Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55226 |
|---|---|
| ensemblid | ENSG00000135372.10 |
| hgncid | 29830 |
| symbol | NAT10 |
| name | N-acetyltransferase 10 |
| refseq_nuc | NM_024662.3 |
| refseq_prot | NP_078938.3 |
| ensembl_nuc | ENST00000257829.8 |
| ensembl_prot | ENSP00000257829.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 34105629 |
| end | 34146908 |
| strand | + |
| ver | v1.2 |
| region | chr11:34105629-34146908 |
| region5000 | chr11:34100629-34151908 |
| regionname0 | NAT10_chr11_34105629_34146908 |
| regionname5000 | NAT10_chr11_34100629_34151908 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1025 | 240 | 81 | 45 | 75 | 8 | 30 | 46 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0002 | 0/0 | 1025 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0003 | 0/0 | 1025 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0004 | 0/0 | 1025 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0005 | 0/0 | 1025 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0006 | 0/0 | 1025 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0007 | 1/0 | 1025 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0008 | 0/0 | 58 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0009 | 0/0 | 1025 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0010 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0011 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0012 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0013 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3078 | 187 | 36 | 41 | 73 | 7 | 29 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0002 | 0/0 | 3078 | 22 | 21 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0003 | 0/0 | 3078 | 11 | 9 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0004 | 0/0 | 3078 | 7 | 7 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0005 | 0/0 | 3078 | 6 | 6 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0006 | 0/0 | 3078 | 4 | 0 | 0 | 4 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0007 | 0/0 | 3078 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0008 | 0/0 | 3078 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0009 | 0/0 | 3078 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0010 | 0/0 | 3078 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0011 | 1/0 | 3078 | 2 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0012 | 0/0 | 3078 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0013 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0014 | 0/0 | 3078 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0015 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0016 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0017 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0018 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0019 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0020 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0021 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0022 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| c0023 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 896 | 168 | 61 | 24 | 50 | 7 | 24 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0002 | 0/0 | 896 | 67 | 8 | 20 | 28 | 1 | 10 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0003 | 0/0 | 896 | 7 | 7 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0004 | 0/0 | 896 | 6 | 6 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0005 | 0/0 | 896 | 5 | 5 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0006 | 0/0 | 896 | 3 | 0 | 0 | 3 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0007 | 0/0 | 896 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0008 | 0/0 | 896 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0009 | 0/0 | 896 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0010 | 0/0 | 896 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| t0011 | 0/0 | 896 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3078 | 187 | 36 | 41 | 73 | 7 | 29 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0002 | 0/0 | 3078 | 22 | 21 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0003 | 0/0 | 3078 | 11 | 9 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0004 | 0/0 | 3078 | 7 | 7 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0005 | 0/0 | 3078 | 6 | 6 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0009 | 0/0 | 3078 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0015 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0016 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0019 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0020 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0022 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0002c0006 | 0/0 | 3078 | 4 | 0 | 0 | 4 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0003c0007 | 0/0 | 3078 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0004c0008 | 0/0 | 3078 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0005c0012 | 0/0 | 3078 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0006c0010 | 0/0 | 3078 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0007c0011 | 1/0 | 3078 | 2 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0008c0013 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0009c0014 | 0/0 | 3078 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0010c0017 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0011c0018 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0012c0023 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0013c0021 | 0/0 | 3078 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3973 | 118 | 28 | 21 | 42 | 7 | 19 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0001t0002 | 0/0 | 3973 | 64 | 7 | 20 | 27 | 0 | 10 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0001t0006 | 0/0 | 3973 | 3 | 0 | 0 | 3 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0001t0010 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0001t0011 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0002t0001 | 0/0 | 3973 | 20 | 20 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0002t0002 | 0/0 | 3973 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0002t0009 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0003t0001 | 0/0 | 3973 | 9 | 7 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0003t0003 | 0/0 | 3973 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0004t0003 | 0/0 | 3973 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0004t0005 | 0/0 | 3973 | 4 | 4 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0004t0008 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0005t0004 | 0/0 | 3973 | 6 | 6 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0009t0007 | 0/0 | 3973 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0015t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0016t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0019t0001 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0020t0005 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0001c0022t0001 | 0/0 | 3973 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0002c0006t0001 | 0/0 | 3973 | 4 | 0 | 0 | 4 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0003c0007t0001 | 0/0 | 3973 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0004c0008t0003 | 0/0 | 3973 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0005c0012t0001 | 0/0 | 3973 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0006c0010t0001 | 0/0 | 3973 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0007c0011t0001 | 1/0 | 3973 | 2 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0008c0013t0002 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0009c0014t0001 | 0/0 | 3973 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0010c0017t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0011c0018t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0012c0023t0001 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| a0013c0021t0002 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | copy fasta | chr11 | 34100629 | 34151908 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0010g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0009t0007g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0015t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0016t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0019t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0020t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0022t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0003c0007t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0003c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0003c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0004c0008t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0004c0008t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0004c0008t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0005c0012t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0005c0012t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0006c0010t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0006c0010t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0007c0011t0001g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0007c0011t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0008c0013t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0009c0014t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0010c0017t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0011c0018t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0012c0023t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0013c0021t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00597 | hp2 | a0002 | c0006 | t0001 | g0168 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00621 | hp2 | a0002 | c0006 | t0001 | g0167 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00639 | hp1 | a0006 | c0010 | t0001 | g0052 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00738 | hp1 | a0001 | c0022 | t0001 | g0036 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01168 | hp1 | a0001 | c0009 | t0007 | g0008 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01169 | hp2 | a0001 | c0009 | t0007 | g0008 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0055 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02145 | hp1 | a0001 | c0004 | t0005 | g0031 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02165 | hp2 | a0010 | c0017 | t0001 | g0059 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02258 | hp1 | a0001 | c0004 | t0003 | g0030 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02258 | hp2 | a0013 | c0021 | t0002 | g0064 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02451 | hp1 | a0001 | c0002 | t0009 | g0225 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02615 | hp1 | a0001 | c0020 | t0005 | g0025 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02717 | hp1 | a0001 | c0019 | t0001 | g0151 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02717 | hp2 | a0003 | c0007 | t0001 | g0091 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02735 | hp2 | a0009 | c0014 | t0001 | g0081 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0044 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02896 | hp2 | a0001 | c0005 | t0004 | g0006 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0006 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0028 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03041 | hp1 | a0001 | c0005 | t0004 | g0045 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0042 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03098 | hp1 | a0007 | c0011 | t0001 | g0234 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03195 | hp2 | a0001 | c0005 | t0004 | g0043 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03209 | hp1 | a0004 | c0008 | t0003 | g0022 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03225 | hp1 | a0001 | c0004 | t0005 | g0026 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03540 | hp2 | a0001 | c0005 | t0004 | g0046 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03654 | hp2 | a0005 | c0012 | t0001 | g0038 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0040 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04184 | hp2 | a0005 | c0012 | t0001 | g0041 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04204 | hp1 | a0006 | c0010 | t0001 | g0053 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0217 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18950 | hp2 | a0011 | c0018 | t0001 | g0125 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18960 | hp1 | a0002 | c0006 | t0001 | g0201 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18968 | hp2 | a0001 | c0016 | t0001 | g0048 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18970 | hp2 | a0002 | c0006 | t0001 | g0005 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18983 | hp2 | a0008 | c0013 | t0002 | g0232 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19011 | hp2 | a0001 | c0015 | t0001 | g0089 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19030 | hp1 | a0004 | c0008 | t0003 | g0021 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0024 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0096 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19240 | hp2 | a0004 | c0008 | t0003 | g0023 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ASW | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ASW | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02109 | hp1 | a0012 | c0023 | t0001 | g0002 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02109 | hp2 | a0003 | c0007 | t0001 | g0092 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0032 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA21309 | hp1 | a0001 | c0004 | t0005 | g0027 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA21309 | hp2 | a0003 | c0007 | t0001 | g0001 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0141 | REF | REF | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| homoSapiens_grch38 | hp1 | a0007 | c0011 | t0001 | g0233 | REF | REF | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34108810
|
T | G | 1 | a0008 | 1 | NA18983.hp2 | stop_gained | HIGH | c.177T>G | p.Tyr59* | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/29 | 356/3973 | 177/3078 | 59/1025 | chr11 | 34108810 | ||
| chr11:34113726
|
C | G | 1 | a0013 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.383C>G | p.Ala128Gly | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/29 | 562/3973 | 383/3078 | 128/1025 | chr11 | 34113726 | ||
| chr11:34118230
|
A | G | 1 | a0012 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.608A>G | p.Gln203Arg | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/29 | 787/3973 | 608/3078 | 203/1025 | chr11 | 34118230 | ||
| chr11:34118259
|
G | A | 1 | a0009 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.637G>A | p.Val213Ile | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/29 | 816/3973 | 637/3078 | 213/1025 | chr11 | 34118259 | ||
| chr11:34118293
|
C | T | 1 | a0003 | 3 | HG02109.hp2 HG02717.hp2 NA21309.hp2 |
missense_variant&splice_region_variant | MODERATE | c.671C>T | p.Pro224Leu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/29 | 850/3973 | 671/3078 | 224/1025 | chr11 | 34118293 | ||
| chr11:34130863
|
G | A | 1 | a0010 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1295G>A | p.Arg432His | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/29 | 1474/3973 | 1295/3078 | 432/1025 | chr11 | 34130863 | ||
| chr11:34131392
|
T | C | 12 | a0001a0002a0003others(9): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
missense_variant | MODERATE | c.1381T>C | p.Tyr461His | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/29 | 1560/3973 | 1381/3078 | 461/1025 | chr11 | 34131392 | ||
| chr11:34133032
|
C | T | 1 | a0006 | 2 | HG00639.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.1624C>T | p.Pro542Ser | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/29 | 1803/3973 | 1624/3078 | 542/1025 | chr11 | 34133032 | ||
| chr11:34133098
|
C | T | 1 | a0002 | 4 | HG00597.hp2 HG00621.hp2 NA18960.hp1 others(1): Show |
missense_variant | MODERATE | c.1690C>T | p.Pro564Ser | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/29 | 1869/3973 | 1690/3078 | 564/1025 | chr11 | 34133098 | ||
| chr11:34135175
|
A | G | 1 | a0005 | 2 | HG03654.hp2 HG04184.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1912A>G | p.Met638Val | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/29 | 2091/3973 | 1912/3078 | 638/1025 | chr11 | 34135175 | ||
| chr11:34142340
|
C | A | 1 | a0011 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.2877C>A | p.Asp959Glu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/29 | 3056/3973 | 2877/3078 | 959/1025 | chr11 | 34142340 | ||
| chr11:34143506
|
G | A | 1 | a0004 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.2947G>A | p.Ala983Thr | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/29 | 3126/3973 | 2947/3078 | 983/1025 | chr11 | 34143506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34108795
|
A | G | 5 | a0001c0003a0001c0022a0004c0008others(2): Show | 18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
synonymous_variant | LOW | c.162A>G | p.Ser54Ser | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/29 | 341/3973 | 162/3078 | 54/1025 | chr11 | 34108795 | ||
| chr11:34108810
|
T | C | 1 | a0001c0005 | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.177T>C | p.Tyr59Tyr | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/29 | 356/3973 | 177/3078 | 59/1025 | chr11 | 34108810 | ||
| chr11:34112220
|
G | A | 1 | a0001c0005 | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.369G>A | p.Leu123Leu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/29 | 548/3973 | 369/3078 | 123/1025 | chr11 | 34112220 | ||
| chr11:34113802
|
C | T | 2 | a0001c0004a0001c0020 | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.459C>T | p.Thr153Thr | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/29 | 638/3973 | 459/3078 | 153/1025 | chr11 | 34113802 | ||
| chr11:34122485
|
G | A | 1 | a0001c0015 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.807G>A | p.Glu269Glu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/29 | 986/3973 | 807/3078 | 269/1025 | chr11 | 34122485 | ||
| chr11:34124397
|
T | C | 1 | a0001c0016 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.1104T>C | p.Ile368Ile | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/29 | 1283/3973 | 1104/3078 | 368/1025 | chr11 | 34124397 | ||
| chr11:34127528
|
C | T | 1 | a0001c0019 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1173C>T | p.Ala391Ala | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/29 | 1352/3973 | 1173/3078 | 391/1025 | chr11 | 34127528 | ||
| chr11:34133094
|
C | T | 13 | a0001c0001a0001c0015a0001c0016others(10): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(202): Show |
synonymous_variant | LOW | c.1686C>T | p.Pro562Pro | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/29 | 1865/3973 | 1686/3078 | 562/1025 | chr11 | 34133094 | ||
| chr11:34140401
|
C | A | 2 | a0001c0009a0004c0008 | 5 | HG01168.hp1 HG01169.hp2 HG03209.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.2421C>A | p.Ala807Ala | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/29 | 2600/3973 | 2421/3078 | 807/1025 | chr11 | 34140401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34105714
|
C | T | 1 | a0001c0001t0011 | 1 | NA19085.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/29 | 2512 | chr11 | 34105714 | |||||
| chr11:34105756
|
T | G | 1 | a0001c0004t0008 | 1 | HG02922.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/29 | chr11 | 34105756 | ||||||
| chr11:34146447
|
C | A | 1 | a0001c0005t0004 | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*255C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 255 | chr11 | 34146447 | |||||
| chr11:34146548
|
T | G | 1 | a0001c0009t0007 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*356T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 356 | chr11 | 34146548 | |||||
| chr11:34146566
|
C | T | 1 | a0001c0001t0006 | 3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*374C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 374 | chr11 | 34146566 | |||||
| chr11:34146606
|
G | A | 5 | a0001c0001t0002a0001c0001t0011a0001c0002t0002others(2): Show | 68 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 414 | chr11 | 34146606 | |||||
| chr11:34146610
|
C | T | 3 | a0001c0004t0005a0001c0004t0008a0001c0020t0005 | 6 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*418C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 418 | chr11 | 34146610 | |||||
| chr11:34146623
|
C | A | 1 | a0001c0002t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 431 | chr11 | 34146623 | |||||
| chr11:34146793
|
C | T | 4 | a0001c0003t0003a0001c0004t0003a0001c0009t0007others(1): Show | 9 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*601C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 601 | chr11 | 34146793 | |||||
| chr11:34146897
|
A | T | 1 | a0001c0001t0010 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 705 | chr11 | 34146897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34105853
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-16+61T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34105853 | ||||||
| chr11:34105916
|
T | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16+124T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34105916 | ||||||
| chr11:34105925
|
A | T | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+133A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34105925 | ||||||
| chr11:34106292
|
A | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16+500A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106292 | ||||||
| chr11:34106362
|
A | G | 1 | a0008c0013t0002g0232 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-16+570A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106362 | ||||||
| chr11:34106379
|
A | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-16+587A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106379 | ||||||
| chr11:34106421
|
A | AT | 17 | a0001c0001t0001g0228a0001c0001t0002g0229a0001c0003t0001g0002others(14): Show | 19 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16+643dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34106421 | |||||
| chr11:34106421
|
A | ATT | 9 | a0001c0003t0003g0042a0001c0004t0003g0029a0001c0004t0003g0030others(6): Show | 9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+642_-16+643dup others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34106421 | |||||
| chr11:34106484
|
A | G | 16 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(13): Show | 18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-16+692A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106484 | ||||||
| chr11:34106710
|
G | C | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+918G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106710 | ||||||
| chr11:34106712
|
C | G | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-16+920C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106712 | ||||||
| chr11:34106786
|
C | T | 2 | a0001c0001t0002g0229a0001c0002t0009g0225 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-16+994C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106786 | ||||||
| chr11:34106863
|
G | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1071G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106863 | ||||||
| chr11:34106906
|
G | C | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-16+1114G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106906 | ||||||
| chr11:34106990
|
T | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-16+1198T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106990 | ||||||
| chr11:34107031
|
C | CT | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(197): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-15-1162dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34107031 | |||||
| chr11:34107031
|
C | CTT | 20 | a0001c0001t0001g0215a0001c0001t0001g0219a0001c0001t0001g0220others(17): Show | 20 | HG01081.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-1163_-15-1162d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34107031 | |||||
| chr11:34107031
|
C | CTTT | 14 | a0001c0001t0001g0224a0001c0003t0001g0002a0001c0003t0001g0033others(11): Show | 16 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1164_-15-1162d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34107031 | |||||
| chr11:34107235
|
T | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG00733.hp2 HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-15-976T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107235 | ||||||
| chr11:34107325
|
T | C | 1 | a0001c0004t0005g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-15-886T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107325 | ||||||
| chr11:34107395
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-816A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107395 | ||||||
| chr11:34107493
|
C | T | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15-718C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107493 | ||||||
| chr11:34107654
|
A | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15-557A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107654 | ||||||
| chr11:34107656
|
G | A | 2 | a0006c0010t0001g0052a0006c0010t0001g0053 | 2 | HG00639.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-15-555G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107656 | ||||||
| chr11:34107847
|
C | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-15-364C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107847 | ||||||
| chr11:34107852
|
C | A | 16 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(13): Show | 18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15-359C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107852 | ||||||
| chr11:34107901
|
G | T | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-15-310G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107901 | ||||||
| chr11:34108421
|
T | G | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.108+88T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108421 | ||||||
| chr11:34108468
|
C | G | 15 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0156others(12): Show | 17 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.108+135C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108468 | ||||||
| chr11:34108476
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18971.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.108+143C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108476 | ||||||
| chr11:34108512
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.108+179C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108512 | ||||||
| chr11:34108608
|
T | C | 2 | a0002c0006t0001g0167a0002c0006t0001g0168 | 2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.109-134T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108608 | ||||||
| chr11:34108617
|
A | G | 25 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(22): Show | 28 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.109-125A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108617 | ||||||
| chr11:34108648
|
G | A | 30 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(27): Show | 34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.109-94G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108648 | ||||||
| chr11:34108847
|
T | G | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.200+14T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34108847 | ||||||
| chr11:34108855
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.200+22T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34108855 | ||||||
| chr11:34108859
|
A | G | 16 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(13): Show | 18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.200+26A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34108859 | ||||||
| chr11:34109010
|
A | C | 1 | a0001c0001t0001g0213 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.200+177A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109010 | ||||||
| chr11:34109164
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.200+331C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109164 | ||||||
| chr11:34109259
|
G | T | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.200+426G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109259 | ||||||
| chr11:34109286
|
A | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.200+453A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109286 | ||||||
| chr11:34109411
|
T | A | 1 | a0001c0003t0003g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.200+578T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109411 | ||||||
| chr11:34109460
|
G | T | 1 | a0001c0002t0001g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.200+627G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109460 | ||||||
| chr11:34109474
|
A | T | 7 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.200+641A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109474 | ||||||
| chr11:34109896
|
T | C | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.200+1063T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109896 | ||||||
| chr11:34110108
|
T | C | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.200+1275T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110108 | ||||||
| chr11:34110169
|
C | T | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.200+1336C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110169 | ||||||
| chr11:34110170
|
G | A | 1 | a0001c0002t0009g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.200+1337G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110170 | ||||||
| chr11:34110248
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.200+1415G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110248 | ||||||
| chr11:34110354
|
A | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.200+1521A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110354 | ||||||
| chr11:34110361
|
C | T | 1 | a0001c0004t0005g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.200+1528C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110361 | ||||||
| chr11:34110410
|
A | G | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.200+1577A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110410 | ||||||
| chr11:34110427
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.200+1594C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110427 | ||||||
| chr11:34110491
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.201-1561A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110491 | ||||||
| chr11:34110559
|
C | CT | 14 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG00597.hp2 HG02040.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.201-1468dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | |||||
| chr11:34110559
|
C | CTT | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-1469_201-1468d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | |||||
| chr11:34110559
|
CT | C | 15 | a0001c0001t0001g0018a0001c0001t0001g0054a0001c0001t0001g0057others(12): Show | 16 | HG00323.hp2 HG01515.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.201-1468delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | |||||
| chr11:34110559
|
CTT | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0156a0001c0003t0001g0040others(4): Show | 8 | HG02976.hp2 HG03209.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-1469_201-1468d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | |||||
| chr11:34110559
|
CTTT | C | 11 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(8): Show | 13 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.201-1470_201-1468d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | |||||
| chr11:34110559
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0005t0004g0043 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.201-1477_201-1468d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | |||||
| chr11:34110915
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.201-1137C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110915 | ||||||
| chr11:34111010
|
G | A | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.201-1042G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111010 | ||||||
| chr11:34111019
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.201-1033T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111019 | ||||||
| chr11:34111062
|
A | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0156a0001c0001t0001g0165others(1): Show | 5 | HG02451.hp2 HG02976.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-990A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111062 | ||||||
| chr11:34111196
|
GC | G | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-852delC | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34111196 | |||||
| chr11:34111417
|
C | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-635C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111417 | ||||||
| chr11:34111842
|
C | T | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.201-210C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111842 | ||||||
| chr11:34111881
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.201-171A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111881 | ||||||
| chr11:34111931
|
T | TTC | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.201-120_201-119dup others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34111931 | |||||
| chr11:34112005
|
T | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-47T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112005 | ||||||
| chr11:34112007
|
C | T | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-45C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112007 | ||||||
| chr11:34112039
|
T | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-13T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112039 | ||||||
| chr11:34112040
|
G | A | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-12G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112040 | ||||||
| chr11:34112331
|
T | C | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.372+108T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112331 | ||||||
| chr11:34112470
|
A | G | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.372+247A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112470 | ||||||
| chr11:34112471
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.372+248C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112471 | ||||||
| chr11:34112600
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.372+377C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112600 | ||||||
| chr11:34112930
|
T | C | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.372+707T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112930 | ||||||
| chr11:34113054
|
C | T | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.373-662C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113054 | ||||||
| chr11:34113151
|
G | A | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.373-565G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113151 | ||||||
| chr11:34113264
|
T | C | 1 | a0010c0017t0001g0059 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.373-452T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113264 | ||||||
| chr11:34113327
|
G | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-389G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113327 | ||||||
| chr11:34113344
|
CGTTTTTG others(4): Show |
C | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-371_373-361del others(11): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113344 | ||||||
| chr11:34113345
|
G | A | 25 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(22): Show | 28 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.373-371G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113345 | ||||||
| chr11:34113366
|
G | A | 7 | a0001c0004t0003g0029a0001c0004t0005g0024a0001c0004t0005g0026others(4): Show | 7 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-350G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113366 | ||||||
| chr11:34113379
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0017others(91): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.373-337C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113379 | ||||||
| chr11:34113525
|
A | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.373-191A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113525 | ||||||
| chr11:34113541
|
G | T | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.373-175G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113541 | ||||||
| chr11:34113636
|
C | CA | 14 | a0001c0001t0001g0171a0001c0001t0001g0215a0001c0003t0001g0033others(11): Show | 14 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-56dupA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | |||||
| chr11:34113636
|
C | CAA | 7 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(4): Show | 9 | HG01168.hp1 HG01169.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.373-57_373-56dupAA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | |||||
| chr11:34113636
|
CA | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(178): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.373-56delA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | |||||
| chr11:34113636
|
CAA | C | 5 | a0001c0002t0001g0007a0001c0002t0001g0047a0001c0002t0001g0218others(2): Show | 6 | HG02451.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-57_373-56delAA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | |||||
| chr11:34113636
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0006t0001g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.373-65_373-56delAA others(8): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | |||||
| chr11:34113703
|
C | T | 1 | a0001c0002t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.373-13C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113703 | ||||||
| chr11:34113709
|
C | T | 6 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.373-7C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113709 | ||||||
| chr11:34114024
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.495+186A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114024 | ||||||
| chr11:34114068
|
C | G | 1 | a0001c0001t0001g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.495+230C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114068 | ||||||
| chr11:34114227
|
C | T | 1 | a0006c0010t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.495+389C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114227 | ||||||
| chr11:34114383
|
G | A | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+545G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114383 | ||||||
| chr11:34114384
|
T | A | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+546T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114384 | ||||||
| chr11:34114385
|
T | C | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+547T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114385 | ||||||
| chr11:34114387
|
C | CTGAT | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+549_495+550ins others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114387 | ||||||
| chr11:34114388
|
C | A | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+550C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114388 | ||||||
| chr11:34114401
|
A | G | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.495+563A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114401 | ||||||
| chr11:34114451
|
C | T | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+613C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114451 | ||||||
| chr11:34114481
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(198): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.495+643T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114481 | ||||||
| chr11:34114549
|
A | G | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.495+711A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114549 | ||||||
| chr11:34114673
|
C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.495+835C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114673 | ||||||
| chr11:34114760
|
G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG00323.hp2 HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.495+922G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114760 | ||||||
| chr11:34114874
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.496-949C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114874 | ||||||
| chr11:34115097
|
G | A | 2 | a0001c0001t0001g0144a0001c0002t0001g0227 | 2 | HG02040.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.496-726G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115097 | ||||||
| chr11:34115251
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.496-572G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115251 | ||||||
| chr11:34115540
|
G | A | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.496-283G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115540 | ||||||
| chr11:34115665
|
A | G | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | HG02080.hp1 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-158A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115665 | ||||||
| chr11:34115805
|
G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.496-18G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115805 | ||||||
| chr11:34115905
|
A | G | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.557+21A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115905 | ||||||
| chr11:34115906
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.557+22A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115906 | ||||||
| chr11:34115929
|
G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.557+45G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115929 | ||||||
| chr11:34115977
|
G | A | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.557+93G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115977 | ||||||
| chr11:34116139
|
T | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+255T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116139 | ||||||
| chr11:34116166
|
T | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+282T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116166 | ||||||
| chr11:34116267
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.557+383T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116267 | ||||||
| chr11:34116314
|
A | C | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0005t0004g0006others(4): Show | 8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.557+430A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116314 | ||||||
| chr11:34116328
|
G | A | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+444G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116328 | ||||||
| chr11:34116385
|
T | C | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.557+501T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116385 | ||||||
| chr11:34116481
|
C | T | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+597C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116481 | ||||||
| chr11:34116904
|
A | G | 17 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(14): Show | 19 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.557+1020A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116904 | ||||||
| chr11:34117172
|
CT | C | 16 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(13): Show | 18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.558-1007delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117172 | ||||||
| chr11:34117208
|
A | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-972A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117208 | ||||||
| chr11:34117210
|
A | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-970A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117210 | ||||||
| chr11:34117211
|
AAATTT | A | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-967_558-963del others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr11 | 34117211 | |||||
| chr11:34117217
|
A | G | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-963A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117217 | ||||||
| chr11:34117224
|
T | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.558-956T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117224 | ||||||
| chr11:34117226
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.558-954A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117226 | ||||||
| chr11:34117396
|
G | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.558-784G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117396 | ||||||
| chr11:34117446
|
G | A | 16 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(13): Show | 18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.558-734G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117446 | ||||||
| chr11:34117670
|
G | A | 27 | a0001c0001t0002g0067a0001c0001t0002g0068a0001c0002t0002g0055others(24): Show | 29 | HG00738.hp1 HG00741.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.558-510G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117670 | ||||||
| chr11:34117691
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.558-489A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117691 | ||||||
| chr11:34117731
|
A | C | 24 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(21): Show | 26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-449A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117731 | ||||||
| chr11:34117803
|
G | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG01168.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.558-377G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117803 | ||||||
| chr11:34117811
|
A | T | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.558-369A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117811 | ||||||
| chr11:34117901
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0057 | 3 | HG02615.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.558-279C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117901 | ||||||
| chr11:34118334
|
C | T | 1 | a0001c0005t0004g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672+40C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/28 | chr11 | 34118334 | ||||||
| chr11:34118347
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.673-49G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/28 | chr11 | 34118347 | ||||||
| chr11:34118392
|
G | A | 1 | a0001c0004t0005g0024 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.673-4G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/28 | chr11 | 34118392 | ||||||
| chr11:34118637
|
C | T | 1 | a0001c0002t0001g0134 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.780+134C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118637 | ||||||
| chr11:34118689
|
G | C | 2 | a0001c0001t0002g0229a0001c0002t0009g0225 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.780+186G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118689 | ||||||
| chr11:34118818
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.780+315C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118818 | ||||||
| chr11:34118954
|
A | G | 5 | a0001c0003t0001g0037a0001c0003t0001g0040a0001c0022t0001g0036others(2): Show | 5 | HG00738.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+451A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118954 | ||||||
| chr11:34119014
|
C | T | 1 | a0005c0012t0001g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.780+511C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119014 | ||||||
| chr11:34119071
|
T | G | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.780+568T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119071 | ||||||
| chr11:34119079
|
G | A | 1 | a0001c0002t0009g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.780+576G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119079 | ||||||
| chr11:34119142
|
G | A | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.780+639G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119142 | ||||||
| chr11:34119159
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.780+656A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119159 | ||||||
| chr11:34119404
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0071a0001c0001t0002g0072 | 5 | HG00733.hp1 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+901T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119404 | ||||||
| chr11:34119415
|
T | C | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.780+912T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119415 | ||||||
| chr11:34119594
|
A | C | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+1091A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119594 | ||||||
| chr11:34119694
|
A | G | 3 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0152 | 3 | HG02559.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.780+1191A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119694 | ||||||
| chr11:34119917
|
A | G | 5 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1414A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119917 | ||||||
| chr11:34119927
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.780+1424G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119927 | ||||||
| chr11:34119946
|
T | C | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+1443T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119946 | ||||||
| chr11:34119981
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(192): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.780+1478C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119981 | ||||||
| chr11:34120085
|
A | G | 21 | a0001c0002t0001g0007a0001c0002t0001g0047a0001c0003t0001g0002others(18): Show | 26 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+1582A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120085 | ||||||
| chr11:34120118
|
TTTG | T | 30 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(27): Show | 34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.780+1631_780+1633d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120118 | |||||
| chr11:34120143
|
G | GT | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.780+1660dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120143 | |||||
| chr11:34120143
|
G | GTT | 19 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(16): Show | 19 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+1659_780+1660d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120143 | |||||
| chr11:34120143
|
GT | G | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+1660delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120143 | |||||
| chr11:34120172
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.780+1669G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120172 | ||||||
| chr11:34120200
|
T | A | 30 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(27): Show | 34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.780+1697T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120200 | ||||||
| chr11:34120222
|
G | A | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.780+1719G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120222 | ||||||
| chr11:34120319
|
A | G | 2 | a0001c0004t0005g0026a0001c0020t0005g0025 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.780+1816A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120319 | ||||||
| chr11:34120328
|
A | G | 30 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(27): Show | 34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.780+1825A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120328 | ||||||
| chr11:34120417
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.780+1914G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120417 | ||||||
| chr11:34120623
|
T | A | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.781-1836T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120623 | ||||||
| chr11:34120769
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781-1690A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120769 | ||||||
| chr11:34120793
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.781-1666G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120793 | ||||||
| chr11:34120825
|
G | T | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1634G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120825 | ||||||
| chr11:34121102
|
C | T | 3 | a0001c0001t0002g0129a0001c0001t0002g0135a0001c0001t0002g0148 | 3 | HG01123.hp1 HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.781-1357C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121102 | ||||||
| chr11:34121103
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.781-1356A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121103 | ||||||
| chr11:34121131
|
T | C | 3 | a0001c0002t0001g0131a0001c0002t0001g0134a0001c0002t0001g0150 | 3 | HG02572.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.781-1328T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121131 | ||||||
| chr11:34121179
|
A | G | 4 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1280A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121179 | ||||||
| chr11:34121206
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.781-1253G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121206 | ||||||
| chr11:34121637
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.781-822G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121637 | ||||||
| chr11:34121689
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.781-770G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121689 | ||||||
| chr11:34121814
|
C | G | 1 | a0001c0001t0006g0121 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.781-645C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121814 | ||||||
| chr11:34121840
|
CAG | C | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.781-616_781-615del others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121840 | |||||
| chr11:34121858
|
C | CA | 126 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(123): Show | 142 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.781-577dupA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | |||||
| chr11:34121858
|
C | CAA | 18 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(15): Show | 18 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-578_781-577dup others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | |||||
| chr11:34121858
|
CAA | C | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-578_781-577del others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | |||||
| chr11:34121858
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0120 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.781-588_781-577del others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | |||||
| chr11:34121882
|
A | T | 1 | a0001c0001t0001g0220 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-577A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121882 | ||||||
| chr11:34121885
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.781-574T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121885 | ||||||
| chr11:34121950
|
C | T | 2 | a0001c0001t0002g0014a0013c0021t0002g0064 | 3 | HG01070.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.781-509C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121950 | ||||||
| chr11:34122048
|
C | T | 1 | a0001c0004t0005g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.781-411C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122048 | ||||||
| chr11:34122049
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.781-410G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122049 | ||||||
| chr11:34122180
|
A | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781-279A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122180 | ||||||
| chr11:34122453
|
C | G | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.781-6C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122453 | ||||||
| chr11:34122931
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.914+339G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34122931 | ||||||
| chr11:34122945
|
C | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.914+353C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34122945 | ||||||
| chr11:34122966
|
T | G | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.914+374T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34122966 | ||||||
| chr11:34123000
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.914+408A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123000 | ||||||
| chr11:34123032
|
T | C | 32 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0003t0001g0002others(29): Show | 36 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.914+440T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123032 | ||||||
| chr11:34123126
|
T | C | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.914+534T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123126 | ||||||
| chr11:34123201
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.915-561G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123201 | ||||||
| chr11:34123291
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.915-471G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123291 | ||||||
| chr11:34123399
|
C | T | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.915-363C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123399 | ||||||
| chr11:34123424
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.915-338C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123424 | ||||||
| chr11:34123456
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.915-306G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123456 | ||||||
| chr11:34123912
|
G | A | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1008+57G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 10/28 | chr11 | 34123912 | ||||||
| chr11:34123965
|
T | G | 1 | a0009c0014t0001g0081 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1008+110T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 10/28 | chr11 | 34123965 | ||||||
| chr11:34124135
|
C | T | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(4): Show | 7 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009-167C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 10/28 | chr11 | 34124135 | ||||||
| chr11:34124558
|
A | G | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1107+158A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124558 | ||||||
| chr11:34124600
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0001g0203 | 2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1107+200T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124600 | ||||||
| chr11:34124686
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1107+286T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124686 | ||||||
| chr11:34124709
|
T | C | 2 | a0001c0001t0002g0229a0001c0002t0009g0225 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1107+309T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124709 | ||||||
| chr11:34124755
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1107+355A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124755 | ||||||
| chr11:34124843
|
A | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0063 | 3 | HG02015.hp1 HG02071.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1107+443A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124843 | ||||||
| chr11:34124856
|
C | T | 1 | a0004c0008t0003g0021 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1107+456C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124856 | ||||||
| chr11:34124955
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(190): Show | 212 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1107+555A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124955 | ||||||
| chr11:34125099
|
C | A | 3 | a0001c0001t0006g0056a0001c0001t0006g0121a0001c0001t0006g0123 | 3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1107+699C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125099 | ||||||
| chr11:34125215
|
A | G | 2 | a0002c0006t0001g0167a0002c0006t0001g0168 | 2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1107+815A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125215 | ||||||
| chr11:34125330
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1107+930T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125330 | ||||||
| chr11:34125798
|
A | G | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1107+1398A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125798 | ||||||
| chr11:34125930
|
G | A | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1107+1530G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125930 | ||||||
| chr11:34125941
|
A | G | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1108-1522A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125941 | ||||||
| chr11:34125959
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG00323.hp2 HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1108-1504C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125959 | ||||||
| chr11:34125998
|
A | G | 1 | a0008c0013t0002g0232 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1108-1465A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125998 | ||||||
| chr11:34126319
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1108-1144A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126319 | ||||||
| chr11:34126691
|
C | T | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1108-772C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126691 | ||||||
| chr11:34126856
|
A | G | 2 | a0001c0001t0002g0060a0001c0001t0002g0109 | 2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1108-607A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126856 | ||||||
| chr11:34126903
|
G | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-560G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126903 | ||||||
| chr11:34126955
|
CAG | C | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-507_1108-506d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126955 | ||||||
| chr11:34126998
|
C | T | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1108-465C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126998 | ||||||
| chr11:34127023
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0156a0001c0001t0001g0166 | 4 | HG02976.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-440C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127023 | ||||||
| chr11:34127100
|
ATC | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(4): Show | 7 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-358_1108-357d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr11 | 34127100 | |||||
| chr11:34127179
|
A | G | 1 | a0001c0004t0005g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1108-284A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127179 | ||||||
| chr11:34127183
|
G | C | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1108-280G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127183 | ||||||
| chr11:34127340
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1108-123A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127340 | ||||||
| chr11:34127445
|
A | T | 3 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0152 | 3 | HG02559.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1108-18A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127445 | ||||||
| chr11:34127619
|
A | T | 13 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(10): Show | 14 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+20A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127619 | ||||||
| chr11:34127652
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1244+53T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127652 | ||||||
| chr11:34127706
|
AGTCTCTG others(3): Show |
A | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1244+110_1244+119d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34127706 | |||||
| chr11:34127708
|
T | G | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1244+109T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127708 | ||||||
| chr11:34127786
|
G | A | 1 | a0001c0022t0001g0036 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1244+187G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127786 | ||||||
| chr11:34128122
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1244+523G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128122 | ||||||
| chr11:34128130
|
C | T | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+531C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128130 | ||||||
| chr11:34128213
|
G | C | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1244+614G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128213 | ||||||
| chr11:34128236
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1244+637C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128236 | ||||||
| chr11:34128293
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1244+694G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128293 | ||||||
| chr11:34128362
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0065a0001c0001t0001g0172others(3): Show | 8 | HG01109.hp1 HG01109.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+779dupA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34128362 | |||||
| chr11:34128362
|
CA | C | 13 | a0001c0002t0001g0227a0001c0004t0003g0029a0001c0004t0003g0030others(10): Show | 14 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+779delA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34128362 | |||||
| chr11:34128367
|
A | C | 31 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(28): Show | 35 | HG00673.hp2 HG00733.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1244+768A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128367 | ||||||
| chr11:34128372
|
A | C | 1 | a0001c0001t0002g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1244+773A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128372 | ||||||
| chr11:34128437
|
A | G | 13 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(10): Show | 14 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+838A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128437 | ||||||
| chr11:34128502
|
A | G | 1 | a0001c0001t0002g0014 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1244+903A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128502 | ||||||
| chr11:34128562
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1244+963G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128562 | ||||||
| chr11:34128680
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1244+1081A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128680 | ||||||
| chr11:34128694
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1244+1095C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128694 | ||||||
| chr11:34128711
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1244+1112A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128711 | ||||||
| chr11:34128836
|
G | C | 1 | a0001c0002t0001g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1244+1237G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128836 | ||||||
| chr11:34128876
|
C | T | 4 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0026others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244+1277C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128876 | ||||||
| chr11:34128888
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1244+1289A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128888 | ||||||
| chr11:34128905
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1244+1306G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128905 | ||||||
| chr11:34128955
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(176): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1244+1356C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128955 | ||||||
| chr11:34129011
|
A | G | 1 | a0001c0003t0001g0034 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1244+1412A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129011 | ||||||
| chr11:34129039
|
T | G | 1 | a0001c0002t0001g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1244+1440T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129039 | ||||||
| chr11:34129165
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1244+1566G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129165 | ||||||
| chr11:34129174
|
T | C | 1 | a0001c0002t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1244+1575T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129174 | ||||||
| chr11:34129186
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1244+1587T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129186 | ||||||
| chr11:34129242
|
G | C | 2 | a0001c0004t0005g0024a0001c0004t0005g0031 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1245-1571G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129242 | ||||||
| chr11:34129278
|
T | C | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1245-1535T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129278 | ||||||
| chr11:34129292
|
C | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(198): Show | 220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1245-1521C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129292 | ||||||
| chr11:34129347
|
G | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-1466G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129347 | ||||||
| chr11:34129407
|
A | G | 5 | a0001c0003t0001g0037a0001c0003t0001g0040a0001c0022t0001g0036others(2): Show | 5 | HG00738.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245-1406A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129407 | ||||||
| chr11:34129584
|
TTTC | T | 6 | a0001c0004t0005g0024a0001c0004t0005g0026a0001c0004t0005g0031others(3): Show | 6 | HG02145.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-1214_1245-121 others(7): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129584 | |||||
| chr11:34129599
|
C | CT | 16 | a0001c0001t0001g0012a0001c0001t0001g0079a0001c0001t0001g0085others(13): Show | 17 | HG00438.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1245-1188dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | |||||
| chr11:34129599
|
CT | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 146 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1245-1188delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | |||||
| chr11:34129599
|
CTT | C | 8 | a0001c0001t0001g0198a0001c0002t0001g0130a0001c0002t0001g0131others(5): Show | 8 | HG01168.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1245-1189_1245-118 others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | |||||
| chr11:34129599
|
CTTTTTTT others(8): Show |
C | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0005t0004g0006others(4): Show | 8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1245-1202_1245-118 others(19): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | |||||
| chr11:34129603
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1245-1210T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129603 | ||||||
| chr11:34129625
|
T | G | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1245-1188T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129625 | ||||||
| chr11:34129709
|
C | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1245-1104C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129709 | ||||||
| chr11:34130044
|
A | ACACT | 15 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0004t0003g0029others(12): Show | 16 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1245-767_1245-766i others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34130044 | |||||
| chr11:34130161
|
T | C | 1 | a0001c0002t0001g0131 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1245-652T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130161 | ||||||
| chr11:34130224
|
A | G | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1245-589A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130224 | ||||||
| chr11:34130247
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245-566A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130247 | ||||||
| chr11:34130342
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1245-471A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130342 | ||||||
| chr11:34130383
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1245-430C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130383 | ||||||
| chr11:34130422
|
A | G | 2 | a0001c0004t0005g0026a0001c0020t0005g0025 | 2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1245-391A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130422 | ||||||
| chr11:34130489
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1245-324A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130489 | ||||||
| chr11:34130527
|
C | G | 1 | a0001c0001t0001g0018 | 2 | HG02015.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1245-286C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130527 | ||||||
| chr11:34130941
|
C | T | 1 | a0001c0002t0009g0225 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.1369+4C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34130941 | ||||||
| chr11:34130977
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1369+40A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34130977 | ||||||
| chr11:34131313
|
C | G | 2 | a0001c0003t0003g0032a0001c0003t0003g0042 | 2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1370-68C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34131313 | ||||||
| chr11:34131333
|
A | C | 1 | a0001c0001t0002g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1370-48A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34131333 | ||||||
| chr11:34131360
|
G | A | 1 | a0001c0001t0011g0096 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1370-21G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34131360 | ||||||
| chr11:34131560
|
G | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG00323.hp2 HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1520+29G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131560 | ||||||
| chr11:34131657
|
TTTCCTTT others(5): Show |
T | 1 | a0001c0016t0001g0048 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1520+136_1520+147d others(14): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr11 | 34131657 | |||||
| chr11:34131685
|
TC | T | 7 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0035others(4): Show | 9 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+155delC | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131685 | ||||||
| chr11:34131686
|
C | T | 5 | a0001c0003t0001g0037a0001c0003t0001g0040a0001c0022t0001g0036others(2): Show | 5 | HG00738.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+155C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131686 | ||||||
| chr11:34131723
|
G | C | 1 | a0001c0003t0003g0042 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1520+192G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131723 | ||||||
| chr11:34131735
|
G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1520+204G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131735 | ||||||
| chr11:34131805
|
C | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0118 | 2 | NA19056.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1520+274C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131805 | ||||||
| chr11:34131842
|
C | T | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1521-283C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131842 | ||||||
| chr11:34131858
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1521-267G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131858 | ||||||
| chr11:34132500
|
CGGT | C | 19 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0051others(16): Show | 20 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617+284_1617+286d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr11 | 34132500 | |||||
| chr11:34132689
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1618-337A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132689 | ||||||
| chr11:34132784
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(234): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1618-242T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132784 | ||||||
| chr11:34132885
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(199): Show | 222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1618-141A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132885 | ||||||
| chr11:34132914
|
C | T | 1 | a0001c0002t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1618-112C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132914 | ||||||
| chr11:34133366
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1734+224C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133366 | ||||||
| chr11:34133374
|
C | G | 3 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134 | 3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1734+232C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133374 | ||||||
| chr11:34133426
|
C | T | 1 | a0001c0002t0001g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734+284C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133426 | ||||||
| chr11:34133463
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1734+321A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133463 | ||||||
| chr11:34133559
|
C | T | 2 | a0001c0001t0002g0060a0001c0001t0002g0109 | 2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1734+417C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133559 | ||||||
| chr11:34133734
|
T | C | 1 | a0001c0004t0005g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1735-585T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133734 | ||||||
| chr11:34133838
|
G | T | 5 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(2): Show | 5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-481G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133838 | ||||||
| chr11:34133882
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.1735-437A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133882 | ||||||
| chr11:34133919
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735-400G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133919 | ||||||
| chr11:34133927
|
C | T | 3 | a0001c0001t0006g0056a0001c0001t0006g0121a0001c0001t0006g0123 | 3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1735-392C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133927 | ||||||
| chr11:34133928
|
G | A | 1 | a0001c0002t0009g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1735-391G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133928 | ||||||
| chr11:34133959
|
T | C | 9 | a0001c0003t0001g0034a0001c0004t0003g0029a0001c0004t0003g0030others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-360T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133959 | ||||||
| chr11:34133968
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1735-351C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133968 | ||||||
| chr11:34134006
|
T | A | 1 | a0001c0001t0002g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1735-313T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134006 | ||||||
| chr11:34134022
|
G | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1735-297G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134022 | ||||||
| chr11:34134032
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1735-287T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134032 | ||||||
| chr11:34134105
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1735-214A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134105 | ||||||
| chr11:34134143
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1735-176G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134143 | ||||||
| chr11:34134425
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0213 | 3 | HG00673.hp1 HG02040.hp1 HG02135.hp2 |
splice_region_variant&intron_variant | LOW | c.1836+5C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 17/28 | chr11 | 34134425 | ||||||
| chr11:34134596
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1911+10C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34134596 | ||||||
| chr11:34134897
|
A | C | 2 | a0001c0004t0003g0029a0001c0004t0003g0030 | 2 | HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1912-278A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34134897 | ||||||
| chr11:34134995
|
A | G | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1912-180A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34134995 | ||||||
| chr11:34135084
|
G | C | 1 | a0001c0002t0009g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1912-91G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34135084 | ||||||
| chr11:34135084
|
G | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1912-91G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34135084 | ||||||
| chr11:34135107
|
A | T | 1 | a0001c0002t0009g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1912-68A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34135107 | ||||||
| chr11:34135325
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2028+34G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135325 | ||||||
| chr11:34135594
|
G | C | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2028+303G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135594 | ||||||
| chr11:34135729
|
T | C | 18 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(15): Show | 21 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2028+438T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135729 | ||||||
| chr11:34135836
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2028+545G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135836 | ||||||
| chr11:34135889
|
A | AG | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(234): Show | 261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.2028+598_2028+599i others(3): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135889 | ||||||
| chr11:34136084
|
A | AT | 5 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0009t0007g0008others(2): Show | 6 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2029-543dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr11 | 34136084 | |||||
| chr11:34136162
|
A | C | 13 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(10): Show | 15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2029-480A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34136162 | ||||||
| chr11:34136345
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134 | 3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2029-297G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34136345 | ||||||
| chr11:34136441
|
T | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2029-201T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34136441 | ||||||
| chr11:34136864
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.2162+89A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 20/28 | chr11 | 34136864 | ||||||
| chr11:34136884
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.2163-94T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 20/28 | chr11 | 34136884 | ||||||
| chr11:34137034
|
A | G | 3 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134 | 3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
splice_region_variant&intron_variant | LOW | c.2211+8A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137034 | ||||||
| chr11:34137038
|
A | G | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0005t0004g0006others(4): Show | 8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2211+12A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137038 | ||||||
| chr11:34137161
|
T | C | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2211+135T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137161 | ||||||
| chr11:34137262
|
G | A | 4 | a0001c0002t0001g0218a0004c0008t0003g0021a0004c0008t0003g0022others(1): Show | 4 | HG02486.hp1 HG03209.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+236G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137262 | ||||||
| chr11:34137337
|
A | C | 1 | a0001c0004t0008g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2211+311A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137337 | ||||||
| chr11:34137375
|
G | A | 6 | a0001c0004t0005g0024a0001c0004t0005g0026a0001c0004t0005g0027others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+349G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137375 | ||||||
| chr11:34137772
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2211+746A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137772 | ||||||
| chr11:34137858
|
G | C | 2 | a0004c0008t0003g0021a0004c0008t0003g0022 | 2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2211+832G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137858 | ||||||
| chr11:34137985
|
G | T | 1 | a0001c0001t0002g0136 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2211+959G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137985 | ||||||
| chr11:34138025
|
A | G | 2 | a0001c0001t0002g0229a0001c0002t0009g0225 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2211+999A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138025 | ||||||
| chr11:34138083
|
G | T | 1 | a0001c0002t0001g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2211+1057G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138083 | ||||||
| chr11:34138226
|
A | G | 2 | a0001c0001t0002g0067a0001c0002t0002g0055 | 2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2212-965A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138226 | ||||||
| chr11:34138285
|
G | A | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2212-906G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138285 | ||||||
| chr11:34138359
|
C | T | 1 | a0007c0011t0001g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2212-832C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138359 | ||||||
| chr11:34138567
|
C | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2212-624C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138567 | ||||||
| chr11:34138646
|
C | G | 14 | a0001c0001t0001g0215a0001c0003t0001g0002a0001c0003t0001g0033others(11): Show | 16 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2212-545C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138646 | ||||||
| chr11:34138665
|
T | G | 3 | a0001c0002t0001g0007a0001c0002t0001g0047a0001c0019t0001g0151 | 4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212-526T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138665 | ||||||
| chr11:34138667
|
T | C | 2 | a0001c0001t0002g0229a0001c0002t0009g0225 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2212-524T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138667 | ||||||
| chr11:34138675
|
G | A | 3 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134 | 3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2212-516G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138675 | ||||||
| chr11:34138779
|
T | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0019others(47): Show | 54 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2212-412T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138779 | ||||||
| chr11:34139024
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0181 | 2 | NA18944.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2212-167G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34139024 | ||||||
| chr11:34139132
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2212-59T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34139132 | ||||||
| chr11:34139309
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2308+22G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 22/28 | chr11 | 34139309 | ||||||
| chr11:34139365
|
T | C | 1 | a0001c0002t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2309-20T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 22/28 | chr11 | 34139365 | ||||||
| chr11:34139917
|
ATG | A | 3 | a0001c0001t0006g0056a0001c0001t0006g0121a0001c0001t0006g0123 | 3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2419+426_2419+427d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr11 | 34139917 | |||||
| chr11:34140039
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2420-361A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140039 | ||||||
| chr11:34140086
|
A | G | 1 | a0001c0001t0001g0009 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2420-314A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140086 | ||||||
| chr11:34140109
|
G | A | 1 | a0004c0008t0003g0021 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2420-291G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140109 | ||||||
| chr11:34140194
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2420-206G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140194 | ||||||
| chr11:34140327
|
G | A | 3 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0152 | 3 | HG02559.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2420-73G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140327 | ||||||
| chr11:34140357
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2420-43C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140357 | ||||||
| chr11:34140360
|
C | T | 7 | a0001c0001t0002g0078a0001c0001t0002g0093a0001c0001t0002g0094others(4): Show | 7 | HG01123.hp1 HG01175.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2420-40C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140360 | ||||||
| chr11:34140641
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA18971.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2592+69G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140641 | ||||||
| chr11:34140676
|
C | A | 1 | a0010c0017t0001g0059 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2592+104C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140676 | ||||||
| chr11:34140683
|
C | T | 1 | a0001c0004t0008g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2592+111C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140683 | ||||||
| chr11:34140684
|
A | C | 1 | a0011c0018t0001g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2592+112A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140684 | ||||||
| chr11:34140953
|
A | G | 7 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0005t0004g0006others(4): Show | 8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2593-136A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140953 | ||||||
| chr11:34141229
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2712+21G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141229 | ||||||
| chr11:34141287
|
CAT | C | 8 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2712+80_2712+81del others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141287 | ||||||
| chr11:34141321
|
T | TCA | 13 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0057others(10): Show | 15 | HG01071.hp1 HG01106.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2712+138_2712+139d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141321 | |||||
| chr11:34141321
|
TCA | T | 30 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0215others(27): Show | 32 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.2712+138_2712+139d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141321 | |||||
| chr11:34141340
|
C | G | 40 | a0001c0001t0001g0165a0001c0001t0002g0003a0001c0001t0002g0013others(37): Show | 44 | HG00673.hp2 HG00733.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2712+132C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141340 | ||||||
| chr11:34141407
|
A | ATC | 26 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0100others(23): Show | 27 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.2712+200_2712+201d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141407 | |||||
| chr11:34141408
|
T | TCACACAC others(3): Show |
1 | a0001c0004t0005g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2712+234_2712+243d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCACACAC others(5): Show |
1 | a0001c0004t0005g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2712+232_2712+243d others(14): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCACACAC others(7): Show |
1 | a0001c0004t0005g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2712+230_2712+243d others(16): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCACACAC others(11): Show |
1 | a0001c0004t0005g0027 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2712+226_2712+243d others(20): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCACACAC others(17): Show |
1 | a0001c0020t0005g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2712+220_2712+243d others(26): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCTCA | 12 | a0001c0001t0001g0061a0001c0001t0001g0079a0001c0001t0001g0090others(9): Show | 12 | HG02071.hp2 HG02129.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2712+201_2712+202i others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCTCACA | 5 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0099others(2): Show | 7 | HG00597.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2712+201_2712+202i others(8): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
T | TCTCACAC others(3): Show |
1 | a0001c0001t0001g0085 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2712+201_2712+202i others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCA | T | 39 | a0001c0001t0001g0016a0001c0001t0001g0157a0001c0001t0001g0163others(36): Show | 46 | HG00673.hp2 HG00733.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.2712+242_2712+243d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCACA | T | 14 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0066others(11): Show | 15 | HG00323.hp2 HG01109.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2712+240_2712+243d others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCACACA | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0076others(15): Show | 19 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2712+238_2712+243d others(8): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCACACAC others(1): Show |
T | 11 | a0001c0001t0001g0049a0001c0001t0001g0075a0001c0001t0001g0111others(8): Show | 12 | HG00733.hp2 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2712+236_2712+243d others(10): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCACACAC others(3): Show |
T | 3 | a0001c0001t0001g0215a0001c0004t0003g0029a0001c0004t0003g0030 | 3 | HG02258.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2712+234_2712+243d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCACACAC others(5): Show |
T | 2 | a0001c0002t0001g0134a0001c0002t0001g0218 | 2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2712+232_2712+243d others(14): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141408
|
TCACACAC others(7): Show |
T | 1 | a0001c0003t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2712+230_2712+243d others(16): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | |||||
| chr11:34141410
|
A | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(94): Show | 108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2712+202A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141410 | ||||||
| chr11:34141412
|
A | T | 39 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0199others(36): Show | 45 | HG00673.hp2 HG00733.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2712+204A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141412 | ||||||
| chr11:34141414
|
A | T | 19 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0066others(16): Show | 20 | HG00323.hp2 HG01109.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.2712+206A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141414 | ||||||
| chr11:34141416
|
A | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0076others(14): Show | 18 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2712+208A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141416 | ||||||
| chr11:34141418
|
A | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0111a0001c0002t0001g0007others(6): Show | 10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2712+210A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141418 | ||||||
| chr11:34141420
|
A | T | 3 | a0001c0001t0001g0215a0001c0004t0003g0029a0001c0004t0003g0030 | 3 | HG02258.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2712+212A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141420 | ||||||
| chr11:34141422
|
A | T | 2 | a0001c0002t0001g0134a0001c0002t0001g0218 | 2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2712+214A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141422 | ||||||
| chr11:34141424
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2712+216A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141424 | ||||||
| chr11:34141424
|
A | T | 1 | a0001c0003t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2712+216A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141424 | ||||||
| chr11:34141452
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2712+244G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141452 | ||||||
| chr11:34141659
|
G | A | 1 | a0001c0001t0002g0004 | 3 | HG03654.hp1 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2713-60G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141659 | ||||||
| chr11:34142019
|
T | G | 6 | a0001c0004t0005g0024a0001c0004t0005g0026a0001c0004t0005g0027others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2811+202T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142019 | ||||||
| chr11:34142069
|
T | C | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2812-206T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142069 | ||||||
| chr11:34142080
|
G | A | 2 | a0001c0002t0001g0226a0001c0002t0001g0227 | 2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2812-195G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142080 | ||||||
| chr11:34142141
|
A | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0177a0001c0001t0001g0179others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2812-134A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142141 | ||||||
| chr11:34142158
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(233): Show | 260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.2812-117T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142158 | ||||||
| chr11:34142229
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2812-46C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142229 | ||||||
| chr11:34142354
|
G | C | 3 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134 | 3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
splice_region_variant&intron_variant | LOW | c.2885+6G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142354 | ||||||
| chr11:34142433
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2885+85C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142433 | ||||||
| chr11:34142501
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2885+153T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142501 | ||||||
| chr11:34142536
|
C | T | 18 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(15): Show | 21 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2885+188C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142536 | ||||||
| chr11:34142549
|
C | T | 2 | a0001c0002t0001g0069a0001c0002t0001g0070 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2885+201C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142549 | ||||||
| chr11:34142550
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2885+202G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142550 | ||||||
| chr11:34142622
|
G | A | 1 | a0001c0002t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2885+274G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142622 | ||||||
| chr11:34142681
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2885+333G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142681 | ||||||
| chr11:34142877
|
G | A | 1 | a0004c0008t0003g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2885+529G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142877 | ||||||
| chr11:34143027
|
A | G | 1 | a0001c0004t0008g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2886-418A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34143027 | ||||||
| chr11:34143313
|
A | G | 1 | a0001c0001t0002g0229 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2886-132A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34143313 | ||||||
| chr11:34143532
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0140 | 2 | HG01081.hp1 HG01261.hp1 |
splice_region_variant&intron_variant | LOW | c.2969+4A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34143532 | ||||||
| chr11:34143696
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2969+168C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34143696 | ||||||
| chr11:34143962
|
C | T | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2969+434C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34143962 | ||||||
| chr11:34144163
|
A | G | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2969+635A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144163 | ||||||
| chr11:34144172
|
C | T | 1 | a0001c0009t0007g0008 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2969+644C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144172 | ||||||
| chr11:34144181
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2969+653T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144181 | ||||||
| chr11:34144246
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2969+718G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144246 | ||||||
| chr11:34144307
|
G | T | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2969+779G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144307 | ||||||
| chr11:34144313
|
T | A | 2 | a0001c0001t0002g0080a0001c0001t0002g0105 | 2 | HG01433.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2969+785T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144313 | ||||||
| chr11:34144332
|
C | T | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2969+804C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144332 | ||||||
| chr11:34144400
|
G | A | 5 | a0001c0005t0004g0006a0001c0005t0004g0043a0001c0005t0004g0044others(2): Show | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2969+872G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144400 | ||||||
| chr11:34144489
|
C | A | 1 | a0001c0001t0001g0010 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2969+961C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144489 | ||||||
| chr11:34144629
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2969+1101C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144629 | ||||||
| chr11:34144746
|
A | G | 4 | a0001c0002t0001g0130a0001c0002t0001g0131a0001c0002t0001g0134others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2969+1218A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144746 | ||||||
| chr11:34145000
|
C | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0002t0001g0069others(12): Show | 17 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2970-1084C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145000 | ||||||
| chr11:34145237
|
C | T | 1 | a0001c0019t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2970-847C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145237 | ||||||
| chr11:34145349
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG00438.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2970-735T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145349 | ||||||
| chr11:34145425
|
G | A | 2 | a0001c0002t0001g0130a0001c0002t0001g0134 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2970-659G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145425 | ||||||
| chr11:34145438
|
G | A | 3 | a0004c0008t0003g0021a0004c0008t0003g0022a0004c0008t0003g0023 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2970-646G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145438 | ||||||
| chr11:34145529
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2970-555T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145529 | ||||||
| chr11:34145633
|
T | C | 12 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(9): Show | 14 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2970-451T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145633 | ||||||
| chr11:34145694
|
G | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2970-390G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145694 | ||||||
| chr11:34145700
|
A | ATATGT | 6 | a0001c0003t0001g0002a0001c0003t0001g0033a0001c0003t0001g0034others(3): Show | 8 | HG01243.hp2 HG02109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-383_2970-379d others(7): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr11 | 34145700 | |||||
| chr11:34145729
|
G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0047 | 3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2970-355G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145729 | ||||||
| chr11:34145825
|
G | A | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-259G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145825 | ||||||
| chr11:34145880
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.2970-204G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145880 | ||||||
| chr11:34145953
|
T | C | 8 | a0001c0004t0003g0029a0001c0004t0003g0030a0001c0004t0005g0024others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-131T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145953 | ||||||
| chr11:34145966
|
C | G | 5 | a0001c0003t0003g0032a0001c0003t0003g0042a0004c0008t0003g0021others(2): Show | 5 | HG03041.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2970-118C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145966 | ||||||
| chr11:34145984
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2970-100C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145984 |