256.hp2 HG01258.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0002c0002t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
13 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(10): Show | 13 | HG00140.hp1 HG00597.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
2 | a0001c0001t0001g0228a0002c0002t0001g0097 | 2 | HG03098.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
12 | a0001c0001t0001g0076a0001c0001t0001g0107a0001c0001t0001g0114others(9): Show | 12 | HG00140.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
1 | a0001c0001t0001g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
1 | a0001c0006t0006g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(319): Show |
1 | a0001c0001t0001g0197 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(326): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
1 | a0001c0020t0001g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(321): Show |
1 | a0007c0008t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(328): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
7 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 7 | HG00323.hp1 HG01071.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
1 | a0001c0001t0001g0202 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
1 | a0001c0001t0001g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
2 | a0011c0016t0001g0170a0011c0016t0001g0171 | 2 | HG00735.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(320): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(327): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(321): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(328): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(317): Show |
2 | a0001c0001t0001g0206a0004c0004t0001g0053 | 2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1334+73_1334+74ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428014
|
G | GGACATTG others(318): Show |
1 | a0001c0001t0001g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1334+73_1334+74ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428014 | ||||||
| chr11:428025
|
C | CTTCATTT others(317): Show |
1 | a0001c0001t0001g0269 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1334+62_1334+63ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428025 | ||||||
| chr11:428025
|
C | CTTCATTT others(318): Show |
1 | a0001c0001t0001g0273 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1334+62_1334+63ins others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428025 | ||||||
| chr11:428026
|
T | TTCATTTT others(317): Show |
1 | a0006c0009t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1334+61_1334+62ins others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428026 | ||||||
| chr11:428046
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1334+42G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 15/22 | chr11 | 428046 | ||||||
| chr11:428657
|
T | C | 1 | a0008c0015t0001g0261 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1021-18A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 12/22 | chr11 | 428657 | ||||||
| chr11:428668
|
C | T | 13 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0240others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1021-29G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 12/22 | chr11 | 428668 | ||||||
| chr11:428711
|
C | T | 1 | a0002c0002t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1020+11G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 12/22 | chr11 | 428711 | ||||||
| chr11:428857
|
A | AGGGACAC others(405): Show |
1 | a0001c0001t0001g0133 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.916-32_916-31insGT others(410): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428857 | ||||||
| chr11:428875
|
T | C | 9 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 10 | HG01884.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.916-49A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428875 | ||||||
| chr11:428894
|
A | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 9 | HG01884.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-68T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428894 | ||||||
| chr11:428894
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.916-68T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428894 | ||||||
| chr11:428900
|
A | G | 8 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 9 | HG01884.hp2 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-74T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428900 | ||||||
| chr11:428921
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.916-95C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428921 | ||||||
| chr11:428945
|
A | AGACAGAC others(56): Show |
1 | a0001c0001t0001g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.916-182_916-120dup others(63): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428945 | ||||||
| chr11:428965
|
C | CCCCACAC others(182): Show |
1 | a0001c0001t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.916-140_916-139ins others(189): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428965 | ||||||
| chr11:428966
|
C | CCCACACG others(56): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG01884.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.916-141_916-140ins others(63): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428966 | ||||||
| chr11:428989
|
AGGGACAC others(21): Show |
A | 1 | a0001c0001t0001g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.916-191_916-164del others(28): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428989 | ||||||
| chr11:428996
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.916-170G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 428996 | ||||||
| chr11:429004
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.916-178C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429004 | ||||||
| chr11:429029
|
A | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0114others(6): Show | 10 | HG01884.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-203T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429029 | ||||||
| chr11:429049
|
C | T | 1 | a0003c0003t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.916-223G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429049 | ||||||
| chr11:429059
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.916-233G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429059 | ||||||
| chr11:429066
|
C | T | 5 | a0001c0001t0001g0254a0001c0013t0005g0003a0001c0013t0008g0275others(2): Show | 6 | HG02280.hp2 HG02976.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.916-240G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429066 | ||||||
| chr11:429091
|
T | C | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-265A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429091 | ||||||
| chr11:429122
|
T | C | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-296A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429122 | ||||||
| chr11:429129
|
T | C | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-303A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429129 | ||||||
| chr11:429129
|
T | TGGGTGGA others(119): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | NA18995.hp2 NA18997.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.915+315_916-304dup others(126): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429129 | ||||||
| chr11:429129
|
T | TGGGTGGA others(468): Show |
1 | a0001c0001t0001g0188 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.916-304_916-303ins others(475): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429129 | ||||||
| chr11:429129
|
T | TGGGTGGA others(434): Show |
1 | a0001c0001t0001g0133 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.916-304_916-303ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429129 | ||||||
| chr11:429185
|
C | T | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-359G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429185 | ||||||
| chr11:429192
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.916-366G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429192 | ||||||
| chr11:429204
|
C | G | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+366G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429204 | ||||||
| chr11:429206
|
C | T | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+364G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429206 | ||||||
| chr11:429214
|
T | G | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+356A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429214 | ||||||
| chr11:429218
|
C | T | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+352G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429218 | ||||||
| chr11:429258
|
GTGGACAG others(17): Show |
G | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.915+288_915+311del others(24): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429258 | ||||||
| chr11:429321
|
C | A | 5 | a0001c0001t0001g0082a0001c0001t0003g0009a0008c0012t0001g0190others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.915+249G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 11/22 | chr11 | 429321 | ||||||
| chr11:429659
|
C | T | 147 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(144): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
splice_region_variant&intron_variant | LOW | c.833-7G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 10/22 | chr11 | 429659 | ||||||
| chr11:429746
|
G | A | 9 | a0001c0001t0001g0082a0001c0001t0001g0193a0001c0001t0001g0249others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.832+12C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 10/22 | chr11 | 429746 | ||||||
| chr11:430014
|
C | G | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.771+69G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 9/22 | chr11 | 430014 | ||||||
| chr11:430024
|
G | A | 3 | a0009c0011t0001g0005a0009c0011t0001g0095a0009c0011t0001g0096 | 4 | HG00733.hp2 HG01081.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+59C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 9/22 | chr11 | 430024 | ||||||
| chr11:430456
|
A | G | 163 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(160): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.540-53T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430456 | ||||||
| chr11:430468
|
G | GGGGTGGG others(27): Show |
1 | a0001c0001t0001g0244 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.540-66_540-65insTC others(32): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430468 | ||||||
| chr11:430487
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0120others(86): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.540-84C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430487 | ||||||
| chr11:430546
|
A | G | 1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540-143T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430546 | ||||||
| chr11:430547
|
C | A | 1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540-144G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430547 | ||||||
| chr11:430548
|
G | C | 1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540-145C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430548 | ||||||
| chr11:430596
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.540-193C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430596 | ||||||
| chr11:430597
|
A | AG | 7 | a0001c0001t0001g0202a0001c0001t0001g0245a0001c0001t0001g0253others(4): Show | 7 | HG00323.hp2 HG01168.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-195dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430597 | ||||||
| chr11:430597
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.540-194T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430597 | ||||||
| chr11:430610
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.540-207C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430610 | ||||||
| chr11:430626
|
A | AG | 18 | a0001c0001t0001g0022a0001c0001t0001g0208a0001c0001t0001g0238others(15): Show | 18 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.540-224dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430626 | ||||||
| chr11:430836
|
T | G | 1 | a0006c0009t0001g0209 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.540-433A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430836 | ||||||
| chr11:430839
|
C | CGCGGCGG others(34): Show |
4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-437_540-436ins others(41): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430839 | ||||||
| chr11:430841
|
C | CG | 11 | a0001c0001t0001g0114a0001c0001t0001g0126a0001c0001t0001g0185others(8): Show | 11 | HG00642.hp1 HG01255.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.540-439dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430841 | ||||||
| chr11:430879
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0120others(100): Show | 107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.540-476A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430879 | ||||||
| chr11:430889
|
T | TGGGGGCT others(34): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.540-487_540-486ins others(41): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430889 | ||||||
| chr11:430902
|
C | G | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540-499G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430902 | ||||||
| chr11:430907
|
T | C | 1 | a0002c0002t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.540-504A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430907 | ||||||
| chr11:430915
|
C | T | 143 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.540-512G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430915 | ||||||
| chr11:430921
|
C | CG | 11 | a0001c0001t0001g0080a0001c0001t0001g0185a0001c0001t0001g0202others(8): Show | 11 | HG01934.hp2 HG02027.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.540-519dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430921 | ||||||
| chr11:430942
|
C | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0220a0001c0013t0005g0003others(3): Show | 7 | HG01433.hp1 HG02280.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-539G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430942 | ||||||
| chr11:430950
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.540-547T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430950 | ||||||
| chr11:430962
|
G | GGGGGGTG others(638): Show |
1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540-560_540-559ins others(645): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430962 | ||||||
| chr11:430975
|
C | T | 1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.540-572G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430975 | ||||||
| chr11:430981
|
C | CGGGTATC others(75): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.540-579_540-578ins others(82): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430981 | ||||||
| chr11:430999
|
C | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0220a0002c0002t0001g0016 | 3 | HG01433.hp1 HG02683.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.540-596G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 430999 | ||||||
| chr11:431016
|
T | G | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540-613A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431016 | ||||||
| chr11:431017
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540-614G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431017 | ||||||
| chr11:431021
|
C | CGGGTATC others(74): Show |
1 | a0001c0001t0001g0076 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.540-619_540-618ins others(81): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431021 | ||||||
| chr11:431034
|
G | A | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-631C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431034 | ||||||
| chr11:431036
|
G | GTCTGCGG others(75): Show |
1 | a0001c0001t0001g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.540-634_540-633ins others(82): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431036 | ||||||
| chr11:431036
|
G | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0220a0001c0013t0005g0003others(2): Show | 6 | HG01433.hp1 HG02280.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.540-633C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431036 | ||||||
| chr11:431039
|
T | C | 5 | a0001c0001t0001g0148a0001c0001t0001g0220a0001c0013t0005g0003others(2): Show | 6 | HG01433.hp1 HG02280.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.540-636A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431039 | ||||||
| chr11:431043
|
G | A | 43 | a0001c0001t0001g0006a0001c0001t0001g0077a0001c0001t0001g0078others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.540-640C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431043 | ||||||
| chr11:431056
|
T | G | 5 | a0001c0001t0001g0148a0001c0013t0005g0003a0001c0013t0008g0275others(2): Show | 6 | HG01433.hp1 HG02280.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+638A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431056 | ||||||
| chr11:431057
|
C | T | 5 | a0001c0001t0001g0148a0001c0013t0005g0003a0001c0013t0008g0275others(2): Show | 6 | HG01433.hp1 HG02280.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+637G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431057 | ||||||
| chr11:431059
|
C | CGTGGGTA others(192): Show |
1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.539+634_539+635ins others(199): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431059 | ||||||
| chr11:431076
|
T | G | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539+618A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431076 | ||||||
| chr11:431079
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539+615G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431079 | ||||||
| chr11:431081
|
C | CG | 6 | a0001c0001t0001g0112a0001c0001t0001g0203a0001c0001t0001g0266others(3): Show | 6 | HG01109.hp1 HG01255.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+612dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431081 | ||||||
| chr11:431081
|
C | CGGGGGTG others(154): Show |
1 | a0001c0001t0001g0076 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.539+612_539+613ins others(161): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431081 | ||||||
| chr11:431082
|
G | A | 4 | a0001c0001t0001g0148a0001c0013t0005g0003a0001c0013t0008g0275others(1): Show | 5 | HG01433.hp1 HG02280.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+612C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431082 | ||||||
| chr11:431091
|
G | A | 3 | a0001c0021t0001g0258a0008c0015t0001g0260a0008c0015t0001g0261 | 3 | HG01943.hp1 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.539+603C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431091 | ||||||
| chr11:431101
|
T | C | 3 | a0001c0001t0001g0076a0001c0001t0001g0220a0002c0002t0001g0016 | 3 | HG02683.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.539+593A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431101 | ||||||
| chr11:431103
|
G | A | 6 | a0001c0006t0003g0011a0001c0006t0003g0013a0001c0006t0003g0014others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+591C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431103 | ||||||
| chr11:431116
|
G | A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117 | 3 | HG02630.hp1 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.539+578C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431116 | ||||||
| chr11:431119
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0148 | 2 | HG01433.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.539+575A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431119 | ||||||
| chr11:431121
|
C | CG | 8 | a0001c0001t0001g0103a0001c0001t0001g0112a0001c0001t0001g0250others(5): Show | 8 | HG00597.hp2 HG01109.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.539+572dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431121 | ||||||
| chr11:431141
|
C | T | 2 | a0001c0001t0001g0148a0002c0002t0001g0016 | 2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.539+553G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431141 | ||||||
| chr11:431156
|
T | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0082a0001c0001t0001g0220others(2): Show | 5 | HG01109.hp1 HG02683.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+538A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431156 | ||||||
| chr11:431159
|
C | CGCAGGGG others(679): Show |
3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+534_539+535ins others(686): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431159 | ||||||
| chr11:431159
|
C | T | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.539+535G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431159 | ||||||
| chr11:431161
|
C | CGGGGGTG others(325): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.539+532_539+533ins others(332): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431161 | ||||||
| chr11:431161
|
C | T | 1 | a0002c0002t0001g0139 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539+533G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431161 | ||||||
| chr11:431162
|
G | GGGGGGTG others(439): Show |
1 | a0006c0019t0001g0142 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(446): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGG others(923): Show |
1 | a0002c0002t0001g0036 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.539+531_539+532ins others(930): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(434): Show |
1 | a0001c0001t0001g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.539+531_539+532ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(195): Show |
1 | a0001c0001t0001g0076 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.539+531_539+532ins others(202): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(442): Show |
1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539+531_539+532ins others(449): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(436): Show |
1 | a0001c0001t0002g0143 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(436): Show |
1 | a0001c0001t0001g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.539+531_539+532ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(438): Show |
1 | a0001c0001t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(445): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(436): Show |
2 | a0001c0001t0001g0145a0001c0001t0002g0141 | 2 | HG01168.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.539+531_539+532ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(435): Show |
24 | a0001c0001t0001g0006a0001c0001t0001g0077a0001c0001t0001g0078others(21): Show | 25 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.539+531_539+532ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(437): Show |
1 | a0001c0001t0001g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(436): Show |
1 | a0004c0004t0001g0030 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.539+531_539+532ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(1355): Show |
1 | a0001c0001t0001g0125 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(1362): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(435): Show |
1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(436): Show |
1 | a0001c0001t0001g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(515): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0117 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.539+531_539+532ins others(522): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(518): Show |
1 | a0001c0001t0001g0114 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(525): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431162
|
G | GGGGGTGT others(436): Show |
1 | a0001c0001t0004g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.539+531_539+532ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431162 | ||||||
| chr11:431163
|
G | GGGGGTGT others(435): Show |
1 | a0001c0001t0001g0250 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.539+530_539+531ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(195): Show |
1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(202): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(438): Show |
1 | a0001c0001t0001g0268 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.539+530_539+531ins others(445): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(434): Show |
1 | a0001c0001t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(434): Show |
1 | a0001c0001t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(435): Show |
1 | a0001c0001t0001g0205 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(436): Show |
1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(436): Show |
1 | a0001c0001t0001g0249 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(434): Show |
2 | a0001c0001t0001g0204a0001c0001t0001g0216 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.539+530_539+531ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(435): Show |
1 | a0001c0001t0001g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.539+530_539+531ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(434): Show |
77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0137others(74): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.539+530_539+531ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(435): Show |
1 | a0001c0001t0001g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.539+530_539+531ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431163
|
G | GGGGTGTG others(434): Show |
1 | a0001c0001t0001g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.539+530_539+531ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431163 | ||||||
| chr11:431165
|
G | GGTGTGGG others(441): Show |
1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.539+528_539+529ins others(448): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431165 | ||||||
| chr11:431202
|
A | AGGGGTGT others(435): Show |
1 | a0001c0001t0001g0203 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.539+491_539+492ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431202 | ||||||
| chr11:431205
|
G | GGTGTGGG others(433): Show |
1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.539+488_539+489ins others(440): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431205 | ||||||
| chr11:431205
|
G | GGTGTGGG others(435): Show |
1 | a0008c0012t0001g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.539+488_539+489ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431205 | ||||||
| chr11:431205
|
G | GGTGTGGG others(434): Show |
2 | a0008c0012t0001g0191a0008c0012t0001g0192 | 2 | HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.539+488_539+489ins others(441): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431205 | ||||||
| chr11:431205
|
G | GGTGTGGG others(435): Show |
1 | a0001c0001t0003g0009 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.539+488_539+489ins others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431205 | ||||||
| chr11:431209
|
T | TGGGGCTC others(436): Show |
1 | a0001c0001t0001g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539+484_539+485ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431209 | ||||||
| chr11:431209
|
TG | T | 9 | a0001c0001t0001g0178a0001c0001t0001g0193a0001c0001t0001g0218others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.539+484delC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431209 | ||||||
| chr11:431210
|
G | GGGGCTCC others(433): Show |
1 | a0001c0001t0001g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.539+483_539+484ins others(440): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431210 | ||||||
| chr11:431241
|
C | CG | 5 | a0001c0001t0001g0078a0001c0001t0001g0210a0002c0002t0001g0081others(2): Show | 5 | HG01891.hp1 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+452dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431241 | ||||||
| chr11:431241
|
C | CGGGGGTG others(1393): Show |
1 | a0001c0001t0001g0112 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.539+452_539+453ins others(1400): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431241 | ||||||
| chr11:431281
|
C | CGGGGGGT others(449): Show |
1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.539+412_539+413ins others(456): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431281 | ||||||
| chr11:431286
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.539+408C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431286 | ||||||
| chr11:431299
|
C | T | 109 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0105others(106): Show | 109 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.539+395G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431299 | ||||||
| chr11:431309
|
T | TG | 148 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(145): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.539+384dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(681): Show |
1 | a0001c0001t0001g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(688): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(923): Show |
1 | a0004c0004t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(930): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(922): Show |
1 | a0002c0002t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(929): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(1381): Show |
1 | a0001c0001t0001g0265 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(1388): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(440): Show |
1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(447): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0002c0002t0001g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(436): Show |
1 | a0001c0001t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0001c0001t0001g0178 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0010c0014t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0001c0001t0001g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(436): Show |
2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.539+384_539+385ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0001c0001t0001g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(436): Show |
80 | a0001c0001t0001g0021a0001c0001t0001g0105a0001c0001t0001g0107others(77): Show | 80 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.539+384_539+385ins others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(920): Show |
1 | a0002c0002t0001g0045 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(927): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0002c0002t0001g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(439): Show |
1 | a0002c0002t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(446): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(440): Show |
1 | a0001c0001t0001g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(447): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(437): Show |
1 | a0001c0001t0001g0152 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(444): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
T | TGGGGGCT others(442): Show |
1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.539+384_539+385ins others(449): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431309
|
TG | T | 8 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+384delC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431309 | ||||||
| chr11:431320
|
T | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+374A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431320 | ||||||
| chr11:431322
|
C | CG | 7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0151others(4): Show | 7 | HG00741.hp1 HG01255.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+371dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431322 | ||||||
| chr11:431362
|
C | CG | 6 | a0001c0001t0001g0080a0001c0001t0001g0148a0001c0001t0001g0205others(3): Show | 6 | HG01175.hp1 HG01433.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+331dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431362 | ||||||
| chr11:431400
|
T | C | 8 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.539+294A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431400 | ||||||
| chr11:431407
|
A | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(9): Show | 13 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.539+287T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431407 | ||||||
| chr11:431443
|
G | GGGGGTGT others(195): Show |
1 | a0001c0006t0003g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539+250_539+251ins others(202): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431443 | ||||||
| chr11:431451
|
G | A | 7 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.539+243C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431451 | ||||||
| chr11:431458
|
C | CCCGCGGG others(398): Show |
1 | a0001c0001t0001g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.539+235_539+236ins others(405): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431458 | ||||||
| chr11:431458
|
C | CCCGCGGG others(398): Show |
1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.539+235_539+236ins others(405): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431458 | ||||||
| chr11:431458
|
C | CCCGCGGG others(397): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0252a0001c0001t0001g0272 | 3 | HG01243.hp1 HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.539+235_539+236ins others(404): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431458 | ||||||
| chr11:431458
|
C | CCCGCGGG others(397): Show |
1 | a0001c0001t0001g0116 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.539+235_539+236ins others(404): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431458 | ||||||
| chr11:431462
|
C | T | 1 | a0001c0006t0003g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539+232G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431462 | ||||||
| chr11:431480
|
T | C | 1 | a0001c0006t0003g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539+214A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431480 | ||||||
| chr11:431483
|
A | AG | 4 | a0001c0001t0001g0080a0001c0001t0001g0178a0001c0001t0001g0184others(1): Show | 4 | HG01981.hp2 HG03654.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+210dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431483 | ||||||
| chr11:431483
|
A | G | 12 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(9): Show | 13 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.539+211T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431483 | ||||||
| chr11:431498
|
C | CCCGTGGG others(34): Show |
1 | a0004c0004t0001g0030 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.539+195_539+196ins others(41): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(36): Show |
3 | a0001c0001t0002g0143a0002c0002t0001g0037a0007c0008t0001g0158 | 3 | HG01169.hp2 HG01928.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.539+195_539+196ins others(43): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(35): Show |
97 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.539+195_539+196ins others(42): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(157): Show |
1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.539+195_539+196ins others(164): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(961): Show |
1 | a0001c0001t0001g0079 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.539+195_539+196ins others(968): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(156): Show |
1 | a0014c0022t0001g0051 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.539+195_539+196ins others(163): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(36): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0145 | 2 | HG01891.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.539+195_539+196ins others(43): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(37): Show |
1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.539+195_539+196ins others(44): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(479): Show |
1 | a0001c0001t0001g0240 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.539+195_539+196ins others(486): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(605): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.539+195_539+196ins others(612): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431498
|
C | CCCGTGGG others(36): Show |
1 | a0001c0001t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539+195_539+196ins others(43): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431498 | ||||||
| chr11:431500
|
C | CGTGGGTA others(278): Show |
1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539+193_539+194ins others(285): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431500
|
C | CGTGGGTA others(277): Show |
1 | a0001c0001t0001g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.539+193_539+194ins others(284): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431500
|
C | CGTGGGTA others(276): Show |
1 | a0001c0001t0001g0076 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.539+193_539+194ins others(283): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431500
|
C | CGTGGGTA others(276): Show |
1 | a0001c0001t0004g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.539+193_539+194ins others(283): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431500
|
C | CGTGGGTA others(276): Show |
1 | a0001c0001t0001g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.539+193_539+194ins others(283): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431500
|
C | CGTGGGTA others(275): Show |
1 | a0001c0001t0001g0157 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.539+193_539+194ins others(282): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431500
|
C | CGTGGGTA others(276): Show |
1 | a0001c0001t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+193_539+194ins others(283): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431500 | ||||||
| chr11:431502
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(127): Show | 134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.539+192G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431502 | ||||||
| chr11:431510
|
T | TGG | 129 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(126): Show | 133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.539+182_539+183dup others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431510 | ||||||
| chr11:431517
|
T | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(127): Show | 134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.539+177A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431517 | ||||||
| chr11:431517
|
T | G | 10 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(7): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+177A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431517 | ||||||
| chr11:431520
|
C | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(137): Show | 145 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.539+174G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431520 | ||||||
| chr11:431523
|
G | A | 9 | a0001c0001t0001g0116a0001c0001t0001g0148a0001c0001t0001g0193others(6): Show | 9 | HG00323.hp2 HG01243.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+171C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431523 | ||||||
| chr11:431535
|
G | T | 106 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(103): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.539+159C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431535 | ||||||
| chr11:431537
|
T | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(126): Show | 133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.539+157A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431537 | ||||||
| chr11:431538
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(126): Show | 133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.539+156G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431538 | ||||||
| chr11:431542
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0076others(134): Show | 141 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.539+152A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431542 | ||||||
| chr11:431544
|
G | A | 1 | a0001c0006t0003g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539+150C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431544 | ||||||
| chr11:431550
|
T | TGG | 10 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(7): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+142_539+143dup others(2): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431550 | ||||||
| chr11:431557
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+137C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431557 | ||||||
| chr11:431557
|
G | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(127): Show | 134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.539+137C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431557 | ||||||
| chr11:431560
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(130): Show | 137 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.539+134A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431560 | ||||||
| chr11:431562
|
C | CG | 5 | a0001c0001t0001g0112a0001c0001t0001g0245a0002c0002t0002g0025others(2): Show | 5 | HG00741.hp2 HG01928.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+131dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431562 | ||||||
| chr11:431577
|
T | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(127): Show | 134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.539+117A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431577 | ||||||
| chr11:431577
|
T | G | 10 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(7): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+117A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431577 | ||||||
| chr11:431578
|
C | T | 10 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(7): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+116G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431578 | ||||||
| chr11:431582
|
C | T | 3 | a0001c0001t0001g0148a0010c0014t0001g0026a0014c0022t0001g0051 | 3 | HG00323.hp2 HG01433.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.539+112G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431582 | ||||||
| chr11:431597
|
T | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0076others(132): Show | 139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.539+97A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431597
|
T | TTCTGCAG others(440): Show |
1 | a0004c0004t0001g0030 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.539+96_539+97insCG others(445): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431597
|
T | TTCTGCAG others(438): Show |
1 | a0002c0002t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.539+96_539+97insCG others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431597
|
T | TTCTGCAG others(438): Show |
1 | a0004c0004t0001g0035 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.539+96_539+97insCG others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431597
|
T | TTCTGCAG others(437): Show |
22 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0027others(19): Show | 22 | HG00280.hp2 HG00438.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.539+96_539+97insCG others(442): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431597
|
T | TTCTGCAG others(438): Show |
1 | a0002c0002t0001g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.539+96_539+97insCG others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431597
|
T | TTCTGCAG others(438): Show |
1 | a0002c0002t0001g0073 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.539+96_539+97insCG others(443): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431597 | ||||||
| chr11:431600
|
C | CGCGGGGG others(33): Show |
10 | a0001c0001t0001g0116a0001c0001t0001g0193a0001c0001t0001g0219others(7): Show | 11 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.539+93_539+94insAG others(38): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGCGGGGG others(318): Show |
1 | a0014c0022t0001g0051 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(323): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGCGGGGG others(320): Show |
1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(325): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(883): Show |
1 | a0001c0001t0001g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(888): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(882): Show |
1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(887): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0001c0001t0001g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(879): Show |
2 | a0001c0001t0001g0105a0001c0001t0004g0118 | 2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.539+93_539+94insAG others(884): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0001c0001t0004g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(876): Show |
1 | a0002c0002t0001g0062 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(881): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(882): Show |
1 | a0010c0014t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(887): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(840): Show |
1 | a0001c0001t0001g0165 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(845): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
2 | a0002c0002t0007g0067a0007c0008t0001g0144 | 2 | HG00738.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(882): Show |
1 | a0001c0001t0001g0145 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(887): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0001c0020t0001g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(881): Show |
1 | a0006c0009t0001g0124 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(886): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(881): Show |
1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(886): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0001c0001t0002g0141 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(882): Show |
1 | a0002c0002t0001g0098 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(887): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(799): Show |
1 | a0002c0002t0002g0074 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(804): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0002c0002t0001g0065 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(879): Show |
45 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0077others(42): Show | 46 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.539+93_539+94insAG others(884): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(879): Show |
1 | a0002c0002t0001g0274 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(884): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(881): Show |
1 | a0002c0002t0001g0066 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(886): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0002c0002t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0011c0016t0001g0170 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0001c0001t0002g0143 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(880): Show |
1 | a0002c0002t0001g0018 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(885): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(883): Show |
1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(888): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(881): Show |
1 | a0001c0001t0001g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(886): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(882): Show |
1 | a0001c0001t0001g0146 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(887): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(879): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.539+93_539+94insAG others(884): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(881): Show |
1 | a0001c0001t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.539+93_539+94insAG others(886): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | CGTGGGGG others(887): Show |
1 | a0006c0019t0001g0142 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.539+93_539+94insAG others(892): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431600
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(154): Show | 161 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.539+94G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431600 | ||||||
| chr11:431602
|
C | CGGGGGTG others(319): Show |
1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.539+91_539+92insCG others(324): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431602 | ||||||
| chr11:431602
|
C | T | 2 | a0001c0001t0001g0240a0002c0002t0001g0081 | 2 | NA18967.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.539+92G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431602 | ||||||
| chr11:431607
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.539+87C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431607 | ||||||
| chr11:431622
|
C | CGGGTATC others(642): Show |
1 | a0001c0001t0001g0076 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.539+71_539+72insAC others(647): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(1578): Show |
1 | a0001c0001t0001g0080 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539+71_539+72insAC others(1583): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(640): Show |
1 | a0001c0001t0001g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.539+71_539+72insAC others(645): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(639): Show |
2 | a0001c0001t0001g0157a0001c0001t0004g0113 | 2 | HG03471.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.539+71_539+72insAC others(644): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(640): Show |
1 | a0001c0001t0001g0149 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.539+71_539+72insAC others(645): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(644): Show |
1 | a0001c0001t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.539+71_539+72insAC others(649): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(878): Show |
1 | a0001c0006t0003g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539+71_539+72insAC others(883): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(887): Show |
1 | a0001c0001t0001g0240 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.539+71_539+72insAC others(892): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(1642): Show |
1 | a0009c0011t0001g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.539+71_539+72insAC others(1647): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(1641): Show |
1 | a0009c0011t0001g0005 | 2 | HG01081.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.539+71_539+72insAC others(1646): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(879): Show |
1 | a0001c0001t0001g0132 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.539+71_539+72insAC others(884): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | CGGGTATC others(1646): Show |
1 | a0009c0011t0001g0095 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.539+71_539+72insAC others(1651): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431622
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(244): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.539+72G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431622 | ||||||
| chr11:431630
|
T | TGGGGGCT others(911): Show |
1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.539+63_539+64insCA others(916): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431630 | ||||||
| chr11:431649
|
C | CG | 4 | a0001c0001t0002g0141a0001c0020t0001g0169a0003c0010t0001g0088others(1): Show | 4 | HG00323.hp2 HG00735.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+44dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 7/22 | chr11 | 431649 | ||||||
| chr11:431834
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.465+14T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 6/22 | chr11 | 431834 | ||||||
| chr11:432213
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0120others(100): Show | 107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.351-159C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432213 | ||||||
| chr11:432436
|
G | A | 146 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.351-382C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432436 | ||||||
| chr11:432558
|
G | A | 1 | a0001c0006t0006g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.351-504C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432558 | ||||||
| chr11:432633
|
C | T | 4 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0016others(1): Show | 5 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.351-579G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432633 | ||||||
| chr11:432664
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.351-610C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432664 | ||||||
| chr11:432746
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0003g0009 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.350+568G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432746 | ||||||
| chr11:432765
|
T | G | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.350+549A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432765 | ||||||
| chr11:432813
|
A | G | 3 | a0008c0012t0001g0190a0008c0012t0001g0191a0008c0012t0001g0192 | 3 | HG02970.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.350+501T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432813 | ||||||
| chr11:432826
|
C | G | 1 | a0001c0001t0002g0156 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.350+488G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432826 | ||||||
| chr11:432836
|
C | G | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.350+478G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432836 | ||||||
| chr11:432876
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.350+438C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432876 | ||||||
| chr11:432964
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.350+350C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 432964 | ||||||
| chr11:433053
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.350+261A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 433053 | ||||||
| chr11:433095
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0003g0009 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.350+219A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 433095 | ||||||
| chr11:433135
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(256): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.350+179A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 433135 | ||||||
| chr11:433248
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.350+66C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 4/22 | chr11 | 433248 | ||||||
| chr11:433514
|
G | GCCTCAGA others(20): Show |
21 | a0001c0001t0001g0204a0001c0001t0001g0210a0001c0001t0001g0211others(18): Show | 21 | HG00741.hp1 HG01358.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.205-56_205-55insTG others(25): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433514 | ||||||
| chr11:433514
|
G | GCCTCAGA others(47): Show |
1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.205-56_205-55insTG others(52): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433514 | ||||||
| chr11:433532
|
C | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0112others(83): Show | 90 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.205-73G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433532 | ||||||
| chr11:433538
|
T | C | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-79A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433538 | ||||||
| chr11:433541
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-82T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433541 | ||||||
| chr11:433541
|
ACCTCAGA others(20): Show |
A | 3 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01981.hp1 NA18971.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.205-109_205-83delC others(26): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433541 | ||||||
| chr11:433554
|
C | T | 91 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(88): Show | 92 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.205-95G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433554 | ||||||
| chr11:433568
|
G | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(251): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.205-109C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433568 | ||||||
| chr11:433568
|
G | GCCTCAGA others(20): Show |
1 | a0003c0003t0001g0093 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.205-110_205-109ins others(27): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433568 | ||||||
| chr11:433617
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(256): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.205-158A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433617 | ||||||
| chr11:433809
|
G | C | 1 | a0010c0014t0001g0026 | 1 | NA18994.hp1 | splice_region_variant&intron_variant | LOW | c.204+6C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 3/22 | chr11 | 433809 | ||||||
| chr11:433965
|
G | A | 65 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.82-28C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 2/22 | chr11 | 433965 | ||||||
| chr11:433995
|
G | A | 147 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(144): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.81+29C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 2/22 | chr11 | 433995 | ||||||
| chr11:434232
|
G | A | 3 | a0002c0002t0001g0099a0002c0002t0001g0100a0002c0002t0001g0101 | 3 | HG00642.hp2 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.7-134C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434232 | ||||||
| chr11:434356
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.7-258C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434356 | ||||||
| chr11:434396
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.7-298G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434396 | ||||||
| chr11:434540
|
G | A | 9 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0178others(6): Show | 9 | HG00558.hp2 HG02129.hp2 HG03704.hp1 others(6): Show |
intron_variant | MODIFIER | c.7-442C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434540 | ||||||
| chr11:434603
|
A | T | 1 | a0003c0003t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7-505T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434603 | ||||||
| chr11:434659
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(109): Show | 116 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.7-561C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434659 | ||||||
| chr11:434895
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7-797C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434895 | ||||||
| chr11:434896
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7-798G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434896 | ||||||
| chr11:434898
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7-800A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434898 | ||||||
| chr11:434899
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7-801G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 434899 | ||||||
| chr11:435195
|
C | CATAGCAT others(3): Show |
3 | a0008c0012t0001g0190a0008c0012t0001g0191a0008c0012t0001g0192 | 3 | HG02970.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.7-1107_7-1098dupAC others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435195 | ||||||
| chr11:435246
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7-1148T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435246 | ||||||
| chr11:435251
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7-1153G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435251 | ||||||
| chr11:435253
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7-1155T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435253 | ||||||
| chr11:435258
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7-1160C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435258 | ||||||
| chr11:435261
|
A | ATAGTC | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(174): Show | 183 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.7-1168_7-1164dupGA others(3): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435261 | ||||||
| chr11:435261
|
A | ATAGTCTA others(3): Show |
5 | a0001c0001t0001g0202a0001c0001t0001g0207a0001c0001t0001g0243others(2): Show | 5 | HG00408.hp2 HG02027.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-1173_7-1164dupGA others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435261 | ||||||
| chr11:435261
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7-1163T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435261 | ||||||
| chr11:435261
|
ATAGTC | A | 65 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.7-1168_7-1164delGA others(3): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435261 | ||||||
| chr11:435354
|
G | T | 146 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(143): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.7-1256C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435354 | ||||||
| chr11:435463
|
A | T | 65 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.7-1365T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435463 | ||||||
| chr11:435476
|
A | G | 1 | a0002c0002t0001g0274 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7-1378T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435476 | ||||||
| chr11:435488
|
G | A | 21 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0028others(18): Show | 21 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.7-1390C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435488 | ||||||
| chr11:435501
|
A | ATAGTCTA others(38): Show |
1 | a0001c0001t0001g0240 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.7-1404_7-1403insGA others(43): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435501 | ||||||
| chr11:435501
|
A | ATAGTCTA others(43): Show |
114 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(111): Show | 119 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.7-1453_7-1404dupGA others(48): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435501 | ||||||
| chr11:435503
|
A | AGTCTAGT others(38): Show |
3 | a0001c0001t0004g0113a0001c0001t0004g0118a0001c0001t0004g0119 | 3 | HG03471.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.7-1406_7-1405insCA others(43): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435503 | ||||||
| chr11:435503
|
A | AGTCTAGT others(38): Show |
138 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.7-1450_7-1406dupCA others(43): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435503 | ||||||
| chr11:435528
|
A | AGTCTAGT others(13): Show |
2 | a0001c0001t0001g0152a0006c0019t0001g0142 | 2 | HG01071.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.7-1450_7-1431dupCA others(18): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435528 | ||||||
| chr11:435658
|
GGTCTAGT others(23): Show |
G | 1 | a0002c0002t0001g0075 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7-1590_7-1561delTA others(28): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435658 | ||||||
| chr11:435683
|
GGTCTA | G | 147 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(144): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.7-1590_7-1586delTA others(3): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435683 | ||||||
| chr11:435763
|
A | C | 7 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0001g0060others(4): Show | 7 | HG01074.hp1 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.7-1665T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435763 | ||||||
| chr11:435833
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7-1735C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435833 | ||||||
| chr11:435836
|
ATAGTC | A | 142 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.7-1743_7-1739delGA others(3): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435836 | ||||||
| chr11:435836
|
ATAGTCTA others(3): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7-1748_7-1739delGA others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435836 | ||||||
| chr11:435904
|
G | A | 146 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(143): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.7-1806C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435904 | ||||||
| chr11:435941
|
A | G | 65 | a0002c0002t0001g0017a0002c0002t0001g0018a0002c0002t0001g0019others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.7-1843T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 435941 | ||||||
| chr11:436063
|
C | CT | 11 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0115others(8): Show | 11 | HG01169.hp1 HG01175.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.7-1966dupA | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436063 | ||||||
| chr11:436063
|
CT | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(112): Show | 119 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.7-1966delA | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436063 | ||||||
| chr11:436068
|
T | A | 5 | a0001c0001t0001g0082a0001c0001t0003g0009a0008c0012t0001g0190others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-1970A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436068 | ||||||
| chr11:436154
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.7-2056T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436154 | ||||||
| chr11:436217
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7-2119C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436217 | ||||||
| chr11:436253
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.7-2155C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436253 | ||||||
| chr11:436287
|
G | A | 1 | a0002c0002t0001g0052 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.7-2189C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436287 | ||||||
| chr11:436313
|
C | T | 1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2215G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436313 | ||||||
| chr11:436461
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(103): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.7-2363A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436461 | ||||||
| chr11:436646
|
G | T | 1 | a0005c0007t0001g0201 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.7-2548C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436646 | ||||||
| chr11:436692
|
GAGCAGGG others(4): Show |
G | 6 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 6 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-2605_7-2595delTA others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436692 | ||||||
| chr11:436697
|
GGGGGTAA others(91): Show |
G | 2 | a0002c0002t0001g0024a0004c0004t0001g0030 | 2 | HG00438.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.7-2697_7-2600delAG others(96): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436697 | ||||||
| chr11:436698
|
GGGGTAAG others(114): Show |
G | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(84): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.7-2721_7-2601del | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436698 | ||||||
| chr11:436703
|
A | G | 163 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(160): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.7-2605T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436703 | ||||||
| chr11:436707
|
A | T | 6 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 6 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.7-2609T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436707 | ||||||
| chr11:436709
|
G | A | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7-2611C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436709 | ||||||
| chr11:436711
|
G | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(160): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.7-2613C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436711 | ||||||
| chr11:436720
|
GGGGTGAG others(92): Show |
G | 70 | a0001c0001t0001g0082a0001c0001t0001g0250a0001c0001t0001g0251others(67): Show | 71 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.7-2721_7-2623delTC others(97): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436720 | ||||||
| chr11:436721
|
G | GAGTGAGC others(4): Show |
1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2624_7-2623insTC others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436721 | ||||||
| chr11:436722
|
G | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.7-2624C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436722 | ||||||
| chr11:436723
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.7-2625C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436723 | ||||||
| chr11:436729
|
T | A | 98 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(95): Show | 99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.7-2631A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436729 | ||||||
| chr11:436732
|
G | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.7-2634C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436732 | ||||||
| chr11:436740
|
A | T | 92 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.7-2642T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436740 | ||||||
| chr11:436744
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2646C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436744 | ||||||
| chr11:436751
|
AGGGGGTA others(103): Show |
A | 1 | a0002c0002t0001g0029 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.7-2763_7-2654del | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436751 | ||||||
| chr11:436755
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(88): Show | 92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.7-2657C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436755 | ||||||
| chr11:436758
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(89): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.7-2660T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436758 | ||||||
| chr11:436773
|
AGGGGGTG others(15): Show |
A | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2697_7-2676delAG others(20): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436773 | ||||||
| chr11:436775
|
G | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2677C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436775 | ||||||
| chr11:436775
|
GGGGTGAG others(115): Show |
G | 1 | a0001c0001t0001g0249 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.7-2799_7-2678del | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436775 | ||||||
| chr11:436776
|
G | A | 1 | a0007c0008t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7-2678C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436776 | ||||||
| chr11:436780
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2682C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436780 | ||||||
| chr11:436784
|
T | A | 81 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(78): Show | 82 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.7-2686A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436784 | ||||||
| chr11:436784
|
T | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2686A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436784 | ||||||
| chr11:436787
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2689C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436787 | ||||||
| chr11:436791
|
G | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.7-2693C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436791 | ||||||
| chr11:436795
|
T | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.7-2697A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436795 | ||||||
| chr11:436795
|
T | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2697A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436795 | ||||||
| chr11:436799
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2701C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436799 | ||||||
| chr11:436806
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2708T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436806 | ||||||
| chr11:436807
|
GGAGGTGA others(3): Show |
G | 1 | a0006c0019t0001g0142 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7-2719_7-2710delTG others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436807 | ||||||
| chr11:436808
|
G | T | 7 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-2710C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436808 | ||||||
| chr11:436809
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(93): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.7-2711T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436809 | ||||||
| chr11:436810
|
G | A | 2 | a0002c0002t0001g0024a0004c0004t0001g0030 | 2 | HG00438.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.7-2712C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436810 | ||||||
| chr11:436811
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2713C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436811 | ||||||
| chr11:436813
|
G | A | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2715C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436813 | ||||||
| chr11:436817
|
A | G | 9 | a0001c0001t0001g0109a0001c0001t0001g0121a0001c0001t0001g0174others(6): Show | 9 | HG01168.hp2 HG01934.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-2719T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436817 | ||||||
| chr11:436817
|
A | T | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.7-2719T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436817 | ||||||
| chr11:436819
|
A | G | 65 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(62): Show | 66 | HG00438.hp2 HG00735.hp1 HG01123.hp2 others(63): Show |
intron_variant | MODIFIER | c.7-2721T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436819 | ||||||
| chr11:436819
|
A | T | 34 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-2721T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436819 | ||||||
| chr11:436820
|
G | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-2722C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436820 | ||||||
| chr11:436821
|
G | A | 71 | a0001c0001t0001g0082a0001c0001t0001g0250a0001c0001t0001g0251others(68): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.7-2723C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436821 | ||||||
| chr11:436827
|
CA | C | 34 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-2730delT | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436827 | ||||||
| chr11:436828
|
A | AGGGGGTG others(48): Show |
1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2731_7-2730insCG others(53): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436828 | ||||||
| chr11:436828
|
A | G | 9 | a0001c0001t0001g0109a0001c0001t0001g0121a0001c0001t0001g0174others(6): Show | 9 | HG01168.hp2 HG01934.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.7-2730T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436828 | ||||||
| chr11:436830
|
G | T | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0108others(22): Show | 25 | HG01123.hp2 HG01255.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.7-2732C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436830 | ||||||
| chr11:436831
|
G | A | 72 | a0001c0001t0001g0082a0001c0001t0001g0250a0001c0001t0001g0251others(69): Show | 73 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.7-2733C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436831 | ||||||
| chr11:436832
|
A | G | 128 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(125): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.7-2734T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436832 | ||||||
| chr11:436832
|
AGTGAGCT others(3): Show |
A | 34 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.7-2744_7-2735delCC others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436832 | ||||||
| chr11:436839
|
T | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(104): Show | 112 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.7-2741A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436839 | ||||||
| chr11:436839
|
T | G | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0108others(25): Show | 28 | HG01123.hp2 HG01168.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.7-2741A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436839 | ||||||
| chr11:436841
|
G | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 19 | HG01256.hp2 HG01258.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.7-2743C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436841 | ||||||
| chr11:436842
|
G | A | 32 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0108others(29): Show | 32 | HG01123.hp2 HG01255.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.7-2744C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436842 | ||||||
| chr11:436843
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(84): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.7-2745C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436843 | ||||||
| chr11:436844
|
G | A | 7 | a0001c0001t0001g0174a0001c0001t0001g0184a0001c0001t0001g0185others(4): Show | 7 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.7-2746C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436844 | ||||||
| chr11:436850
|
G | A | 167 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(164): Show | 172 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.7-2752C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436850 | ||||||
| chr11:436853
|
G | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(104): Show | 112 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.7-2755C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436853 | ||||||
| chr11:436853
|
GAGTGAGC others(37): Show |
G | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7-2799_7-2756delTC others(42): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436853 | ||||||
| chr11:436854
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 129 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.7-2756T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436854 | ||||||
| chr11:436858
|
A | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2760T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436858 | ||||||
| chr11:436861
|
T | A | 80 | a0001c0001t0001g0082a0001c0001t0001g0250a0001c0001t0001g0251others(77): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.7-2763A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436861 | ||||||
| chr11:436861
|
T | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(26): Show | 30 | HG00735.hp1 HG01168.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.7-2763A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436861 | ||||||
| chr11:436861
|
TGGGGGTG others(26): Show |
T | 4 | a0001c0001t0001g0112a0001c0001t0001g0120a0001c0001t0001g0147others(1): Show | 4 | HG01433.hp1 HG01496.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-2796_7-2764delTG others(31): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436861 | ||||||
| chr11:436863
|
G | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2765C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436863 | ||||||
| chr11:436864
|
G | A | 55 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0102others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.7-2766C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436864 | ||||||
| chr11:436865
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(18): Show | 22 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.7-2767C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436865 | ||||||
| chr11:436866
|
G | A | 55 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0102others(52): Show | 55 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.7-2768C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436866 | ||||||
| chr11:436866
|
GTGAGCAG others(147): Show |
G | 5 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG01934.hp2 HG01975.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.7-2922_7-2769del | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436866 | ||||||
| chr11:436869
|
A | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0121a0002c0002t0001g0097 | 3 | HG01168.hp2 HG02683.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.7-2771T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436869 | ||||||
| chr11:436871
|
CAGGGGGT others(146): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.7-2926_7-2774del | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436871 | ||||||
| chr11:436872
|
A | G | 66 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0102others(63): Show | 66 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.7-2774T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436872 | ||||||
| chr11:436872
|
A | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(17): Show | 21 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-2774T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436872 | ||||||
| chr11:436875
|
G | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(25): Show | 29 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.7-2777C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436875 | ||||||
| chr11:436875
|
GGGTGAGC others(15): Show |
G | 52 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0102others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.7-2799_7-2778delTC others(20): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436875 | ||||||
| chr11:436875
|
GGGTGAGC others(48): Show |
G | 1 | a0001c0001t0001g0138 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7-2832_7-2778delTC others(53): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436875 | ||||||
| chr11:436876
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(84): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.7-2778C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436876 | ||||||
| chr11:436877
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(17): Show | 21 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.7-2779C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436877 | ||||||
| chr11:436883
|
A | G | 30 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(27): Show | 31 | HG00735.hp1 HG01099.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.7-2785T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436883 | ||||||
| chr11:436883
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2785T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436883 | ||||||
| chr11:436884
|
GGGGGTAA others(14): Show |
G | 2 | a0001c0001t0001g0149a0006c0019t0001g0142 | 2 | HG01099.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.7-2807_7-2787delTG others(19): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436884 | ||||||
| chr11:436886
|
GGGTAAGC others(4): Show |
G | 16 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(13): Show | 17 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.7-2799_7-2789delTC others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436886 | ||||||
| chr11:436887
|
G | A | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2789C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436887 | ||||||
| chr11:436888
|
G | T | 1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.7-2790C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436888 | ||||||
| chr11:436889
|
T | A | 1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.7-2791A>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436889 | ||||||
| chr11:436890
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(100): Show | 107 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.7-2792T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436890 | ||||||
| chr11:436894
|
A | G | 4 | a0001c0001t0001g0145a0001c0001t0004g0113a0005c0007t0001g0198others(1): Show | 4 | HG03471.hp2 HG03942.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-2796T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436894 | ||||||
| chr11:436894
|
A | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(5): Show | 8 | HG01943.hp1 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.7-2796T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436894 | ||||||
| chr11:436895
|
GGAGGTGA others(3): Show |
G | 1 | a0001c0001t0004g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7-2807_7-2798delTG others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436895 | ||||||
| chr11:436897
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(163): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.7-2799T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436897 | ||||||
| chr11:436899
|
G | A | 12 | a0001c0001t0001g0112a0001c0001t0001g0120a0001c0001t0001g0147others(9): Show | 12 | HG01433.hp1 HG01496.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.7-2801C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436899 | ||||||
| chr11:436905
|
A | AGTGGGTG others(202): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0121 | 2 | HG01168.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.7-2808_7-2807insCG others(207): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436905 | ||||||
| chr11:436905
|
A | G | 84 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(81): Show | 85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.7-2807T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436905 | ||||||
| chr11:436912
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(84): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.7-2814C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436912 | ||||||
| chr11:436913
|
A | C | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.7-2815T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436913 | ||||||
| chr11:436915
|
C | T | 1 | a0003c0005t0001g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.7-2817G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436915 | ||||||
| chr11:436916
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(148): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.7-2818C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436916 | ||||||
| chr11:436916
|
G | T | 10 | a0001c0001t0001g0082a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 11 | HG01109.hp1 HG01433.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.7-2818C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436916 | ||||||
| chr11:436917
|
G | A | 1 | a0002c0002t0001g0069 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.7-2819C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436917 | ||||||
| chr11:436919
|
GGGTGAGC others(4): Show |
G | 2 | a0001c0001t0001g0082a0001c0001t0003g0009 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7-2832_7-2822delTC others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436919 | ||||||
| chr11:436920
|
GGTGAGCA others(3): Show |
G | 1 | a0001c0001t0001g0145 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7-2832_7-2823delTC others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436920 | ||||||
| chr11:436923
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2825C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436923 | ||||||
| chr11:436924
|
A | C | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.7-2826T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436924 | ||||||
| chr11:436926
|
C | CG | 6 | a0001c0001t0001g0112a0001c0001t0001g0120a0001c0001t0001g0121others(3): Show | 6 | HG01168.hp1 HG01168.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-2829_7-2828insC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436926 | ||||||
| chr11:436926
|
C | T | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.7-2828G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436926 | ||||||
| chr11:436927
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.7-2829T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436927 | ||||||
| chr11:436930
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(245): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.7-2832T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436930 | ||||||
| chr11:436930
|
AGGTGAGC others(4): Show |
A | 1 | a0003c0003t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.7-2843_7-2833delCC others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436930 | ||||||
| chr11:436935
|
A | C | 83 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(80): Show | 84 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.7-2837T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436935 | ||||||
| chr11:436937
|
C | CGGGGGGG others(6): Show |
1 | a0001c0001t0001g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.7-2840_7-2839insCG others(11): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436937 | ||||||
| chr11:436938
|
A | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.7-2840T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436938 | ||||||
| chr11:436938
|
A | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(87): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.7-2840T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436938 | ||||||
| chr11:436940
|
G | T | 21 | a0001c0001t0001g0250a0001c0001t0001g0251a0002c0002t0001g0019others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.7-2842C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436940 | ||||||
| chr11:436946
|
A | C | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.7-2848T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436946 | ||||||
| chr11:436948
|
C | CGGGGGGT others(5): Show |
1 | a0001c0001t0001g0112 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.7-2851_7-2850insCG others(10): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436948 | ||||||
| chr11:436948
|
C | CGGGGGGT others(4): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.7-2851_7-2850insAC others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436948 | ||||||
| chr11:436948
|
C | T | 60 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 61 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.7-2850G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436948 | ||||||
| chr11:436949
|
A | G | 109 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(106): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.7-2851T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436949 | ||||||
| chr11:436951
|
G | T | 49 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0017others(46): Show | 50 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.7-2853C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436951 | ||||||
| chr11:436952
|
G | A | 21 | a0001c0001t0001g0250a0001c0001t0001g0251a0002c0002t0001g0019others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.7-2854C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436952 | ||||||
| chr11:436954
|
GTGAGCAG others(59): Show |
G | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.7-2922_7-2857delTC others(64): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436954 | ||||||
| chr11:436960
|
A | G | 72 | a0001c0001t0001g0138a0001c0001t0001g0250a0001c0001t0001g0251others(69): Show | 73 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.7-2862T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436960 | ||||||
| chr11:436960
|
A | T | 87 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.7-2862T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436960 | ||||||
| chr11:436962
|
G | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(87): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.7-2864C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436962 | ||||||
| chr11:436963
|
G | A | 50 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0017others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-2865C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436963 | ||||||
| chr11:436964
|
G | A | 22 | a0001c0001t0001g0138a0001c0001t0001g0250a0001c0001t0001g0251others(19): Show | 22 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.7-2866C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436964 | ||||||
| chr11:436971
|
A | AG | 5 | a0001c0001t0001g0112a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG00741.hp2 HG01496.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.7-2874dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436971 | ||||||
| chr11:436971
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(137): Show | 145 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.7-2873T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436971 | ||||||
| chr11:436971
|
A | T | 21 | a0001c0001t0001g0250a0001c0001t0001g0251a0002c0002t0001g0019others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.7-2873T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436971 | ||||||
| chr11:436974
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(108): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.7-2876C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436974 | ||||||
| chr11:436975
|
G | A | 50 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0017others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-2877C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436975 | ||||||
| chr11:436976
|
G | A | 21 | a0001c0001t0001g0250a0001c0001t0001g0251a0002c0002t0001g0019others(18): Show | 21 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.7-2878C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436976 | ||||||
| chr11:436982
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(108): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.7-2884T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436982 | ||||||
| chr11:436982
|
A | T | 50 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0017others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-2884T>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436982 | ||||||
| chr11:436984
|
T | G | 161 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(158): Show | 166 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.7-2886A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436984 | ||||||
| chr11:436985
|
G | A | 50 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0017others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-2887C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436985 | ||||||
| chr11:436986
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(87): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.7-2888C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436986 | ||||||
| chr11:436987
|
G | A | 50 | a0001c0013t0005g0003a0001c0013t0008g0275a0002c0002t0001g0017others(47): Show | 51 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.7-2889C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436987 | ||||||
| chr11:436993
|
G | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(87): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.7-2895C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436993 | ||||||
| chr11:436993
|
GGGAGGTG others(3): Show |
G | 1 | a0001c0001t0001g0250 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.7-2905_7-2896delGC others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436993 | ||||||
| chr11:436996
|
A | G | 70 | a0001c0001t0001g0251a0001c0013t0005g0003a0001c0013t0008g0275others(67): Show | 71 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.7-2898T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436996 | ||||||
| chr11:436998
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(87): Show | 94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.7-2900C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 436998 | ||||||
| chr11:437003
|
C | T | 1 | a0002c0002t0001g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7-2905G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437003 | ||||||
| chr11:437004
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.7-2906C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437004 | ||||||
| chr11:437007
|
GAGTGAGC others(4): Show |
G | 18 | a0001c0001t0001g0251a0002c0002t0001g0019a0002c0002t0001g0020others(15): Show | 18 | HG00280.hp1 HG00323.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.7-2920_7-2910delTC others(9): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437007 | ||||||
| chr11:437008
|
A | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(140): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.7-2910T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437008 | ||||||
| chr11:437014
|
C | CG | 6 | a0001c0001t0001g0193a0001c0001t0001g0202a0001c0001t0001g0203others(3): Show | 6 | HG01243.hp1 HG02027.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.7-2917_7-2916insC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437014 | ||||||
| chr11:437014
|
CTGGAGAT others(3): Show |
C | 2 | a0002c0002t0002g0025a0010c0014t0001g0026 | 2 | HG02074.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.7-2926_7-2917delCT others(8): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437014 | ||||||
| chr11:437015
|
T | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(138): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.7-2917A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437015 | ||||||
| chr11:437018
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(138): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.7-2920T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437018 | ||||||
| chr11:437020
|
A | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(156): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.7-2922T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437020 | ||||||
| chr11:437025
|
C | CG | 10 | a0001c0001t0001g0076a0001c0001t0001g0110a0001c0001t0001g0265others(7): Show | 10 | HG00438.hp2 HG00738.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.7-2928dupC | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437025 | ||||||
| chr11:437025
|
C | G | 3 | a0001c0001t0001g0174a0002c0002t0002g0025a0010c0014t0001g0026 | 3 | HG01993.hp2 HG02074.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.7-2927G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437025 | ||||||
| chr11:437025
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7-2927G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437025 | ||||||
| chr11:437034
|
A | AGCGGGGG others(26): Show |
1 | a0002c0002t0001g0097 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-2937_7-2936insGC others(31): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437034 | ||||||
| chr11:437034
|
A | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(165): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.7-2936T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437034 | ||||||
| chr11:437045
|
C | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.7-2947G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437045 | ||||||
| chr11:437047
|
T | C | 89 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.7-2949A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437047 | ||||||
| chr11:437048
|
G | A | 2 | a0008c0015t0001g0260a0008c0015t0001g0261 | 2 | HG01943.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.7-2950C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437048 | ||||||
| chr11:437050
|
G | A | 88 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(85): Show | 89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.7-2952C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437050 | ||||||
| chr11:437050
|
G | GGGGTGAG others(26): Show |
1 | a0001c0001t0001g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.7-2953_7-2952insTC others(31): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437050 | ||||||
| chr11:437059
|
T | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.7-2961A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437059 | ||||||
| chr11:437088
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.7-2990A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437088 | ||||||
| chr11:437362
|
C | G | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-3264G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437362 | ||||||
| chr11:437401
|
C | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.7-3303G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437401 | ||||||
| chr11:437403
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.7-3305C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437403 | ||||||
| chr11:437409
|
A | C | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG02486.hp2 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.7-3311T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437409 | ||||||
| chr11:437432
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7-3334C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437432 | ||||||
| chr11:437559
|
C | T | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.7-3461G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437559 | ||||||
| chr11:437582
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7-3484G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437582 | ||||||
| chr11:437719
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.7-3621C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437719 | ||||||
| chr11:437781
|
G | C | 155 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.7-3683C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437781 | ||||||
| chr11:437795
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.7-3697T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437795 | ||||||
| chr11:437811
|
T | G | 153 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(150): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.7-3713A>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437811 | ||||||
| chr11:437866
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.7-3768A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 437866 | ||||||
| chr11:438353
|
TCCCCCCA others(25): Show |
T | 2 | a0005c0007t0001g0198a0005c0007t0001g0199 | 2 | NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.6+3536_6+3567delGC others(30): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438353 | ||||||
| chr11:438369
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0003g0009 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6+3552T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438369 | ||||||
| chr11:438391
|
C | G | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+3530G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438391 | ||||||
| chr11:438391
|
C | T | 2 | a0002c0002t0001g0070a0002c0002t0001g0071 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.6+3530G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438391 | ||||||
| chr11:438445
|
G | A | 6 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0001g0060others(3): Show | 6 | HG01074.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+3476C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438445 | ||||||
| chr11:438459
|
T | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.6+3462A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438459 | ||||||
| chr11:438571
|
GTCCATCT others(89): Show |
G | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6+3254_6+3349delTG others(94): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438571 | ||||||
| chr11:438662
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(197): Show | 206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.6+3259T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438662 | ||||||
| chr11:438683
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0003g0009 | 2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6+3238C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438683 | ||||||
| chr11:438755
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(187): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.6+3166T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438755 | ||||||
| chr11:438875
|
G | A | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6+3046C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438875 | ||||||
| chr11:438926
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.6+2995T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438926 | ||||||
| chr11:438928
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.6+2993T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438928 | ||||||
| chr11:438939
|
G | C | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.6+2982C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 438939 | ||||||
| chr11:439012
|
C | T | 1 | a0003c0003t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6+2909G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439012 | ||||||
| chr11:439039
|
G | A | 142 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6+2882C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439039 | ||||||
| chr11:439065
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6+2856C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439065 | ||||||
| chr11:439073
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(255): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.6+2848T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439073 | ||||||
| chr11:439205
|
C | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(113): Show | 121 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.6+2716G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439205 | ||||||
| chr11:439219
|
G | A | 142 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.6+2702C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439219 | ||||||
| chr11:439263
|
C | G | 2 | a0001c0001t0002g0007a0001c0001t0002g0196 | 3 | HG01081.hp1 HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6+2658G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439263 | ||||||
| chr11:439328
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG01243.hp2 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+2593C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439328 | ||||||
| chr11:439503
|
C | A | 9 | a0001c0006t0003g0011a0001c0006t0003g0013a0001c0006t0003g0014others(6): Show | 10 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+2418G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439503 | ||||||
| chr11:439514
|
G | C | 1 | a0002c0002t0001g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6+2407C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439514 | ||||||
| chr11:439523
|
C | CAGGCCTG others(66): Show |
116 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0082others(113): Show | 121 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.6+2397_6+2398insCT others(71): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439523 | ||||||
| chr11:439671
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6+2250G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439671 | ||||||
| chr11:439699
|
C | T | 2 | a0002c0002t0001g0065a0010c0014t0001g0064 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.6+2222G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439699 | ||||||
| chr11:439744
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6+2177G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439744 | ||||||
| chr11:439802
|
C | CTCCTCGG others(1): Show |
40 | a0001c0001t0001g0082a0001c0001t0001g0105a0001c0001t0001g0193others(37): Show | 41 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.6+2118_6+2119insTC others(6): Show |
ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439802 | ||||||
| chr11:439805
|
T | C | 40 | a0001c0001t0001g0082a0001c0001t0001g0105a0001c0001t0001g0193others(37): Show | 41 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.6+2116A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439805 | ||||||
| chr11:439828
|
C | T | 3 | a0001c0013t0005g0003a0001c0013t0008g0275a0012c0017t0003g0010 | 4 | HG02280.hp2 HG03486.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.6+2093G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439828 | ||||||
| chr11:439879
|
G | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0080others(37): Show | 41 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.6+2042C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439879 | ||||||
| chr11:439916
|
T | C | 1 | a0002c0002t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.6+2005A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 439916 | ||||||
| chr11:440053
|
C | T | 5 | a0001c0001t0001g0082a0001c0001t0003g0009a0008c0012t0001g0190others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+1868G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440053 | ||||||
| chr11:440065
|
CAT | C | 3 | a0009c0011t0001g0005a0009c0011t0001g0095a0009c0011t0001g0096 | 4 | HG00733.hp2 HG01081.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+1854_6+1855delAT | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440065 | ||||||
| chr11:440287
|
G | A | 3 | a0008c0012t0001g0190a0008c0012t0001g0191a0008c0012t0001g0192 | 3 | HG02970.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.6+1634C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440287 | ||||||
| chr11:440343
|
A | C | 151 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0022others(148): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.6+1578T>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440343 | ||||||
| chr11:440571
|
T | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG00408.hp1 HG00673.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+1350A>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440571 | ||||||
| chr11:440601
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.6+1320G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440601 | ||||||
| chr11:440612
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.6+1309G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440612 | ||||||
| chr11:440686
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6+1235G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440686 | ||||||
| chr11:440722
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6+1199G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440722 | ||||||
| chr11:440736
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6+1185G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440736 | ||||||
| chr11:440758
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6+1163G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440758 | ||||||
| chr11:440765
|
G | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0105others(86): Show | 93 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.6+1156C>G | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440765 | ||||||
| chr11:440857
|
C | T | 6 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0001g0060others(3): Show | 6 | HG01074.hp1 HG02451.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.6+1064G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440857 | ||||||
| chr11:440998
|
C | T | 2 | a0002c0002t0001g0097a0002c0002t0001g0098 | 2 | HG00642.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.6+923G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 440998 | ||||||
| chr11:441106
|
G | A | 4 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0056others(1): Show | 4 | HG02559.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.6+815C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441106 | ||||||
| chr11:441111
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.6+810C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441111 | ||||||
| chr11:441140
|
C | T | 47 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0102others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.6+781G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441140 | ||||||
| chr11:441143
|
C | T | 1 | a0012c0017t0003g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6+778G>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441143 | ||||||
| chr11:441313
|
G | A | 8 | a0001c0006t0003g0011a0001c0006t0003g0013a0001c0006t0003g0014others(5): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+608C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441313 | ||||||
| chr11:441366
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6+555C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441366 | ||||||
| chr11:441454
|
G | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0018 | 2 | HG00609.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.6+467C>A | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441454 | ||||||
| chr11:441710
|
A | G | 9 | a0001c0001t0003g0009a0001c0006t0003g0011a0001c0006t0003g0013others(6): Show | 10 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+211T>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441710 | ||||||
| chr11:441762
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6+159C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441762 | ||||||
| chr11:441776
|
G | A | 5 | a0002c0002t0001g0097a0002c0002t0001g0098a0002c0002t0001g0099others(2): Show | 5 | HG00642.hp1 HG00642.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.6+145C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441776 | ||||||
| chr11:441806
|
C | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(175): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.6+115G>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441806 | ||||||
| chr11:441844
|
G | A | 1 | a0002c0002t0001g0274 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.6+77C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441844 | ||||||
| chr11:441854
|
G | A | 8 | a0001c0006t0003g0011a0001c0006t0003g0013a0001c0006t0003g0014others(5): Show | 9 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.6+67C>T | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441854 | ||||||
| chr11:441859
|
C | G | 9 | a0001c0001t0003g0009a0001c0006t0003g0011a0001c0006t0003g0013others(6): Show | 10 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.6+62G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441859 | ||||||
| chr11:441862
|
C | G | 1 | a0002c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6+59G>C | ANO9 | ENSG00000185101.13 | transcript | ENST00000332826.7 | protein_coding | 1/22 | chr11 | 441862 |