Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 60560 |
|---|---|
| ensemblid | ENSG00000135040.16 |
| hgncid | 24340 |
| symbol | NAA35 |
| name | N-alpha-acetyltransferase 35, NatC auxiliary subunit |
| refseq_nuc | NM_024635.4 |
| refseq_prot | NP_078911.3 |
| ensembl_nuc | ENST00000361671.10 |
| ensembl_prot | ENSP00000354972.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 85941146 |
| end | 86025462 |
| strand | + |
| ver | v1.2 |
| region | chr9:85941146-86025462 |
| region5000 | chr9:85936146-86030462 |
| regionname0 | NAA35_chr9_85941146_86025462 |
| regionname5000 | NAA35_chr9_85936146_86030462 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 725 | 282 | 78 | 42 | 126 | 8 | 26 | 100 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0002 | 0/0 | 725 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0003 | 0/0 | 725 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0004 | 0/0 | 725 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0005 | 0/0 | 725 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2178 | 279 | 78 | 41 | 125 | 8 | 25 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| c0002 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| c0003 | 0/0 | 2178 | 2 | 0 | 0 | 1 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| c0004 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| c0005 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| c0006 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| c0007 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3636 | 127 | 25 | 17 | 66 | 5 | 13 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0002 | 0/0 | 3636 | 65 | 5 | 5 | 52 | 0 | 3 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0003 | 0/1 | 3636 | 43 | 19 | 12 | 4 | 1 | 6 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0004 | 0/0 | 3636 | 26 | 25 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0005 | 0/0 | 3636 | 5 | 0 | 4 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0006 | 0/0 | 3636 | 4 | 0 | 2 | 0 | 1 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0007 | 0/0 | 3636 | 3 | 3 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0008 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0009 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0010 | 0/0 | 3636 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0011 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0012 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0013 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0014 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0015 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0016 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0017 | 0/0 | 3636 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0018 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0019 | 0/0 | 3636 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0020 | 0/0 | 3636 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0021 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| t0022 | 0/0 | 3636 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2178 | 279 | 78 | 41 | 125 | 8 | 25 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0003 | 0/0 | 2178 | 2 | 0 | 0 | 1 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0006 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0002c0004 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0003c0002 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0004c0005 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0005c0007 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5813 | 125 | 25 | 15 | 66 | 5 | 13 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0002 | 0/0 | 5813 | 63 | 4 | 4 | 52 | 0 | 3 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0003 | 0/1 | 5813 | 41 | 17 | 12 | 4 | 1 | 6 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0004 | 0/0 | 5813 | 26 | 25 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0005 | 0/0 | 5813 | 5 | 0 | 4 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0006 | 0/0 | 5813 | 4 | 0 | 2 | 0 | 1 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0007 | 0/0 | 5813 | 3 | 3 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0008 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0011 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0012 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0014 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0015 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0016 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0017 | 0/0 | 5813 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0018 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0019 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0020 | 0/0 | 5813 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0021 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0001t0022 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0003t0009 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0003t0010 | 0/0 | 5813 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0001c0006t0001 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0002c0004t0002 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0002c0004t0013 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0003c0002t0003 | 0/0 | 5813 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0004c0005t0001 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| a0005c0007t0002 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | copy fasta | chr9 | 85936146 | 86030462 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0007g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0008g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0011g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0012g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0014g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0016g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0017g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0018g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0019g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0020g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0021g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0003t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0003t0010g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0006t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0002c0004t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0002c0004t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0003c0002t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0003c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0004c0005t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0005c0007t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0114 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0231 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00673 | hp1 | a0001 | c0003 | t0009 | g0015 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0237 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01106 | hp1 | a0001 | c0001 | t0016 | g0238 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0273 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01243 | hp1 | a0001 | c0006 | t0001 | g0220 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01243 | hp2 | a0005 | c0007 | t0002 | g0060 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0227 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0011 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01346 | hp2 | a0004 | c0005 | t0001 | g0132 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0232 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01433 | hp2 | a0001 | c0001 | t0021 | g0140 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0151 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0272 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0100 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0233 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02647 | hp2 | a0002 | c0004 | t0013 | g0016 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02717 | hp1 | a0003 | c0002 | t0003 | g0099 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02723 | hp1 | a0003 | c0002 | t0003 | g0098 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0234 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0017 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0097 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0263 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03017 | hp1 | a0001 | c0003 | t0010 | g0014 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0269 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04204 | hp1 | a0001 | c0001 | t0020 | g0196 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18970 | hp2 | a0001 | c0001 | t0018 | g0239 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19066 | hp1 | a0001 | c0001 | t0019 | g0155 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | ASW | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | ASW | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0222 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0221 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0111 | REF | REF | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:85978322
|
C | G | 1 | a0002 | 2 | HG02647.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.818C>G | p.Ser273Cys | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/23 | 951/5813 | 818/2178 | 273/725 | chr9 | 85978322 | ||
| chr9:85978360
|
C | A | 1 | a0004 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.856C>A | p.Gln286Lys | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/23 | 989/5813 | 856/2178 | 286/725 | chr9 | 85978360 | ||
| chr9:86013837
|
A | C | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1508A>C | p.Tyr503Ser | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/23 | 1641/5813 | 1508/2178 | 503/725 | chr9 | 86013837 | ||
| chr9:86018741
|
C | T | 1 | a0003 | 2 | HG02717.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1957C>T | p.Pro653Ser | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/23 | 2090/5813 | 1957/2178 | 653/725 | chr9 | 86018741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:86013129
|
C | T | 1 | a0001c0003 | 2 | HG00673.hp1 HG03017.hp1 |
synonymous_variant | LOW | c.1374C>T | p.Ala458Ala | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/23 | 1507/5813 | 1374/2178 | 458/725 | chr9 | 86013129 | ||
| chr9:86016581
|
G | A | 1 | a0001c0006 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1611G>A | p.Leu537Leu | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/23 | 1744/5813 | 1611/2178 | 537/725 | chr9 | 86016581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:85941169
|
G | A | 1 | a0001c0001t0008 | 1 | HG01975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/23 | 991 | chr9 | 85941169 | |||||
| chr9:85941206
|
C | A | 2 | a0001c0003t0009a0001c0003t0010 | 2 | HG00673.hp1 HG03017.hp1 |
5_prime_UTR_variant | MODIFIER | c.-73C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/23 | 954 | chr9 | 85941206 | |||||
| chr9:86021972
|
G | A | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(11): Show | 142 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*12G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 12 | chr9 | 86021972 | |||||
| chr9:86022045
|
C | T | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 85 | chr9 | 86022045 | |||||
| chr9:86022511
|
A | G | 1 | a0001c0001t0006 | 4 | HG00280.hp2 HG00738.hp2 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*551A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 551 | chr9 | 86022511 | |||||
| chr9:86023024
|
A | C | 1 | a0001c0001t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1064A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1064 | chr9 | 86023024 | |||||
| chr9:86023030
|
A | G | 1 | a0001c0001t0007 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1070A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1070 | chr9 | 86023030 | |||||
| chr9:86023065
|
G | T | 5 | a0001c0001t0002a0001c0001t0012a0002c0004t0002others(2): Show | 67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1105G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1105 | chr9 | 86023065 | |||||
| chr9:86023252
|
A | T | 11 | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(8): Show | 98 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1292A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1292 | chr9 | 86023252 | |||||
| chr9:86023266
|
C | T | 1 | a0002c0004t0013 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1306C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1306 | chr9 | 86023266 | |||||
| chr9:86023362
|
T | C | 1 | a0001c0001t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1402 | chr9 | 86023362 | |||||
| chr9:86023482
|
A | C | 1 | a0001c0001t0021 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1522A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1522 | chr9 | 86023482 | |||||
| chr9:86023609
|
C | G | 1 | a0001c0001t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1649 | chr9 | 86023609 | |||||
| chr9:86023858
|
T | C | 1 | a0001c0001t0017 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1898T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1898 | chr9 | 86023858 | |||||
| chr9:86024059
|
C | G | 1 | a0001c0001t0020 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2099 | chr9 | 86024059 | |||||
| chr9:86024247
|
G | C | 1 | a0001c0001t0005 | 5 | HG00639.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2287G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2287 | chr9 | 86024247 | |||||
| chr9:86024462
|
A | G | 1 | a0001c0001t0012 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2502A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2502 | chr9 | 86024462 | |||||
| chr9:86024543
|
T | A | 1 | a0001c0001t0018 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2583T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2583 | chr9 | 86024543 | |||||
| chr9:86024616
|
G | A | 1 | a0001c0003t0009 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2656G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2656 | chr9 | 86024616 | |||||
| chr9:86024815
|
A | G | 2 | a0001c0003t0009a0001c0003t0010 | 2 | HG00673.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2855A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2855 | chr9 | 86024815 | |||||
| chr9:86025163
|
T | C | 2 | a0001c0003t0009a0001c0003t0010 | 2 | HG00673.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3203T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 3203 | chr9 | 86025163 | |||||
| chr9:86025237
|
C | T | 1 | a0001c0001t0019 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3277C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 3277 | chr9 | 86025237 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:85941328
|
C | T | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6+55C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941328 | ||||||
| chr9:85941338
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6+65C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941338 | ||||||
| chr9:85941354
|
T | C | 4 | a0001c0003t0009g0015a0001c0003t0010g0014a0002c0004t0002g0017others(1): Show | 4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+81T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941354 | ||||||
| chr9:85941414
|
G | C | 39 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0022others(36): Show | 40 | HG00673.hp1 HG00741.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.-6+141G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941414 | ||||||
| chr9:85941450
|
C | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG00558.hp2 HG02027.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+177C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941450 | ||||||
| chr9:85941517
|
A | T | 35 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0022others(32): Show | 36 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6+244A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941517 | ||||||
| chr9:85941677
|
G | T | 1 | a0001c0001t0004g0254 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-6+404G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941677 | ||||||
| chr9:85941772
|
C | G | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-5-383C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941772 | ||||||
| chr9:85941950
|
A | G | 3 | a0001c0001t0001g0253a0001c0003t0009g0015a0001c0003t0010g0014 | 3 | HG00597.hp2 HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-5-205A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941950 | ||||||
| chr9:85941988
|
G | T | 1 | a0001c0001t0004g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-5-167G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941988 | ||||||
| chr9:85942097
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-5-58C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85942097 | ||||||
| chr9:85942349
|
AAACTT | A | 7 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+68_124+72delAC others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85942349 | |||||
| chr9:85942496
|
A | G | 2 | a0001c0001t0002g0251a0001c0001t0002g0252 | 2 | NA18944.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.124+213A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85942496 | ||||||
| chr9:85942920
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 6 | NA18612.hp2 NA18947.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+637C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85942920 | ||||||
| chr9:85943004
|
A | AT | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.124+722dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85943004 | |||||
| chr9:85943153
|
T | C | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124+870T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943153 | ||||||
| chr9:85943168
|
C | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+885C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943168 | ||||||
| chr9:85943592
|
G | GT | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124+1310dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85943592 | |||||
| chr9:85943629
|
A | G | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.124+1346A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943629 | ||||||
| chr9:85943702
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.124+1419G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943702 | ||||||
| chr9:85944217
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.124+1934A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85944217 | ||||||
| chr9:85944513
|
A | G | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.124+2230A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85944513 | ||||||
| chr9:85944660
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+2377G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85944660 | ||||||
| chr9:85945250
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.124+2967G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945250 | ||||||
| chr9:85945358
|
T | A | 3 | a0001c0001t0011g0097a0003c0002t0003g0098a0003c0002t0003g0099 | 3 | HG02717.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.124+3075T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945358 | ||||||
| chr9:85945472
|
T | G | 39 | a0001c0001t0001g0105a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 41 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.124+3189T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945472 | ||||||
| chr9:85945558
|
C | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | NA18972.hp1 NA18974.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+3275C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945558 | ||||||
| chr9:85945591
|
T | TCTCGGCT others(2): Show |
37 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(34): Show | 38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3313_124+3321d others(11): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85945591 | |||||
| chr9:85945594
|
C | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.124+3311C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945594 | ||||||
| chr9:85945595
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | NA18944.hp2 NA18960.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.124+3312G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945595 | ||||||
| chr9:85945744
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+3461C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945744 | ||||||
| chr9:85945747
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | NA18953.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.124+3464C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945747 | ||||||
| chr9:85945771
|
G | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124+3488G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945771 | ||||||
| chr9:85945785
|
C | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124+3502C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945785 | ||||||
| chr9:85945810
|
T | C | 37 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(34): Show | 38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3527T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945810 | ||||||
| chr9:85945910
|
C | T | 2 | a0001c0001t0003g0127a0001c0001t0003g0128 | 2 | HG01257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.124+3627C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945910 | ||||||
| chr9:85946375
|
C | A | 1 | a0001c0001t0004g0256 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.124+4092C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946375 | ||||||
| chr9:85946669
|
A | T | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124+4386A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946669 | ||||||
| chr9:85946684
|
A | AT | 110 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0039others(107): Show | 119 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.124+4413dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85946684 | |||||
| chr9:85946684
|
A | ATT | 30 | a0001c0001t0002g0092a0001c0001t0003g0026a0001c0001t0003g0027others(27): Show | 31 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.124+4412_124+4413d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85946684 | |||||
| chr9:85946684
|
A | ATTT | 9 | a0001c0001t0001g0253a0001c0001t0003g0022a0001c0001t0003g0029others(6): Show | 9 | HG00597.hp2 HG00673.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+4411_124+4413d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85946684 | |||||
| chr9:85946830
|
C | A | 1 | a0004c0005t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.124+4547C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946830 | ||||||
| chr9:85946969
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.124+4686A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946969 | ||||||
| chr9:85947015
|
G | A | 3 | a0001c0001t0001g0253a0001c0003t0009g0015a0001c0003t0010g0014 | 3 | HG00597.hp2 HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+4732G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947015 | ||||||
| chr9:85947036
|
T | A | 1 | a0001c0001t0001g0133 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.124+4753T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947036 | ||||||
| chr9:85947080
|
A | G | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.124+4797A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947080 | ||||||
| chr9:85947236
|
A | AT | 7 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0124others(4): Show | 7 | HG01346.hp1 HG01496.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+4962dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85947236 | |||||
| chr9:85947283
|
A | G | 1 | a0001c0001t0003g0111 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.124+5000A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947283 | ||||||
| chr9:85947326
|
T | G | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0254 | 3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.124+5043T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947326 | ||||||
| chr9:85947445
|
A | T | 1 | a0001c0001t0002g0091 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.124+5162A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947445 | ||||||
| chr9:85947477
|
C | T | 3 | a0001c0001t0006g0231a0001c0001t0006g0232a0001c0001t0006g0233 | 3 | HG00280.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.124+5194C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947477 | ||||||
| chr9:85947591
|
C | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+5308C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947591 | ||||||
| chr9:85947640
|
A | G | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0003g0110 | 3 | HG03017.hp2 HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.124+5357A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947640 | ||||||
| chr9:85947644
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+5361G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947644 | ||||||
| chr9:85947650
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+5367G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947650 | ||||||
| chr9:85947654
|
C | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124+5371C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947654 | ||||||
| chr9:85947713
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124+5430C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947713 | ||||||
| chr9:85947768
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.124+5485C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947768 | ||||||
| chr9:85947810
|
C | T | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+5527C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947810 | ||||||
| chr9:85947810
|
CCT | C | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124+5531_124+5532d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85947810 | |||||
| chr9:85948039
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+5756A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948039 | ||||||
| chr9:85948149
|
G | A | 140 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0001g0134others(137): Show | 149 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.124+5866G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948149 | ||||||
| chr9:85948172
|
T | C | 1 | a0001c0001t0002g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.124+5889T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948172 | ||||||
| chr9:85948696
|
T | C | 10 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+6413T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948696 | ||||||
| chr9:85948746
|
G | A | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124+6463G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948746 | ||||||
| chr9:85948983
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124+6700A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948983 | ||||||
| chr9:85949003
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02027.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.124+6720C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949003 | ||||||
| chr9:85949045
|
C | G | 1 | a0001c0001t0001g0228 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.124+6762C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949045 | ||||||
| chr9:85949292
|
T | C | 1 | a0001c0001t0004g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124+7009T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949292 | ||||||
| chr9:85949299
|
C | CT | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.124+7028dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85949299 | |||||
| chr9:85949406
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.125-6954T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949406 | ||||||
| chr9:85949432
|
C | T | 2 | a0001c0001t0004g0273a0001c0001t0022g0272 | 2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.125-6928C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949432 | ||||||
| chr9:85949434
|
A | G | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.125-6926A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949434 | ||||||
| chr9:85949600
|
T | G | 1 | a0001c0001t0003g0112 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.125-6760T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949600 | ||||||
| chr9:85949790
|
A | G | 2 | a0001c0001t0005g0011a0001c0001t0005g0227 | 3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.125-6570A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949790 | ||||||
| chr9:85949801
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.125-6559G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949801 | ||||||
| chr9:85949822
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125-6538A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949822 | ||||||
| chr9:85949833
|
T | C | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.125-6527T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949833 | ||||||
| chr9:85949903
|
T | C | 1 | a0001c0001t0011g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-6457T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949903 | ||||||
| chr9:85949925
|
G | A | 19 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(16): Show | 22 | HG00597.hp1 HG00609.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-6435G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949925 | ||||||
| chr9:85950118
|
A | G | 2 | a0001c0001t0005g0011a0001c0001t0005g0227 | 3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.125-6242A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950118 | ||||||
| chr9:85950244
|
T | A | 37 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(34): Show | 38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-6116T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950244 | ||||||
| chr9:85950333
|
T | C | 136 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0002g0001others(133): Show | 145 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.125-6027T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950333 | ||||||
| chr9:85950465
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.125-5895G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950465 | ||||||
| chr9:85950485
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5875A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950485 | ||||||
| chr9:85950492
|
G | A | 1 | a0001c0001t0003g0122 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.125-5868G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950492 | ||||||
| chr9:85950564
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5796C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950564 | ||||||
| chr9:85950617
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5743G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950617 | ||||||
| chr9:85950684
|
C | G | 97 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(94): Show | 104 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.125-5676C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950684 | ||||||
| chr9:85950728
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.125-5632C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950728 | ||||||
| chr9:85950733
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.125-5627C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950733 | ||||||
| chr9:85950745
|
C | A | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-5615C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950745 | ||||||
| chr9:85950790
|
A | G | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-5570A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950790 | ||||||
| chr9:85950795
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5565T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950795 | ||||||
| chr9:85950818
|
G | A | 39 | a0001c0001t0001g0105a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 41 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.125-5542G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950818 | ||||||
| chr9:85950846
|
A | C | 3 | a0001c0001t0007g0221a0001c0001t0007g0222a0001c0001t0007g0223 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.125-5514A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950846 | ||||||
| chr9:85950874
|
C | T | 1 | a0001c0006t0001g0220 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-5486C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950874 | ||||||
| chr9:85950887
|
A | G | 1 | a0001c0001t0002g0089 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.125-5473A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950887 | ||||||
| chr9:85950890
|
A | G | 14 | a0001c0001t0001g0105a0001c0001t0003g0018a0001c0001t0003g0019others(11): Show | 14 | HG00741.hp2 HG01167.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-5470A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950890 | ||||||
| chr9:85950907
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5453C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950907 | ||||||
| chr9:85951131
|
C | T | 56 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-5229C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951131 | ||||||
| chr9:85951137
|
CA | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0242others(3): Show | 6 | HG01167.hp2 HG02055.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-5208delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85951137 | |||||
| chr9:85951190
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5170A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951190 | ||||||
| chr9:85951207
|
G | A | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-5153G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951207 | ||||||
| chr9:85951293
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5067A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951293 | ||||||
| chr9:85951294
|
T | C | 1 | a0001c0001t0003g0127 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.125-5066T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951294 | ||||||
| chr9:85951681
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.125-4679A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951681 | ||||||
| chr9:85951739
|
C | T | 56 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-4621C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951739 | ||||||
| chr9:85951743
|
C | T | 1 | a0002c0004t0002g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125-4617C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951743 | ||||||
| chr9:85951835
|
T | A | 1 | a0001c0001t0002g0062 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.125-4525T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951835 | ||||||
| chr9:85951849
|
G | A | 1 | a0002c0004t0013g0016 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.125-4511G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951849 | ||||||
| chr9:85951861
|
T | C | 22 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(19): Show | 23 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.125-4499T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951861 | ||||||
| chr9:85951994
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.125-4366A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951994 | ||||||
| chr9:85952010
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-4350C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952010 | ||||||
| chr9:85952082
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.125-4278C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952082 | ||||||
| chr9:85952181
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-4179T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952181 | ||||||
| chr9:85952281
|
G | GT | 3 | a0001c0001t0003g0026a0001c0001t0003g0028a0001c0001t0003g0029 | 3 | HG02055.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.125-4073dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85952281 | |||||
| chr9:85952288
|
G | GT | 61 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0001g0250others(58): Show | 67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.125-4058dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85952288 | |||||
| chr9:85952288
|
G | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4072G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952288 | ||||||
| chr9:85952517
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.125-3843T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952517 | ||||||
| chr9:85952585
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-3775G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952585 | ||||||
| chr9:85952593
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-3767G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952593 | ||||||
| chr9:85952593
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-3767G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952593 | ||||||
| chr9:85952601
|
T | C | 1 | a0001c0001t0003g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.125-3759T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952601 | ||||||
| chr9:85952654
|
AT | A | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.125-3699delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85952654 | |||||
| chr9:85952684
|
A | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-3676A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952684 | ||||||
| chr9:85952845
|
T | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01168.hp2 HG01433.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3515T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952845 | ||||||
| chr9:85952865
|
G | T | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-3495G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952865 | ||||||
| chr9:85952867
|
T | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.125-3493T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952867 | ||||||
| chr9:85952882
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.125-3478A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952882 | ||||||
| chr9:85953009
|
A | C | 33 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(30): Show | 34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.125-3351A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953009 | ||||||
| chr9:85953217
|
A | AT | 17 | a0001c0001t0001g0041a0001c0001t0001g0095a0001c0001t0001g0137others(14): Show | 17 | HG00597.hp2 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.125-3121dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | |||||
| chr9:85953217
|
A | ATT | 44 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(41): Show | 50 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.125-3122_125-3121d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | |||||
| chr9:85953217
|
A | ATTT | 14 | a0001c0001t0001g0084a0001c0001t0002g0045a0001c0001t0002g0046others(11): Show | 14 | HG01106.hp2 HG01358.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-3123_125-3121d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | |||||
| chr9:85953217
|
AT | A | 6 | a0001c0001t0001g0139a0001c0001t0001g0242a0001c0001t0001g0250others(3): Show | 6 | HG01167.hp2 HG01168.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3121delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | |||||
| chr9:85953218
|
T | A | 33 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(30): Show | 34 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-3142T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953218 | ||||||
| chr9:85953239
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.125-3121T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953239 | ||||||
| chr9:85953329
|
C | G | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-3031C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953329 | ||||||
| chr9:85953394
|
C | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.125-2966C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953394 | ||||||
| chr9:85953778
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-2582C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953778 | ||||||
| chr9:85954022
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-2338C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954022 | ||||||
| chr9:85954239
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.125-2121C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954239 | ||||||
| chr9:85954253
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-2107G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954253 | ||||||
| chr9:85954324
|
C | G | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-2036C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954324 | ||||||
| chr9:85954345
|
A | G | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-2015A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954345 | ||||||
| chr9:85954430
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.125-1930C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954430 | ||||||
| chr9:85954509
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1851A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954509 | ||||||
| chr9:85954639
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.125-1721C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954639 | ||||||
| chr9:85954910
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1450T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954910 | ||||||
| chr9:85954991
|
C | T | 1 | a0001c0001t0003g0112 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.125-1369C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954991 | ||||||
| chr9:85955000
|
C | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1360C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955000 | ||||||
| chr9:85955126
|
G | A | 4 | a0001c0003t0009g0015a0001c0003t0010g0014a0002c0004t0002g0017others(1): Show | 4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1234G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955126 | ||||||
| chr9:85955128
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1232G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955128 | ||||||
| chr9:85955148
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.125-1212C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955148 | ||||||
| chr9:85955228
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1132G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955228 | ||||||
| chr9:85955327
|
C | CAT | 3 | a0001c0001t0001g0033a0001c0001t0001g0157a0001c0001t0001g0228 | 3 | HG02040.hp1 NA18945.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.125-1000_125-999du others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | |||||
| chr9:85955327
|
CAT | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0034a0001c0001t0001g0035others(81): Show | 86 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.125-1000_125-999de others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | |||||
| chr9:85955327
|
CATAT | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0135others(12): Show | 15 | HG00741.hp2 HG01106.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-1002_125-999de others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | |||||
| chr9:85955327
|
CATATAT | C | 9 | a0001c0001t0001g0242a0001c0001t0003g0022a0001c0001t0003g0109others(6): Show | 9 | HG01167.hp2 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-1004_125-999de others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | |||||
| chr9:85955327
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0092others(1): Show | 5 | HG01243.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-1006_125-999de others(9): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | |||||
| chr9:85955327
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125-1008_125-999de others(11): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | |||||
| chr9:85955345
|
TATATA | T | 4 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0271others(1): Show | 4 | HG02257.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1014_125-1010d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955345 | ||||||
| chr9:85955346
|
ATATATAT others(8): Show |
A | 1 | a0001c0003t0009g0015 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.125-1012_125-998de others(16): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955346 | |||||
| chr9:85955347
|
TATATA | T | 4 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0270others(1): Show | 5 | HG02258.hp2 HG02280.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-1012_125-1008d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955347 | ||||||
| chr9:85955348
|
ATATATAT others(7): Show |
A | 1 | a0001c0003t0010g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.125-1010_125-997de others(15): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955348 | |||||
| chr9:85955349
|
TATA | T | 8 | a0001c0001t0003g0009a0001c0001t0003g0111a0001c0001t0003g0112others(5): Show | 9 | HG00738.hp1 HG01952.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-1010_125-1008d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955349 | ||||||
| chr9:85955349
|
TATATA | T | 12 | a0001c0001t0003g0029a0001c0001t0004g0256a0001c0001t0004g0259others(9): Show | 12 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-1010_125-1006d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955349 | ||||||
| chr9:85955350
|
A | T | 3 | a0001c0001t0003g0108a0001c0001t0004g0025a0002c0004t0002g0017 | 3 | HG02818.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.125-1010A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955350 | ||||||
| chr9:85955351
|
TATA | T | 7 | a0001c0001t0003g0008a0001c0001t0003g0114a0001c0001t0003g0121others(4): Show | 8 | HG00280.hp1 HG01346.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-1008_125-1006d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955351 | ||||||
| chr9:85955352
|
A | T | 21 | a0001c0001t0002g0082a0001c0001t0002g0090a0001c0001t0003g0019others(18): Show | 21 | HG00741.hp2 HG01496.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-1008A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955352 | ||||||
| chr9:85955354
|
A | ATT | 3 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0089 | 3 | NA18961.hp2 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.125-1005_125-1004i others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955354 | |||||
| chr9:85955354
|
A | T | 56 | a0001c0001t0001g0105a0001c0001t0001g0137a0001c0001t0002g0006others(53): Show | 60 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.125-1006A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955354 | ||||||
| chr9:85955355
|
TATA | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0203a0001c0001t0011g0097 | 3 | HG01168.hp2 HG01515.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.125-1004_125-1002d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955355 | ||||||
| chr9:85955356
|
A | ATT | 15 | a0001c0001t0001g0084a0001c0001t0002g0003a0001c0001t0002g0004others(12): Show | 16 | HG01106.hp2 HG01256.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-1003_125-1002i others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955356 | |||||
| chr9:85955356
|
A | T | 118 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0001g0135others(115): Show | 127 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.125-1004A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955356 | ||||||
| chr9:85955357
|
TATA | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0095a0001c0001t0001g0130 | 3 | NA18960.hp1 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.125-1002_125-1000d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955357 | ||||||
| chr9:85955358
|
A | T | 170 | a0001c0001t0001g0037a0001c0001t0001g0084a0001c0001t0001g0105others(167): Show | 180 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.125-1002A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955358 | ||||||
| chr9:85955359
|
TA | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0129others(4): Show | 8 | HG02735.hp2 HG03139.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-1000delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955359 | ||||||
| chr9:85955360
|
A | T | 201 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0037others(198): Show | 211 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.125-1000A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955360 | ||||||
| chr9:85955362
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0019g0155 | 2 | NA19066.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.125-998T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955362 | ||||||
| chr9:85955393
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.125-967C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955393 | ||||||
| chr9:85955394
|
G | C | 3 | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054 | 3 | HG00597.hp1 HG02132.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.125-966G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955394 | ||||||
| chr9:85955511
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.125-849C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955511 | ||||||
| chr9:85955610
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-750G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955610 | ||||||
| chr9:85955830
|
C | T | 141 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0001g0134others(138): Show | 150 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.125-530C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955830 | ||||||
| chr9:85955835
|
T | G | 2 | a0001c0001t0005g0011a0001c0001t0005g0227 | 3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.125-525T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955835 | ||||||
| chr9:85956164
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0077 | 3 | NA19007.hp2 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.125-196G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85956164 | ||||||
| chr9:85956346
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-14C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85956346 | ||||||
| chr9:85956346
|
CT | C | 7 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0003g0018others(4): Show | 7 | HG00280.hp1 HG01167.hp2 HG01934.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.125-3delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85956346 | |||||
| chr9:85956665
|
A | T | 2 | a0001c0001t0004g0243a0001c0001t0004g0244 | 2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.158+272A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956665 | ||||||
| chr9:85956708
|
A | G | 2 | a0001c0001t0004g0023a0001c0001t0004g0024 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.158+315A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956708 | ||||||
| chr9:85956721
|
A | G | 1 | a0001c0003t0009g0015 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158+328A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956721 | ||||||
| chr9:85956793
|
A | C | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.158+400A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956793 | ||||||
| chr9:85956831
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01975.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.158+438A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956831 | ||||||
| chr9:85956970
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158+577G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956970 | ||||||
| chr9:85957017
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.158+624C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957017 | ||||||
| chr9:85957188
|
T | G | 1 | a0001c0001t0002g0067 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.158+795T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957188 | ||||||
| chr9:85957764
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0002g0065a0001c0001t0002g0066others(1): Show | 4 | NA18940.hp1 NA18945.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-708A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957764 | ||||||
| chr9:85957777
|
C | T | 3 | a0001c0001t0004g0013a0001c0001t0004g0268a0001c0001t0004g0270 | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-695C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957777 | ||||||
| chr9:85957817
|
A | C | 1 | a0001c0001t0003g0127 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.159-655A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957817 | ||||||
| chr9:85957890
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-582C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957890 | ||||||
| chr9:85957895
|
G | T | 56 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.159-577G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957895 | ||||||
| chr9:85957967
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.159-505G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957967 | ||||||
| chr9:85957988
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.159-484C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957988 | ||||||
| chr9:85958035
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159-437G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958035 | ||||||
| chr9:85958139
|
C | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.159-333C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958139 | ||||||
| chr9:85958219
|
G | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.159-253G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958219 | ||||||
| chr9:85958404
|
C | G | 1 | a0001c0001t0003g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.159-68C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958404 | ||||||
| chr9:85958404
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.159-68C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958404 | ||||||
| chr9:85958405
|
G | A | 6 | a0001c0001t0001g0212a0001c0001t0003g0022a0001c0001t0003g0026others(3): Show | 6 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-67G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958405 | ||||||
| chr9:85959094
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.273+508C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959094 | ||||||
| chr9:85959143
|
G | A | 3 | a0001c0001t0004g0013a0001c0001t0004g0268a0001c0001t0004g0270 | 4 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+557G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959143 | ||||||
| chr9:85959270
|
G | A | 1 | a0001c0001t0014g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.274-523G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959270 | ||||||
| chr9:85959293
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.274-500G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959293 | ||||||
| chr9:85959296
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.274-497G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959296 | ||||||
| chr9:85959320
|
G | T | 1 | a0001c0001t0004g0268 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-473G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959320 | ||||||
| chr9:85959333
|
G | A | 1 | a0001c0001t0004g0271 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.274-460G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959333 | ||||||
| chr9:85959376
|
C | CA | 16 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0245others(13): Show | 16 | HG00741.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.274-404dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 85959376 | |||||
| chr9:85959415
|
T | C | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-378T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959415 | ||||||
| chr9:85959512
|
A | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-281A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959512 | ||||||
| chr9:85959612
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.274-181T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959612 | ||||||
| chr9:85959682
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274-111G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959682 | ||||||
| chr9:85959911
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.348+44C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85959911 | ||||||
| chr9:85960300
|
A | G | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+433A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960300 | ||||||
| chr9:85960339
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.348+472C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960339 | ||||||
| chr9:85960699
|
A | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.348+832A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960699 | ||||||
| chr9:85960917
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+1050T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960917 | ||||||
| chr9:85960939
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.348+1072G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960939 | ||||||
| chr9:85961045
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.349-968A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961045 | ||||||
| chr9:85961183
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.349-830A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961183 | ||||||
| chr9:85961204
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.349-809G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961204 | ||||||
| chr9:85961765
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.349-248A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961765 | ||||||
| chr9:85961816
|
G | T | 140 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0001g0134others(137): Show | 149 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.349-197G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961816 | ||||||
| chr9:85961953
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.349-60A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961953 | ||||||
| chr9:85962321
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.516+141T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962321 | ||||||
| chr9:85962490
|
C | CA | 8 | a0001c0001t0001g0037a0001c0001t0001g0129a0001c0001t0001g0130others(5): Show | 8 | HG02027.hp1 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.516+329dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | |||||
| chr9:85962490
|
C | CAAA | 30 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(27): Show | 31 | HG01168.hp1 HG01255.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.516+327_516+329dup others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | |||||
| chr9:85962490
|
C | CAAAA | 102 | a0001c0001t0001g0039a0001c0001t0001g0084a0001c0001t0001g0105others(99): Show | 110 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.516+326_516+329dup others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | |||||
| chr9:85962490
|
C | CAAAAA | 77 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(74): Show | 80 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.516+325_516+329dup others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | |||||
| chr9:85962490
|
C | CAAAAAA | 9 | a0001c0001t0001g0170a0001c0001t0001g0200a0001c0001t0001g0210others(6): Show | 9 | HG00741.hp2 HG02027.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.516+324_516+329dup others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | |||||
| chr9:85962510
|
G | A | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(2): Show | 5 | HG02040.hp1 HG02071.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+330G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962510 | ||||||
| chr9:85962557
|
G | A | 1 | a0001c0001t0003g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516+377G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962557 | ||||||
| chr9:85962562
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+382A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962562 | ||||||
| chr9:85962735
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.516+555G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962735 | ||||||
| chr9:85962815
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.516+635T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962815 | ||||||
| chr9:85962875
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+695T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962875 | ||||||
| chr9:85963186
|
C | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.516+1006C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963186 | ||||||
| chr9:85963231
|
C | T | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+1051C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963231 | ||||||
| chr9:85963263
|
C | CT | 16 | a0001c0001t0001g0043a0001c0001t0001g0165a0001c0001t0001g0169others(13): Show | 16 | HG00597.hp2 HG00741.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.516+1107dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85963263 | |||||
| chr9:85963263
|
CT | C | 103 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0001g0134others(100): Show | 111 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(108): Show |
intron_variant | MODIFIER | c.516+1107delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85963263 | |||||
| chr9:85963363
|
C | T | 42 | a0001c0001t0001g0105a0001c0001t0003g0008a0001c0001t0003g0009others(39): Show | 44 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.516+1183C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963363 | ||||||
| chr9:85963364
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.516+1184G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963364 | ||||||
| chr9:85963371
|
A | G | 23 | a0001c0001t0004g0013a0001c0001t0004g0023a0001c0001t0004g0024others(20): Show | 24 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.516+1191A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963371 | ||||||
| chr9:85963396
|
G | T | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1216G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963396 | ||||||
| chr9:85963449
|
A | G | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+1269A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963449 | ||||||
| chr9:85963489
|
G | C | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.516+1309G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963489 | ||||||
| chr9:85963622
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1442T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963622 | ||||||
| chr9:85963712
|
T | A | 4 | a0001c0003t0009g0015a0001c0003t0010g0014a0002c0004t0002g0017others(1): Show | 4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+1532T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963712 | ||||||
| chr9:85963768
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.516+1588A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963768 | ||||||
| chr9:85963887
|
G | T | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+1707G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963887 | ||||||
| chr9:85963980
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1800T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963980 | ||||||
| chr9:85964063
|
A | T | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1883A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964063 | ||||||
| chr9:85964092
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.516+1912A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964092 | ||||||
| chr9:85964128
|
CT | C | 10 | a0001c0001t0001g0137a0001c0001t0001g0159a0001c0001t0001g0198others(7): Show | 10 | HG00673.hp1 HG01516.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.516+1966delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85964128 | |||||
| chr9:85964128
|
CTT | C | 33 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(30): Show | 34 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.516+1965_516+1966d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85964128 | |||||
| chr9:85964189
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2009T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964189 | ||||||
| chr9:85964399
|
A | T | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2219A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964399 | ||||||
| chr9:85964459
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2279T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964459 | ||||||
| chr9:85964493
|
C | CA | 18 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(15): Show | 19 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.516+2315dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85964493 | |||||
| chr9:85964574
|
T | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2394T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964574 | ||||||
| chr9:85964782
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2602A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964782 | ||||||
| chr9:85964783
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+2603G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964783 | ||||||
| chr9:85964823
|
A | C | 1 | a0001c0001t0001g0249 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.516+2643A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964823 | ||||||
| chr9:85964999
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.516+2819C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964999 | ||||||
| chr9:85965165
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.516+2985G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965165 | ||||||
| chr9:85965236
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+3056A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965236 | ||||||
| chr9:85965310
|
G | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+3130G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965310 | ||||||
| chr9:85965311
|
A | G | 54 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(51): Show | 59 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.516+3131A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965311 | ||||||
| chr9:85965311
|
A | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+3131A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965311 | ||||||
| chr9:85965345
|
G | A | 3 | a0001c0001t0011g0097a0003c0002t0003g0098a0003c0002t0003g0099 | 3 | HG02717.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.516+3165G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965345 | ||||||
| chr9:85965370
|
T | G | 1 | a0001c0001t0005g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.516+3190T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965370 | ||||||
| chr9:85965518
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+3338C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965518 | ||||||
| chr9:85965688
|
A | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+3508A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965688 | ||||||
| chr9:85965690
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+3510T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965690 | ||||||
| chr9:85965694
|
A | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0164 | 3 | HG02132.hp1 NA18968.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.516+3514A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965694 | ||||||
| chr9:85965716
|
G | C | 1 | a0001c0001t0019g0155 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.516+3536G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965716 | ||||||
| chr9:85965779
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+3599T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965779 | ||||||
| chr9:85965942
|
T | C | 6 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(3): Show | 6 | HG01167.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+3762T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965942 | ||||||
| chr9:85966033
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.516+3853A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966033 | ||||||
| chr9:85966099
|
G | A | 1 | a0001c0001t0006g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516+3919G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966099 | ||||||
| chr9:85966100
|
T | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.516+3920T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966100 | ||||||
| chr9:85966113
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+3933A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966113 | ||||||
| chr9:85966216
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+4036T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966216 | ||||||
| chr9:85966268
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+4088G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966268 | ||||||
| chr9:85966324
|
A | T | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+4144A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966324 | ||||||
| chr9:85966544
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.516+4364G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966544 | ||||||
| chr9:85966600
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.516+4420C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966600 | ||||||
| chr9:85966685
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.516+4505A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966685 | ||||||
| chr9:85966882
|
A | G | 223 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(220): Show | 235 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.516+4702A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966882 | ||||||
| chr9:85966910
|
C | A | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+4730C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966910 | ||||||
| chr9:85966999
|
TGGGAGGC others(25): Show |
T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+4850_516+4881d others(34): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85966999 | |||||
| chr9:85967070
|
C | T | 33 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(30): Show | 34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.516+4890C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967070 | ||||||
| chr9:85967194
|
G | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.516+5014G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967194 | ||||||
| chr9:85967234
|
T | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0240a0001c0001t0001g0241 | 4 | NA19004.hp1 NA19064.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+5054T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967234 | ||||||
| chr9:85967394
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.516+5214A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967394 | ||||||
| chr9:85967496
|
A | G | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.516+5316A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967496 | ||||||
| chr9:85967548
|
A | T | 136 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0002g0001others(133): Show | 145 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.516+5368A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967548 | ||||||
| chr9:85967596
|
A | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+5416A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967596 | ||||||
| chr9:85967607
|
C | G | 1 | a0002c0004t0013g0016 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.516+5427C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967607 | ||||||
| chr9:85967629
|
C | T | 10 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+5449C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967629 | ||||||
| chr9:85967663
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+5483A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967663 | ||||||
| chr9:85967719
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+5539G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967719 | ||||||
| chr9:85967727
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.516+5547G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967727 | ||||||
| chr9:85967799
|
C | CA | 106 | a0001c0001t0001g0084a0001c0001t0001g0180a0001c0001t0002g0001others(103): Show | 115 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.516+5631dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85967799 | |||||
| chr9:85967836
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.516+5656T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967836 | ||||||
| chr9:85968146
|
G | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+5966G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968146 | ||||||
| chr9:85968178
|
G | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0187 | 2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.516+5998G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968178 | ||||||
| chr9:85968246
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516+6066T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968246 | ||||||
| chr9:85968539
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+6359G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968539 | ||||||
| chr9:85968541
|
G | A | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.516+6361G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968541 | ||||||
| chr9:85968660
|
C | T | 37 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(34): Show | 38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.517-6307C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968660 | ||||||
| chr9:85968708
|
A | G | 56 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.517-6259A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968708 | ||||||
| chr9:85968779
|
A | G | 1 | a0001c0001t0020g0196 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-6188A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968779 | ||||||
| chr9:85968800
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-6167T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968800 | ||||||
| chr9:85968870
|
T | C | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.517-6097T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968870 | ||||||
| chr9:85968888
|
C | G | 33 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(30): Show | 34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.517-6079C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968888 | ||||||
| chr9:85969270
|
C | CAAAAAAA others(291): Show |
2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-5683_517-5682i others(300): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969270 | |||||
| chr9:85969270
|
CA | C | 85 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0001g0135others(82): Show | 91 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.517-5678delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969270 | |||||
| chr9:85969270
|
CAA | C | 49 | a0001c0001t0001g0084a0001c0001t0002g0005a0001c0001t0002g0006others(46): Show | 52 | HG00558.hp1 HG01106.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.517-5679_517-5678d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969270 | |||||
| chr9:85969438
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-5529T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969438 | ||||||
| chr9:85969574
|
A | C | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-5393A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969574 | ||||||
| chr9:85969615
|
G | A | 10 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-5352G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969615 | ||||||
| chr9:85969616
|
C | T | 10 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-5351C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969616 | ||||||
| chr9:85969661
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-5306C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969661 | ||||||
| chr9:85969836
|
G | A | 13 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(10): Show | 13 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.517-5131G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969836 | ||||||
| chr9:85969859
|
T | TA | 8 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0027others(5): Show | 8 | HG00741.hp2 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-5090dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969859 | |||||
| chr9:85969859
|
TA | T | 17 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0152others(14): Show | 17 | HG00323.hp1 HG01516.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.517-5090delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969859 | |||||
| chr9:85969931
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517-5036C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969931 | ||||||
| chr9:85970099
|
T | C | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-4868T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970099 | ||||||
| chr9:85970099
|
TC | T | 4 | a0001c0001t0003g0101a0001c0001t0011g0097a0003c0002t0003g0098others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-4865delC | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85970099 | |||||
| chr9:85970321
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.517-4646A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970321 | ||||||
| chr9:85970343
|
A | G | 1 | a0001c0001t0003g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.517-4624A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970343 | ||||||
| chr9:85970737
|
TG | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(42): Show | 47 | HG00558.hp2 HG00597.hp2 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.517-4229delG | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970737 | ||||||
| chr9:85970747
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-4220G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970747 | ||||||
| chr9:85970794
|
C | T | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-4173C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970794 | ||||||
| chr9:85970803
|
G | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.517-4164G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970803 | ||||||
| chr9:85970880
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517-4087G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970880 | ||||||
| chr9:85970984
|
A | G | 1 | a0001c0001t0003g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.517-3983A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970984 | ||||||
| chr9:85971099
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-3868A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971099 | ||||||
| chr9:85971358
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-3609T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971358 | ||||||
| chr9:85971535
|
A | G | 1 | a0001c0001t0003g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.517-3432A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971535 | ||||||
| chr9:85971801
|
A | C | 1 | a0001c0001t0003g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.517-3166A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971801 | ||||||
| chr9:85971836
|
A | AT | 123 | a0001c0001t0001g0042a0001c0001t0001g0084a0001c0001t0001g0105others(120): Show | 132 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.517-3115dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85971836 | |||||
| chr9:85971852
|
T | TA | 3 | a0001c0001t0002g0076a0001c0003t0009g0015a0001c0003t0010g0014 | 3 | HG00673.hp1 HG03017.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.517-3113dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85971852 | |||||
| chr9:85971880
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.517-3087G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971880 | ||||||
| chr9:85972004
|
A | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0193 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.517-2963A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972004 | ||||||
| chr9:85972173
|
T | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.517-2794T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972173 | ||||||
| chr9:85972243
|
C | T | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-2724C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972243 | ||||||
| chr9:85972248
|
G | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-2719G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972248 | ||||||
| chr9:85972303
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-2664C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972303 | ||||||
| chr9:85972332
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-2635C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972332 | ||||||
| chr9:85972438
|
C | G | 172 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0033others(169): Show | 178 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.517-2529C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972438 | ||||||
| chr9:85972480
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0002g0065a0001c0001t0002g0066others(1): Show | 4 | NA18940.hp1 NA18945.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2487C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972480 | ||||||
| chr9:85972509
|
C | CA | 62 | a0001c0001t0001g0041a0001c0001t0001g0084a0001c0001t0001g0146others(59): Show | 67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.517-2435dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85972509 | |||||
| chr9:85972509
|
C | CAA | 22 | a0001c0001t0002g0048a0001c0001t0002g0050a0001c0001t0002g0052others(19): Show | 23 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.517-2436_517-2435d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85972509 | |||||
| chr9:85972509
|
CA | C | 32 | a0001c0001t0001g0105a0001c0001t0001g0139a0001c0001t0001g0203others(29): Show | 34 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.517-2435delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85972509 | |||||
| chr9:85972879
|
T | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-2088T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972879 | ||||||
| chr9:85972893
|
C | G | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.517-2074C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972893 | ||||||
| chr9:85972914
|
A | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.517-2053A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972914 | ||||||
| chr9:85973186
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.517-1781G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973186 | ||||||
| chr9:85973229
|
C | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-1738C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973229 | ||||||
| chr9:85973452
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0016g0238 | 2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.517-1515A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973452 | ||||||
| chr9:85973526
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-1441T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973526 | ||||||
| chr9:85973598
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-1369G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973598 | ||||||
| chr9:85973745
|
G | A | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.517-1222G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973745 | ||||||
| chr9:85973748
|
T | G | 1 | a0001c0001t0003g0121 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.517-1219T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973748 | ||||||
| chr9:85973749
|
GT | G | 59 | a0001c0001t0001g0084a0001c0001t0001g0199a0001c0001t0002g0001others(56): Show | 64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.517-1206delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85973749 | |||||
| chr9:85974019
|
C | T | 18 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(15): Show | 19 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.517-948C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974019 | ||||||
| chr9:85974097
|
C | T | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.517-870C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974097 | ||||||
| chr9:85974213
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-754T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974213 | ||||||
| chr9:85974271
|
T | G | 7 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0202others(4): Show | 7 | HG01071.hp1 NA18940.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-696T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974271 | ||||||
| chr9:85974275
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517-692T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974275 | ||||||
| chr9:85974494
|
C | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-473C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974494 | ||||||
| chr9:85974505
|
T | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-462T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974505 | ||||||
| chr9:85974620
|
A | G | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.517-347A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974620 | ||||||
| chr9:85974918
|
T | G | 1 | a0002c0004t0002g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.517-49T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974918 | ||||||
| chr9:85974955
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.517-12C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974955 | ||||||
| chr9:85975313
|
T | C | 1 | a0001c0001t0004g0261 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.627+156T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975313 | ||||||
| chr9:85975352
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.627+195C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975352 | ||||||
| chr9:85975502
|
T | C | 167 | a0001c0001t0001g0084a0001c0001t0001g0105a0001c0001t0001g0134others(164): Show | 177 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.627+345T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975502 | ||||||
| chr9:85975560
|
G | A | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.627+403G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975560 | ||||||
| chr9:85975640
|
T | A | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.627+483T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975640 | ||||||
| chr9:85975644
|
C | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+487C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975644 | ||||||
| chr9:85975660
|
A | G | 1 | a0004c0005t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.627+503A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975660 | ||||||
| chr9:85975806
|
A | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.627+649A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975806 | ||||||
| chr9:85976046
|
A | G | 37 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(34): Show | 38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.628-639A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976046 | ||||||
| chr9:85976109
|
T | G | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.628-576T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976109 | ||||||
| chr9:85976215
|
A | G | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.628-470A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976215 | ||||||
| chr9:85976227
|
C | A | 1 | a0001c0003t0009g0015 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.628-458C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976227 | ||||||
| chr9:85976252
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.628-433T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976252 | ||||||
| chr9:85976301
|
T | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.628-384T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976301 | ||||||
| chr9:85976535
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.628-150T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976535 | ||||||
| chr9:85976928
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.678+193T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85976928 | ||||||
| chr9:85976997
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.678+262C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85976997 | ||||||
| chr9:85977134
|
G | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.679-229G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977134 | ||||||
| chr9:85977141
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.679-222A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977141 | ||||||
| chr9:85977173
|
C | T | 1 | a0002c0004t0013g0016 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.679-190C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977173 | ||||||
| chr9:85977250
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.679-113C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977250 | ||||||
| chr9:85977251
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.679-112C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977251 | ||||||
| chr9:85977278
|
A | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.679-85A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977278 | ||||||
| chr9:85977870
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.763-397A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 10/22 | chr9 | 85977870 | ||||||
| chr9:85977929
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.763-338T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 10/22 | chr9 | 85977929 | ||||||
| chr9:85978034
|
A | G | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.763-233A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 10/22 | chr9 | 85978034 | ||||||
| chr9:85978393
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.877+12A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978393 | ||||||
| chr9:85978403
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+22A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978403 | ||||||
| chr9:85978486
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+105G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978486 | ||||||
| chr9:85978558
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.877+177T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978558 | ||||||
| chr9:85978651
|
T | G | 1 | a0001c0001t0003g0120 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+270T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978651 | ||||||
| chr9:85978756
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.877+375C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978756 | ||||||
| chr9:85978929
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+548G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978929 | ||||||
| chr9:85979000
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+619T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979000 | ||||||
| chr9:85979007
|
T | C | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.877+626T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979007 | ||||||
| chr9:85979063
|
A | C | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.877+682A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979063 | ||||||
| chr9:85979138
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.877+757C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979138 | ||||||
| chr9:85979210
|
C | T | 2 | a0001c0001t0003g0101a0001c0001t0011g0097 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.877+829C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979210 | ||||||
| chr9:85979637
|
A | G | 29 | a0001c0001t0003g0029a0001c0001t0004g0013a0001c0001t0004g0020others(26): Show | 30 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.877+1256A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979637 | ||||||
| chr9:85979717
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+1336T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979717 | ||||||
| chr9:85979770
|
T | A | 1 | a0001c0001t0004g0256 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.877+1389T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979770 | ||||||
| chr9:85979797
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.877+1416C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979797 | ||||||
| chr9:85979890
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.877+1509C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979890 | ||||||
| chr9:85979952
|
A | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1571A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979952 | ||||||
| chr9:85980087
|
A | C | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.877+1706A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980087 | ||||||
| chr9:85980207
|
C | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1826C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980207 | ||||||
| chr9:85980263
|
C | T | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.877+1882C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980263 | ||||||
| chr9:85980330
|
C | G | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.877+1949C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980330 | ||||||
| chr9:85980355
|
G | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1974G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980355 | ||||||
| chr9:85980356
|
G | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1975G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980356 | ||||||
| chr9:85980357
|
G | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1976G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980357 | ||||||
| chr9:85980358
|
G | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1977G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980358 | ||||||
| chr9:85980359
|
T | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1978T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980359 | ||||||
| chr9:85980360
|
G | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1979G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980360 | ||||||
| chr9:85980364
|
C | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1983C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980364 | ||||||
| chr9:85980366
|
G | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1985G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980366 | ||||||
| chr9:85980367
|
A | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1986A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980367 | ||||||
| chr9:85980370
|
G | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1989G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980370 | ||||||
| chr9:85980371
|
T | TTGTACCC others(1): Show |
5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1991_877+1992i others(10): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85980371 | |||||
| chr9:85980577
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+2196C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980577 | ||||||
| chr9:85981283
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.877+2902C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85981283 | ||||||
| chr9:85981568
|
A | G | 4 | a0001c0001t0005g0011a0001c0001t0005g0145a0001c0001t0005g0151others(1): Show | 5 | HG00639.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+3187A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85981568 | ||||||
| chr9:85981846
|
G | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0193 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.877+3465G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85981846 | ||||||
| chr9:85982209
|
G | C | 1 | a0001c0001t0003g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.877+3828G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982209 | ||||||
| chr9:85982219
|
A | G | 1 | a0001c0001t0008g0100 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.877+3838A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982219 | ||||||
| chr9:85982347
|
A | C | 54 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0038others(51): Show | 56 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.877+3966A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982347 | ||||||
| chr9:85982426
|
A | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0163 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.877+4045A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982426 | ||||||
| chr9:85982712
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.877+4331C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982712 | ||||||
| chr9:85982769
|
C | G | 6 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0078others(3): Show | 6 | NA18947.hp2 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+4388C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982769 | ||||||
| chr9:85982898
|
A | G | 1 | a0001c0001t0003g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.877+4517A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982898 | ||||||
| chr9:85982929
|
T | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG01167.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.877+4548T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982929 | ||||||
| chr9:85982967
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.877+4586G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982967 | ||||||
| chr9:85983006
|
A | G | 1 | a0002c0004t0002g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.877+4625A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983006 | ||||||
| chr9:85983022
|
A | C | 2 | a0001c0001t0004g0273a0001c0001t0022g0272 | 2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.877+4641A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983022 | ||||||
| chr9:85983072
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.877+4691C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983072 | ||||||
| chr9:85983159
|
G | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0254 | 3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.877+4778G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983159 | ||||||
| chr9:85983238
|
G | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+4857G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983238 | ||||||
| chr9:85983239
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+4858A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983239 | ||||||
| chr9:85983254
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.877+4873C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983254 | ||||||
| chr9:85983387
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.877+5006T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983387 | ||||||
| chr9:85983444
|
C | T | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+5063C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983444 | ||||||
| chr9:85983627
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+5246G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983627 | ||||||
| chr9:85983668
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.877+5287G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983668 | ||||||
| chr9:85983677
|
C | G | 226 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0038others(223): Show | 238 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.877+5296C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983677 | ||||||
| chr9:85983746
|
A | G | 1 | a0001c0001t0006g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.877+5365A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983746 | ||||||
| chr9:85983903
|
G | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.877+5522G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983903 | ||||||
| chr9:85983915
|
A | G | 2 | a0001c0001t0004g0273a0001c0001t0022g0272 | 2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.877+5534A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983915 | ||||||
| chr9:85984024
|
C | CA | 34 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0030others(31): Show | 36 | HG00741.hp2 HG01167.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.877+5661dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984024 | |||||
| chr9:85984024
|
C | CAA | 8 | a0001c0001t0003g0022a0001c0001t0003g0101a0001c0001t0004g0020others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.877+5660_877+5661d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984024 | |||||
| chr9:85984024
|
CA | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(55): Show | 64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.877+5661delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984024 | |||||
| chr9:85984191
|
G | A | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.877+5810G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984191 | ||||||
| chr9:85984192
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+5811G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984192 | ||||||
| chr9:85984305
|
G | C | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0045others(4): Show | 8 | HG01256.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.877+5924G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984305 | ||||||
| chr9:85984332
|
AAAAC | A | 36 | a0001c0001t0002g0092a0001c0001t0003g0022a0001c0001t0003g0026others(33): Show | 37 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.877+5973_877+5976d others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984332 | |||||
| chr9:85984567
|
G | A | 33 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(30): Show | 34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.877+6186G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984567 | ||||||
| chr9:85984583
|
G | A | 1 | a0001c0001t0017g0234 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.877+6202G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984583 | ||||||
| chr9:85984607
|
A | G | 2 | a0001c0001t0003g0008a0001c0001t0003g0118 | 3 | NA18977.hp2 NA18990.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.877+6226A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984607 | ||||||
| chr9:85984613
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+6232C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984613 | ||||||
| chr9:85984821
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+6440C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984821 | ||||||
| chr9:85984832
|
G | A | 1 | a0001c0001t0002g0090 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.877+6451G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984832 | ||||||
| chr9:85984933
|
A | G | 61 | a0001c0001t0001g0084a0001c0001t0001g0229a0001c0001t0002g0001others(58): Show | 67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.877+6552A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984933 | ||||||
| chr9:85984977
|
TA | T | 3 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082 | 3 | NA18995.hp1 NA19012.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.877+6603delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984977 | |||||
| chr9:85985341
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+6960A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85985341 | ||||||
| chr9:85985694
|
TA | T | 5 | a0001c0001t0002g0066a0001c0003t0009g0015a0001c0003t0010g0014others(2): Show | 5 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+7320delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85985694 | |||||
| chr9:85985810
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+7429G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85985810 | ||||||
| chr9:85985962
|
G | A | 1 | a0001c0001t0003g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.877+7581G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85985962 | ||||||
| chr9:85986104
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+7723C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986104 | ||||||
| chr9:85986236
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+7855G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986236 | ||||||
| chr9:85986300
|
T | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.877+7919T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986300 | ||||||
| chr9:85986357
|
A | T | 6 | a0001c0001t0002g0068a0001c0001t0002g0070a0001c0001t0002g0072others(3): Show | 6 | NA18953.hp2 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+7976A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986357 | ||||||
| chr9:85986364
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+7983A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986364 | ||||||
| chr9:85986421
|
A | G | 2 | a0001c0001t0004g0273a0001c0001t0022g0272 | 2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.877+8040A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986421 | ||||||
| chr9:85986461
|
C | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+8080C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986461 | ||||||
| chr9:85986496
|
G | A | 3 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | HG01167.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.877+8115G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986496 | ||||||
| chr9:85986569
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+8188G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986569 | ||||||
| chr9:85986589
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0193 | 2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.877+8208A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986589 | ||||||
| chr9:85986660
|
A | G | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.877+8279A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986660 | ||||||
| chr9:85987101
|
A | G | 5 | a0001c0001t0001g0105a0001c0001t0003g0110a0001c0001t0003g0111others(2): Show | 5 | HG01257.hp1 HG02559.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+8720A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987101 | ||||||
| chr9:85987149
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.877+8768C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987149 | ||||||
| chr9:85987161
|
A | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.877+8780A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987161 | ||||||
| chr9:85987219
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.877+8838G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987219 | ||||||
| chr9:85987480
|
G | A | 97 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(94): Show | 104 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.878-8919G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987480 | ||||||
| chr9:85987574
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-8825G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987574 | ||||||
| chr9:85987587
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.878-8812T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987587 | ||||||
| chr9:85987785
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.878-8614T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987785 | ||||||
| chr9:85987810
|
G | T | 1 | a0001c0001t0001g0039 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.878-8589G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987810 | ||||||
| chr9:85987873
|
A | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-8526A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987873 | ||||||
| chr9:85987892
|
G | C | 1 | a0001c0001t0011g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.878-8507G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987892 | ||||||
| chr9:85988045
|
T | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-8354T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988045 | ||||||
| chr9:85988054
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-8345A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988054 | ||||||
| chr9:85988077
|
A | G | 1 | a0001c0001t0003g0018 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.878-8322A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988077 | ||||||
| chr9:85988402
|
G | A | 60 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0003others(57): Show | 66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.878-7997G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988402 | ||||||
| chr9:85988566
|
G | A | 1 | a0002c0004t0002g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.878-7833G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988566 | ||||||
| chr9:85988628
|
C | A | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.878-7771C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988628 | ||||||
| chr9:85988710
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-7689C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988710 | ||||||
| chr9:85988925
|
G | A | 6 | a0001c0001t0002g0068a0001c0001t0002g0070a0001c0001t0002g0072others(3): Show | 6 | NA18953.hp2 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-7474G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988925 | ||||||
| chr9:85988949
|
A | T | 1 | a0001c0001t0003g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.878-7450A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988949 | ||||||
| chr9:85989010
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.878-7389C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989010 | ||||||
| chr9:85989078
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.878-7321T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989078 | ||||||
| chr9:85989177
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-7222A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989177 | ||||||
| chr9:85989199
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.878-7200G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989199 | ||||||
| chr9:85989210
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.878-7189C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989210 | ||||||
| chr9:85989215
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-7184G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989215 | ||||||
| chr9:85989278
|
CT | C | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-7120delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989278 | ||||||
| chr9:85989380
|
A | C | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-7019A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989380 | ||||||
| chr9:85989478
|
AAAAC | A | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-6909_878-6906d others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85989478 | |||||
| chr9:85989548
|
A | G | 5 | a0001c0001t0001g0218a0001c0001t0003g0102a0001c0001t0003g0106others(2): Show | 5 | HG01255.hp2 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-6851A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989548 | ||||||
| chr9:85989591
|
A | G | 36 | a0001c0001t0001g0105a0001c0001t0001g0218a0001c0001t0003g0018others(33): Show | 37 | HG00741.hp2 HG01168.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.878-6808A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989591 | ||||||
| chr9:85989673
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.878-6726A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989673 | ||||||
| chr9:85989756
|
T | C | 1 | a0001c0001t0002g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.878-6643T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989756 | ||||||
| chr9:85990242
|
T | C | 2 | a0001c0001t0004g0271a0001c0001t0004g0274 | 2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.878-6157T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990242 | ||||||
| chr9:85990290
|
G | T | 30 | a0001c0001t0001g0105a0001c0001t0003g0008a0001c0001t0003g0009others(27): Show | 32 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.878-6109G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990290 | ||||||
| chr9:85990321
|
C | G | 1 | a0001c0001t0001g0168 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.878-6078C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990321 | ||||||
| chr9:85990380
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-6019G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990380 | ||||||
| chr9:85990546
|
A | C | 1 | a0004c0005t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.878-5853A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990546 | ||||||
| chr9:85990581
|
T | C | 22 | a0001c0001t0003g0027a0001c0001t0003g0028a0001c0001t0004g0013others(19): Show | 23 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.878-5818T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990581 | ||||||
| chr9:85990822
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.878-5577G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990822 | ||||||
| chr9:85991377
|
T | G | 2 | a0001c0001t0004g0271a0001c0001t0004g0274 | 2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.878-5022T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991377 | ||||||
| chr9:85991458
|
G | T | 2 | a0001c0001t0004g0257a0001c0001t0004g0258 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.878-4941G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991458 | ||||||
| chr9:85991632
|
G | C | 21 | a0001c0001t0003g0022a0001c0001t0004g0013a0001c0001t0004g0256others(18): Show | 22 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.878-4767G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991632 | ||||||
| chr9:85991810
|
T | C | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.878-4589T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991810 | ||||||
| chr9:85991904
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-4495G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991904 | ||||||
| chr9:85991998
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.878-4401C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991998 | ||||||
| chr9:85992169
|
G | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.878-4230G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992169 | ||||||
| chr9:85992173
|
C | CA | 221 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(218): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.878-4213dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85992173 | |||||
| chr9:85992173
|
C | CAA | 12 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG01168.hp1 HG01257.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.878-4214_878-4213d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85992173 | |||||
| chr9:85992184
|
A | AAT | 28 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(25): Show | 29 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.878-4214_878-4213i others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85992184 | |||||
| chr9:85992184
|
A | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0254 | 3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.878-4215A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992184 | ||||||
| chr9:85992187
|
T | A | 2 | a0001c0001t0001g0134a0001c0001t0003g0106 | 2 | HG01255.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.878-4212T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992187 | ||||||
| chr9:85992193
|
A | T | 14 | a0001c0001t0001g0105a0001c0001t0003g0018a0001c0001t0003g0019others(11): Show | 14 | HG00741.hp2 HG01255.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.878-4206A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992193 | ||||||
| chr9:85992266
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 6 | NA18612.hp2 NA18947.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-4133C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992266 | ||||||
| chr9:85992543
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.878-3856A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992543 | ||||||
| chr9:85993006
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.878-3393T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993006 | ||||||
| chr9:85993073
|
C | G | 39 | a0001c0001t0001g0105a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 41 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.878-3326C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993073 | ||||||
| chr9:85993144
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.878-3255C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993144 | ||||||
| chr9:85993153
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-3246T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993153 | ||||||
| chr9:85993195
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191 | 3 | HG02622.hp1 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.878-3204C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993195 | ||||||
| chr9:85993552
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-2847A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993552 | ||||||
| chr9:85993559
|
G | A | 1 | a0001c0001t0004g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.878-2840G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993559 | ||||||
| chr9:85993747
|
G | A | 1 | a0001c0001t0004g0262 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.878-2652G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993747 | ||||||
| chr9:85993766
|
CT | C | 95 | a0001c0001t0001g0169a0001c0001t0001g0247a0001c0001t0002g0001others(92): Show | 102 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.878-2625delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85993766 | |||||
| chr9:85993897
|
G | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-2502G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993897 | ||||||
| chr9:85993905
|
C | G | 1 | a0001c0001t0001g0158 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.878-2494C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993905 | ||||||
| chr9:85993942
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-2457A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993942 | ||||||
| chr9:85993975
|
AT | A | 5 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0092others(2): Show | 6 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-2409delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85993975 | |||||
| chr9:85994000
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.878-2399G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994000 | ||||||
| chr9:85994245
|
A | G | 1 | a0001c0003t0010g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.878-2154A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994245 | ||||||
| chr9:85994338
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.878-2061C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994338 | ||||||
| chr9:85994414
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-1985G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994414 | ||||||
| chr9:85994436
|
A | G | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.878-1963A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994436 | ||||||
| chr9:85994734
|
T | G | 1 | a0002c0004t0002g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.878-1665T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994734 | ||||||
| chr9:85994760
|
A | G | 2 | a0001c0001t0004g0271a0001c0001t0004g0274 | 2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.878-1639A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994760 | ||||||
| chr9:85994793
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.878-1606G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994793 | ||||||
| chr9:85994876
|
G | T | 6 | a0001c0001t0004g0260a0001c0001t0004g0261a0001c0001t0004g0262others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-1523G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994876 | ||||||
| chr9:85995272
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-1127A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995272 | ||||||
| chr9:85995302
|
ATTATT | A | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.878-1085_878-1081d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85995302 | |||||
| chr9:85995325
|
A | G | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.878-1074A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995325 | ||||||
| chr9:85995598
|
T | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.878-801T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995598 | ||||||
| chr9:85995621
|
A | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-778A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995621 | ||||||
| chr9:85995666
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.878-733G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995666 | ||||||
| chr9:85995720
|
C | T | 4 | a0001c0003t0009g0015a0001c0003t0010g0014a0002c0004t0002g0017others(1): Show | 4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.878-679C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995720 | ||||||
| chr9:85995845
|
A | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-554A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995845 | ||||||
| chr9:85996000
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-399G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996000 | ||||||
| chr9:85996063
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.878-336G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996063 | ||||||
| chr9:85996188
|
T | C | 9 | a0001c0001t0001g0084a0001c0001t0001g0133a0001c0001t0001g0138others(6): Show | 9 | HG02015.hp1 HG02083.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.878-211T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996188 | ||||||
| chr9:85996312
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.878-87A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996312 | ||||||
| chr9:85996352
|
A | G | 4 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(1): Show | 4 | HG00280.hp1 HG01934.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-47A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996352 | ||||||
| chr9:85996363
|
A | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-36A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996363 | ||||||
| chr9:85996764
|
T | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1056+187T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996764 | ||||||
| chr9:85996913
|
G | A | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1056+336G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996913 | ||||||
| chr9:85996935
|
T | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+358T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996935 | ||||||
| chr9:85996954
|
T | A | 55 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(52): Show | 60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1056+377T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996954 | ||||||
| chr9:85997018
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1056+441T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997018 | ||||||
| chr9:85997045
|
G | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+468G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997045 | ||||||
| chr9:85997194
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1056+617T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997194 | ||||||
| chr9:85997328
|
T | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1056+751T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997328 | ||||||
| chr9:85997346
|
A | AT | 13 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0172others(10): Show | 13 | HG00673.hp1 HG01071.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1056+782dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 85997346 | |||||
| chr9:85997704
|
G | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+1127G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997704 | ||||||
| chr9:85997890
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1056+1313T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997890 | ||||||
| chr9:85997970
|
A | G | 22 | a0001c0001t0004g0013a0001c0001t0004g0023a0001c0001t0004g0024others(19): Show | 23 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1056+1393A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997970 | ||||||
| chr9:85998024
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+1447C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998024 | ||||||
| chr9:85998060
|
G | A | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1056+1483G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998060 | ||||||
| chr9:85998072
|
G | A | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1056+1495G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998072 | ||||||
| chr9:85998104
|
C | T | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+1527C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998104 | ||||||
| chr9:85998149
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+1572C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998149 | ||||||
| chr9:85998297
|
A | G | 10 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0177others(7): Show | 10 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1056+1720A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998297 | ||||||
| chr9:85998390
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1056+1813T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998390 | ||||||
| chr9:85998464
|
T | C | 2 | a0001c0001t0004g0023a0001c0001t0004g0024 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1056+1887T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998464 | ||||||
| chr9:85998471
|
C | T | 11 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0067others(8): Show | 11 | HG01106.hp2 HG02083.hp1 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1056+1894C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998471 | ||||||
| chr9:85999046
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1056+2469G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999046 | ||||||
| chr9:85999072
|
C | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0045others(4): Show | 8 | HG01256.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1056+2495C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999072 | ||||||
| chr9:85999241
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1056+2664C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999241 | ||||||
| chr9:85999503
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1056+2926G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999503 | ||||||
| chr9:85999879
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1056+3302C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999879 | ||||||
| chr9:85999947
|
A | G | 24 | a0001c0001t0001g0105a0001c0001t0001g0139a0001c0001t0001g0141others(21): Show | 25 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1056+3370A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999947 | ||||||
| chr9:86000248
|
C | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0092others(1): Show | 5 | HG01243.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-3337C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000248 | ||||||
| chr9:86000327
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1057-3258G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000327 | ||||||
| chr9:86000439
|
TCA | T | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1057-3145_1057-314 others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000439 | ||||||
| chr9:86000557
|
T | C | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1057-3028T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000557 | ||||||
| chr9:86000604
|
G | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(271): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1057-2981G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000604 | ||||||
| chr9:86000736
|
G | C | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1057-2849G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000736 | ||||||
| chr9:86001514
|
G | C | 4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0089others(1): Show | 4 | HG01106.hp2 HG02083.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-2071G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001514 | ||||||
| chr9:86001547
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1057-2038C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001547 | ||||||
| chr9:86001561
|
G | A | 1 | a0001c0001t0003g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1057-2024G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001561 | ||||||
| chr9:86001607
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1057-1978C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001607 | ||||||
| chr9:86001693
|
C | T | 3 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1057-1892C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001693 | ||||||
| chr9:86001838
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1057-1747T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001838 | ||||||
| chr9:86001839
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(130): Show | 142 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1057-1746C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001839 | ||||||
| chr9:86001844
|
G | T | 1 | a0001c0001t0003g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1057-1741G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001844 | ||||||
| chr9:86001847
|
G | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-1738G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001847 | ||||||
| chr9:86001869
|
C | G | 34 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(31): Show | 35 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.1057-1716C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001869 | ||||||
| chr9:86002107
|
T | A | 1 | a0001c0001t0002g0047 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1057-1478T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002107 | ||||||
| chr9:86002210
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1057-1375T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002210 | ||||||
| chr9:86002228
|
CT | C | 133 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(130): Show | 142 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1057-1352delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 86002228 | |||||
| chr9:86002291
|
A | C | 1 | a0001c0001t0002g0073 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1057-1294A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002291 | ||||||
| chr9:86002414
|
T | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-1171T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002414 | ||||||
| chr9:86002681
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1057-904T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002681 | ||||||
| chr9:86002745
|
C | A | 10 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(7): Show | 10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1057-840C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002745 | ||||||
| chr9:86002952
|
TTCTCA | T | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-628_1057-624d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 86002952 | |||||
| chr9:86003022
|
T | C | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-563T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003022 | ||||||
| chr9:86003255
|
A | G | 2 | a0001c0001t0004g0023a0001c0001t0004g0024 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1057-330A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003255 | ||||||
| chr9:86003305
|
A | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1057-280A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003305 | ||||||
| chr9:86003547
|
C | G | 26 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0142others(23): Show | 27 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1057-38C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003547 | ||||||
| chr9:86003574
|
A | G | 1 | a0001c0001t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1057-11A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003574 | ||||||
| chr9:86003764
|
A | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1116+120A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86003764 | ||||||
| chr9:86003764
|
AT | A | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+130delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr9 | 86003764 | |||||
| chr9:86003846
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1116+202G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86003846 | ||||||
| chr9:86003935
|
A | C | 6 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0078others(3): Show | 6 | NA18947.hp2 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+291A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86003935 | ||||||
| chr9:86004036
|
A | G | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+392A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004036 | ||||||
| chr9:86004074
|
G | A | 1 | a0001c0001t0004g0273 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1116+430G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004074 | ||||||
| chr9:86004164
|
G | C | 1 | a0001c0001t0004g0259 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1116+520G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004164 | ||||||
| chr9:86004190
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1116+546C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004190 | ||||||
| chr9:86004198
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1116+554G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004198 | ||||||
| chr9:86004294
|
G | A | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1116+650G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004294 | ||||||
| chr9:86004391
|
A | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02257.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+747A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004391 | ||||||
| chr9:86004423
|
G | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1116+779G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004423 | ||||||
| chr9:86004438
|
CA | C | 274 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(271): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1116+796delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr9 | 86004438 | |||||
| chr9:86004569
|
G | T | 1 | a0001c0003t0010g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1116+925G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004569 | ||||||
| chr9:86004570
|
A | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1116+926A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004570 | ||||||
| chr9:86004617
|
A | G | 58 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0038others(55): Show | 60 | HG00558.hp2 HG00597.hp2 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.1116+973A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004617 | ||||||
| chr9:86004855
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1116+1211G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004855 | ||||||
| chr9:86004928
|
G | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1116+1284G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004928 | ||||||
| chr9:86004990
|
A | G | 1 | a0001c0001t0006g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1116+1346A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004990 | ||||||
| chr9:86005002
|
A | G | 5 | a0001c0001t0003g0022a0001c0001t0003g0026a0001c0001t0003g0027others(2): Show | 5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+1358A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005002 | ||||||
| chr9:86005018
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1116+1374C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005018 | ||||||
| chr9:86005061
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1116+1417C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005061 | ||||||
| chr9:86005209
|
A | G | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1116+1565A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005209 | ||||||
| chr9:86005356
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1116+1712A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005356 | ||||||
| chr9:86005448
|
C | T | 3 | a0001c0001t0001g0167a0001c0003t0009g0015a0001c0003t0010g0014 | 3 | HG00673.hp1 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1116+1804C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005448 | ||||||
| chr9:86005692
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1666T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005692 | ||||||
| chr9:86005695
|
T | G | 4 | a0001c0003t0009g0015a0001c0003t0010g0014a0002c0004t0002g0017others(1): Show | 4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-1663T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005695 | ||||||
| chr9:86005715
|
CAAACT | C | 59 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(56): Show | 65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1117-1641_1117-163 others(9): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr9 | 86005715 | |||||
| chr9:86005765
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0150 | 3 | HG02965.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1117-1593A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005765 | ||||||
| chr9:86005910
|
C | A | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1117-1448C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005910 | ||||||
| chr9:86005910
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0001g0035 | 2 | NA18957.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1117-1448C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005910 | ||||||
| chr9:86005946
|
T | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1412T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005946 | ||||||
| chr9:86005954
|
C | T | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-1404C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005954 | ||||||
| chr9:86006063
|
C | T | 10 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0115others(7): Show | 10 | HG00280.hp1 HG01346.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-1295C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006063 | ||||||
| chr9:86006092
|
G | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1266G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006092 | ||||||
| chr9:86006262
|
T | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0214 | 2 | HG01934.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1117-1096T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006262 | ||||||
| chr9:86006267
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG00609.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1117-1091C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006267 | ||||||
| chr9:86006285
|
A | G | 2 | a0001c0001t0002g0055a0001c0001t0002g0058 | 2 | NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1117-1073A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006285 | ||||||
| chr9:86006748
|
A | G | 55 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(52): Show | 60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1117-610A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006748 | ||||||
| chr9:86006769
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1117-589C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006769 | ||||||
| chr9:86006797
|
T | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1117-561T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006797 | ||||||
| chr9:86007038
|
A | G | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1117-320A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86007038 | ||||||
| chr9:86007188
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1117-170A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86007188 | ||||||
| chr9:86007538
|
T | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+74T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007538 | ||||||
| chr9:86007539
|
T | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+75T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007539 | ||||||
| chr9:86007541
|
T | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+77T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007541 | ||||||
| chr9:86007542
|
A | G | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+78A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007542 | ||||||
| chr9:86007543
|
G | C | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+79G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007543 | ||||||
| chr9:86007615
|
C | T | 20 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(17): Show | 21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1223+151C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007615 | ||||||
| chr9:86007692
|
C | T | 134 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(131): Show | 143 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(140): Show |
intron_variant | MODIFIER | c.1223+228C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007692 | ||||||
| chr9:86007754
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1223+290C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007754 | ||||||
| chr9:86007775
|
A | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0118 | 3 | NA18977.hp2 NA18990.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1223+311A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007775 | ||||||
| chr9:86007899
|
C | A | 1 | a0001c0001t0003g0107 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1223+435C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007899 | ||||||
| chr9:86007974
|
A | G | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1223+510A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007974 | ||||||
| chr9:86008054
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1223+590A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008054 | ||||||
| chr9:86008080
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1223+616G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008080 | ||||||
| chr9:86008126
|
C | T | 59 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(56): Show | 65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1223+662C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008126 | ||||||
| chr9:86008259
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1223+795C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008259 | ||||||
| chr9:86008706
|
G | T | 1 | a0001c0001t0003g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1224-1159G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008706 | ||||||
| chr9:86008742
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1224-1123T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008742 | ||||||
| chr9:86008930
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1224-935T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008930 | ||||||
| chr9:86009125
|
A | G | 1 | a0001c0001t0003g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1224-740A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009125 | ||||||
| chr9:86009182
|
A | G | 1 | a0002c0004t0013g0016 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1224-683A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009182 | ||||||
| chr9:86009284
|
C | A | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1224-581C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009284 | ||||||
| chr9:86009378
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1224-487C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009378 | ||||||
| chr9:86009505
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1224-360T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009505 | ||||||
| chr9:86009675
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1224-190C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009675 | ||||||
| chr9:86009803
|
G | T | 2 | a0001c0001t0004g0273a0001c0001t0022g0272 | 2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1224-62G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009803 | ||||||
| chr9:86009829
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1224-36T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009829 | ||||||
| chr9:86010002
|
T | TCATGCCT others(10): Show |
2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+73_1290+74ins others(17): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010002 | |||||
| chr9:86010116
|
C | T | 6 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0078others(3): Show | 6 | NA18947.hp2 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+185C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010116 | ||||||
| chr9:86010130
|
G | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+199G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010130 | ||||||
| chr9:86010209
|
T | A | 2 | a0001c0001t0003g0103a0001c0001t0003g0104 | 2 | HG01167.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1290+278T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010209 | ||||||
| chr9:86010248
|
C | CATAATA | 3 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082 | 3 | NA18995.hp1 NA19012.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1290+337_1290+342d others(8): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010248 | |||||
| chr9:86010250
|
T | TAAC | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290+321_1290+322i others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010250 | |||||
| chr9:86010279
|
T | A | 1 | a0001c0001t0002g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1290+348T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010279 | ||||||
| chr9:86010286
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+355C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010286 | ||||||
| chr9:86010480
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1290+549T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010480 | ||||||
| chr9:86010569
|
A | AT | 11 | a0001c0001t0001g0037a0001c0001t0001g0144a0001c0001t0001g0146others(8): Show | 11 | HG01243.hp1 HG02027.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1290+661dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010569 | |||||
| chr9:86010569
|
AT | A | 118 | a0001c0001t0001g0105a0001c0001t0001g0139a0001c0001t0001g0148others(115): Show | 126 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1290+661delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010569 | |||||
| chr9:86010569
|
ATT | A | 19 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0092others(16): Show | 20 | HG01243.hp2 HG01255.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.1290+660_1290+661d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010569 | |||||
| chr9:86010605
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1290+674C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010605 | ||||||
| chr9:86010622
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1290+691G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010622 | ||||||
| chr9:86010635
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1290+704C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010635 | ||||||
| chr9:86010665
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1290+734C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010665 | ||||||
| chr9:86010667
|
C | T | 3 | a0001c0001t0001g0139a0002c0004t0002g0017a0002c0004t0013g0016 | 3 | HG01168.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1290+736C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010667 | ||||||
| chr9:86010734
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+803T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010734 | ||||||
| chr9:86010802
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1290+871C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010802 | ||||||
| chr9:86010810
|
C | T | 4 | a0001c0001t0005g0011a0001c0001t0005g0145a0001c0001t0005g0151others(1): Show | 5 | HG00639.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1290+879C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010810 | ||||||
| chr9:86010812
|
C | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0254 | 3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1290+881C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010812 | ||||||
| chr9:86011072
|
G | A | 19 | a0001c0001t0004g0013a0001c0001t0004g0256a0001c0001t0004g0257others(16): Show | 20 | HG01168.hp1 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1290+1141G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011072 | ||||||
| chr9:86011127
|
A | G | 13 | a0001c0001t0001g0105a0001c0001t0003g0018a0001c0001t0003g0019others(10): Show | 13 | HG00741.hp2 HG01255.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1290+1196A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011127 | ||||||
| chr9:86011233
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1290+1302G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011233 | ||||||
| chr9:86011449
|
C | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1290+1518C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011449 | ||||||
| chr9:86011459
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1290+1528A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011459 | ||||||
| chr9:86011522
|
T | C | 35 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(32): Show | 36 | HG00673.hp1 HG01168.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1291-1524T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011522 | ||||||
| chr9:86011602
|
G | A | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1291-1444G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011602 | ||||||
| chr9:86011614
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291-1432C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011614 | ||||||
| chr9:86011662
|
A | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0164 | 3 | HG02132.hp1 NA18968.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1291-1384A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011662 | ||||||
| chr9:86011679
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-1367T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011679 | ||||||
| chr9:86011872
|
A | AATATATA others(17): Show |
2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-1167_1291-114 others(28): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011872 | |||||
| chr9:86011912
|
T | TTATATAT others(26): Show |
2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1291-1129_1291-109 others(37): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011912 | |||||
| chr9:86011951
|
T | C | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1291-1095T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011951 | ||||||
| chr9:86011966
|
GTATATAA | G | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG01167.hp1 HG01243.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291-1066_1291-106 others(11): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011966 | |||||
| chr9:86011968
|
A | ATATAATA others(19): Show |
1 | a0001c0001t0003g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1291-1077_1291-105 others(30): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011968 | |||||
| chr9:86012117
|
C | CT | 58 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(55): Show | 64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1291-919dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86012117 | |||||
| chr9:86012128
|
G | T | 1 | a0001c0001t0002g0052 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1291-918G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012128 | ||||||
| chr9:86012182
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291-864C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012182 | ||||||
| chr9:86012422
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-624C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012422 | ||||||
| chr9:86012426
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1291-620A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012426 | ||||||
| chr9:86012639
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-407A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012639 | ||||||
| chr9:86012789
|
T | C | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(15): Show | 20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1291-257T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012789 | ||||||
| chr9:86012878
|
G | T | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1291-168G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012878 | ||||||
| chr9:86012897
|
C | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-149C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012897 | ||||||
| chr9:86013291
|
A | G | 59 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(56): Show | 65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1389+147A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013291 | ||||||
| chr9:86013335
|
T | G | 4 | a0001c0001t0002g0005a0001c0001t0002g0061a0001c0001t0002g0092others(1): Show | 5 | HG01243.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+191T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013335 | ||||||
| chr9:86013413
|
AAATATT | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0236 | 3 | HG00558.hp2 NA18970.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1389+274_1389+279d others(8): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 86013413 | |||||
| chr9:86013510
|
G | C | 1 | a0001c0001t0003g0109 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1390-209G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013510 | ||||||
| chr9:86013632
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1390-87T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013632 | ||||||
| chr9:86013932
|
G | A | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1568+35G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86013932 | ||||||
| chr9:86014195
|
T | C | 1 | a0001c0001t0003g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1568+298T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014195 | ||||||
| chr9:86014258
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1568+361G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014258 | ||||||
| chr9:86014396
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1568+499C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014396 | ||||||
| chr9:86014651
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1568+754T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014651 | ||||||
| chr9:86014829
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0174a0001c0001t0001g0217 | 3 | NA18965.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1568+932C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014829 | ||||||
| chr9:86015042
|
A | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1568+1145A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015042 | ||||||
| chr9:86015134
|
G | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1568+1237G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015134 | ||||||
| chr9:86015150
|
A | C | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1568+1253A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015150 | ||||||
| chr9:86015473
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1569-1066C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015473 | ||||||
| chr9:86015764
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1569-775T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015764 | ||||||
| chr9:86015871
|
C | T | 3 | a0001c0001t0006g0231a0001c0001t0006g0232a0001c0001t0006g0233 | 3 | HG00280.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1569-668C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015871 | ||||||
| chr9:86016019
|
T | A | 7 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1569-520T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016019 | ||||||
| chr9:86016057
|
T | G | 2 | a0001c0001t0003g0022a0001c0001t0003g0107 | 2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1569-482T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016057 | ||||||
| chr9:86016138
|
CAAGT | C | 28 | a0001c0001t0004g0013a0001c0001t0004g0020a0001c0001t0004g0021others(25): Show | 29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1569-398_1569-395d others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 86016138 | |||||
| chr9:86016467
|
C | CGTT | 133 | a0001c0001t0001g0105a0001c0001t0002g0001a0001c0001t0002g0003others(130): Show | 142 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1569-71_1569-69dup others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 86016467 | |||||
| chr9:86016467
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1569-72C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016467 | ||||||
| chr9:86016489
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1569-50G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016489 | ||||||
| chr9:86016817
|
C | A | 6 | a0001c0001t0002g0068a0001c0001t0002g0070a0001c0001t0002g0072others(3): Show | 6 | NA18953.hp2 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1705+142C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016817 | ||||||
| chr9:86016817
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1705+142C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016817 | ||||||
| chr9:86016819
|
A | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1705+144A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016819 | ||||||
| chr9:86016865
|
C | A | 31 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(28): Show | 32 | HG01168.hp1 HG02055.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1705+190C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016865 | ||||||
| chr9:86017033
|
C | T | 3 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0254 | 3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1705+358C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017033 | ||||||
| chr9:86017139
|
T | C | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1706-359T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017139 | ||||||
| chr9:86017453
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1706-45G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017453 | ||||||
| chr9:86017477
|
C | T | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1706-21C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017477 | ||||||
| chr9:86017727
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02027.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1773+162A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017727 | ||||||
| chr9:86017803
|
T | C | 1 | a0001c0001t0002g0076 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1773+238T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017803 | ||||||
| chr9:86017842
|
G | A | 1 | a0001c0001t0003g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1773+277G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017842 | ||||||
| chr9:86017865
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1773+300G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017865 | ||||||
| chr9:86018205
|
A | T | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1774-50A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86018205 | ||||||
| chr9:86018458
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0083 | 2 | NA18940.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1914+63G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 20/22 | chr9 | 86018458 | ||||||
| chr9:86018550
|
T | G | 1 | a0001c0001t0001g0181 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1915-149T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 20/22 | chr9 | 86018550 | ||||||
| chr9:86019320
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2037+499C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019320 | ||||||
| chr9:86019328
|
A | G | 3 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025 | 3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2037+507A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019328 | ||||||
| chr9:86019568
|
A | C | 2 | a0001c0001t0002g0075a0001c0001t0002g0078 | 2 | NA18947.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2037+747A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019568 | ||||||
| chr9:86019707
|
C | G | 1 | a0001c0001t0001g0175 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2037+886C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019707 | ||||||
| chr9:86019733
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2037+912C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019733 | ||||||
| chr9:86019747
|
C | T | 5 | a0001c0001t0003g0009a0001c0001t0003g0112a0001c0001t0003g0116others(2): Show | 6 | HG00738.hp1 HG01952.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2037+926C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019747 | ||||||
| chr9:86019835
|
T | C | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2037+1014T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019835 | ||||||
| chr9:86020101
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2038-788G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020101 | ||||||
| chr9:86020145
|
A | G | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2038-744A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020145 | ||||||
| chr9:86020163
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2038-726T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020163 | ||||||
| chr9:86020460
|
T | C | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-429T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020460 | ||||||
| chr9:86020621
|
T | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2038-268T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020621 | ||||||
| chr9:86020659
|
CA | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0077others(1): Show | 6 | HG00558.hp1 NA18974.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.2038-229delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020659 | ||||||
| chr9:86020833
|
AAG | A | 3 | a0001c0001t0006g0231a0001c0001t0006g0232a0001c0001t0006g0233 | 3 | HG00280.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2038-52_2038-51del others(2): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr9 | 86020833 | |||||
| chr9:86020860
|
G | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-29G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020860 | ||||||
| chr9:86020984
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2118+15G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86020984 | ||||||
| chr9:86021024
|
G | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(130): Show | 142 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.2118+55G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021024 | ||||||
| chr9:86021057
|
A | G | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0243others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2118+88A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021057 | ||||||
| chr9:86021141
|
G | A | 2 | a0001c0003t0009g0015a0001c0003t0010g0014 | 2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2118+172G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021141 | ||||||
| chr9:86021417
|
C | T | 2 | a0002c0004t0002g0017a0002c0004t0013g0016 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2118+448C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021417 | ||||||
| chr9:86021435
|
C | T | 1 | a0004c0005t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2118+466C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021435 | ||||||
| chr9:86021461
|
C | T | 55 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(52): Show | 60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2119-440C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021461 | ||||||
| chr9:86021566
|
A | G | 1 | a0001c0001t0003g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2119-335A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021566 | ||||||
| chr9:86021599
|
C | G | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2119-302C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021599 | ||||||
| chr9:86021622
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2119-279C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021622 | ||||||
| chr9:86021624
|
A | G | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0112others(35): Show | 41 | HG00280.hp1 HG00738.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.2119-277A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021624 | ||||||
| chr9:86021683
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2119-218C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021683 | ||||||
| chr9:86021694
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2119-207T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021694 | ||||||
| chr9:86021836
|
CTT | C | 59 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(56): Show | 65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2119-63_2119-62del others(2): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr9 | 86021836 |