Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 408050 |
|---|---|
| ensemblid | ENSG00000103226.19 |
| hgncid | 25242 |
| symbol | NOMO3 |
| name | NODAL modulator 3 |
| refseq_nuc | NM_001004067.4 |
| refseq_prot | NP_001004067.1 |
| ensembl_nuc | ENST00000399336.9 |
| ensembl_prot | ENSP00000382274.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 16232528 |
| end | 16294811 |
| strand | + |
| ver | v1.2 |
| region | chr16:16232528-16294811 |
| region5000 | chr16:16227528-16299811 |
| regionname0 | NOMO3_chr16_16232528_16294811 |
| regionname5000 | NOMO3_chr16_16227528_16299811 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1222 | 95 | 14 | 34 | 28 | 5 | 14 | 14 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0002 | 0/0 | 1222 | 17 | 3 | 5 | 5 | 2 | 2 | 3 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0003 | 0/0 | 1222 | 4 | 0 | 3 | 1 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0004 | 0/0 | 707 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0005 | 0/0 | 1222 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0006 | 0/0 | 1222 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0007 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0008 | 0/0 | 379 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0009 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0010 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0011 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0012 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0013 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0014 | 0/0 | 1227 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0015 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3669 | 63 | 10 | 27 | 10 | 3 | 13 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0002 | 0/0 | 3669 | 21 | 1 | 6 | 13 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0003 | 0/0 | 3669 | 16 | 3 | 4 | 5 | 2 | 2 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0004 | 0/0 | 3669 | 4 | 0 | 3 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0005 | 0/0 | 3669 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0006 | 0/0 | 3669 | 3 | 0 | 1 | 0 | 1 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0007 | 0/0 | 3669 | 2 | 0 | 0 | 0 | 1 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0008 | 0/0 | 3669 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0009 | 0/0 | 3669 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0010 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0011 | 0/0 | 3684 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0012 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0013 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0014 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0015 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0016 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0017 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0018 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0019 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0020 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0021 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0022 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0023 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0024 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| c0025 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 652 | 100 | 16 | 35 | 28 | 6 | 15 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| t0002 | 0/0 | 652 | 28 | 7 | 9 | 7 | 2 | 3 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| t0003 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| t0004 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| t0005 | 0/0 | 652 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| t0006 | 0/0 | 652 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3669 | 63 | 10 | 27 | 10 | 3 | 13 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0002 | 0/0 | 3669 | 21 | 1 | 6 | 13 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0005 | 0/0 | 3669 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0007 | 0/0 | 3669 | 2 | 0 | 0 | 0 | 1 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0018 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0019 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0020 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0023 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0024 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0025 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0002c0003 | 0/0 | 3669 | 16 | 3 | 4 | 5 | 2 | 2 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0002c0016 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0003c0004 | 0/0 | 3669 | 4 | 0 | 3 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0004c0006 | 0/0 | 3669 | 3 | 0 | 1 | 0 | 1 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0005c0008 | 0/0 | 3669 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0006c0009 | 0/0 | 3669 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0007c0012 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0008c0021 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0009c0013 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0010c0014 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0011c0015 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0012c0017 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0013c0022 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0014c0011 | 0/0 | 3684 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0015c0010 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4320 | 62 | 10 | 27 | 9 | 3 | 13 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0001t0004 | 0/0 | 4320 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0002t0001 | 0/0 | 4320 | 21 | 1 | 6 | 13 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0005t0001 | 0/0 | 4320 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0007t0001 | 0/0 | 4320 | 2 | 0 | 0 | 0 | 1 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0018t0001 | 0/0 | 4320 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0019t0001 | 0/0 | 4320 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0020t0001 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0023t0001 | 0/0 | 4320 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0024t0001 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0001c0025t0001 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0002c0003t0002 | 0/0 | 4320 | 16 | 3 | 4 | 5 | 2 | 2 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0002c0016t0002 | 0/0 | 4320 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0003c0004t0002 | 0/0 | 4320 | 4 | 0 | 3 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0004c0006t0001 | 0/0 | 4320 | 3 | 0 | 1 | 0 | 1 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0005c0008t0002 | 0/0 | 4320 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0006c0009t0002 | 0/0 | 4320 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0007c0012t0005 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0008c0021t0006 | 0/0 | 4320 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0009c0013t0001 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0010c0014t0002 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0011c0015t0002 | 0/0 | 4320 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0012c0017t0002 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0013c0022t0001 | 0/0 | 4320 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0014c0011t0003 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| a0015c0010t0001 | 0/0 | 4320 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | copy fasta | chr16 | 16227528 | 16299811 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0018t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0019t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0020t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0023t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0024t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0001c0025t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0002c0016t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0003c0004t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0003c0004t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0003c0004t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0003c0004t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0004c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0004c0006t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0004c0006t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0005c0008t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0005c0008t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0006c0009t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0006c0009t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0007c0012t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0008c0021t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0009c0013t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0010c0014t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0011c0015t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0012c0017t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0013c0022t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0014c0011t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| a0015c0010t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | GBR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | GBR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0122 | EUR | GBR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00642 | hp1 | a0002 | c0016 | t0002 | g0110 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00673 | hp1 | a0002 | c0003 | t0002 | g0113 | EAS | CHS | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01074 | hp1 | a0006 | c0009 | t0002 | g0106 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01074 | hp2 | a0004 | c0006 | t0001 | g0017 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01099 | hp1 | a0003 | c0004 | t0002 | g0129 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0114 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01168 | hp2 | a0003 | c0004 | t0002 | g0128 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01257 | hp1 | a0003 | c0004 | t0002 | g0127 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0102 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0024 | AMR | CLM | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01515 | hp1 | a0001 | c0007 | t0001 | g0044 | EUR | IBS | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0100 | EUR | IBS | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01884 | hp2 | a0001 | c0020 | t0001 | g0036 | AFR | ACB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01943 | hp1 | a0001 | c0018 | t0001 | g0014 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01943 | hp2 | a0008 | c0021 | t0006 | g0063 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01993 | hp1 | a0014 | c0011 | t0003 | g0034 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02015 | hp1 | a0001 | c0019 | t0001 | g0045 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02300 | hp2 | a0002 | c0003 | t0002 | g0109 | AMR | PEL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02451 | hp1 | a0005 | c0008 | t0002 | g0084 | AFR | ACB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02451 | hp2 | a0007 | c0012 | t0005 | g0130 | AFR | ACB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02683 | hp2 | a0002 | c0003 | t0002 | g0115 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03130 | hp1 | a0002 | c0003 | t0002 | g0116 | AFR | ESN | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03130 | hp2 | a0005 | c0008 | t0002 | g0083 | AFR | ESN | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03209 | hp1 | a0009 | c0013 | t0001 | g0098 | AFR | MSL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03209 | hp2 | a0001 | c0025 | t0001 | g0123 | AFR | MSL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03486 | hp1 | a0002 | c0003 | t0002 | g0117 | AFR | MSL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03490 | hp1 | a0004 | c0006 | t0001 | g0016 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03688 | hp1 | a0001 | c0007 | t0001 | g0046 | SAS | STU | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0108 | SAS | STU | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18612 | hp2 | a0002 | c0003 | t0002 | g0105 | EAS | CHB | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18906 | hp1 | a0012 | c0017 | t0002 | g0104 | AFR | YRI | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18906 | hp2 | a0002 | c0003 | t0002 | g0118 | AFR | YRI | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18944 | hp1 | a0001 | c0005 | t0001 | g0074 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18944 | hp2 | a0003 | c0004 | t0002 | g0126 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0111 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19009 | hp1 | a0002 | c0003 | t0002 | g0112 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19010 | hp2 | a0001 | c0005 | t0001 | g0095 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19066 | hp1 | a0011 | c0015 | t0002 | g0103 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19068 | hp2 | a0001 | c0005 | t0001 | g0073 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19079 | hp1 | a0001 | c0023 | t0001 | g0042 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19079 | hp2 | a0002 | c0003 | t0002 | g0101 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA19080 | hp2 | a0015 | c0010 | t0001 | g0069 | EAS | JPT | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA20805 | hp1 | a0004 | c0006 | t0001 | g0009 | EUR | TSI | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA20905 | hp1 | a0006 | c0009 | t0002 | g0107 | SAS | GIH | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG03471 | hp2 | a0001 | c0024 | t0001 | g0099 | AFR | MSL | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG06807 | hp1 | a0013 | c0022 | t0001 | g0026 | AFR | USA | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| HG06807 | hp2 | a0010 | c0014 | t0002 | g0121 | AFR | USA | NOMO3_chr16_16227528_16299811 | NOMO3 | chr16 | 16227528 | 16299811 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16232682
|
G | A | 1 | a0015 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.16G>A | p.Gly6Ser | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/31 | 155/4320 | 16/3669 | 6/1222 | chr16 | 16232682 | ||
| chr16:16232700
|
C | CCCGCGGT others(8): Show |
1 | a0014 | 1 | HG01993.hp1 | disruptive_inframe_insertion | MODERATE | c.45_59dupCACCGCCGCG others(5): Show |
p.Val20_Leu21insThrA others(11): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/31 | 199/4320 | 60/3669 | 20/1222 | INFO_REALIGN_3_PRIME | chr16 | 16232700 | |
| chr16:16236901
|
A | G | 1 | a0006 | 2 | HG01074.hp1 NA20905.hp1 |
missense_variant&splice_region_variant | MODERATE | c.166A>G | p.Ile56Val | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/31 | 305/4320 | 166/3669 | 56/1222 | chr16 | 16236901 | ||
| chr16:16251019
|
G | A | 2 | a0003a0007 | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
missense_variant | MODERATE | c.674G>A | p.Ser225Asn | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/31 | 813/4320 | 674/3669 | 225/1222 | chr16 | 16251019 | ||
| chr16:16251079
|
A | T | 1 | a0013 | 1 | HG06807.hp1 | missense_variant&splice_region_variant | MODERATE | c.734A>T | p.Glu245Val | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/31 | 873/4320 | 734/3669 | 245/1222 | chr16 | 16251079 | ||
| chr16:16256076
|
C | T | 1 | a0008 | 1 | HG01943.hp2 | stop_gained | HIGH | c.1138C>T | p.Gln380* | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/31 | 1277/4320 | 1138/3669 | 380/1222 | chr16 | 16256076 | ||
| chr16:16261655
|
C | A | 2 | a0003a0007 | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
missense_variant | MODERATE | c.1374C>A | p.Asn458Lys | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/31 | 1513/4320 | 1374/3669 | 458/1222 | chr16 | 16261655 | ||
| chr16:16265087
|
G | A | 3 | a0003a0005a0007 | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
missense_variant | MODERATE | c.1714G>A | p.Glu572Lys | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/31 | 1853/4320 | 1714/3669 | 572/1222 | chr16 | 16265087 | ||
| chr16:16265111
|
G | A | 1 | a0010 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1738G>A | p.Val580Met | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/31 | 1877/4320 | 1738/3669 | 580/1222 | chr16 | 16265111 | ||
| chr16:16265112
|
T | C | 1 | a0009 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1739T>C | p.Val580Ala | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/31 | 1878/4320 | 1739/3669 | 580/1222 | chr16 | 16265112 | ||
| chr16:16267111
|
G | A | 1 | a0011 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.1874G>A | p.Arg625Gln | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/31 | 2013/4320 | 1874/3669 | 625/1222 | chr16 | 16267111 | ||
| chr16:16273756
|
G | T | 1 | a0004 | 3 | HG01074.hp2 HG03490.hp1 NA20805.hp1 |
stop_gained | HIGH | c.2122G>T | p.Glu708* | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/31 | 2261/4320 | 2122/3669 | 708/1222 | chr16 | 16273756 | ||
| chr16:16273812
|
T | A | 7 | a0002a0003a0005others(4): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
missense_variant | MODERATE | c.2178T>A | p.Asn726Lys | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/31 | 2317/4320 | 2178/3669 | 726/1222 | chr16 | 16273812 | ||
| chr16:16273906
|
C | T | 1 | a0005 | 2 | HG02451.hp1 HG03130.hp2 |
missense_variant&splice_region_variant | MODERATE | c.2272C>T | p.Arg758Trp | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/31 | 2411/4320 | 2272/3669 | 758/1222 | chr16 | 16273906 | ||
| chr16:16285423
|
G | A | 2 | a0003a0005 | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
missense_variant | MODERATE | c.3241G>A | p.Glu1081Lys | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/31 | 3380/4320 | 3241/3669 | 1081/1222 | chr16 | 16285423 | ||
| chr16:16287839
|
A | T | 7 | a0002a0003a0005others(4): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
missense_variant | MODERATE | c.3421A>T | p.Ile1141Phe | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/31 | 3560/4320 | 3421/3669 | 1141/1222 | chr16 | 16287839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16232756
|
C | T | 1 | a0001c0025 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.90C>T | p.His30His | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/31 | 229/4320 | 90/3669 | 30/1222 | chr16 | 16232756 | ||
| chr16:16251041
|
C | G | 4 | a0001c0023a0001c0024a0003c0004others(1): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
synonymous_variant | LOW | c.696C>G | p.Gly232Gly | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/31 | 835/4320 | 696/3669 | 232/1222 | chr16 | 16251041 | ||
| chr16:16252040
|
G | A | 1 | a0009c0013 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.813G>A | p.Thr271Thr | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 8/31 | 952/4320 | 813/3669 | 271/1222 | chr16 | 16252040 | ||
| chr16:16256123
|
A | G | 4 | a0001c0020a0001c0024a0003c0004others(1): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
synonymous_variant | LOW | c.1185A>G | p.Pro395Pro | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/31 | 1324/4320 | 1185/3669 | 395/1222 | chr16 | 16256123 | ||
| chr16:16263154
|
T | C | 4 | a0001c0007a0003c0004a0007c0012others(1): Show | 8 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(5): Show |
synonymous_variant | LOW | c.1476T>C | p.Pro492Pro | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 13/31 | 1615/4320 | 1476/3669 | 492/1222 | chr16 | 16263154 | ||
| chr16:16265149
|
G | A | 1 | a0007c0012 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1776G>A | p.Leu592Leu | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/31 | 1915/4320 | 1776/3669 | 592/1222 | chr16 | 16265149 | ||
| chr16:16273821
|
T | C | 9 | a0002c0003a0002c0016a0003c0004others(6): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
synonymous_variant | LOW | c.2187T>C | p.Gly729Gly | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/31 | 2326/4320 | 2187/3669 | 729/1222 | chr16 | 16273821 | ||
| chr16:16273845
|
T | C | 25 | a0001c0001a0001c0002a0001c0005others(22): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
synonymous_variant | LOW | c.2211T>C | p.Pro737Pro | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/31 | 2350/4320 | 2211/3669 | 737/1222 | chr16 | 16273845 | ||
| chr16:16274053
|
A | G | 1 | a0001c0019 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2334A>G | p.Ser778Ser | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/31 | 2473/4320 | 2334/3669 | 778/1222 | chr16 | 16274053 | ||
| chr16:16275169
|
C | T | 1 | a0002c0016 | 1 | HG00642.hp1 | splice_region_variant&synonymous_variant | LOW | c.2514C>T | p.Tyr838Tyr | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 21/31 | 2653/4320 | 2514/3669 | 838/1222 | chr16 | 16275169 | ||
| chr16:16275386
|
A | G | 9 | a0002c0003a0002c0016a0003c0004others(6): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
synonymous_variant | LOW | c.2586A>G | p.Ala862Ala | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/31 | 2725/4320 | 2586/3669 | 862/1222 | chr16 | 16275386 | ||
| chr16:16277420
|
T | C | 13 | a0001c0002a0001c0018a0001c0025others(10): Show | 55 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(52): Show |
synonymous_variant | LOW | c.2694T>C | p.Ser898Ser | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/31 | 2833/4320 | 2694/3669 | 898/1222 | chr16 | 16277420 | ||
| chr16:16277462
|
C | A | 9 | a0002c0003a0002c0016a0003c0004others(6): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
synonymous_variant | LOW | c.2736C>A | p.Gly912Gly | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/31 | 2875/4320 | 2736/3669 | 912/1222 | chr16 | 16277462 | ||
| chr16:16281256
|
C | T | 1 | a0001c0005 | 3 | NA18944.hp1 NA19010.hp2 NA19068.hp2 |
synonymous_variant | LOW | c.3045C>T | p.His1015His | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/31 | 3184/4320 | 3045/3669 | 1015/1222 | chr16 | 16281256 | ||
| chr16:16283033
|
C | T | 1 | a0001c0018 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.3129C>T | p.Ile1043Ile | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/31 | 3268/4320 | 3129/3669 | 1043/1222 | chr16 | 16283033 | ||
| chr16:16285500
|
T | C | 2 | a0003c0004a0005c0008 | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
synonymous_variant | LOW | c.3318T>C | p.Asp1106Asp | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/31 | 3457/4320 | 3318/3669 | 1106/1222 | chr16 | 16285500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16232539
|
G | T | 1 | a0008c0021t0006 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/31 | 128 | chr16 | 16232539 | |||||
| chr16:16232629
|
G | A | 1 | a0014c0011t0003 | 1 | HG01993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/31 | 38 | chr16 | 16232629 | |||||
| chr16:16294640
|
G | C | 1 | a0001c0001t0004 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 31/31 | 341 | chr16 | 16294640 | |||||
| chr16:16294656
|
T | C | 8 | a0002c0003t0002a0002c0016t0002a0003c0004t0002others(5): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*357T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 31/31 | 357 | chr16 | 16294656 | |||||
| chr16:16294674
|
G | C | 1 | a0007c0012t0005 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*375G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 31/31 | 375 | chr16 | 16294674 | |||||
| chr16:16294744
|
G | A | 8 | a0002c0003t0002a0002c0016t0002a0003c0004t0002others(5): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*445G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 31/31 | 445 | chr16 | 16294744 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:16232933
|
C | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+102C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16232933 | ||||||
| chr16:16232961
|
T | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+130T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16232961 | ||||||
| chr16:16233348
|
A | T | 33 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.165+517A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16233348 | ||||||
| chr16:16233502
|
G | GT | 31 | a0001c0001t0001g0002a0001c0001t0001g0064a0001c0001t0001g0065others(28): Show | 32 | HG00642.hp2 HG00741.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.165+691dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 16233502 | |||||
| chr16:16233502
|
G | GTT | 6 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | HG00099.hp1 HG01256.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+690_165+691dup others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 16233502 | |||||
| chr16:16233502
|
GT | G | 7 | a0001c0001t0001g0003a0003c0004t0002g0126a0003c0004t0002g0127others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+691delT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 16233502 | |||||
| chr16:16233522
|
T | A | 7 | a0001c0024t0001g0099a0002c0003t0002g0100a0002c0003t0002g0101others(4): Show | 7 | HG01346.hp1 HG01515.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+691T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16233522 | ||||||
| chr16:16233522
|
T | TA | 11 | a0002c0003t0002g0105a0002c0003t0002g0108a0002c0003t0002g0109others(8): Show | 11 | HG00642.hp1 HG00673.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+693dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 16233522 | |||||
| chr16:16233544
|
T | G | 1 | a0008c0021t0006g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.165+713T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16233544 | ||||||
| chr16:16233711
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+880G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16233711 | ||||||
| chr16:16233836
|
G | C | 1 | a0001c0001t0001g0092 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.165+1005G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16233836 | ||||||
| chr16:16234028
|
A | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(36): Show | 39 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.165+1197A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234028 | ||||||
| chr16:16234080
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1249A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234080 | ||||||
| chr16:16234207
|
A | G | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.165+1376A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234207 | ||||||
| chr16:16234271
|
C | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1440C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234271 | ||||||
| chr16:16234350
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.165+1519C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234350 | ||||||
| chr16:16234418
|
C | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1587C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234418 | ||||||
| chr16:16234434
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1603C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234434 | ||||||
| chr16:16234461
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1630A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234461 | ||||||
| chr16:16234540
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1709T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234540 | ||||||
| chr16:16234565
|
C | T | 33 | a0001c0001t0001g0062a0001c0001t0001g0120a0001c0001t0001g0125others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.165+1734C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234565 | ||||||
| chr16:16234574
|
T | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1743T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234574 | ||||||
| chr16:16234676
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1845T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234676 | ||||||
| chr16:16234700
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1869C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234700 | ||||||
| chr16:16234777
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1946T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234777 | ||||||
| chr16:16234819
|
TAA | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+2001_165+2002d others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 16234819 | |||||
| chr16:16234863
|
A | C | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.165+2032A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234863 | ||||||
| chr16:16234907
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.166-1994G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234907 | ||||||
| chr16:16234914
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.166-1987G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16234914 | ||||||
| chr16:16235114
|
T | G | 1 | a0001c0002t0001g0004 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-1787T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235114 | ||||||
| chr16:16235149
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG02683.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.166-1752T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235149 | ||||||
| chr16:16235205
|
G | A | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.166-1696G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235205 | ||||||
| chr16:16235222
|
C | G | 1 | a0013c0022t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.166-1679C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235222 | ||||||
| chr16:16235252
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-1649G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235252 | ||||||
| chr16:16235483
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1418T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235483 | ||||||
| chr16:16235487
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1414G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235487 | ||||||
| chr16:16235514
|
T | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-1387T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235514 | ||||||
| chr16:16235743
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1158A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235743 | ||||||
| chr16:16235800
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-1101G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235800 | ||||||
| chr16:16235894
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-1007T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235894 | ||||||
| chr16:16235901
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-1000A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235901 | ||||||
| chr16:16235907
|
G | A | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-994G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235907 | ||||||
| chr16:16235946
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-955G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16235946 | ||||||
| chr16:16236088
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-813G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236088 | ||||||
| chr16:16236187
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-714G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236187 | ||||||
| chr16:16236241
|
A | G | 1 | a0001c0002t0001g0025 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.166-660A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236241 | ||||||
| chr16:16236246
|
A | ATTTTT | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-651_166-650ins others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 16236246 | |||||
| chr16:16236361
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.166-540C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236361 | ||||||
| chr16:16236501
|
C | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-400C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236501 | ||||||
| chr16:16236635
|
G | A | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-266G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236635 | ||||||
| chr16:16236655
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-246A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236655 | ||||||
| chr16:16236693
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-208G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236693 | ||||||
| chr16:16236788
|
C | T | 10 | a0001c0001t0001g0059a0001c0001t0001g0120a0001c0001t0001g0125others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-113C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236788 | ||||||
| chr16:16236794
|
A | G | 10 | a0001c0001t0001g0059a0001c0001t0001g0120a0001c0001t0001g0125others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.166-107A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 1/30 | chr16 | 16236794 | ||||||
| chr16:16237061
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+71T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237061 | ||||||
| chr16:16237126
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+136C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237126 | ||||||
| chr16:16237192
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+202A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237192 | ||||||
| chr16:16237287
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+297T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237287 | ||||||
| chr16:16237342
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+352T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237342 | ||||||
| chr16:16237393
|
A | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+403A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237393 | ||||||
| chr16:16237484
|
G | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+494G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237484 | ||||||
| chr16:16237547
|
GT | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+568delT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 16237547 | |||||
| chr16:16237547
|
GTT | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+567_255+568del others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 16237547 | |||||
| chr16:16237570
|
T | A | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+580T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237570 | ||||||
| chr16:16237665
|
C | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+675C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237665 | ||||||
| chr16:16237666
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+676A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237666 | ||||||
| chr16:16237673
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+683T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237673 | ||||||
| chr16:16237695
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+705T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237695 | ||||||
| chr16:16237738
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+748T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237738 | ||||||
| chr16:16237758
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+768T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237758 | ||||||
| chr16:16237869
|
T | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+879T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237869 | ||||||
| chr16:16237908
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+918A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237908 | ||||||
| chr16:16237937
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+947T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16237937 | ||||||
| chr16:16238012
|
A | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+1022A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238012 | ||||||
| chr16:16238185
|
G | GT | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.255+1201dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 16238185 | |||||
| chr16:16238261
|
C | G | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.255+1271C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238261 | ||||||
| chr16:16238329
|
TTCCAGTG others(4): Show |
T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.255+1341_255+1351d others(13): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 16238329 | |||||
| chr16:16238400
|
T | C | 6 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(3): Show | 6 | HG00140.hp1 HG00438.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+1410T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238400 | ||||||
| chr16:16238479
|
G | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0064a0001c0001t0001g0065others(24): Show | 28 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.256-1372G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238479 | ||||||
| chr16:16238526
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.256-1325A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238526 | ||||||
| chr16:16238554
|
G | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-1297G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238554 | ||||||
| chr16:16238705
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-1146T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238705 | ||||||
| chr16:16238848
|
T | C | 33 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.256-1003T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16238848 | ||||||
| chr16:16239077
|
CA | C | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0120others(3): Show | 6 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-762delA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 16239077 | |||||
| chr16:16239098
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-753A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239098 | ||||||
| chr16:16239102
|
C | CAA | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-748_256-747ins others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 16239102 | |||||
| chr16:16239158
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-693C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239158 | ||||||
| chr16:16239180
|
C | T | 10 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-671C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239180 | ||||||
| chr16:16239183
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-668T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239183 | ||||||
| chr16:16239193
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-658C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239193 | ||||||
| chr16:16239260
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-591T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239260 | ||||||
| chr16:16239296
|
G | A | 1 | a0014c0011t0003g0034 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.256-555G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239296 | ||||||
| chr16:16239316
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.256-535A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239316 | ||||||
| chr16:16239476
|
C | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-375C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239476 | ||||||
| chr16:16239730
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-121T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239730 | ||||||
| chr16:16239803
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.256-48G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 2/30 | chr16 | 16239803 | ||||||
| chr16:16239974
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.301+78G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16239974 | ||||||
| chr16:16240085
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+189C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240085 | ||||||
| chr16:16240214
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+318A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240214 | ||||||
| chr16:16240241
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+345C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240241 | ||||||
| chr16:16240255
|
G | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+359G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240255 | ||||||
| chr16:16240379
|
G | A | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+483G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240379 | ||||||
| chr16:16240418
|
C | G | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+522C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240418 | ||||||
| chr16:16240427
|
T | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+531T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240427 | ||||||
| chr16:16240498
|
G | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG03492.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.301+602G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240498 | ||||||
| chr16:16240573
|
A | AGAAC | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+677_301+678ins others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240573 | ||||||
| chr16:16240643
|
G | A | 2 | a0006c0009t0002g0106a0006c0009t0002g0107 | 2 | HG01074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.301+747G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240643 | ||||||
| chr16:16240799
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+903A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240799 | ||||||
| chr16:16240888
|
C | G | 33 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.301+992C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240888 | ||||||
| chr16:16240942
|
C | T | 1 | a0002c0003t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.301+1046C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16240942 | ||||||
| chr16:16241116
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+1220A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241116 | ||||||
| chr16:16241287
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+1391G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241287 | ||||||
| chr16:16241315
|
T | C | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1419T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241315 | ||||||
| chr16:16241320
|
G | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+1424G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241320 | ||||||
| chr16:16241404
|
C | T | 11 | a0001c0001t0001g0023a0001c0001t0001g0120a0001c0001t0001g0125others(8): Show | 11 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.301+1508C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241404 | ||||||
| chr16:16241419
|
A | C | 1 | a0007c0012t0005g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.301+1523A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241419 | ||||||
| chr16:16241449
|
G | A | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.301+1553G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241449 | ||||||
| chr16:16241495
|
T | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.301+1599T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241495 | ||||||
| chr16:16241527
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+1631C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241527 | ||||||
| chr16:16241549
|
G | A | 2 | a0002c0003t0002g0116a0002c0003t0002g0117 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.302-1612G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241549 | ||||||
| chr16:16241550
|
G | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-1611G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241550 | ||||||
| chr16:16241675
|
T | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-1486T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241675 | ||||||
| chr16:16241863
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-1298A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16241863 | ||||||
| chr16:16242009
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-1152A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242009 | ||||||
| chr16:16242117
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.302-1044C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242117 | ||||||
| chr16:16242201
|
T | TTG | 6 | a0001c0001t0001g0032a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG00438.hp2 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-933_302-932dup others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 16242201 | |||||
| chr16:16242201
|
TTG | T | 26 | a0001c0001t0001g0041a0001c0002t0001g0082a0001c0023t0001g0042others(23): Show | 26 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.302-933_302-932del others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 16242201 | |||||
| chr16:16242201
|
TTGTG | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-935_302-932del others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 16242201 | |||||
| chr16:16242503
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-658A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242503 | ||||||
| chr16:16242664
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-497T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242664 | ||||||
| chr16:16242676
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-485T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242676 | ||||||
| chr16:16242698
|
G | C | 1 | a0003c0004t0002g0126 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.302-463G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242698 | ||||||
| chr16:16242862
|
A | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-299A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16242862 | ||||||
| chr16:16243001
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-160C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | chr16 | 16243001 | ||||||
| chr16:16243023
|
CA | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.302-136delA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 16243023 | |||||
| chr16:16243280
|
A | G | 1 | a0001c0002t0001g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.402+19A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243280 | ||||||
| chr16:16243428
|
A | G | 12 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(9): Show | 12 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.402+167A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243428 | ||||||
| chr16:16243447
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+186A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243447 | ||||||
| chr16:16243540
|
C | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+279C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243540 | ||||||
| chr16:16243832
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.402+571C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243832 | ||||||
| chr16:16243840
|
T | TCAGGGAT others(9): Show |
1 | a0001c0002t0001g0019 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.402+588_402+603dup others(16): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 16243840 | |||||
| chr16:16243880
|
A | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+619A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243880 | ||||||
| chr16:16243964
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+703T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243964 | ||||||
| chr16:16243974
|
G | C | 11 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(8): Show | 11 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.402+713G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16243974 | ||||||
| chr16:16244068
|
T | C | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+807T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244068 | ||||||
| chr16:16244100
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+839C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244100 | ||||||
| chr16:16244120
|
C | A | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+859C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244120 | ||||||
| chr16:16244235
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.403-833G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244235 | ||||||
| chr16:16244296
|
C | T | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.403-772C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244296 | ||||||
| chr16:16244400
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-668A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244400 | ||||||
| chr16:16244505
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 8 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-563C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244505 | ||||||
| chr16:16244511
|
C | CT | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG01109.hp1 HG02027.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.403-533dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 16244511 | |||||
| chr16:16244511
|
C | CTTTT | 4 | a0001c0001t0001g0039a0001c0001t0001g0120a0001c0001t0001g0125others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-536_403-533dup others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 16244511 | |||||
| chr16:16244511
|
CT | C | 35 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 35 | HG00741.hp2 HG01099.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.403-533delT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 16244511 | |||||
| chr16:16244535
|
T | A | 1 | a0002c0003t0002g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.403-533T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244535 | ||||||
| chr16:16244599
|
C | G | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403-469C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244599 | ||||||
| chr16:16244675
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.403-393G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 4/30 | chr16 | 16244675 | ||||||
| chr16:16245253
|
G | GC | 20 | a0001c0024t0001g0099a0002c0003t0002g0100a0002c0003t0002g0101others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.509+79_509+80insC | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245253 | ||||||
| chr16:16245296
|
G | C | 10 | a0001c0001t0001g0058a0001c0001t0001g0120a0001c0001t0001g0125others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+122G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245296 | ||||||
| chr16:16245417
|
G | A | 10 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+243G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245417 | ||||||
| chr16:16245457
|
T | G | 9 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(6): Show | 9 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+283T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245457 | ||||||
| chr16:16245518
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG02132.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+344G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245518 | ||||||
| chr16:16245561
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.509+387T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245561 | ||||||
| chr16:16245562
|
G | C | 1 | a0003c0004t0002g0128 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.509+388G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245562 | ||||||
| chr16:16245605
|
T | C | 14 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0004g0124others(11): Show | 14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+431T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245605 | ||||||
| chr16:16245758
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+584C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245758 | ||||||
| chr16:16245830
|
C | T | 2 | a0001c0002t0001g0018a0001c0002t0001g0025 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.509+656C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245830 | ||||||
| chr16:16245996
|
A | T | 1 | a0001c0002t0001g0119 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.509+822A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16245996 | ||||||
| chr16:16246009
|
T | C | 7 | a0001c0001t0001g0125a0001c0002t0001g0119a0003c0004t0002g0126others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+835T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246009 | ||||||
| chr16:16246037
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+863A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246037 | ||||||
| chr16:16246077
|
A | G | 7 | a0001c0001t0001g0125a0001c0002t0001g0119a0003c0004t0002g0126others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+903A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246077 | ||||||
| chr16:16246110
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+936T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246110 | ||||||
| chr16:16246209
|
G | A | 4 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+1035G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246209 | ||||||
| chr16:16246245
|
G | A | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509+1071G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246245 | ||||||
| chr16:16246291
|
A | T | 6 | a0001c0001t0001g0125a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-1104A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246291 | ||||||
| chr16:16246374
|
G | C | 6 | a0001c0001t0001g0125a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-1021G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246374 | ||||||
| chr16:16246397
|
G | A | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.510-998G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246397 | ||||||
| chr16:16246484
|
C | T | 4 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-911C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246484 | ||||||
| chr16:16246543
|
C | G | 32 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0125others(29): Show | 32 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.510-852C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246543 | ||||||
| chr16:16246583
|
A | C | 9 | a0001c0001t0001g0125a0002c0003t0002g0116a0002c0003t0002g0117others(6): Show | 9 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-812A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246583 | ||||||
| chr16:16246613
|
C | T | 6 | a0001c0001t0001g0125a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-782C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246613 | ||||||
| chr16:16246900
|
A | G | 6 | a0001c0001t0001g0125a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-495A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16246900 | ||||||
| chr16:16247069
|
C | A | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510-326C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16247069 | ||||||
| chr16:16247105
|
A | G | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.510-290A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16247105 | ||||||
| chr16:16247134
|
T | G | 1 | a0010c0014t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-261T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 5/30 | chr16 | 16247134 | ||||||
| chr16:16247773
|
G | T | 2 | a0002c0003t0002g0116a0002c0003t0002g0117 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.582+306G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16247773 | ||||||
| chr16:16248042
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+575T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16248042 | ||||||
| chr16:16248081
|
C | CT | 8 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00140.hp1 HG01109.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.582+636dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 16248081 | |||||
| chr16:16248081
|
CTT | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+635_582+636del others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 16248081 | |||||
| chr16:16248109
|
C | T | 17 | a0001c0024t0001g0099a0002c0003t0002g0100a0002c0003t0002g0101others(14): Show | 17 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.582+642C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16248109 | ||||||
| chr16:16248118
|
G | A | 7 | a0001c0024t0001g0099a0002c0003t0002g0100a0002c0003t0002g0101others(4): Show | 7 | HG00642.hp1 HG01346.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.582+651G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16248118 | ||||||
| chr16:16248153
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.582+686T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16248153 | ||||||
| chr16:16248337
|
C | T | 1 | a0002c0003t0002g0100 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.582+870C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16248337 | ||||||
| chr16:16248395
|
C | CT | 12 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0054others(9): Show | 12 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.582+949dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 16248395 | |||||
| chr16:16248661
|
G | A | 3 | a0002c0003t0002g0105a0002c0003t0002g0111a0002c0003t0002g0112 | 3 | NA18612.hp2 NA18969.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.582+1194G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16248661 | ||||||
| chr16:16249238
|
G | A | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.583-1690G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249238 | ||||||
| chr16:16249297
|
G | A | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.583-1631G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249297 | ||||||
| chr16:16249436
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1492G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249436 | ||||||
| chr16:16249474
|
C | T | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.583-1454C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249474 | ||||||
| chr16:16249513
|
T | G | 1 | a0001c0002t0001g0010 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.583-1415T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249513 | ||||||
| chr16:16249581
|
C | CA | 6 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0002t0001g0018others(3): Show | 6 | HG02135.hp1 HG02135.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.583-1328dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 16249581 | |||||
| chr16:16249652
|
G | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1276G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249652 | ||||||
| chr16:16249758
|
T | C | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-1170T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249758 | ||||||
| chr16:16249778
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1150G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249778 | ||||||
| chr16:16249788
|
G | C | 1 | a0003c0004t0002g0128 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.583-1140G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249788 | ||||||
| chr16:16249816
|
A | C | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-1112A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249816 | ||||||
| chr16:16249830
|
T | C | 29 | a0001c0024t0001g0099a0001c0025t0001g0123a0002c0003t0002g0100others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.583-1098T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249830 | ||||||
| chr16:16249910
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.583-1018A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16249910 | ||||||
| chr16:16250007
|
T | C | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-921T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250007 | ||||||
| chr16:16250032
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-896C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250032 | ||||||
| chr16:16250233
|
A | AC | 3 | a0001c0024t0001g0099a0003c0004t0002g0127a0003c0004t0002g0128 | 3 | HG01168.hp2 HG01257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.583-695_583-694ins others(1): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250233 | ||||||
| chr16:16250302
|
A | G | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-626A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250302 | ||||||
| chr16:16250557
|
G | A | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-371G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250557 | ||||||
| chr16:16250647
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-281G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250647 | ||||||
| chr16:16250671
|
C | T | 1 | a0004c0006t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.583-257C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250671 | ||||||
| chr16:16250825
|
A | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0048a0001c0001t0001g0049others(10): Show | 13 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.583-103A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250825 | ||||||
| chr16:16250858
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-70G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 6/30 | chr16 | 16250858 | ||||||
| chr16:16251148
|
G | A | 6 | a0001c0002t0001g0010a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01106.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+68G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/30 | chr16 | 16251148 | ||||||
| chr16:16251502
|
A | C | 2 | a0002c0003t0002g0116a0002c0003t0002g0117 | 2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.735+422A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/30 | chr16 | 16251502 | ||||||
| chr16:16251581
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.736-382G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/30 | chr16 | 16251581 | ||||||
| chr16:16251635
|
A | G | 2 | a0001c0001t0001g0058a0001c0024t0001g0099 | 2 | HG02300.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.736-328A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/30 | chr16 | 16251635 | ||||||
| chr16:16251730
|
G | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-233G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/30 | chr16 | 16251730 | ||||||
| chr16:16251834
|
T | G | 29 | a0001c0024t0001g0099a0001c0025t0001g0123a0002c0003t0002g0100others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.736-129T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 7/30 | chr16 | 16251834 | ||||||
| chr16:16252214
|
T | C | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.873+114T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 8/30 | chr16 | 16252214 | ||||||
| chr16:16252258
|
C | T | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.873+158C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 8/30 | chr16 | 16252258 | ||||||
| chr16:16252295
|
A | G | 6 | a0001c0024t0001g0099a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.874-138A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 8/30 | chr16 | 16252295 | ||||||
| chr16:16252379
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.874-54T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 8/30 | chr16 | 16252379 | ||||||
| chr16:16252652
|
G | A | 1 | a0002c0003t0002g0109 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.963+130G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16252652 | ||||||
| chr16:16252824
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+302C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16252824 | ||||||
| chr16:16252828
|
A | AT | 22 | a0001c0001t0001g0030a0001c0020t0001g0036a0001c0024t0001g0099others(19): Show | 22 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.963+329dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 16252828 | |||||
| chr16:16252828
|
A | ATT | 6 | a0001c0025t0001g0123a0002c0003t0002g0116a0002c0003t0002g0117others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.963+328_963+329dup others(2): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 16252828 | |||||
| chr16:16252856
|
C | T | 2 | a0001c0002t0001g0004a0001c0020t0001g0036 | 2 | HG01884.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.963+334C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16252856 | ||||||
| chr16:16252930
|
T | C | 7 | a0001c0020t0001g0036a0001c0024t0001g0099a0003c0004t0002g0126others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+408T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16252930 | ||||||
| chr16:16253162
|
T | C | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.963+640T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253162 | ||||||
| chr16:16253246
|
A | C | 11 | a0001c0002t0001g0010a0001c0020t0001g0036a0001c0024t0001g0099others(8): Show | 11 | HG01099.hp1 HG01106.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+724A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253246 | ||||||
| chr16:16253329
|
G | T | 2 | a0009c0013t0001g0098a0012c0017t0002g0104 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.963+807G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253329 | ||||||
| chr16:16253402
|
C | T | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.963+880C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253402 | ||||||
| chr16:16253416
|
G | A | 3 | a0001c0001t0004g0124a0001c0002t0001g0021a0001c0002t0001g0022 | 3 | HG00438.hp1 HG00438.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.963+894G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253416 | ||||||
| chr16:16253441
|
G | A | 10 | a0002c0003t0002g0105a0002c0003t0002g0108a0002c0003t0002g0111others(7): Show | 10 | HG00140.hp2 HG00673.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.963+919G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253441 | ||||||
| chr16:16253506
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.963+984C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253506 | ||||||
| chr16:16253558
|
T | C | 31 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123others(28): Show | 31 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.963+1036T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253558 | ||||||
| chr16:16253900
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.963+1378A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253900 | ||||||
| chr16:16253962
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+1440T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16253962 | ||||||
| chr16:16253973
|
TA | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+1453delA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 16253973 | |||||
| chr16:16254089
|
C | T | 2 | a0001c0020t0001g0036a0001c0025t0001g0123 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.963+1567C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254089 | ||||||
| chr16:16254285
|
T | C | 8 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123others(5): Show | 8 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-1435T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254285 | ||||||
| chr16:16254365
|
C | A | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-1355C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254365 | ||||||
| chr16:16254430
|
T | G | 30 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123others(27): Show | 30 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.964-1290T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254430 | ||||||
| chr16:16254638
|
A | T | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.964-1082A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254638 | ||||||
| chr16:16254741
|
T | C | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-979T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254741 | ||||||
| chr16:16254748
|
A | G | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-972A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254748 | ||||||
| chr16:16254818
|
C | G | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-902C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254818 | ||||||
| chr16:16254835
|
G | A | 2 | a0001c0020t0001g0036a0001c0025t0001g0123 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.964-885G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254835 | ||||||
| chr16:16254842
|
G | GCACAGA | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-861_964-856dup others(6): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 16254842 | |||||
| chr16:16254872
|
C | T | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-848C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254872 | ||||||
| chr16:16254946
|
A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0064others(27): Show | 31 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.964-774A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254946 | ||||||
| chr16:16254959
|
T | G | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-761T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254959 | ||||||
| chr16:16254977
|
A | G | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-743A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254977 | ||||||
| chr16:16254998
|
T | C | 8 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123others(5): Show | 8 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-722T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16254998 | ||||||
| chr16:16255015
|
T | C | 3 | a0001c0020t0001g0036a0001c0024t0001g0099a0001c0025t0001g0123 | 3 | HG01884.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-705T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255015 | ||||||
| chr16:16255029
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0075 | 2 | HG01261.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.964-691C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255029 | ||||||
| chr16:16255061
|
C | T | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-659C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255061 | ||||||
| chr16:16255120
|
C | T | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-600C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255120 | ||||||
| chr16:16255156
|
G | T | 1 | a0001c0002t0001g0007 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.964-564G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255156 | ||||||
| chr16:16255297
|
C | T | 4 | a0001c0002t0001g0020a0004c0006t0001g0009a0004c0006t0001g0016others(1): Show | 4 | HG01074.hp2 HG01891.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-423C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255297 | ||||||
| chr16:16255322
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-398G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255322 | ||||||
| chr16:16255330
|
T | G | 7 | a0001c0020t0001g0036a0001c0024t0001g0099a0003c0004t0002g0126others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-390T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255330 | ||||||
| chr16:16255521
|
T | C | 2 | a0001c0002t0001g0001a0001c0002t0001g0008 | 3 | HG01928.hp2 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.964-199T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255521 | ||||||
| chr16:16255574
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.964-146G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255574 | ||||||
| chr16:16255617
|
G | A | 1 | a0007c0012t0005g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-103G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255617 | ||||||
| chr16:16255648
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0087 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.964-72C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | chr16 | 16255648 | ||||||
| chr16:16255697
|
C | CCTT | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-19_964-17dupCT others(1): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 16255697 | |||||
| chr16:16255862
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1069+37G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 10/30 | chr16 | 16255862 | ||||||
| chr16:16255967
|
G | A | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1070-41G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 10/30 | chr16 | 16255967 | ||||||
| chr16:16256169
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1220+11C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16256169 | ||||||
| chr16:16256276
|
C | CTTT | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+131_1220+133d others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 16256276 | |||||
| chr16:16256416
|
C | T | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1220+258C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16256416 | ||||||
| chr16:16256762
|
T | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+604T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16256762 | ||||||
| chr16:16257044
|
C | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+886C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257044 | ||||||
| chr16:16257091
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0064others(27): Show | 31 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.1220+933G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257091 | ||||||
| chr16:16257185
|
G | A | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1220+1027G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257185 | ||||||
| chr16:16257287
|
A | G | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1220+1129A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257287 | ||||||
| chr16:16257337
|
G | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+1179G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257337 | ||||||
| chr16:16257467
|
T | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(46): Show | 49 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1220+1309T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257467 | ||||||
| chr16:16257502
|
A | G | 3 | a0004c0006t0001g0009a0004c0006t0001g0016a0004c0006t0001g0017 | 3 | HG01074.hp2 HG03490.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1220+1344A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257502 | ||||||
| chr16:16257641
|
AG | A | 7 | a0001c0020t0001g0036a0001c0024t0001g0099a0003c0004t0002g0126others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1220+1490delG | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 16257641 | |||||
| chr16:16257660
|
C | G | 2 | a0001c0020t0001g0036a0001c0024t0001g0099 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1220+1502C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257660 | ||||||
| chr16:16257716
|
G | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(118): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1220+1558G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257716 | ||||||
| chr16:16257809
|
A | G | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1220+1651A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257809 | ||||||
| chr16:16257946
|
A | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.1220+1788A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257946 | ||||||
| chr16:16257996
|
A | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1220+1838A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16257996 | ||||||
| chr16:16258086
|
T | C | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1220+1928T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258086 | ||||||
| chr16:16258090
|
C | T | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1220+1932C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258090 | ||||||
| chr16:16258097
|
C | A | 4 | a0001c0002t0001g0020a0004c0006t0001g0009a0004c0006t0001g0016others(1): Show | 4 | HG01074.hp2 HG01891.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+1939C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258097 | ||||||
| chr16:16258136
|
C | G | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1220+1978C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258136 | ||||||
| chr16:16258143
|
C | A | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1220+1985C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258143 | ||||||
| chr16:16258192
|
A | AAAAT | 4 | a0001c0002t0001g0020a0004c0006t0001g0009a0004c0006t0001g0016others(1): Show | 4 | HG01074.hp2 HG01891.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+2042_1220+204 others(8): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 16258192 | |||||
| chr16:16258217
|
A | AAAAAT | 5 | a0001c0002t0001g0020a0001c0020t0001g0036a0004c0006t0001g0009others(2): Show | 5 | HG01074.hp2 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+2062_1220+206 others(9): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 16258217 | |||||
| chr16:16258234
|
T | A | 5 | a0001c0002t0001g0020a0001c0020t0001g0036a0004c0006t0001g0009others(2): Show | 5 | HG01074.hp2 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+2076T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258234 | ||||||
| chr16:16258243
|
CAAAA | C | 4 | a0001c0002t0001g0020a0004c0006t0001g0009a0004c0006t0001g0016others(1): Show | 4 | HG01074.hp2 HG01891.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+2088_1220+209 others(8): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 16258243 | |||||
| chr16:16258283
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1220+2125A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258283 | ||||||
| chr16:16258294
|
G | A | 4 | a0001c0002t0001g0020a0004c0006t0001g0009a0004c0006t0001g0016others(1): Show | 4 | HG01074.hp2 HG01891.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220+2136G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258294 | ||||||
| chr16:16258661
|
C | G | 1 | a0003c0004t0002g0126 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1220+2503C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258661 | ||||||
| chr16:16258720
|
C | T | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1220+2562C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258720 | ||||||
| chr16:16258821
|
C | T | 19 | a0002c0003t0002g0100a0002c0003t0002g0101a0002c0003t0002g0102others(16): Show | 19 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1220+2663C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258821 | ||||||
| chr16:16258860
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2642G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16258860 | ||||||
| chr16:16259011
|
C | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2491C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259011 | ||||||
| chr16:16259012
|
A | G | 28 | a0001c0025t0001g0123a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1221-2490A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259012 | ||||||
| chr16:16259202
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2300A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259202 | ||||||
| chr16:16259214
|
C | T | 4 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(1): Show | 4 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221-2288C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259214 | ||||||
| chr16:16259309
|
T | C | 16 | a0002c0003t0002g0100a0002c0003t0002g0101a0002c0003t0002g0102others(13): Show | 16 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1221-2193T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259309 | ||||||
| chr16:16259364
|
G | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2138G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259364 | ||||||
| chr16:16259370
|
C | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2132C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259370 | ||||||
| chr16:16259404
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-2098G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16259404 | ||||||
| chr16:16260330
|
A | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-1172A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16260330 | ||||||
| chr16:16260646
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-856G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16260646 | ||||||
| chr16:16260749
|
T | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-753T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16260749 | ||||||
| chr16:16260757
|
C | T | 1 | a0001c0002t0001g0015 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1221-745C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16260757 | ||||||
| chr16:16260911
|
ACATTGTG others(30): Show |
A | 4 | a0002c0003t0002g0100a0002c0003t0002g0102a0002c0003t0002g0109others(1): Show | 4 | HG00642.hp1 HG01346.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221-589_1221-553d others(39): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 16260911 | |||||
| chr16:16260986
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1221-516A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16260986 | ||||||
| chr16:16261039
|
C | T | 1 | a0002c0003t0002g0114 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1221-463C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16261039 | ||||||
| chr16:16261063
|
T | A | 2 | a0005c0008t0002g0083a0005c0008t0002g0084 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1221-439T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16261063 | ||||||
| chr16:16261429
|
T | G | 2 | a0009c0013t0001g0098a0012c0017t0002g0104 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1221-73T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16261429 | ||||||
| chr16:16261465
|
A | G | 1 | a0001c0018t0001g0014 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1221-37A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 11/30 | chr16 | 16261465 | ||||||
| chr16:16261763
|
G | A | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+87G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16261763 | ||||||
| chr16:16261840
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+164C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16261840 | ||||||
| chr16:16261883
|
G | C | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+207G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16261883 | ||||||
| chr16:16261885
|
T | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0125 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1395+209T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16261885 | ||||||
| chr16:16261887
|
T | G | 19 | a0002c0003t0002g0100a0002c0003t0002g0101a0002c0003t0002g0102others(16): Show | 19 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1395+211T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16261887 | ||||||
| chr16:16262014
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1395+338G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262014 | ||||||
| chr16:16262134
|
G | A | 2 | a0001c0001t0001g0023a0002c0003t0002g0024 | 2 | HG01496.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1395+458G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262134 | ||||||
| chr16:16262152
|
A | C | 1 | a0002c0003t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1395+476A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262152 | ||||||
| chr16:16262154
|
C | T | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1395+478C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262154 | ||||||
| chr16:16262291
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1395+615A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262291 | ||||||
| chr16:16262347
|
C | T | 2 | a0006c0009t0002g0106a0006c0009t0002g0107 | 2 | HG01074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1395+671C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262347 | ||||||
| chr16:16262477
|
A | C | 8 | a0001c0005t0001g0073a0001c0005t0001g0074a0001c0005t0001g0095others(5): Show | 8 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1396-597A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262477 | ||||||
| chr16:16262506
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0125 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1396-568G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262506 | ||||||
| chr16:16262656
|
C | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.1396-418C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262656 | ||||||
| chr16:16262674
|
A | G | 1 | a0002c0003t0002g0112 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1396-400A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262674 | ||||||
| chr16:16262809
|
T | C | 20 | a0001c0001t0001g0043a0002c0003t0002g0100a0002c0003t0002g0101others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1396-265T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262809 | ||||||
| chr16:16262893
|
C | T | 6 | a0001c0001t0001g0080a0003c0004t0002g0126a0003c0004t0002g0127others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-181C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262893 | ||||||
| chr16:16262943
|
A | G | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-131A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16262943 | ||||||
| chr16:16263036
|
C | T | 2 | a0001c0001t0001g0033a0001c0020t0001g0036 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1396-38C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16263036 | ||||||
| chr16:16263052
|
C | T | 5 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-22C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 12/30 | chr16 | 16263052 | ||||||
| chr16:16263276
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1537+61G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 13/30 | chr16 | 16263276 | ||||||
| chr16:16263363
|
G | C | 20 | a0001c0001t0001g0043a0002c0003t0002g0100a0002c0003t0002g0101others(17): Show | 20 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1537+148G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 13/30 | chr16 | 16263363 | ||||||
| chr16:16263380
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1538-133G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 13/30 | chr16 | 16263380 | ||||||
| chr16:16263645
|
G | A | 6 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(3): Show | 6 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(3): Show |
splice_donor_variant&intron_variant | HIGH | c.1669+1G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16263645 | ||||||
| chr16:16263834
|
G | A | 3 | a0002c0003t0002g0114a0002c0003t0002g0115a0002c0003t0002g0122 | 3 | HG00140.hp2 HG01106.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1669+190G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16263834 | ||||||
| chr16:16263838
|
C | G | 13 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0047others(10): Show | 13 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1669+194C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16263838 | ||||||
| chr16:16263924
|
G | T | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG03130.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669+280G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16263924 | ||||||
| chr16:16263926
|
G | T | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG03130.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669+282G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16263926 | ||||||
| chr16:16263989
|
G | A | 1 | a0004c0006t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1669+345G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16263989 | ||||||
| chr16:16264040
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0035others(35): Show | 39 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1669+396A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264040 | ||||||
| chr16:16264045
|
A | G | 6 | a0001c0001t0001g0002a0001c0002t0001g0005a0001c0002t0001g0006others(3): Show | 7 | HG00140.hp1 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1669+401A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264045 | ||||||
| chr16:16264233
|
C | T | 2 | a0002c0003t0002g0118a0007c0012t0005g0130 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1669+589C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264233 | ||||||
| chr16:16264268
|
T | G | 1 | a0005c0008t0002g0083 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1669+624T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264268 | ||||||
| chr16:16264321
|
G | A | 11 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0067others(8): Show | 11 | HG00673.hp1 HG01074.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1669+677G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264321 | ||||||
| chr16:16264398
|
C | G | 3 | a0002c0003t0002g0105a0002c0003t0002g0108a0002c0003t0002g0113 | 3 | HG00673.hp1 HG04115.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1670-645C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264398 | ||||||
| chr16:16264405
|
T | C | 1 | a0001c0002t0001g0004 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1670-638T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264405 | ||||||
| chr16:16264554
|
C | CT | 19 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0047others(16): Show | 19 | HG00642.hp1 HG01099.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-480dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | 16264554 | |||||
| chr16:16264577
|
G | A | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1670-466G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264577 | ||||||
| chr16:16264713
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0125 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1670-330A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264713 | ||||||
| chr16:16264718
|
T | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(38): Show | 41 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.1670-325T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264718 | ||||||
| chr16:16264790
|
C | CA | 13 | a0001c0001t0001g0030a0002c0003t0002g0115a0002c0003t0002g0116others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1670-252dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | 16264790 | |||||
| chr16:16264792
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(2): Show | 5 | HG01361.hp2 HG01515.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-251C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264792 | ||||||
| chr16:16264793
|
T | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(2): Show | 5 | HG01361.hp2 HG01515.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-250T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264793 | ||||||
| chr16:16264794
|
G | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(2): Show | 5 | HG01361.hp2 HG01515.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-249G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264794 | ||||||
| chr16:16264795
|
C | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(2): Show | 5 | HG01361.hp2 HG01515.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-248C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264795 | ||||||
| chr16:16264800
|
G | A | 7 | a0001c0001t0001g0030a0002c0003t0002g0114a0002c0003t0002g0115others(4): Show | 7 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1670-243G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264800 | ||||||
| chr16:16264840
|
G | A | 4 | a0001c0002t0001g0020a0004c0006t0001g0009a0004c0006t0001g0016others(1): Show | 4 | HG01074.hp2 HG01891.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670-203G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264840 | ||||||
| chr16:16264954
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(2): Show | 5 | HG01361.hp2 HG01515.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-89A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264954 | ||||||
| chr16:16264955
|
G | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(2): Show | 5 | HG01361.hp2 HG01515.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670-88G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264955 | ||||||
| chr16:16264987
|
C | G | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1670-56C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 14/30 | chr16 | 16264987 | ||||||
| chr16:16265195
|
G | T | 1 | a0010c0014t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1806+16G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265195 | ||||||
| chr16:16265220
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0004g0124others(5): Show | 8 | HG00438.hp1 HG01109.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+41T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265220 | ||||||
| chr16:16265278
|
C | T | 1 | a0010c0014t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1806+99C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265278 | ||||||
| chr16:16265299
|
G | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0067others(3): Show | 6 | HG00438.hp1 HG01109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+120G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265299 | ||||||
| chr16:16265305
|
A | G | 16 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0067others(13): Show | 16 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1806+126A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265305 | ||||||
| chr16:16265347
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1806+168C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265347 | ||||||
| chr16:16265441
|
T | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0086a0001c0001t0004g0124others(2): Show | 5 | HG00438.hp1 HG00642.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806+262T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265441 | ||||||
| chr16:16265480
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0004g0124 | 2 | HG00438.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1806+301T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265480 | ||||||
| chr16:16265491
|
A | G | 2 | a0001c0001t0004g0124a0010c0014t0002g0121 | 2 | HG00438.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1806+312A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265491 | ||||||
| chr16:16265637
|
G | GAT | 2 | a0001c0001t0001g0055a0002c0003t0002g0111 | 2 | NA18612.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1806+491_1806+492d others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265637 | |||||
| chr16:16265637
|
G | GATATATA others(3): Show |
1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1806+483_1806+492d others(12): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265637 | |||||
| chr16:16265637
|
GATATATA others(1): Show |
G | 2 | a0002c0003t0002g0118a0010c0014t0002g0121 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1806+485_1806+492d others(10): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265637 | |||||
| chr16:16265657
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1806+479_1806+491d others(15): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265657 | ||||||
| chr16:16265658
|
ATATATAT others(6): Show |
A | 5 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806+481_1806+493d others(15): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265658 | |||||
| chr16:16265660
|
A | G | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+481A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265660 | ||||||
| chr16:16265662
|
ATATATAT others(8): Show |
A | 4 | a0003c0004t0002g0126a0003c0004t0002g0127a0005c0008t0002g0083others(1): Show | 4 | HG01257.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+485_1806+499d others(17): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265662 | |||||
| chr16:16265662
|
ATATATAT others(9): Show |
A | 3 | a0003c0004t0002g0128a0003c0004t0002g0129a0007c0012t0005g0130 | 3 | HG01099.hp1 HG01168.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1806+485_1806+500d others(18): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265662 | |||||
| chr16:16265666
|
A | AT | 2 | a0001c0001t0001g0067a0001c0001t0001g0081 | 2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1806+488dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265666 | |||||
| chr16:16265666
|
A | ATT | 4 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | HG00741.hp2 HG01106.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+488_1806+489i others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265666 | |||||
| chr16:16265666
|
A | ATTT | 6 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0059others(3): Show | 6 | HG01109.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+488_1806+489i others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265666 | |||||
| chr16:16265666
|
A | T | 1 | a0001c0001t0001g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1806+487A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265666 | ||||||
| chr16:16265666
|
ATATATTT others(7): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1806+489_1806+502d others(16): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265666 | |||||
| chr16:16265668
|
A | AT | 9 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0066others(6): Show | 10 | HG01255.hp2 HG01256.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1806+490dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265668 | |||||
| chr16:16265668
|
A | ATT | 4 | a0001c0001t0001g0035a0001c0001t0001g0070a0002c0003t0002g0122others(1): Show | 4 | HG00140.hp2 HG00741.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+490_1806+491i others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265668 | |||||
| chr16:16265668
|
A | ATTT | 10 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0060others(7): Show | 11 | HG01099.hp2 HG01168.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.1806+490_1806+491i others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265668 | |||||
| chr16:16265668
|
A | ATTTTTTT others(4): Show |
1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1806+490_1806+491i others(13): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265668 | |||||
| chr16:16265668
|
A | T | 16 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1806+489A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265668 | ||||||
| chr16:16265669
|
TA | T | 2 | a0004c0006t0001g0016a0004c0006t0001g0017 | 2 | HG01074.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1806+491delA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265669 | ||||||
| chr16:16265670
|
A | ATAT | 4 | a0001c0001t0001g0056a0002c0003t0002g0100a0002c0003t0002g0105others(1): Show | 4 | HG01515.hp2 HG03492.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+492_1806+493i others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265670 | |||||
| chr16:16265670
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1806+492_1806+493i others(12): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265670 | |||||
| chr16:16265670
|
A | ATATTT | 6 | a0001c0001t0001g0097a0001c0002t0001g0004a0001c0002t0001g0019others(3): Show | 6 | HG01106.hp2 HG01175.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+492_1806+493i others(7): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265670 | |||||
| chr16:16265670
|
A | ATT | 7 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0078others(4): Show | 7 | HG01346.hp2 HG02015.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806+518_1806+519d others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265670 | |||||
| chr16:16265670
|
A | ATTT | 10 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0064others(7): Show | 10 | HG01261.hp1 HG01928.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1806+517_1806+519d others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265670 | |||||
| chr16:16265670
|
A | T | 50 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0029others(47): Show | 52 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1806+491A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265670 | ||||||
| chr16:16265670
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1806+510_1806+519d others(12): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265670 | |||||
| chr16:16265671
|
T | TATA | 2 | a0002c0003t0002g0024a0002c0016t0002g0110 | 2 | HG00642.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1806+492_1806+493i others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265671 | ||||||
| chr16:16265672
|
T | A | 2 | a0001c0001t0001g0055a0009c0013t0001g0098 | 2 | HG03209.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1806+493T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265672 | ||||||
| chr16:16265673
|
T | G | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1806+494T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265673 | ||||||
| chr16:16265674
|
T | A | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1806+495T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265674 | ||||||
| chr16:16265674
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1806+495T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265674 | ||||||
| chr16:16265675
|
T | A | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1806+496T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265675 | ||||||
| chr16:16265676
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0020t0001g0036 | 3 | HG01109.hp1 HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1806+497T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265676 | ||||||
| chr16:16265676
|
T | G | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1806+497T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265676 | ||||||
| chr16:16265678
|
T | A | 3 | a0001c0001t0001g0033a0001c0020t0001g0036a0009c0013t0001g0098 | 3 | HG01884.hp1 HG01884.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+499T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265678 | ||||||
| chr16:16265680
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1806+501T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265680 | ||||||
| chr16:16265682
|
T | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0091 | 2 | HG01433.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1806+503T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265682 | ||||||
| chr16:16265684
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1806+505T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265684 | ||||||
| chr16:16265707
|
G | A | 1 | a0001c0025t0001g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1806+528G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265707 | ||||||
| chr16:16265741
|
T | C | 10 | a0001c0001t0001g0030a0001c0001t0001g0070a0001c0001t0004g0124others(7): Show | 10 | HG00438.hp1 HG00741.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1806+562T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265741 | ||||||
| chr16:16265749
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1806+570C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265749 | ||||||
| chr16:16265840
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+661C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265840 | ||||||
| chr16:16265845
|
TA | T | 2 | a0001c0001t0001g0030a0009c0013t0001g0098 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+668delA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16265845 | |||||
| chr16:16265846
|
A | T | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1806+667A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265846 | ||||||
| chr16:16265847
|
A | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+668A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265847 | ||||||
| chr16:16265941
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+762C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265941 | ||||||
| chr16:16265943
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+764C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265943 | ||||||
| chr16:16265974
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1806+795C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16265974 | ||||||
| chr16:16266017
|
T | C | 10 | a0001c0001t0001g0030a0001c0001t0004g0124a0003c0004t0002g0126others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1806+838T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266017 | ||||||
| chr16:16266060
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1806+881C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266060 | ||||||
| chr16:16266113
|
T | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0010c0014t0002g0121 | 3 | HG03490.hp2 HG03492.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1807-931T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266113 | ||||||
| chr16:16266152
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1807-892C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266152 | ||||||
| chr16:16266156
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1807-888C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266156 | ||||||
| chr16:16266172
|
C | T | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-872C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266172 | ||||||
| chr16:16266267
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1807-777C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266267 | ||||||
| chr16:16266268
|
C | G | 21 | a0001c0001t0001g0030a0001c0001t0004g0124a0002c0003t0002g0024others(18): Show | 21 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1807-776C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266268 | ||||||
| chr16:16266281
|
G | A | 2 | a0001c0002t0001g0001a0001c0002t0001g0008 | 3 | HG01928.hp2 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1807-763G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266281 | ||||||
| chr16:16266305
|
G | A | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-739G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266305 | ||||||
| chr16:16266387
|
CT | C | 25 | a0001c0001t0001g0030a0001c0001t0004g0124a0001c0002t0001g0001others(22): Show | 26 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.1807-639delT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16266387 | |||||
| chr16:16266387
|
CTT | C | 12 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0097others(9): Show | 12 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1807-640_1807-639d others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 16266387 | |||||
| chr16:16266553
|
A | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(41): Show | 44 | HG00099.hp2 HG00438.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1807-491A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266553 | ||||||
| chr16:16266574
|
G | T | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-470G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266574 | ||||||
| chr16:16266598
|
T | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(46): Show | 49 | HG00099.hp2 HG00438.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1807-446T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266598 | ||||||
| chr16:16266639
|
G | A | 2 | a0001c0001t0001g0033a0001c0020t0001g0036 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1807-405G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266639 | ||||||
| chr16:16266653
|
T | G | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1807-391T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266653 | ||||||
| chr16:16266654
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1807-390C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266654 | ||||||
| chr16:16266738
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1807-306T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266738 | ||||||
| chr16:16266802
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1807-242A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266802 | ||||||
| chr16:16266914
|
C | A | 14 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(11): Show | 14 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.1807-130C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16266914 | ||||||
| chr16:16267016
|
A | T | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1807-28A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 15/30 | chr16 | 16267016 | ||||||
| chr16:16267217
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+86G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267217 | ||||||
| chr16:16267360
|
A | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1894+229A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267360 | ||||||
| chr16:16267375
|
T | G | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+244T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267375 | ||||||
| chr16:16267418
|
G | A | 17 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(14): Show | 17 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1894+287G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267418 | ||||||
| chr16:16267437
|
T | TC | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+306_1894+307i others(3): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267437 | ||||||
| chr16:16267440
|
TC | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+310delC | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267440 | ||||||
| chr16:16267445
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+314C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267445 | ||||||
| chr16:16267497
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+366C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267497 | ||||||
| chr16:16267535
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+404G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267535 | ||||||
| chr16:16267546
|
T | A | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1894+415T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267546 | ||||||
| chr16:16267559
|
C | T | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894+428C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267559 | ||||||
| chr16:16267646
|
C | G | 1 | a0001c0002t0001g0011 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1894+515C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267646 | ||||||
| chr16:16267734
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+603C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267734 | ||||||
| chr16:16267754
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+623C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267754 | ||||||
| chr16:16267782
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+651A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267782 | ||||||
| chr16:16267849
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0004g0124a0007c0012t0005g0130others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+718T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267849 | ||||||
| chr16:16267867
|
A | T | 1 | a0001c0001t0004g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1894+736A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267867 | ||||||
| chr16:16267907
|
G | A | 14 | a0001c0001t0001g0030a0001c0001t0004g0124a0002c0003t0002g0116others(11): Show | 14 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1894+776G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16267907 | ||||||
| chr16:16268188
|
A | G | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1894+1057A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268188 | ||||||
| chr16:16268206
|
A | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+1075A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268206 | ||||||
| chr16:16268234
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+1103G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268234 | ||||||
| chr16:16268279
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+1148G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268279 | ||||||
| chr16:16268284
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0004g0124a0009c0013t0001g0098 | 3 | HG00438.hp1 HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1894+1153G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268284 | ||||||
| chr16:16268445
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+1314C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268445 | ||||||
| chr16:16268446
|
G | A | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894+1315G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268446 | ||||||
| chr16:16268455
|
T | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(8): Show | 11 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1894+1324T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268455 | ||||||
| chr16:16268502
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894+1371C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268502 | ||||||
| chr16:16268503
|
G | A | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1894+1372G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268503 | ||||||
| chr16:16268629
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1895-1492G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268629 | ||||||
| chr16:16268663
|
T | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1895-1458T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268663 | ||||||
| chr16:16268674
|
A | G | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1895-1447A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268674 | ||||||
| chr16:16268794
|
C | T | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1895-1327C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268794 | ||||||
| chr16:16268817
|
G | T | 6 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(3): Show | 6 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1895-1304G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268817 | ||||||
| chr16:16268843
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1895-1278G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16268843 | ||||||
| chr16:16269098
|
C | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(8): Show | 11 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1895-1023C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269098 | ||||||
| chr16:16269151
|
T | TC | 5 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(2): Show | 5 | HG00438.hp1 HG01109.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1895-968dupC | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr16 | 16269151 | |||||
| chr16:16269277
|
C | G | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1895-844C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269277 | ||||||
| chr16:16269324
|
C | T | 1 | a0010c0014t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1895-797C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269324 | ||||||
| chr16:16269373
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(2): Show | 5 | HG00438.hp1 HG01109.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1895-748A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269373 | ||||||
| chr16:16269429
|
A | AT | 10 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0059others(7): Show | 11 | HG01109.hp2 HG01255.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1895-671dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr16 | 16269429 | |||||
| chr16:16269429
|
AT | A | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0002c0003t0002g0105others(7): Show | 10 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1895-671delT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr16 | 16269429 | |||||
| chr16:16269429
|
ATTTTTT | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0004g0124others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1895-676_1895-671d others(8): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr16 | 16269429 | |||||
| chr16:16269440
|
T | G | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1895-681T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269440 | ||||||
| chr16:16269544
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(2): Show | 5 | HG00438.hp1 HG01109.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1895-577C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269544 | ||||||
| chr16:16269694
|
AC | A | 2 | a0005c0008t0002g0083a0005c0008t0002g0084 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1895-425delC | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr16 | 16269694 | |||||
| chr16:16269774
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1895-347G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269774 | ||||||
| chr16:16269840
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1895-281T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269840 | ||||||
| chr16:16269869
|
T | G | 22 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(19): Show | 22 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1895-252T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16269869 | ||||||
| chr16:16270014
|
A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(2): Show | 5 | HG00438.hp1 HG01109.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1895-107A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16270014 | ||||||
| chr16:16270027
|
C | T | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1895-94C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16270027 | ||||||
| chr16:16270060
|
G | A | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1895-61G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 16/30 | chr16 | 16270060 | ||||||
| chr16:16270274
|
G | GT | 5 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG00438.hp1 HG01109.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1958+98dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 16270274 | |||||
| chr16:16270513
|
C | A | 9 | a0001c0001t0001g0033a0001c0020t0001g0036a0003c0004t0002g0126others(6): Show | 9 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1959-220C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 17/30 | chr16 | 16270513 | ||||||
| chr16:16270513
|
C | T | 22 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(19): Show | 22 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1959-220C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 17/30 | chr16 | 16270513 | ||||||
| chr16:16270553
|
G | A | 1 | a0013c0022t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1959-180G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 17/30 | chr16 | 16270553 | ||||||
| chr16:16270581
|
A | G | 1 | a0001c0002t0001g0015 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1959-152A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 17/30 | chr16 | 16270581 | ||||||
| chr16:16270622
|
A | G | 9 | a0001c0001t0001g0033a0001c0020t0001g0036a0003c0004t0002g0126others(6): Show | 9 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1959-111A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 17/30 | chr16 | 16270622 | ||||||
| chr16:16271010
|
A | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.2054+182A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271010 | ||||||
| chr16:16271208
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2054+380T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271208 | ||||||
| chr16:16271349
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2054+521C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271349 | ||||||
| chr16:16271350
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2054+522G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271350 | ||||||
| chr16:16271374
|
A | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0041a0001c0001t0001g0094others(3): Show | 6 | HG00099.hp1 HG02132.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.2054+546A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271374 | ||||||
| chr16:16271418
|
T | C | 26 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0094others(23): Show | 26 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.2054+590T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271418 | ||||||
| chr16:16271461
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2054+633C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271461 | ||||||
| chr16:16271506
|
G | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0068others(3): Show | 6 | HG00642.hp2 HG01361.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2054+678G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271506 | ||||||
| chr16:16271614
|
G | A | 1 | a0002c0003t0002g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2054+786G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271614 | ||||||
| chr16:16271663
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2054+835G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271663 | ||||||
| chr16:16271802
|
G | GA | 12 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(9): Show | 12 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2054+976dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 16271802 | |||||
| chr16:16271820
|
C | T | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2054+992C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271820 | ||||||
| chr16:16271877
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2054+1049G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271877 | ||||||
| chr16:16271886
|
G | A | 2 | a0002c0003t0002g0102a0002c0016t0002g0110 | 2 | HG00642.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2054+1058G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16271886 | ||||||
| chr16:16272053
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2054+1225G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16272053 | ||||||
| chr16:16272063
|
C | T | 26 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(23): Show | 27 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.2054+1235C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16272063 | ||||||
| chr16:16272169
|
G | A | 27 | a0002c0003t0002g0100a0002c0003t0002g0101a0002c0003t0002g0102others(24): Show | 27 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.2054+1341G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16272169 | ||||||
| chr16:16272288
|
T | TC | 50 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0005others(47): Show | 51 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.2055-1397dupC | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 16272288 | |||||
| chr16:16272484
|
A | G | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2055-1205A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16272484 | ||||||
| chr16:16272548
|
T | C | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2055-1141T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16272548 | ||||||
| chr16:16272708
|
CCAGCTGG others(69): Show |
C | 1 | a0001c0002t0001g0004 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2055-967_2055-892d others(78): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 16272708 | |||||
| chr16:16272759
|
C | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0004g0124 | 3 | HG00438.hp1 HG01109.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2055-930C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16272759 | ||||||
| chr16:16273127
|
T | C | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2055-562T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16273127 | ||||||
| chr16:16273319
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2055-370C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 18/30 | chr16 | 16273319 | ||||||
| chr16:16273956
|
T | C | 35 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(32): Show | 35 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2274-37T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/30 | chr16 | 16273956 | ||||||
| chr16:16273977
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0004g0124 | 3 | HG00438.hp1 HG01109.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.2274-16A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 19/30 | chr16 | 16273977 | ||||||
| chr16:16274096
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2356+21C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274096 | ||||||
| chr16:16274222
|
T | TTGGA | 7 | a0001c0001t0001g0030a0001c0001t0001g0088a0001c0001t0001g0120others(4): Show | 7 | HG00438.hp1 HG01109.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.2356+175_2356+178d others(6): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 16274222 | |||||
| chr16:16274246
|
A | T | 1 | a0004c0006t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2356+171A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274246 | ||||||
| chr16:16274250
|
A | T | 3 | a0004c0006t0001g0009a0004c0006t0001g0016a0004c0006t0001g0017 | 3 | HG01074.hp2 HG03490.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2356+175A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274250 | ||||||
| chr16:16274253
|
G | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0076a0001c0001t0001g0077others(4): Show | 8 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2356+178G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274253 | ||||||
| chr16:16274254
|
T | G | 1 | a0004c0006t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2356+179T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274254 | ||||||
| chr16:16274256
|
G | T | 1 | a0004c0006t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2356+181G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274256 | ||||||
| chr16:16274259
|
T | A | 1 | a0004c0006t0001g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2356+184T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274259 | ||||||
| chr16:16274259
|
T | TTGGA | 86 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0030others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.2356+223_2356+226d others(6): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 16274259 | |||||
| chr16:16274259
|
T | TTGGATGG others(1): Show |
3 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0002t0001g0082 | 3 | HG03492.hp2 NA18612.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2356+219_2356+226d others(10): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 16274259 | |||||
| chr16:16274263
|
A | G | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.2356+188A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274263 | ||||||
| chr16:16274298
|
GATGA | G | 18 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(15): Show | 18 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.2356+232_2356+235d others(6): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 16274298 | |||||
| chr16:16274302
|
A | G | 11 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(8): Show | 11 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2356+227A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274302 | ||||||
| chr16:16274366
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2356+291A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274366 | ||||||
| chr16:16274461
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2356+386T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274461 | ||||||
| chr16:16274482
|
T | A | 1 | a0002c0003t0002g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2356+407T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274482 | ||||||
| chr16:16274599
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2357-413C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274599 | ||||||
| chr16:16274657
|
G | A | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2357-355G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 20/30 | chr16 | 16274657 | ||||||
| chr16:16275195
|
T | G | 2 | a0001c0001t0001g0033a0001c0020t0001g0036 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2516+24T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 21/30 | chr16 | 16275195 | ||||||
| chr16:16275456
|
G | A | 1 | a0007c0012t0005g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2643+13G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16275456 | ||||||
| chr16:16275646
|
C | G | 7 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(4): Show | 7 | HG01891.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2643+203C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16275646 | ||||||
| chr16:16275795
|
A | G | 49 | a0001c0002t0001g0001a0001c0002t0001g0004a0001c0002t0001g0005others(46): Show | 50 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.2643+352A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16275795 | ||||||
| chr16:16275948
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0004g0124a0001c0007t0001g0046others(1): Show | 4 | HG00438.hp1 HG01109.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2643+505C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16275948 | ||||||
| chr16:16276021
|
A | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0064others(25): Show | 29 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643+578A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276021 | ||||||
| chr16:16276213
|
A | G | 1 | a0007c0012t0005g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2643+770A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276213 | ||||||
| chr16:16276236
|
A | G | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643+793A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276236 | ||||||
| chr16:16276279
|
G | C | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643+836G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276279 | ||||||
| chr16:16276287
|
G | A | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643+844G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276287 | ||||||
| chr16:16276289
|
AG | A | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2643+848delG | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 16276289 | |||||
| chr16:16276317
|
G | A | 9 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(6): Show | 9 | HG00099.hp2 HG01099.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2643+874G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276317 | ||||||
| chr16:16276338
|
A | G | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2643+895A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276338 | ||||||
| chr16:16276407
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2644-963C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276407 | ||||||
| chr16:16276558
|
G | GAAATAA | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2644-809_2644-804d others(8): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 16276558 | |||||
| chr16:16276872
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2644-498C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | chr16 | 16276872 | ||||||
| chr16:16277151
|
C | CA | 33 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0033others(30): Show | 34 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2644-200dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 16277151 | |||||
| chr16:16277151
|
C | CAAAA | 17 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(14): Show | 17 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.2644-203_2644-200d others(6): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 16277151 | |||||
| chr16:16277151
|
C | CAAAAA | 12 | a0002c0003t0002g0111a0002c0003t0002g0116a0002c0003t0002g0117others(9): Show | 12 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2644-204_2644-200d others(7): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 16277151 | |||||
| chr16:16277151
|
CA | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0054others(4): Show | 7 | HG00099.hp2 HG01168.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.2644-200delA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 16277151 | |||||
| chr16:16277486
|
A | G | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2757+3A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277486 | ||||||
| chr16:16277556
|
T | C | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2757+73T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277556 | ||||||
| chr16:16277685
|
G | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.2757+202G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277685 | ||||||
| chr16:16277772
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2757+289C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277772 | ||||||
| chr16:16277781
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0075 | 2 | HG01261.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2757+298A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277781 | ||||||
| chr16:16277783
|
A | G | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2757+300A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277783 | ||||||
| chr16:16277792
|
T | C | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2757+309T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277792 | ||||||
| chr16:16277877
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2757+394T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277877 | ||||||
| chr16:16277878
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2757+395C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277878 | ||||||
| chr16:16277881
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2757+398T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277881 | ||||||
| chr16:16277996
|
T | C | 30 | a0001c0001t0001g0057a0002c0003t0002g0024a0002c0003t0002g0100others(27): Show | 30 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.2757+513T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277996 | ||||||
| chr16:16277997
|
G | A | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2757+514G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16277997 | ||||||
| chr16:16278294
|
C | T | 3 | a0004c0006t0001g0009a0004c0006t0001g0016a0004c0006t0001g0017 | 3 | HG01074.hp2 HG03490.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2758-368C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16278294 | ||||||
| chr16:16278496
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2758-166C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16278496 | ||||||
| chr16:16278540
|
T | C | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2758-122T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 23/30 | chr16 | 16278540 | ||||||
| chr16:16279017
|
A | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2885+228A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16279017 | ||||||
| chr16:16279365
|
C | A | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2885+576C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16279365 | ||||||
| chr16:16279368
|
C | T | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2885+579C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16279368 | ||||||
| chr16:16279538
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2886-651C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16279538 | ||||||
| chr16:16279722
|
A | G | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2886-467A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16279722 | ||||||
| chr16:16279858
|
A | G | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2886-331A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16279858 | ||||||
| chr16:16280027
|
G | A | 7 | a0003c0004t0002g0126a0003c0004t0002g0127a0003c0004t0002g0128others(4): Show | 7 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2886-162G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16280027 | ||||||
| chr16:16280166
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2886-23C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 24/30 | chr16 | 16280166 | ||||||
| chr16:16280346
|
T | G | 1 | a0007c0012t0005g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3027+16T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 25/30 | chr16 | 16280346 | ||||||
| chr16:16280579
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3027+249A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 25/30 | chr16 | 16280579 | ||||||
| chr16:16280595
|
C | T | 1 | a0001c0019t0001g0045 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3027+265C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 25/30 | chr16 | 16280595 | ||||||
| chr16:16280644
|
G | A | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3027+314G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 25/30 | chr16 | 16280644 | ||||||
| chr16:16280755
|
G | A | 29 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.3027+425G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 25/30 | chr16 | 16280755 | ||||||
| chr16:16281040
|
C | T | 2 | a0001c0002t0001g0021a0001c0002t0001g0022 | 2 | HG00438.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3028-199C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 25/30 | chr16 | 16281040 | ||||||
| chr16:16281407
|
T | G | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3111+85T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281407 | ||||||
| chr16:16281557
|
G | A | 1 | a0009c0013t0001g0098 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3111+235G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281557 | ||||||
| chr16:16281643
|
C | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3111+321C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281643 | ||||||
| chr16:16281775
|
A | G | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3111+453A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281775 | ||||||
| chr16:16281871
|
T | C | 2 | a0001c0005t0001g0073a0001c0005t0001g0095 | 2 | NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.3111+549T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281871 | ||||||
| chr16:16281933
|
G | A | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3111+611G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281933 | ||||||
| chr16:16281984
|
C | CT | 29 | a0001c0001t0001g0030a0001c0001t0001g0125a0001c0001t0004g0124others(26): Show | 29 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.3111+676dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr16 | 16281984 | |||||
| chr16:16281984
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3111+662C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281984 | ||||||
| chr16:16281997
|
T | G | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3111+675T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16281997 | ||||||
| chr16:16282003
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3111+681T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282003 | ||||||
| chr16:16282122
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3111+800T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282122 | ||||||
| chr16:16282800
|
A | C | 2 | a0001c0002t0001g0021a0001c0002t0001g0022 | 2 | HG00438.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3112-216A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282800 | ||||||
| chr16:16282812
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3112-204C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282812 | ||||||
| chr16:16282856
|
G | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3112-160G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282856 | ||||||
| chr16:16282896
|
A | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3112-120A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282896 | ||||||
| chr16:16282988
|
T | C | 17 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(14): Show | 17 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.3112-28T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 26/30 | chr16 | 16282988 | ||||||
| chr16:16283217
|
G | A | 2 | a0006c0009t0002g0106a0006c0009t0002g0107 | 2 | HG01074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3222+91G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283217 | ||||||
| chr16:16283277
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3222+151A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283277 | ||||||
| chr16:16283778
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3222+652C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283778 | ||||||
| chr16:16283810
|
A | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3222+684A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283810 | ||||||
| chr16:16283813
|
G | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3222+687G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283813 | ||||||
| chr16:16283969
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3222+843C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283969 | ||||||
| chr16:16283995
|
G | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3222+869G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16283995 | ||||||
| chr16:16284108
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3222+982T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284108 | ||||||
| chr16:16284121
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3222+995C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284121 | ||||||
| chr16:16284163
|
G | A | 29 | a0001c0024t0001g0099a0002c0003t0002g0024a0002c0003t0002g0100others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.3222+1037G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284163 | ||||||
| chr16:16284509
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3223-896G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284509 | ||||||
| chr16:16284569
|
A | G | 1 | a0013c0022t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3223-836A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284569 | ||||||
| chr16:16284620
|
G | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3223-785G>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284620 | ||||||
| chr16:16284780
|
C | G | 18 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(15): Show | 18 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.3223-625C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16284780 | ||||||
| chr16:16285254
|
A | T | 1 | a0001c0002t0001g0010 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3223-151A>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16285254 | ||||||
| chr16:16285313
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3223-92T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16285313 | ||||||
| chr16:16285324
|
C | T | 1 | a0010c0014t0002g0121 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3223-81C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 27/30 | chr16 | 16285324 | ||||||
| chr16:16285767
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3324+261T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16285767 | ||||||
| chr16:16285873
|
A | G | 3 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118 | 3 | HG03130.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3324+367A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16285873 | ||||||
| chr16:16285893
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.3324+387C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16285893 | ||||||
| chr16:16285941
|
C | CT | 25 | a0001c0001t0001g0023a0001c0001t0001g0089a0001c0001t0001g0120others(22): Show | 25 | HG00642.hp1 HG01074.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.3324+451dupT | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr16 | 16285941 | |||||
| chr16:16285941
|
C | CTT | 4 | a0002c0003t0002g0113a0003c0004t0002g0126a0005c0008t0002g0083others(1): Show | 4 | HG00673.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3324+450_3324+451d others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr16 | 16285941 | |||||
| chr16:16286062
|
C | T | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3324+556C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286062 | ||||||
| chr16:16286117
|
TG | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3324+612delG | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286117 | ||||||
| chr16:16286299
|
G | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3324+793G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286299 | ||||||
| chr16:16286438
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3324+932T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286438 | ||||||
| chr16:16286523
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3324+1017C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286523 | ||||||
| chr16:16286859
|
A | G | 1 | a0002c0003t0002g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3325-884A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286859 | ||||||
| chr16:16286971
|
C | G | 1 | a0002c0003t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3325-772C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16286971 | ||||||
| chr16:16287062
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3325-681A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16287062 | ||||||
| chr16:16287085
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3325-658C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16287085 | ||||||
| chr16:16287313
|
T | C | 1 | a0002c0003t0002g0113 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3325-430T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16287313 | ||||||
| chr16:16287404
|
C | T | 27 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(24): Show | 27 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3325-339C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16287404 | ||||||
| chr16:16287602
|
A | G | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3325-141A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 28/30 | chr16 | 16287602 | ||||||
| chr16:16287891
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3444+29T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16287891 | ||||||
| chr16:16287969
|
G | A | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3444+107G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16287969 | ||||||
| chr16:16288072
|
A | G | 27 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(24): Show | 27 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3444+210A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16288072 | ||||||
| chr16:16288108
|
G | C | 1 | a0001c0002t0001g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3444+246G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16288108 | ||||||
| chr16:16288184
|
G | GAA | 21 | a0002c0003t0002g0100a0002c0003t0002g0101a0002c0003t0002g0102others(18): Show | 21 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.3444+324_3444+325d others(4): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16288184 | |||||
| chr16:16288184
|
G | GAAACA | 8 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0070others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.3444+354_3444+358d others(7): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16288184 | |||||
| chr16:16288184
|
GAAACAAA others(3): Show |
G | 1 | a0001c0020t0001g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3444+349_3444+358d others(12): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16288184 | |||||
| chr16:16288185
|
AAAC | A | 5 | a0003c0004t0002g0127a0003c0004t0002g0128a0003c0004t0002g0129others(2): Show | 5 | HG01099.hp1 HG01168.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3444+326_3444+328d others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16288185 | |||||
| chr16:16288234
|
A | G | 56 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0037others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.3444+372A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16288234 | ||||||
| chr16:16288255
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3444+393A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16288255 | ||||||
| chr16:16288533
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0087 | 2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3444+671G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16288533 | ||||||
| chr16:16288665
|
AACC | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0064others(21): Show | 25 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.3444+805_3444+807d others(5): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16288665 | |||||
| chr16:16289043
|
G | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3444+1181G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289043 | ||||||
| chr16:16289096
|
G | A | 27 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(24): Show | 27 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.3444+1234G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289096 | ||||||
| chr16:16289122
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3444+1260C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289122 | ||||||
| chr16:16289153
|
G | A | 1 | a0003c0004t0002g0129 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3444+1291G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289153 | ||||||
| chr16:16289496
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3444+1634C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289496 | ||||||
| chr16:16289708
|
C | T | 29 | a0001c0001t0001g0125a0002c0003t0002g0024a0002c0003t0002g0100others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.3444+1846C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289708 | ||||||
| chr16:16289864
|
C | G | 29 | a0001c0001t0001g0125a0002c0003t0002g0024a0002c0003t0002g0100others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.3444+2002C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289864 | ||||||
| chr16:16289919
|
T | G | 29 | a0001c0001t0001g0125a0002c0003t0002g0024a0002c0003t0002g0100others(26): Show | 29 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.3444+2057T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289919 | ||||||
| chr16:16289996
|
A | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.3444+2134A>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16289996 | ||||||
| chr16:16290426
|
C | T | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3444+2564C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16290426 | ||||||
| chr16:16290470
|
T | C | 4 | a0002c0003t0002g0100a0002c0003t0002g0102a0002c0003t0002g0109others(1): Show | 4 | HG00642.hp1 HG01346.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.3444+2608T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16290470 | ||||||
| chr16:16290723
|
C | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3444+2861C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16290723 | ||||||
| chr16:16290840
|
G | A | 1 | a0001c0024t0001g0099 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3445-2812G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16290840 | ||||||
| chr16:16290893
|
C | CA | 11 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0053others(8): Show | 11 | HG00099.hp2 HG00438.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.3445-2741dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16290893 | |||||
| chr16:16290995
|
T | A | 1 | a0001c0002t0001g0013 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3445-2657T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16290995 | ||||||
| chr16:16291014
|
G | A | 1 | a0001c0002t0001g0013 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3445-2638G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291014 | ||||||
| chr16:16291151
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3445-2501G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291151 | ||||||
| chr16:16291165
|
T | A | 1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3445-2487T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291165 | ||||||
| chr16:16291220
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-2432T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291220 | ||||||
| chr16:16291265
|
T | TA | 5 | a0001c0002t0001g0082a0002c0003t0002g0101a0002c0003t0002g0105others(2): Show | 5 | HG01257.hp1 NA18612.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.3445-2371dupA | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16291265 | |||||
| chr16:16291265
|
T | TAA | 22 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0102others(19): Show | 22 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.3445-2372_3445-237 others(6): Show |
NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 16291265 | |||||
| chr16:16291285
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0096 | 2 | HG01109.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3445-2367G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291285 | ||||||
| chr16:16291311
|
G | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-2341G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291311 | ||||||
| chr16:16291367
|
C | A | 1 | a0002c0003t0002g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3445-2285C>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291367 | ||||||
| chr16:16291398
|
A | G | 19 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(16): Show | 19 | HG00642.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.3445-2254A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291398 | ||||||
| chr16:16291400
|
G | A | 2 | a0006c0009t0002g0106a0006c0009t0002g0107 | 2 | HG01074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3445-2252G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291400 | ||||||
| chr16:16291489
|
A | G | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-2163A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291489 | ||||||
| chr16:16291642
|
T | A | 1 | a0005c0008t0002g0084 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3445-2010T>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291642 | ||||||
| chr16:16291728
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | HG02300.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3445-1924A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291728 | ||||||
| chr16:16291938
|
G | C | 41 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0047others(38): Show | 41 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.3445-1714G>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16291938 | ||||||
| chr16:16292206
|
G | A | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-1446G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292206 | ||||||
| chr16:16292292
|
C | G | 31 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0076others(28): Show | 31 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.3445-1360C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292292 | ||||||
| chr16:16292309
|
A | G | 1 | a0014c0011t0003g0034 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3445-1343A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292309 | ||||||
| chr16:16292323
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-1329C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292323 | ||||||
| chr16:16292390
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3445-1262T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292390 | ||||||
| chr16:16292534
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-1118T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292534 | ||||||
| chr16:16292888
|
T | G | 1 | a0012c0017t0002g0104 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3445-764T>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292888 | ||||||
| chr16:16292894
|
T | C | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-758T>C | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292894 | ||||||
| chr16:16292950
|
A | G | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-702A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16292950 | ||||||
| chr16:16293095
|
C | T | 1 | a0007c0012t0005g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3445-557C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16293095 | ||||||
| chr16:16293454
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-198C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16293454 | ||||||
| chr16:16293478
|
C | T | 28 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(25): Show | 28 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.3445-174C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16293478 | ||||||
| chr16:16293489
|
C | T | 2 | a0001c0001t0004g0124a0001c0023t0001g0042 | 2 | HG00438.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3445-163C>T | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 29/30 | chr16 | 16293489 | ||||||
| chr16:16293815
|
G | A | 22 | a0002c0003t0002g0024a0002c0003t0002g0100a0002c0003t0002g0101others(19): Show | 22 | HG00140.hp2 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.3537+71G>A | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 30/30 | chr16 | 16293815 | ||||||
| chr16:16293821
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3537+77A>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 30/30 | chr16 | 16293821 | ||||||
| chr16:16293856
|
C | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.3537+112C>G | NOMO3 | ENSG00000103226.19 | transcript | ENST00000399336.9 | protein_coding | 30/30 | chr16 | 16293856 |