Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23420 |
|---|---|
| ensemblid | ENSG00000103512.16 |
| hgncid | 30060 |
| symbol | NOMO1 |
| name | NODAL modulator 1 |
| refseq_nuc | NM_014287.4 |
| refseq_prot | NP_055102.3 |
| ensembl_nuc | ENST00000287667.12 |
| ensembl_prot | ENSP00000287667.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 14833721 |
| end | 14896157 |
| strand | + |
| ver | v1.2 |
| region | chr16:14833721-14896157 |
| region5000 | chr16:14828721-14901157 |
| regionname0 | NOMO1_chr16_14833721_14896157 |
| regionname5000 | NOMO1_chr16_14828721_14901157 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1222 | 219 | 47 | 50 | 82 | 6 | 33 | 58 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002 | 0/0 | 1222 | 57 | 3 | 0 | 45 | 1 | 8 | 31 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0003 | 0/0 | 1222 | 21 | 6 | 0 | 15 | 0 | 0 | 14 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0004 | 0/0 | 1222 | 12 | 3 | 8 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0005 | 0/0 | 1222 | 5 | 0 | 1 | 0 | 1 | 3 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0006 | 0/0 | 1222 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0007 | 0/0 | 1222 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0008 | 0/0 | 1222 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0009 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0010 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0011 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0012 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0013 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0014 | 0/0 | 1222 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0015 | 0/0 | 1222 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0016 | 0/0 | 1222 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0017 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0018 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0019 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3669 | 201 | 42 | 45 | 76 | 6 | 31 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0002 | 0/0 | 3669 | 49 | 3 | 0 | 37 | 1 | 8 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0003 | 0/0 | 3669 | 20 | 5 | 0 | 15 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0004 | 0/0 | 3669 | 12 | 3 | 8 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0005 | 0/0 | 3669 | 7 | 0 | 0 | 7 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0006 | 0/0 | 3669 | 5 | 0 | 1 | 0 | 1 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0007 | 0/0 | 3669 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0008 | 0/0 | 3669 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0009 | 0/0 | 3669 | 5 | 0 | 2 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0010 | 0/0 | 3669 | 4 | 3 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0011 | 0/0 | 3669 | 3 | 1 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0012 | 0/0 | 3669 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0013 | 0/0 | 3669 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0014 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0015 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0016 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0017 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0018 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0019 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0020 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0021 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0022 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0023 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0024 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0025 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0026 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0027 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0028 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0029 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| c0030 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 644 | 252 | 37 | 57 | 118 | 5 | 35 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0002 | 0/1 | 644 | 68 | 23 | 3 | 30 | 3 | 8 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0003 | 0/0 | 645 | 7 | 2 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0004 | 0/0 | 644 | 3 | 3 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0005 | 0/0 | 644 | 3 | 0 | 0 | 1 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0006 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0007 | 0/0 | 644 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0008 | 0/0 | 644 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| t0009 | 0/0 | 644 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3669 | 201 | 42 | 45 | 76 | 6 | 31 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0008 | 0/0 | 3669 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0010 | 0/0 | 3669 | 4 | 3 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0011 | 0/0 | 3669 | 3 | 1 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0013 | 0/0 | 3669 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0014 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0015 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0020 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0021 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0002 | 0/0 | 3669 | 49 | 3 | 0 | 37 | 1 | 8 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0005 | 0/0 | 3669 | 7 | 0 | 0 | 7 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0018 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0003c0003 | 0/0 | 3669 | 20 | 5 | 0 | 15 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0003c0028 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0004c0004 | 0/0 | 3669 | 12 | 3 | 8 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0005c0006 | 0/0 | 3669 | 5 | 0 | 1 | 0 | 1 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0006c0009 | 0/0 | 3669 | 5 | 0 | 2 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0007c0007 | 0/0 | 3669 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0008c0012 | 0/0 | 3669 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0009c0026 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0010c0029 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0011c0027 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0012c0024 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0013c0023 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0014c0022 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0015c0019 | 0/0 | 3669 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0016c0016 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0017c0017 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0018c0025 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0019c0030 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4312 | 130 | 20 | 41 | 44 | 3 | 22 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0001t0002 | 0/1 | 4312 | 63 | 21 | 3 | 29 | 3 | 6 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0001t0003 | 0/0 | 4313 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0001t0005 | 0/0 | 4312 | 2 | 0 | 0 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0001t0006 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0001t0007 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0001t0008 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0008t0001 | 0/0 | 4312 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0010t0001 | 0/0 | 4312 | 4 | 3 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0011t0001 | 0/0 | 4312 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0011t0002 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0013t0001 | 0/0 | 4312 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0014t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0015t0001 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0020t0002 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0001c0021t0003 | 0/0 | 4313 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0002t0001 | 0/0 | 4312 | 46 | 0 | 0 | 37 | 1 | 8 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0002t0004 | 0/0 | 4312 | 3 | 3 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0005t0001 | 0/0 | 4312 | 7 | 0 | 0 | 7 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0002c0018t0001 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0003c0003t0001 | 0/0 | 4312 | 20 | 5 | 0 | 15 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0003c0028t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0004c0004t0001 | 0/0 | 4312 | 9 | 1 | 7 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0004c0004t0003 | 0/0 | 4313 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0004c0004t0009 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0005c0006t0001 | 0/0 | 4312 | 5 | 0 | 1 | 0 | 1 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0006c0009t0001 | 0/0 | 4312 | 4 | 0 | 2 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0006c0009t0003 | 0/0 | 4313 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0007c0007t0001 | 0/0 | 4312 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0008c0012t0001 | 0/0 | 4312 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0009c0026t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0010c0029t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0011c0027t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0012c0024t0001 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0013c0023t0002 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0014c0022t0002 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0015c0019t0001 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0016c0016t0001 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0017c0017t0005 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0018c0025t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| a0019c0030t0002 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | copy fasta | chr16 | 14828721 | 14901157 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0267 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0011t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0011t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0011t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0013t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0013t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0014t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0015t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0020t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0021t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0018t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0028t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0009g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0008c0012t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0008c0012t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0009c0026t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0010c0029t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0011c0027t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0012c0024t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0013c0023t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0014c0022t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0015c0019t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0016c0016t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0017c0017t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0018c0025t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0019c0030t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0289 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00140 | hp2 | a0005 | c0006 | t0001 | g0282 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0313 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00673 | hp2 | a0002 | c0005 | t0001 | g0254 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01074 | hp1 | a0001 | c0015 | t0001 | g0263 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01074 | hp2 | a0006 | c0009 | t0001 | g0280 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01106 | hp2 | a0001 | c0013 | t0001 | g0247 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01109 | hp1 | a0004 | c0004 | t0009 | g0140 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01109 | hp2 | a0001 | c0010 | t0001 | g0011 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01255 | hp1 | a0006 | c0009 | t0001 | g0285 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01255 | hp2 | a0004 | c0004 | t0001 | g0139 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01257 | hp1 | a0001 | c0011 | t0001 | g0031 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01258 | hp2 | a0001 | c0011 | t0001 | g0032 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01358 | hp2 | a0005 | c0006 | t0001 | g0226 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01361 | hp2 | a0015 | c0019 | t0001 | g0224 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0269 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01928 | hp2 | a0004 | c0004 | t0001 | g0134 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01943 | hp1 | a0004 | c0004 | t0001 | g0142 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01952 | hp1 | a0004 | c0004 | t0001 | g0137 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01978 | hp2 | a0004 | c0004 | t0001 | g0136 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02004 | hp1 | a0004 | c0004 | t0001 | g0135 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02071 | hp2 | a0001 | c0008 | t0001 | g0108 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0317 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02074 | hp2 | a0013 | c0023 | t0002 | g0205 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0309 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02145 | hp1 | a0008 | c0012 | t0001 | g0128 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0248 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02148 | hp2 | a0004 | c0004 | t0001 | g0138 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02451 | hp2 | a0003 | c0028 | t0001 | g0196 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02523 | hp2 | a0001 | c0008 | t0001 | g0109 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0184 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02572 | hp2 | a0010 | c0029 | t0001 | g0272 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02602 | hp2 | a0016 | c0016 | t0001 | g0273 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02647 | hp1 | a0004 | c0004 | t0003 | g0012 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02698 | hp2 | a0001 | c0013 | t0001 | g0148 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02723 | hp1 | a0002 | c0002 | t0004 | g0143 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02723 | hp2 | a0004 | c0004 | t0003 | g0013 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02735 | hp2 | a0005 | c0006 | t0001 | g0281 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02886 | hp1 | a0001 | c0010 | t0001 | g0210 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02895 | hp1 | a0011 | c0027 | t0001 | g0127 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03098 | hp2 | a0008 | c0012 | t0001 | g0129 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0019 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03139 | hp1 | a0018 | c0025 | t0001 | g0275 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03209 | hp1 | a0019 | c0030 | t0002 | g0008 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0130 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03239 | hp1 | a0005 | c0006 | t0001 | g0283 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03453 | hp1 | a0001 | c0014 | t0001 | g0113 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0265 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03486 | hp2 | a0001 | c0011 | t0002 | g0187 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0144 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03579 | hp2 | a0001 | c0010 | t0001 | g0207 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03654 | hp1 | a0005 | c0006 | t0001 | g0279 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0132 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03669 | hp1 | a0001 | c0020 | t0002 | g0179 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0195 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0131 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0235 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0102 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0163 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18947 | hp2 | a0007 | c0007 | t0001 | g0296 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18950 | hp1 | a0006 | c0009 | t0001 | g0133 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18952 | hp2 | a0002 | c0005 | t0001 | g0237 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18956 | hp2 | a0002 | c0005 | t0001 | g0091 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18957 | hp1 | a0006 | c0009 | t0003 | g0075 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18961 | hp1 | a0001 | c0021 | t0003 | g0088 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18962 | hp1 | a0007 | c0007 | t0001 | g0010 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18963 | hp1 | a0002 | c0005 | t0001 | g0253 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18970 | hp1 | a0012 | c0024 | t0001 | g0086 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18978 | hp2 | a0007 | c0007 | t0001 | g0297 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18982 | hp1 | a0001 | c0008 | t0001 | g0040 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18983 | hp2 | a0007 | c0007 | t0001 | g0010 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18987 | hp1 | a0006 | c0009 | t0001 | g0293 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18993 | hp2 | a0017 | c0017 | t0005 | g0303 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18999 | hp2 | a0002 | c0018 | t0001 | g0298 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19001 | hp2 | a0002 | c0005 | t0001 | g0236 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19030 | hp1 | a0009 | c0026 | t0001 | g0322 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19060 | hp1 | a0007 | c0007 | t0001 | g0295 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19060 | hp2 | a0002 | c0005 | t0001 | g0245 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19062 | hp2 | a0001 | c0008 | t0001 | g0268 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19065 | hp2 | a0001 | c0008 | t0001 | g0039 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19077 | hp2 | a0002 | c0005 | t0001 | g0238 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ASW | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20905 | hp2 | a0014 | c0022 | t0002 | g0192 | SAS | GIH | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG06807 | hp1 | a0001 | c0010 | t0001 | g0164 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0267 | REF | REF | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14848912
|
A | C | 1 | a0019 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.523A>C | p.Lys175Gln | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/31 | 654/4312 | 523/3669 | 175/1222 | chr16 | 14848912 | ||
| chr16:14863125
|
G | A | 1 | a0005 | 5 | HG00140.hp2 HG01358.hp2 HG02735.hp2 others(2): Show |
missense_variant | MODERATE | c.1333G>A | p.Val445Met | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/31 | 1464/4312 | 1333/3669 | 445/1222 | chr16 | 14863125 | ||
| chr16:14864657
|
A | G | 5 | a0005a0006a0009others(2): Show | 13 | HG00140.hp2 HG01074.hp2 HG01255.hp1 others(10): Show |
missense_variant | MODERATE | c.1468A>G | p.Asn490Asp | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/31 | 1599/4312 | 1468/3669 | 490/1222 | chr16 | 14864657 | ||
| chr16:14864666
|
A | G | 4 | a0008a0009a0010others(1): Show | 5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.1477A>G | p.Met493Val | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/31 | 1608/4312 | 1477/3669 | 493/1222 | chr16 | 14864666 | ||
| chr16:14866623
|
A | G | 5 | a0003a0004a0008others(2): Show | 37 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(34): Show |
missense_variant | MODERATE | c.1738A>G | p.Met580Val | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/31 | 1869/4312 | 1738/3669 | 580/1222 | chr16 | 14866623 | ||
| chr16:14868572
|
C | T | 1 | a0012 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1831C>T | p.Arg611Cys | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/31 | 1962/4312 | 1831/3669 | 611/1222 | chr16 | 14868572 | ||
| chr16:14872311
|
A | C | 1 | a0013 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2036A>C | p.Asp679Ala | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/31 | 2167/4312 | 2036/3669 | 679/1222 | chr16 | 14872311 | ||
| chr16:14875363
|
C | T | 1 | a0014 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.2297C>T | p.Thr766Ile | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/31 | 2428/4312 | 2297/3669 | 766/1222 | chr16 | 14875363 | ||
| chr16:14882663
|
C | G | 1 | a0015 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.3097C>G | p.His1033Asp | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/31 | 3228/4312 | 3097/3669 | 1033/1222 | chr16 | 14882663 | ||
| chr16:14886792
|
A | G | 1 | a0007 | 5 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(2): Show |
missense_variant | MODERATE | c.3254A>G | p.Asn1085Ser | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/31 | 3385/4312 | 3254/3669 | 1085/1222 | chr16 | 14886792 | ||
| chr16:14889192
|
A | T | 1 | a0009 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.3421A>T | p.Ile1141Phe | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/31 | 3552/4312 | 3421/3669 | 1141/1222 | chr16 | 14889192 | ||
| chr16:14895011
|
A | G | 1 | a0017 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.3458A>G | p.Glu1153Gly | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 30/31 | 3589/4312 | 3458/3669 | 1153/1222 | chr16 | 14895011 | ||
| chr16:14895559
|
C | G | 2 | a0016a0018 | 2 | HG02602.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.3583C>G | p.Arg1195Gly | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3714/4312 | 3583/3669 | 1195/1222 | chr16 | 14895559 | ||
| chr16:14895563
|
C | T | 4 | a0002a0004a0007others(1): Show | 75 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
missense_variant | MODERATE | c.3587C>T | p.Ala1196Val | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3718/4312 | 3587/3669 | 1196/1222 | chr16 | 14895563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14844684
|
C | T | 1 | a0001c0013 | 2 | HG01106.hp2 HG02698.hp2 |
synonymous_variant | LOW | c.312C>T | p.Thr104Thr | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/31 | 443/4312 | 312/3669 | 104/1222 | chr16 | 14844684 | ||
| chr16:14846678
|
C | A | 1 | a0001c0014 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.504C>A | p.Gly168Gly | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/31 | 635/4312 | 504/3669 | 168/1222 | chr16 | 14846678 | ||
| chr16:14857264
|
C | T | 3 | a0001c0010a0003c0028a0010c0029 | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.1011C>T | p.Asn337Asn | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 10/31 | 1142/4312 | 1011/3669 | 337/1222 | chr16 | 14857264 | ||
| chr16:14864665
|
C | T | 1 | a0010c0029 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1476C>T | p.Pro492Pro | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/31 | 1607/4312 | 1476/3669 | 492/1222 | chr16 | 14864665 | ||
| chr16:14872249
|
C | T | 1 | a0001c0008 | 5 | HG02071.hp2 HG02523.hp2 NA18982.hp1 others(2): Show |
synonymous_variant | LOW | c.1974C>T | p.Ile658Ile | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/31 | 2105/4312 | 1974/3669 | 658/1222 | chr16 | 14872249 | ||
| chr16:14875367
|
G | A | 1 | a0002c0005 | 7 | HG00673.hp2 NA18952.hp2 NA18956.hp2 others(4): Show |
synonymous_variant | LOW | c.2301G>A | p.Pro767Pro | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/31 | 2432/4312 | 2301/3669 | 767/1222 | chr16 | 14875367 | ||
| chr16:14876733
|
G | A | 2 | a0001c0011a0009c0026 | 4 | HG01257.hp1 HG01258.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.2586G>A | p.Ala862Ala | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/31 | 2717/4312 | 2586/3669 | 862/1222 | chr16 | 14876733 | ||
| chr16:14878723
|
A | T | 1 | a0001c0021 | 1 | NA18961.hp1 | splice_region_variant&synonymous_variant | LOW | c.2646A>T | p.Ile882Ile | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/31 | 2777/4312 | 2646/3669 | 882/1222 | chr16 | 14878723 | ||
| chr16:14878771
|
C | T | 2 | a0001c0014a0001c0020 | 2 | HG03453.hp1 HG03669.hp1 |
synonymous_variant | LOW | c.2694C>T | p.Ser898Ser | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/31 | 2825/4312 | 2694/3669 | 898/1222 | chr16 | 14878771 | ||
| chr16:14882656
|
C | T | 1 | a0001c0008 | 5 | HG02071.hp2 HG02523.hp2 NA18982.hp1 others(2): Show |
synonymous_variant | LOW | c.3090C>T | p.Leu1030Leu | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/31 | 3221/4312 | 3090/3669 | 1030/1222 | chr16 | 14882656 | ||
| chr16:14884476
|
A | G | 2 | a0001c0020a0002c0018 | 2 | HG03669.hp1 NA18999.hp2 |
synonymous_variant | LOW | c.3216A>G | p.Thr1072Thr | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/31 | 3347/4312 | 3216/3669 | 1072/1222 | chr16 | 14884476 | ||
| chr16:14886856
|
C | T | 1 | a0002c0018 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.3318C>T | p.Asp1106Asp | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/31 | 3449/4312 | 3318/3669 | 1106/1222 | chr16 | 14886856 | ||
| chr16:14895591
|
C | T | 1 | a0001c0015 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.3615C>T | p.Ser1205Ser | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3746/4312 | 3615/3669 | 1205/1222 | chr16 | 14895591 | ||
| chr16:14895642
|
T | G | 1 | a0018c0025 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.3666T>G | p.Thr1222Thr | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3797/4312 | 3666/3669 | 1222/1222 | chr16 | 14895642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14833723
|
C | CG | 5 | a0001c0001t0003a0001c0001t0006a0001c0021t0003others(2): Show | 8 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-129_-128insG | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/31 | 128 | chr16 | 14833723 | |||||
| chr16:14833724
|
T | G | 5 | a0001c0001t0003a0001c0001t0006a0001c0021t0003others(2): Show | 8 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-128T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/31 | 128 | chr16 | 14833724 | |||||
| chr16:14833773
|
G | A | 1 | a0002c0002t0004 | 3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/31 | 79 | chr16 | 14833773 | |||||
| chr16:14895759
|
C | T | 1 | a0004c0004t0009 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 114 | chr16 | 14895759 | |||||
| chr16:14895953
|
A | C | 2 | a0001c0001t0005a0017c0017t0005 | 3 | HG03654.hp2 HG03710.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*308A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 308 | chr16 | 14895953 | |||||
| chr16:14895970
|
C | T | 1 | a0001c0001t0008 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 325 | chr16 | 14895970 | |||||
| chr16:14895987
|
G | A | 33 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(30): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*342G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 342 | chr16 | 14895987 | |||||
| chr16:14896090
|
A | G | 1 | a0001c0001t0007 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 445 | chr16 | 14896090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14834057
|
C | A | 1 | a0001c0010t0001g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.165+41C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834057 | ||||||
| chr16:14834306
|
C | T | 1 | a0009c0026t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+290C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834306 | ||||||
| chr16:14834322
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+306C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834322 | ||||||
| chr16:14834360
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+344C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834360 | ||||||
| chr16:14834489
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.165+473C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834489 | ||||||
| chr16:14834533
|
T | A | 2 | a0004c0004t0003g0012a0004c0004t0003g0013 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.165+517T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834533 | ||||||
| chr16:14834687
|
G | GT | 10 | a0001c0001t0001g0291a0001c0001t0002g0286a0001c0001t0002g0287others(7): Show | 10 | HG00099.hp1 HG01261.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+689dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14834687 | |||||
| chr16:14834687
|
G | GTT | 25 | a0002c0002t0001g0299a0002c0002t0001g0300a0002c0002t0001g0301others(22): Show | 26 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.165+688_165+689dup others(2): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14834687 | |||||
| chr16:14834687
|
GT | G | 126 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(123): Show | 133 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.165+689delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14834687 | |||||
| chr16:14834706
|
A | T | 3 | a0001c0001t0002g0294a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.165+690A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834706 | ||||||
| chr16:14834728
|
T | G | 9 | a0002c0002t0001g0141a0004c0004t0001g0134a0004c0004t0001g0135others(6): Show | 9 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+712T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834728 | ||||||
| chr16:14834961
|
G | A | 2 | a0002c0002t0004g0143a0002c0002t0004g0144 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.165+945G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834961 | ||||||
| chr16:14835251
|
A | G | 10 | a0001c0001t0001g0284a0004c0004t0003g0012a0004c0004t0003g0013others(7): Show | 10 | HG00140.hp2 HG01074.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+1235A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835251 | ||||||
| chr16:14835365
|
G | T | 2 | a0004c0004t0003g0012a0004c0004t0003g0013 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.165+1349G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835365 | ||||||
| chr16:14835391
|
G | A | 2 | a0004c0004t0003g0012a0004c0004t0003g0013 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.165+1375G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835391 | ||||||
| chr16:14835416
|
C | T | 1 | a0006c0009t0001g0133 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.165+1400C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835416 | ||||||
| chr16:14835531
|
C | G | 1 | a0001c0001t0002g0278 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165+1515C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835531 | ||||||
| chr16:14835754
|
A | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.165+1738A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835754 | ||||||
| chr16:14835765
|
C | T | 2 | a0001c0001t0005g0131a0001c0001t0005g0132 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.165+1749C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835765 | ||||||
| chr16:14835797
|
T | C | 1 | a0002c0002t0001g0145 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.165+1781T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835797 | ||||||
| chr16:14835868
|
A | G | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.165+1852A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835868 | ||||||
| chr16:14836113
|
A | C | 4 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127others(1): Show | 4 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2097A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836113 | ||||||
| chr16:14836176
|
C | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 7 | HG02027.hp2 NA18612.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+2160C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836176 | ||||||
| chr16:14836189
|
G | T | 1 | a0016c0016t0001g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.165+2173G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836189 | ||||||
| chr16:14836224
|
T | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.166-2183T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836224 | ||||||
| chr16:14836544
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.166-1863A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836544 | ||||||
| chr16:14836577
|
C | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18978.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.166-1830C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836577 | ||||||
| chr16:14836694
|
C | CT | 13 | a0001c0001t0001g0116a0001c0001t0001g0271a0001c0001t0001g0319others(10): Show | 13 | HG01255.hp1 HG01433.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-1691dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14836694 | |||||
| chr16:14836694
|
CT | C | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0149others(3): Show | 6 | HG02135.hp1 HG02165.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1691delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14836694 | |||||
| chr16:14836730
|
G | A | 5 | a0002c0018t0001g0298a0007c0007t0001g0010a0007c0007t0001g0295others(2): Show | 6 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1677G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836730 | ||||||
| chr16:14836761
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.166-1646A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836761 | ||||||
| chr16:14836778
|
T | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-1629T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836778 | ||||||
| chr16:14836809
|
C | T | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.166-1598C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836809 | ||||||
| chr16:14836952
|
G | A | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127 | 3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1455G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836952 | ||||||
| chr16:14837021
|
ATTTTG | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1381_166-1377d others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14837021 | |||||
| chr16:14837134
|
C | T | 1 | a0002c0002t0001g0266 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.166-1273C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837134 | ||||||
| chr16:14837155
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.166-1252C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837155 | ||||||
| chr16:14837308
|
C | T | 3 | a0004c0004t0001g0265a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-1099C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837308 | ||||||
| chr16:14837589
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.166-818G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837589 | ||||||
| chr16:14837688
|
C | G | 1 | a0018c0025t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-719C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837688 | ||||||
| chr16:14837754
|
T | A | 1 | a0007c0007t0001g0295 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-653T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837754 | ||||||
| chr16:14837773
|
C | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0015t0001g0263 | 3 | HG01074.hp1 HG01167.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.166-634C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837773 | ||||||
| chr16:14837906
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.166-501A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837906 | ||||||
| chr16:14838043
|
C | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.166-364C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14838043 | ||||||
| chr16:14838320
|
T | G | 21 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0151others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-87T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14838320 | ||||||
| chr16:14838632
|
C | T | 2 | a0002c0002t0001g0316a0002c0002t0001g0317 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.255+136C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838632 | ||||||
| chr16:14838660
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.255+164C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838660 | ||||||
| chr16:14838785
|
G | A | 7 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+289G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838785 | ||||||
| chr16:14838848
|
C | G | 1 | a0006c0009t0001g0133 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.255+352C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838848 | ||||||
| chr16:14838990
|
C | G | 26 | a0002c0002t0001g0292a0002c0002t0001g0299a0002c0002t0001g0300others(23): Show | 27 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.255+494C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838990 | ||||||
| chr16:14839024
|
T | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+528T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839024 | ||||||
| chr16:14839056
|
T | G | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.255+560T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839056 | ||||||
| chr16:14839067
|
T | C | 6 | a0001c0001t0001g0284a0005c0006t0001g0279a0005c0006t0001g0281others(3): Show | 6 | HG00140.hp2 HG01074.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+571T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839067 | ||||||
| chr16:14839159
|
A | G | 1 | a0002c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.255+663A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839159 | ||||||
| chr16:14839169
|
C | T | 1 | a0002c0002t0001g0260 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.255+673C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839169 | ||||||
| chr16:14839189
|
G | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 11 | HG02027.hp2 HG02040.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.255+693G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839189 | ||||||
| chr16:14839334
|
G | T | 1 | a0003c0003t0001g0003 | 3 | NA18973.hp2 NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.255+838G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839334 | ||||||
| chr16:14839414
|
A | T | 1 | a0003c0003t0001g0110 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.255+918A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839414 | ||||||
| chr16:14839770
|
G | C | 1 | a0002c0002t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.255+1274G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839770 | ||||||
| chr16:14839792
|
A | G | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.255+1296A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839792 | ||||||
| chr16:14839850
|
T | G | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.255+1354T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839850 | ||||||
| chr16:14839971
|
C | G | 2 | a0001c0008t0001g0108a0001c0008t0001g0109 | 2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.256-1391C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839971 | ||||||
| chr16:14840063
|
C | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0100others(14): Show | 23 | HG01993.hp2 HG02486.hp2 HG02717.hp1 others(20): Show |
intron_variant | MODIFIER | c.256-1299C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840063 | ||||||
| chr16:14840162
|
A | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-1200A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840162 | ||||||
| chr16:14840572
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.256-790G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840572 | ||||||
| chr16:14840578
|
C | T | 1 | a0001c0001t0002g0004 | 3 | NA18948.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.256-784C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840578 | ||||||
| chr16:14840592
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.256-770A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840592 | ||||||
| chr16:14840623
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.256-739G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840623 | ||||||
| chr16:14840669
|
T | C | 2 | a0004c0004t0003g0012a0004c0004t0003g0013 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.256-693T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840669 | ||||||
| chr16:14840824
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.256-538G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840824 | ||||||
| chr16:14840954
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-408G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840954 | ||||||
| chr16:14841015
|
T | G | 1 | a0004c0004t0001g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.256-347T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14841015 | ||||||
| chr16:14841527
|
G | A | 1 | a0001c0010t0001g0164 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.301+120G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841527 | ||||||
| chr16:14841596
|
T | C | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.301+189T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841596 | ||||||
| chr16:14841754
|
T | A | 2 | a0002c0002t0001g0299a0002c0002t0001g0300 | 2 | NA18971.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.301+347T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841754 | ||||||
| chr16:14841968
|
C | G | 2 | a0001c0010t0001g0164a0010c0029t0001g0272 | 2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.301+561C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841968 | ||||||
| chr16:14842223
|
C | G | 4 | a0003c0003t0001g0003a0003c0003t0001g0105a0003c0003t0001g0106others(1): Show | 6 | NA18973.hp2 NA18995.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+816C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842223 | ||||||
| chr16:14842251
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.301+844C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842251 | ||||||
| chr16:14842400
|
G | C | 321 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(318): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.301+993G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842400 | ||||||
| chr16:14842496
|
T | A | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.301+1089T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842496 | ||||||
| chr16:14842513
|
C | G | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+1106C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842513 | ||||||
| chr16:14842814
|
A | G | 1 | a0001c0001t0002g0256 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.301+1407A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842814 | ||||||
| chr16:14843011
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.301+1604G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843011 | ||||||
| chr16:14843013
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301+1606G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843013 | ||||||
| chr16:14843063
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.302-1611G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843063 | ||||||
| chr16:14843292
|
C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0024others(165): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.302-1382C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843292 | ||||||
| chr16:14843462
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1212G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843462 | ||||||
| chr16:14843520
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0161 | 2 | HG02040.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.302-1154G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843520 | ||||||
| chr16:14843610
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1064T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843610 | ||||||
| chr16:14843611
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1063A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843611 | ||||||
| chr16:14843612
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1062A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843612 | ||||||
| chr16:14843613
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1061A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843613 | ||||||
| chr16:14843616
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1058A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843616 | ||||||
| chr16:14843619
|
A | G | 4 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127others(1): Show | 4 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-1055A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843619 | ||||||
| chr16:14843631
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1043T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843631 | ||||||
| chr16:14843679
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0255others(2): Show | 5 | NA18950.hp1 NA18960.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-995C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843679 | ||||||
| chr16:14843715
|
T | TTG | 201 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.302-932_302-931dup others(2): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | |||||
| chr16:14843715
|
T | TTGTG | 6 | a0001c0001t0001g0259a0001c0001t0002g0166a0001c0001t0002g0213others(3): Show | 6 | HG00673.hp2 HG03195.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-934_302-931dup others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | |||||
| chr16:14843715
|
TTG | T | 21 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 21 | HG00140.hp2 HG01074.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.302-932_302-931del others(2): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | |||||
| chr16:14843715
|
TTGTG | T | 5 | a0001c0001t0001g0098a0003c0003t0001g0016a0003c0003t0001g0017others(2): Show | 5 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-934_302-931del others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | |||||
| chr16:14844017
|
G | A | 3 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0268 | 3 | NA18982.hp1 NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.302-657G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844017 | ||||||
| chr16:14844070
|
G | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0042others(9): Show | 12 | HG00323.hp2 HG00733.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-604G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844070 | ||||||
| chr16:14844178
|
T | C | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-496T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844178 | ||||||
| chr16:14844328
|
T | G | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-346T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844328 | ||||||
| chr16:14844376
|
A | C | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-298A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844376 | ||||||
| chr16:14844478
|
T | C | 1 | a0001c0015t0001g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.302-196T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844478 | ||||||
| chr16:14844808
|
C | G | 1 | a0002c0002t0001g0252 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.402+34C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844808 | ||||||
| chr16:14844876
|
C | T | 1 | a0008c0012t0001g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+102C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844876 | ||||||
| chr16:14844941
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402+167G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844941 | ||||||
| chr16:14844964
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.402+190G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844964 | ||||||
| chr16:14845014
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402+240G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845014 | ||||||
| chr16:14845058
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.402+284G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845058 | ||||||
| chr16:14845376
|
T | C | 1 | a0009c0026t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402+602T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845376 | ||||||
| chr16:14845464
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03834.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.402+690A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845464 | ||||||
| chr16:14845487
|
C | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03834.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.402+713C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845487 | ||||||
| chr16:14845531
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.402+757G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845531 | ||||||
| chr16:14845560
|
T | C | 5 | a0003c0003t0001g0130a0008c0012t0001g0128a0008c0012t0001g0129others(2): Show | 5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+786T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845560 | ||||||
| chr16:14845858
|
C | T | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127 | 3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.403-719C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845858 | ||||||
| chr16:14845896
|
C | G | 13 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0151others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-681C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845896 | ||||||
| chr16:14845913
|
G | A | 1 | a0002c0002t0001g0318 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.403-664G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845913 | ||||||
| chr16:14846024
|
CT | C | 13 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(10): Show | 13 | HG01192.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.403-533delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 14846024 | |||||
| chr16:14846113
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0061others(12): Show | 16 | HG00735.hp2 HG00738.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.403-464G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14846113 | ||||||
| chr16:14846295
|
A | G | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403-282A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14846295 | ||||||
| chr16:14846323
|
G | A | 14 | a0001c0001t0002g0008a0001c0001t0002g0162a0001c0001t0002g0168others(11): Show | 14 | HG01496.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-254G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14846323 | ||||||
| chr16:14846912
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.509+229G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14846912 | ||||||
| chr16:14847004
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+321A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847004 | ||||||
| chr16:14847009
|
T | A | 2 | a0001c0001t0002g0168a0003c0003t0001g0099 | 2 | NA18961.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.509+326T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847009 | ||||||
| chr16:14847069
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.509+386G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847069 | ||||||
| chr16:14847175
|
C | T | 1 | a0004c0004t0001g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.509+492C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847175 | ||||||
| chr16:14847334
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.509+651C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847334 | ||||||
| chr16:14847868
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.510-1031G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847868 | ||||||
| chr16:14847971
|
T | G | 1 | a0001c0001t0002g0178 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.510-928T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847971 | ||||||
| chr16:14848052
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510-847A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14848052 | ||||||
| chr16:14848117
|
C | T | 1 | a0002c0002t0001g0215 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.510-782C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14848117 | ||||||
| chr16:14848609
|
G | A | 1 | a0001c0020t0002g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510-290G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14848609 | ||||||
| chr16:14849896
|
C | CT | 80 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(77): Show | 82 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.582+946dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 14849896 | |||||
| chr16:14849896
|
CT | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG02109.hp1 HG03139.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.582+946delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 14849896 | |||||
| chr16:14850002
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.582+1031C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850002 | ||||||
| chr16:14850140
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.582+1169G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850140 | ||||||
| chr16:14850156
|
C | T | 2 | a0004c0004t0003g0012a0004c0004t0003g0013 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.582+1185C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850156 | ||||||
| chr16:14850253
|
T | C | 1 | a0009c0026t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.582+1282T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850253 | ||||||
| chr16:14850317
|
G | A | 1 | a0001c0015t0001g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.582+1346G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850317 | ||||||
| chr16:14850368
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.582+1397G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850368 | ||||||
| chr16:14850374
|
T | C | 1 | a0018c0025t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.582+1403T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850374 | ||||||
| chr16:14850658
|
T | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+1687T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850658 | ||||||
| chr16:14850675
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.582+1704C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850675 | ||||||
| chr16:14850740
|
A | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.583-1690A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850740 | ||||||
| chr16:14850808
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.583-1622C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850808 | ||||||
| chr16:14851083
|
CA | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(253): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.583-1329delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 14851083 | |||||
| chr16:14851231
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.583-1199G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851231 | ||||||
| chr16:14851302
|
T | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.583-1128T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851302 | ||||||
| chr16:14851612
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.583-818A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851612 | ||||||
| chr16:14851739
|
T | G | 234 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(231): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.583-691T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851739 | ||||||
| chr16:14852032
|
A | G | 1 | a0002c0002t0001g0246 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.583-398A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852032 | ||||||
| chr16:14852058
|
C | T | 1 | a0002c0005t0001g0245 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.583-372C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852058 | ||||||
| chr16:14852059
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.583-371G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852059 | ||||||
| chr16:14852086
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.583-344G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852086 | ||||||
| chr16:14852161
|
A | G | 4 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127others(1): Show | 4 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-269A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852161 | ||||||
| chr16:14852405
|
A | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(47): Show | 50 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.583-25A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852405 | ||||||
| chr16:14852619
|
GGTAGGAG others(19): Show |
G | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+39_735+64delTA others(24): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | 14852619 | |||||
| chr16:14852949
|
G | A | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+367G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14852949 | ||||||
| chr16:14852960
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.735+378A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14852960 | ||||||
| chr16:14852995
|
T | A | 53 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(50): Show | 54 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.735+413T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14852995 | ||||||
| chr16:14852998
|
C | CA | 12 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.735+434dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | 14852998 | |||||
| chr16:14852998
|
CA | C | 61 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(58): Show | 62 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.735+434delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | 14852998 | |||||
| chr16:14853030
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.736-437T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853030 | ||||||
| chr16:14853201
|
T | C | 1 | a0001c0008t0001g0039 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.736-266T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853201 | ||||||
| chr16:14853246
|
C | G | 2 | a0002c0002t0001g0218a0002c0002t0001g0219 | 2 | HG02523.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.736-221C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853246 | ||||||
| chr16:14853290
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.736-177T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853290 | ||||||
| chr16:14853674
|
TG | T | 14 | a0002c0002t0001g0092a0002c0002t0001g0145a0002c0002t0001g0217others(11): Show | 14 | HG00597.hp1 HG03834.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+73delG | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr16 | 14853674 | |||||
| chr16:14853775
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.874-162A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 8/30 | chr16 | 14853775 | ||||||
| chr16:14853920
|
C | G | 5 | a0001c0001t0001g0035a0001c0001t0001g0036a0008c0012t0001g0128others(2): Show | 5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-17C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 8/30 | chr16 | 14853920 | ||||||
| chr16:14854332
|
A | AT | 10 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0125others(7): Show | 10 | HG01261.hp2 HG02486.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+326dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 14854332 | |||||
| chr16:14854332
|
AT | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0096a0001c0001t0001g0097others(12): Show | 15 | HG00280.hp2 HG02145.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.963+326delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 14854332 | |||||
| chr16:14854355
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.963+329G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854355 | ||||||
| chr16:14854357
|
T | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(46): Show | 49 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+331T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854357 | ||||||
| chr16:14854379
|
A | C | 3 | a0004c0004t0001g0265a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.963+353A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854379 | ||||||
| chr16:14854563
|
G | A | 1 | a0001c0008t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.963+537G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854563 | ||||||
| chr16:14854644
|
T | G | 233 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.963+618T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854644 | ||||||
| chr16:14854747
|
C | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+721C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854747 | ||||||
| chr16:14854903
|
C | T | 1 | a0013c0023t0002g0205 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.963+877C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854903 | ||||||
| chr16:14854982
|
A | G | 2 | a0001c0001t0003g0117a0001c0021t0003g0088 | 2 | NA18961.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.963+956A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854982 | ||||||
| chr16:14855059
|
C | T | 1 | a0001c0013t0001g0247 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.963+1033C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855059 | ||||||
| chr16:14855342
|
G | T | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127 | 3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.963+1316G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855342 | ||||||
| chr16:14855463
|
C | T | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1437C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855463 | ||||||
| chr16:14855474
|
T | TA | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1449dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 14855474 | |||||
| chr16:14855653
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.964-1564A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855653 | ||||||
| chr16:14856146
|
A | G | 5 | a0003c0003t0001g0130a0008c0012t0001g0128a0008c0012t0001g0129others(2): Show | 5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-1071A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856146 | ||||||
| chr16:14856224
|
A | C | 9 | a0002c0002t0001g0092a0002c0002t0001g0240a0002c0002t0001g0241others(6): Show | 9 | HG03834.hp1 NA18974.hp1 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.964-993A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856224 | ||||||
| chr16:14856309
|
A | G | 1 | a0001c0001t0002g0165 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.964-908A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856309 | ||||||
| chr16:14856315
|
C | A | 2 | a0002c0002t0001g0261a0002c0002t0001g0302 | 2 | HG00597.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.964-902C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856315 | ||||||
| chr16:14856317
|
G | C | 1 | a0002c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.964-900G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856317 | ||||||
| chr16:14856444
|
C | T | 1 | a0009c0026t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-773C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856444 | ||||||
| chr16:14856709
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.964-508G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856709 | ||||||
| chr16:14856852
|
T | A | 15 | a0002c0002t0001g0292a0002c0002t0001g0299a0002c0002t0001g0300others(12): Show | 15 | HG00438.hp1 HG00609.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-365T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856852 | ||||||
| chr16:14856864
|
T | C | 3 | a0002c0002t0001g0092a0002c0002t0001g0240a0002c0002t0001g0270 | 3 | NA18985.hp1 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.964-353T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856864 | ||||||
| chr16:14856874
|
C | T | 1 | a0016c0016t0001g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.964-343C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856874 | ||||||
| chr16:14856993
|
T | A | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.964-224T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856993 | ||||||
| chr16:14857042
|
G | T | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127 | 3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.964-175G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14857042 | ||||||
| chr16:14857110
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.964-107C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14857110 | ||||||
| chr16:14857327
|
G | A | 2 | a0004c0004t0003g0012a0004c0004t0003g0013 | 2 | HG02647.hp1 HG02723.hp2 |
splice_region_variant&intron_variant | LOW | c.1069+5G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 10/30 | chr16 | 14857327 | ||||||
| chr16:14857683
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1220+28G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14857683 | ||||||
| chr16:14857773
|
CT | C | 318 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(315): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1220+136delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 14857773 | |||||
| chr16:14857921
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1220+266G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14857921 | ||||||
| chr16:14858410
|
A | G | 1 | a0001c0001t0008g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1220+755A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858410 | ||||||
| chr16:14858441
|
A | C | 55 | a0001c0001t0001g0114a0001c0001t0002g0197a0001c0001t0003g0087others(52): Show | 56 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1220+786A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858441 | ||||||
| chr16:14858567
|
C | T | 2 | a0002c0018t0001g0298a0007c0007t0001g0295 | 2 | NA18999.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1220+912C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858567 | ||||||
| chr16:14858614
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1220+959A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858614 | ||||||
| chr16:14858651
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1220+996C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858651 | ||||||
| chr16:14858682
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0002g0197 | 2 | NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1220+1027G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858682 | ||||||
| chr16:14858837
|
C | G | 1 | a0002c0002t0001g0311 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1220+1182C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858837 | ||||||
| chr16:14859091
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1220+1436C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859091 | ||||||
| chr16:14859319
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1220+1664G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859319 | ||||||
| chr16:14859381
|
G | A | 1 | a0002c0002t0001g0223 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1220+1726G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859381 | ||||||
| chr16:14859590
|
G | A | 3 | a0002c0002t0001g0302a0002c0002t0001g0304a0017c0017t0005g0303 | 3 | NA18975.hp1 NA18977.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1220+1935G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859590 | ||||||
| chr16:14859602
|
C | G | 1 | a0001c0001t0002g0193 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1220+1947C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859602 | ||||||
| chr16:14859746
|
A | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0167 | 2 | HG00733.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1220+2091A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859746 | ||||||
| chr16:14859975
|
G | A | 1 | a0001c0013t0001g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1220+2320G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859975 | ||||||
| chr16:14860176
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1220+2521T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860176 | ||||||
| chr16:14860223
|
C | T | 1 | a0002c0002t0001g0239 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1220+2568C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860223 | ||||||
| chr16:14860755
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1221-2258T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860755 | ||||||
| chr16:14860828
|
A | T | 1 | a0001c0001t0002g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1221-2185A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860828 | ||||||
| chr16:14860891
|
G | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221-2122G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860891 | ||||||
| chr16:14860894
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1221-2119G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860894 | ||||||
| chr16:14860964
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1221-2049C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860964 | ||||||
| chr16:14861506
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 5 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-1507G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14861506 | ||||||
| chr16:14861837
|
AT | A | 241 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(238): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1221-1163delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 14861837 | |||||
| chr16:14862333
|
A | G | 9 | a0002c0002t0001g0141a0004c0004t0001g0134a0004c0004t0001g0135others(6): Show | 9 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221-680A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862333 | ||||||
| chr16:14862387
|
G | C | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1221-626G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862387 | ||||||
| chr16:14862689
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1221-324G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862689 | ||||||
| chr16:14862797
|
G | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0015t0001g0263 | 3 | HG01074.hp1 HG01167.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1221-216G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862797 | ||||||
| chr16:14862841
|
G | A | 1 | a0018c0025t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1221-172G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862841 | ||||||
| chr16:14862950
|
T | G | 2 | a0002c0005t0001g0236a0009c0026t0001g0322 | 2 | NA19001.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1221-63T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862950 | ||||||
| chr16:14862963
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1221-50C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862963 | ||||||
| chr16:14863213
|
A | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0152others(2): Show | 5 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+26A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863213 | ||||||
| chr16:14863310
|
T | G | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG02083.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1395+123T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863310 | ||||||
| chr16:14863592
|
C | T | 2 | a0001c0001t0005g0131a0001c0001t0005g0132 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1395+405C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863592 | ||||||
| chr16:14863663
|
A | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1395+476A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863663 | ||||||
| chr16:14863951
|
C | T | 5 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0108others(2): Show | 5 | HG02071.hp2 HG02523.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-634C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863951 | ||||||
| chr16:14863988
|
C | A | 6 | a0001c0001t0002g0277a0003c0003t0001g0105a0003c0003t0001g0106others(3): Show | 6 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-597C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863988 | ||||||
| chr16:14864167
|
G | C | 4 | a0001c0001t0002g0277a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-418G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864167 | ||||||
| chr16:14864318
|
A | G | 3 | a0001c0001t0001g0098a0001c0014t0001g0113a0006c0009t0001g0293 | 3 | HG03453.hp1 NA18987.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1396-267A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864318 | ||||||
| chr16:14864347
|
T | C | 1 | a0015c0019t0001g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1396-238T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864347 | ||||||
| chr16:14864404
|
T | C | 4 | a0001c0001t0002g0277a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-181T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864404 | ||||||
| chr16:14864453
|
C | T | 8 | a0001c0001t0001g0161a0002c0005t0001g0091a0002c0005t0001g0236others(5): Show | 8 | HG00673.hp2 HG02040.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396-132C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864453 | ||||||
| chr16:14864581
|
A | G | 17 | a0001c0001t0001g0049a0001c0001t0001g0158a0001c0001t0002g0008others(14): Show | 17 | HG00140.hp1 HG01496.hp1 HG01884.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1396-4A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864581 | ||||||
| chr16:14864891
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0116 | 2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1538-133A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/30 | chr16 | 14864891 | ||||||
| chr16:14864965
|
A | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | HG00099.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1538-59A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/30 | chr16 | 14864965 | ||||||
| chr16:14864989
|
G | A | 1 | a0001c0008t0001g0268 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1538-35G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/30 | chr16 | 14864989 | ||||||
| chr16:14865349
|
G | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1669+194G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865349 | ||||||
| chr16:14865435
|
G | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 19 | HG01993.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1669+280G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865435 | ||||||
| chr16:14865437
|
G | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 19 | HG01993.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1669+282G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865437 | ||||||
| chr16:14865551
|
G | A | 12 | a0001c0001t0001g0041a0001c0001t0001g0259a0001c0001t0002g0211others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1669+396G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865551 | ||||||
| chr16:14865556
|
A | G | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0012c0024t0001g0086 | 3 | HG02145.hp1 HG03098.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1669+401A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865556 | ||||||
| chr16:14865779
|
T | G | 4 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0171others(1): Show | 4 | HG01496.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669+624T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865779 | ||||||
| chr16:14865832
|
G | A | 30 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0050others(27): Show | 30 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1669+677G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865832 | ||||||
| chr16:14865909
|
C | G | 7 | a0001c0001t0005g0131a0001c0001t0005g0132a0003c0003t0001g0003others(4): Show | 9 | HG02257.hp1 HG03130.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.1670-646C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865909 | ||||||
| chr16:14865912
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1670-643G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865912 | ||||||
| chr16:14866065
|
CT | C | 39 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(36): Show | 50 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1670-480delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | 14866065 | |||||
| chr16:14866106
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1670-449G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866106 | ||||||
| chr16:14866191
|
C | T | 1 | a0009c0026t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1670-364C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866191 | ||||||
| chr16:14866225
|
A | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0093a0003c0003t0001g0002others(10): Show | 18 | HG01346.hp1 HG01433.hp1 HG03139.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-330A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866225 | ||||||
| chr16:14866230
|
T | C | 213 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(210): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1670-325T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866230 | ||||||
| chr16:14866304
|
A | C | 4 | a0002c0002t0001g0242a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-251A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866304 | ||||||
| chr16:14866305
|
G | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0093a0003c0003t0001g0002others(10): Show | 18 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-250G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866305 | ||||||
| chr16:14866305
|
G | T | 4 | a0002c0002t0001g0242a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-250G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866305 | ||||||
| chr16:14866306
|
T | G | 4 | a0002c0002t0001g0242a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-249T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866306 | ||||||
| chr16:14866307
|
G | C | 4 | a0002c0002t0001g0242a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-248G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866307 | ||||||
| chr16:14866307
|
G | GC | 13 | a0001c0001t0001g0027a0001c0001t0001g0093a0003c0003t0001g0002others(10): Show | 18 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-247dupC | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | 14866307 | |||||
| chr16:14866312
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0093a0003c0003t0001g0002others(10): Show | 18 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-243G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866312 | ||||||
| chr16:14866466
|
G | A | 14 | a0001c0001t0001g0206a0003c0003t0001g0002a0003c0003t0001g0003others(11): Show | 19 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-89G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866466 | ||||||
| chr16:14866467
|
A | G | 14 | a0001c0001t0001g0206a0003c0003t0001g0002a0003c0003t0001g0003others(11): Show | 19 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-88A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866467 | ||||||
| chr16:14866499
|
G | C | 14 | a0001c0001t0001g0206a0003c0003t0001g0002a0003c0003t0001g0003others(11): Show | 19 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-56G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866499 | ||||||
| chr16:14866707
|
T | G | 18 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079others(15): Show | 23 | HG01192.hp2 HG02572.hp2 HG02647.hp1 others(20): Show |
intron_variant | MODIFIER | c.1806+16T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866707 | ||||||
| chr16:14866732
|
C | T | 3 | a0004c0004t0001g0265a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+41C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866732 | ||||||
| chr16:14866749
|
G | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1806+58G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866749 | ||||||
| chr16:14866790
|
T | C | 22 | a0003c0003t0001g0002a0003c0003t0001g0003a0003c0003t0001g0007others(19): Show | 27 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(24): Show |
intron_variant | MODIFIER | c.1806+99T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866790 | ||||||
| chr16:14866811
|
C | G | 3 | a0004c0004t0001g0265a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+120C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866811 | ||||||
| chr16:14866817
|
G | A | 3 | a0004c0004t0001g0265a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+126G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866817 | ||||||
| chr16:14866829
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1806+138C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866829 | ||||||
| chr16:14866931
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1806+240C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866931 | ||||||
| chr16:14866943
|
T | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1806+252T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866943 | ||||||
| chr16:14866953
|
C | T | 3 | a0004c0004t0001g0265a0004c0004t0003g0012a0004c0004t0003g0013 | 3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+262C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866953 | ||||||
| chr16:14866992
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1806+301T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866992 | ||||||
| chr16:14867003
|
G | A | 4 | a0001c0001t0002g0211a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG01261.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+312G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867003 | ||||||
| chr16:14867065
|
G | T | 1 | a0001c0001t0001g0250 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1806+374G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867065 | ||||||
| chr16:14867094
|
A | G | 9 | a0002c0002t0001g0141a0004c0004t0001g0134a0004c0004t0001g0135others(6): Show | 9 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1806+403A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867094 | ||||||
| chr16:14867149
|
G | GAT | 3 | a0001c0001t0002g0258a0001c0010t0001g0207a0018c0025t0001g0275 | 3 | HG03139.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1806+485_1806+486d others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | |||||
| chr16:14867149
|
G | GATATATA others(9): Show |
1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1806+471_1806+486d others(18): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | |||||
| chr16:14867149
|
GAT | G | 13 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0098others(10): Show | 13 | HG00280.hp2 HG00621.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1806+485_1806+486d others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | |||||
| chr16:14867149
|
GATATATA others(3): Show |
G | 1 | a0001c0001t0001g0320 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1806+477_1806+486d others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | |||||
| chr16:14867163
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1806+473_1806+483d others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867163 | ||||||
| chr16:14867163
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1806+473_1806+485d others(15): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867163 | ||||||
| chr16:14867168
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1806+477A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867168 | ||||||
| chr16:14867170
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1806+479A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867170 | ||||||
| chr16:14867172
|
A | T | 3 | a0001c0001t0001g0123a0001c0001t0001g0160a0002c0002t0004g0144 | 3 | HG03540.hp1 HG04204.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1806+481A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867172 | ||||||
| chr16:14867174
|
A | ATTTT | 3 | a0001c0001t0001g0076a0002c0002t0001g0089a0002c0002t0001g0216 | 3 | HG03491.hp1 HG03492.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1806+484_1806+485i others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | |||||
| chr16:14867174
|
A | ATTTTT | 4 | a0002c0002t0001g0215a0002c0005t0001g0238a0002c0005t0001g0245others(1): Show | 4 | HG00673.hp2 HG02040.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+484_1806+485i others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | |||||
| chr16:14867174
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1806+484_1806+485i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | |||||
| chr16:14867174
|
A | ATTTTTTT others(5): Show |
1 | a0001c0013t0001g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1806+484_1806+485i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | |||||
| chr16:14867174
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1806+483A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867174 | ||||||
| chr16:14867174
|
A | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0123a0001c0001t0001g0159others(7): Show | 10 | HG01346.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1806+483A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867174 | ||||||
| chr16:14867174
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0095 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1806+485_1806+496d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | |||||
| chr16:14867175
|
TA | T | 3 | a0001c0001t0002g0200a0001c0001t0002g0211a0003c0003t0001g0102 | 3 | HG01261.hp2 HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1806+485delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867175 | ||||||
| chr16:14867176
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0035a0006c0009t0001g0293 | 2 | NA18948.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(23): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0044 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(35): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(30): Show |
1 | a0001c0008t0001g0109 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(42): Show |
1 | a0001c0001t0001g0051 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(51): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(40): Show |
1 | a0001c0001t0001g0052 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(49): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0125 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(54): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0048 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(46): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(33): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0212 | 2 | NA18947.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(42): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(31): Show |
3 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0161 | 3 | HG00741.hp1 HG01981.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(40): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0118 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(44): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0014 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(36): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0054a0001c0011t0001g0031 | 2 | HG01257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(38): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(30): Show |
1 | a0001c0011t0001g0032 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(41): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(42): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(35): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0033 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(36): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(38): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0274 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(41): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0026a0001c0008t0001g0108 | 2 | HG02071.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(32): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0007g0269 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(33): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0124 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(36): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(37): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0047 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(29): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0122 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(37): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0126 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0034a0006c0009t0001g0285 | 2 | HG01255.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(26): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(19): Show |
1 | a0001c0008t0001g0268 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(28): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(20): Show |
2 | a0001c0008t0001g0039a0001c0008t0001g0040 | 2 | NA18982.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(29): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(32): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0152 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(26): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(19): Show |
1 | a0016c0016t0001g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(28): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0167 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(29): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(14): Show |
1 | a0005c0006t0001g0279 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(23): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(25): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0024a0006c0009t0001g0280 | 2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(21): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(7): Show |
1 | a0005c0006t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(16): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0153a0001c0001t0001g0154a0005c0006t0001g0226others(1): Show | 4 | HG00099.hp2 HG00140.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0151 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(18): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0227 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0249others(1): Show | 4 | HG01123.hp1 HG01358.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(15): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(16): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(8): Show |
1 | a0005c0006t0001g0283 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(11): Show |
1 | a0004c0004t0003g0012 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(20): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0229a0015c0019t0001g0224 | 2 | HG01361.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0037a0001c0001t0001g0250 | 2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(15): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0262others(2): Show | 5 | HG00323.hp1 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0090a0001c0001t0001g0232others(1): Show | 4 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATTT | 7 | a0002c0002t0001g0220a0004c0004t0001g0135a0004c0004t0001g0136others(4): Show | 7 | HG01109.hp1 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(9): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0063a0001c0001t0001g0080a0001c0001t0001g0264 | 3 | HG00609.hp2 HG01167.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATTT others(4): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0003g0087 | 3 | HG00738.hp1 HG01243.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATATTT others(5): Show |
6 | a0001c0001t0001g0072a0001c0001t0001g0150a0001c0001t0001g0271others(3): Show | 6 | HG01074.hp1 HG02723.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATTT | 5 | a0002c0002t0001g0239a0002c0002t0001g0312a0002c0002t0001g0316others(2): Show | 6 | HG02015.hp2 HG02074.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATTTTT | 7 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0304others(4): Show | 7 | HG00438.hp1 HG00609.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(9): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATTTTT others(2): Show |
7 | a0001c0001t0001g0064a0001c0001t0001g0077a0001c0001t0001g0081others(4): Show | 7 | HG00621.hp1 HG01346.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(11): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATTTTT others(3): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0093others(1): Show | 4 | HG01433.hp1 NA19012.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0015a0001c0001t0003g0060 | 2 | NA18968.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATATTTTT others(5): Show |
2 | a0001c0001t0001g0066a0006c0009t0003g0075 | 2 | HG00735.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTT | 16 | a0002c0002t0001g0092a0002c0002t0001g0145a0002c0002t0001g0218others(13): Show | 16 | HG02027.hp1 HG02523.hp1 HG03688.hp1 others(13): Show |
intron_variant | MODIFIER | c.1806+510_1806+514d others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTTT | 7 | a0002c0002t0001g0235a0002c0002t0001g0240a0002c0002t0001g0242others(4): Show | 7 | HG02080.hp2 HG03927.hp2 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+509_1806+514d others(8): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTTTT | 6 | a0002c0002t0001g0217a0002c0002t0001g0261a0002c0002t0001g0299others(3): Show | 6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+508_1806+514d others(9): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0073others(5): Show | 8 | HG00642.hp1 HG01123.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+506_1806+514d others(11): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | NA18960.hp1 NA18973.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+505_1806+514d others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTTTT others(5): Show |
1 | a0001c0013t0001g0247 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1806+503_1806+514d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0068 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1806+501_1806+514d others(16): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
A | T | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00621.hp2 HG00673.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1806+485A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867176 | ||||||
| chr16:14867176
|
AT | A | 12 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0115others(9): Show | 12 | HG02145.hp1 HG02572.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1806+514delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
ATT | A | 13 | a0001c0001t0001g0189a0001c0001t0002g0166a0001c0001t0002g0178others(10): Show | 13 | HG00323.hp2 HG01258.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1806+513_1806+514d others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867176
|
ATTTT | A | 12 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0009others(9): Show | 18 | HG00438.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1806+511_1806+514d others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | |||||
| chr16:14867177
|
T | TA | 10 | a0001c0001t0001g0114a0001c0001t0002g0008a0001c0001t0002g0162others(7): Show | 10 | HG01496.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(3): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867177 | ||||||
| chr16:14867177
|
T | TATATATA others(8): Show |
1 | a0011c0027t0001g0127 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867177 | ||||||
| chr16:14867178
|
T | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0186a0001c0001t0001g0222others(3): Show | 6 | HG01952.hp2 HG01993.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+487T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867178 | ||||||
| chr16:14867179
|
T | A | 12 | a0001c0001t0001g0114a0001c0001t0002g0038a0001c0001t0002g0146others(9): Show | 12 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1806+488T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867179 | ||||||
| chr16:14867180
|
T | A | 2 | a0001c0001t0002g0201a0018c0025t0001g0275 | 2 | HG00323.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1806+489T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867180 | ||||||
| chr16:14867181
|
T | A | 8 | a0001c0001t0006g0184a0003c0003t0001g0016a0003c0003t0001g0017others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+490T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867181 | ||||||
| chr16:14867182
|
T | A | 9 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0193others(6): Show | 12 | HG00438.hp2 HG02056.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.1806+491T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867182 | ||||||
| chr16:14867183
|
T | A | 7 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+492T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867183 | ||||||
| chr16:14867184
|
T | A | 2 | a0001c0001t0002g0198a0018c0025t0001g0275 | 2 | HG00438.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1806+493T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867184 | ||||||
| chr16:14867185
|
T | A | 7 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+494T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867185 | ||||||
| chr16:14867186
|
T | A | 2 | a0001c0001t0002g0198a0018c0025t0001g0275 | 2 | HG00438.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1806+495T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867186 | ||||||
| chr16:14867187
|
T | A | 6 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+496T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867187 | ||||||
| chr16:14867189
|
T | A | 2 | a0003c0003t0001g0017a0008c0012t0001g0128 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1806+498T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867189 | ||||||
| chr16:14867230
|
C | T | 1 | a0006c0009t0003g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1806+539C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867230 | ||||||
| chr16:14867248
|
T | C | 5 | a0003c0003t0001g0102a0008c0012t0001g0128a0008c0012t0001g0129others(2): Show | 5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806+557T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867248 | ||||||
| chr16:14867311
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1806+620C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867311 | ||||||
| chr16:14867324
|
A | G | 8 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+633A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867324 | ||||||
| chr16:14867333
|
G | A | 2 | a0002c0002t0001g0309a0002c0002t0001g0311 | 2 | HG02080.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1806+642G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867333 | ||||||
| chr16:14867347
|
C | T | 29 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0151others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.1806+656C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867347 | ||||||
| chr16:14867481
|
T | C | 238 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(235): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1806+790T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867481 | ||||||
| chr16:14867524
|
T | C | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1806+833T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867524 | ||||||
| chr16:14867620
|
C | T | 2 | a0001c0001t0002g0165a0018c0025t0001g0275 | 2 | HG03139.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1807-928C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867620 | ||||||
| chr16:14867644
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0103a0001c0001t0001g0114others(11): Show | 20 | HG01993.hp2 HG02486.hp2 HG03490.hp2 others(17): Show |
intron_variant | MODIFIER | c.1807-904A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867644 | ||||||
| chr16:14867679
|
C | T | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1807-869C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867679 | ||||||
| chr16:14867774
|
C | T | 2 | a0001c0013t0001g0148a0001c0013t0001g0247 | 2 | HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1807-774C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867774 | ||||||
| chr16:14867775
|
G | C | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1807-773G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867775 | ||||||
| chr16:14867812
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1807-736G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867812 | ||||||
| chr16:14867894
|
C | CT | 29 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0100others(26): Show | 29 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1807-638dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867894 | |||||
| chr16:14868033
|
T | C | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127 | 3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1807-515T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868033 | ||||||
| chr16:14868058
|
T | A | 1 | a0001c0001t0002g0004 | 3 | NA18948.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1807-490T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868058 | ||||||
| chr16:14868103
|
T | C | 320 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1807-445T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868103 | ||||||
| chr16:14868441
|
A | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(49): Show | 53 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1807-107A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868441 | ||||||
| chr16:14868449
|
T | C | 1 | a0003c0003t0001g0007 | 2 | NA19062.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1807-99T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868449 | ||||||
| chr16:14868508
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1807-40A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868508 | ||||||
| chr16:14868541
|
T | C | 10 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1807-7T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868541 | ||||||
| chr16:14868682
|
G | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG01192.hp2 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1894+47G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14868682 | ||||||
| chr16:14868909
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1894+274T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14868909 | ||||||
| chr16:14868978
|
A | G | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894+343A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14868978 | ||||||
| chr16:14869001
|
T | C | 1 | a0005c0006t0001g0281 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1894+366T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869001 | ||||||
| chr16:14869185
|
G | A | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894+550G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869185 | ||||||
| chr16:14869223
|
C | T | 1 | a0006c0009t0001g0293 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1894+588C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869223 | ||||||
| chr16:14869340
|
A | G | 1 | a0018c0025t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1894+705A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869340 | ||||||
| chr16:14869353
|
T | C | 73 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0024others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1894+718T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869353 | ||||||
| chr16:14869411
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894+776G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869411 | ||||||
| chr16:14869707
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1894+1072C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869707 | ||||||
| chr16:14869843
|
G | A | 255 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(252): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1894+1208G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869843 | ||||||
| chr16:14869854
|
C | A | 1 | a0007c0007t0001g0296 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1894+1219C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869854 | ||||||
| chr16:14869935
|
G | A | 1 | a0001c0001t0002g0171 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1894+1300G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869935 | ||||||
| chr16:14870074
|
C | A | 216 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(213): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1894+1439C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870074 | ||||||
| chr16:14870265
|
G | T | 3 | a0002c0002t0004g0143a0002c0002t0004g0144a0002c0002t0004g0248 | 3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1895-1356G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870265 | ||||||
| chr16:14870386
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0104 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1895-1235T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870386 | ||||||
| chr16:14870434
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1895-1187C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870434 | ||||||
| chr16:14870623
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1895-998G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870623 | ||||||
| chr16:14870653
|
C | G | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1895-968C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870653 | ||||||
| chr16:14870711
|
A | C | 46 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(43): Show | 46 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1895-910A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870711 | ||||||
| chr16:14870711
|
A | G | 1 | a0002c0002t0001g0309 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1895-910A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870711 | ||||||
| chr16:14870717
|
A | G | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1895-904A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870717 | ||||||
| chr16:14870887
|
C | T | 5 | a0001c0001t0003g0060a0001c0001t0003g0087a0001c0001t0003g0117others(2): Show | 5 | NA18957.hp1 NA18961.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1895-734C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870887 | ||||||
| chr16:14871139
|
G | C | 1 | a0004c0004t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1895-482G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871139 | ||||||
| chr16:14871140
|
C | T | 1 | a0004c0004t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1895-481C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871140 | ||||||
| chr16:14871383
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1895-238A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871383 | ||||||
| chr16:14871403
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1895-218G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871403 | ||||||
| chr16:14871434
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1895-187T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871434 | ||||||
| chr16:14871467
|
G | A | 1 | a0018c0025t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1895-154G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871467 | ||||||
| chr16:14871576
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1895-45A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871576 | ||||||
| chr16:14871729
|
G | A | 1 | a0013c0023t0002g0205 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1958+45G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 17/30 | chr16 | 14871729 | ||||||
| chr16:14871969
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1959-265G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 17/30 | chr16 | 14871969 | ||||||
| chr16:14872123
|
G | A | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1959-111G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 17/30 | chr16 | 14872123 | ||||||
| chr16:14872835
|
G | A | 1 | a0002c0002t0001g0261 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2054+506G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14872835 | ||||||
| chr16:14872875
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2054+546C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14872875 | ||||||
| chr16:14872919
|
T | C | 36 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0151others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.2054+590T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14872919 | ||||||
| chr16:14873006
|
C | T | 8 | a0005c0006t0001g0226a0005c0006t0001g0279a0005c0006t0001g0281others(5): Show | 8 | HG00140.hp2 HG01074.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.2054+677C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873006 | ||||||
| chr16:14873007
|
G | A | 68 | a0002c0002t0001g0089a0002c0002t0001g0092a0002c0002t0001g0141others(65): Show | 69 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2054+678G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873007 | ||||||
| chr16:14873151
|
T | TA | 175 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0024others(172): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.2054+825dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 14873151 | |||||
| chr16:14873302
|
GA | G | 68 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2054+976delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 14873302 | |||||
| chr16:14873439
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2054+1110G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873439 | ||||||
| chr16:14873564
|
C | T | 9 | a0001c0001t0001g0077a0001c0010t0001g0164a0002c0005t0001g0091others(6): Show | 9 | HG00673.hp2 HG06807.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.2054+1235C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873564 | ||||||
| chr16:14873565
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2054+1236G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873565 | ||||||
| chr16:14873670
|
A | G | 21 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(18): Show | 21 | HG01255.hp1 HG02027.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2054+1341A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873670 | ||||||
| chr16:14873799
|
G | A | 6 | a0001c0013t0001g0247a0001c0020t0002g0179a0003c0003t0001g0016others(3): Show | 6 | HG01106.hp2 HG02257.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2055-1237G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873799 | ||||||
| chr16:14873803
|
T | G | 8 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0013t0001g0247others(5): Show | 8 | HG01106.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2055-1233T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873803 | ||||||
| chr16:14873824
|
C | T | 48 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(45): Show | 48 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.2055-1212C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873824 | ||||||
| chr16:14873972
|
A | G | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2055-1064A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873972 | ||||||
| chr16:14873986
|
G | A | 2 | a0001c0001t0002g0213a0002c0002t0001g0266 | 2 | NA18997.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2055-1050G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873986 | ||||||
| chr16:14874022
|
TTGGTCTG others(69): Show |
T | 167 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0024others(164): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.2055-986_2055-911d others(78): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 14874022 | |||||
| chr16:14874098
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2055-938C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874098 | ||||||
| chr16:14874119
|
G | A | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0255others(5): Show | 8 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2055-917G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874119 | ||||||
| chr16:14874136
|
C | T | 5 | a0001c0001t0001g0053a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | NA18960.hp1 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2055-900C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874136 | ||||||
| chr16:14874141
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2055-895T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874141 | ||||||
| chr16:14874144
|
C | G | 28 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0100others(25): Show | 34 | HG01109.hp2 HG01993.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.2055-892C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874144 | ||||||
| chr16:14874185
|
G | A | 5 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0193others(2): Show | 8 | HG00438.hp2 HG02056.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.2055-851G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874185 | ||||||
| chr16:14874625
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2055-411A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874625 | ||||||
| chr16:14874925
|
T | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0100others(21): Show | 30 | HG01109.hp2 HG01993.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.2055-111T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874925 | ||||||
| chr16:14875002
|
C | T | 49 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(46): Show | 49 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.2055-34C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14875002 | ||||||
| chr16:14875021
|
C | T | 1 | a0013c0023t0002g0205 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2055-15C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14875021 | ||||||
| chr16:14875023
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2055-13G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14875023 | ||||||
| chr16:14875271
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2273+17G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 19/30 | chr16 | 14875271 | ||||||
| chr16:14875569
|
TTGGATGG others(5): Show |
T | 22 | a0001c0001t0001g0024a0001c0001t0001g0150a0001c0001t0001g0151others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(19): Show |
intron_variant | MODIFIER | c.2356+163_2356+174d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875569 | |||||
| chr16:14875602
|
T | TTGGA | 15 | a0001c0001t0001g0023a0001c0001t0001g0081a0001c0001t0001g0094others(12): Show | 15 | HG00621.hp1 HG01884.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.2356+219_2356+222d others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875602 | |||||
| chr16:14875602
|
TTGGA | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0025others(55): Show | 59 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.2356+219_2356+222d others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875602 | |||||
| chr16:14875602
|
TTGGATGG others(13): Show |
T | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2356+203_2356+222d others(22): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875602 | |||||
| chr16:14875645
|
A | G | 1 | a0002c0002t0001g0316 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2356+223A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14875645 | ||||||
| chr16:14875892
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0189 | 2 | HG01258.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2357-467T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14875892 | ||||||
| chr16:14875937
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2357-422T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14875937 | ||||||
| chr16:14876067
|
C | G | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2357-292C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876067 | ||||||
| chr16:14876104
|
C | G | 233 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2357-255C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876104 | ||||||
| chr16:14876180
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2357-179G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876180 | ||||||
| chr16:14876206
|
C | T | 1 | a0002c0005t0001g0245 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2357-153C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876206 | ||||||
| chr16:14876333
|
C | T | 1 | a0001c0001t0002g0180 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2357-26C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876333 | ||||||
| chr16:14876542
|
G | T | 1 | a0001c0010t0001g0207 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2516+24G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 21/30 | chr16 | 14876542 | ||||||
| chr16:14876817
|
C | G | 3 | a0002c0002t0004g0143a0002c0002t0004g0144a0002c0002t0004g0248 | 3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2643+27C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14876817 | ||||||
| chr16:14876953
|
T | C | 240 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(237): Show | 242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2643+163T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14876953 | ||||||
| chr16:14877012
|
C | T | 1 | a0001c0020t0002g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2643+222C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877012 | ||||||
| chr16:14877155
|
G | GT | 59 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(56): Show | 60 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2643+381dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14877155 | |||||
| chr16:14877158
|
T | G | 4 | a0001c0001t0002g0277a0004c0004t0001g0265a0004c0004t0003g0012others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2643+368T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877158 | ||||||
| chr16:14877506
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2643+716C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877506 | ||||||
| chr16:14877625
|
G | A | 1 | a0001c0001t0001g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2643+835G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877625 | ||||||
| chr16:14877626
|
C | G | 1 | a0002c0002t0001g0312 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2643+836C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877626 | ||||||
| chr16:14877738
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2643+948G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877738 | ||||||
| chr16:14877809
|
G | GTGGTTAC others(8): Show |
1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-908_2644-894d others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14877809 | |||||
| chr16:14877888
|
A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-833A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877888 | ||||||
| chr16:14877891
|
A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-830A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877891 | ||||||
| chr16:14877892
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-829A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877892 | ||||||
| chr16:14877893
|
T | A | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-828T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877893 | ||||||
| chr16:14877911
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-810A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877911 | ||||||
| chr16:14877915
|
T | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-806T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877915 | ||||||
| chr16:14877915
|
T | TAAAAC | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(314): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.2644-806_2644-805i others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877915 | ||||||
| chr16:14877935
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2644-786A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877935 | ||||||
| chr16:14877950
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-771A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877950 | ||||||
| chr16:14878086
|
A | T | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2644-635A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878086 | ||||||
| chr16:14878271
|
A | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG01243.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2644-450A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878271 | ||||||
| chr16:14878404
|
G | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-317G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878404 | ||||||
| chr16:14878407
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-314T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878407 | ||||||
| chr16:14878493
|
C | CA | 32 | a0001c0001t0001g0030a0001c0001t0001g0036a0001c0001t0001g0051others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.2644-200dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14878493 | |||||
| chr16:14878493
|
CA | C | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 30 | HG00438.hp2 HG01109.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.2644-200delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14878493 | |||||
| chr16:14878493
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2644-211_2644-200d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14878493 | |||||
| chr16:14878516
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-205A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878516 | ||||||
| chr16:14878517
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-204A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878517 | ||||||
| chr16:14878638
|
A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-83A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878638 | ||||||
| chr16:14878668
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-53T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878668 | ||||||
| chr16:14878899
|
G | A | 3 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0268 | 3 | NA18982.hp1 NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2757+65G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878899 | ||||||
| chr16:14878907
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2757+73C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878907 | ||||||
| chr16:14878916
|
T | A | 1 | a0002c0002t0001g0235 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2757+82T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878916 | ||||||
| chr16:14878923
|
G | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2757+89G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878923 | ||||||
| chr16:14878935
|
A | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2757+101A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878935 | ||||||
| chr16:14879019
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2757+185T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879019 | ||||||
| chr16:14879033
|
C | A | 1 | a0002c0002t0001g0309 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2757+199C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879033 | ||||||
| chr16:14879058
|
A | G | 6 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055others(3): Show | 6 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2757+224A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879058 | ||||||
| chr16:14879060
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2757+226T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879060 | ||||||
| chr16:14879116
|
A | G | 7 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055others(4): Show | 7 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.2757+282A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879116 | ||||||
| chr16:14879123
|
C | T | 1 | a0004c0004t0001g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2757+289C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879123 | ||||||
| chr16:14879134
|
G | A | 5 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055others(2): Show | 5 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757+300G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879134 | ||||||
| chr16:14879143
|
C | T | 9 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055others(6): Show | 11 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.2757+309C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879143 | ||||||
| chr16:14879310
|
C | A | 1 | a0001c0010t0001g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2757+476C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879310 | ||||||
| chr16:14879347
|
C | T | 3 | a0001c0001t0001g0156a0001c0020t0002g0179a0002c0018t0001g0298 | 3 | HG03669.hp1 HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2757+513C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879347 | ||||||
| chr16:14879503
|
C | T | 2 | a0001c0001t0005g0131a0001c0001t0005g0132 | 2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2758-512C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879503 | ||||||
| chr16:14879588
|
T | A | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-427T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879588 | ||||||
| chr16:14879589
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-426A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879589 | ||||||
| chr16:14879659
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-356T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879659 | ||||||
| chr16:14879740
|
GA | G | 6 | a0001c0001t0001g0095a0001c0001t0001g0230a0001c0001t0001g0321others(3): Show | 6 | HG00323.hp1 HG02735.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.2758-257delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr16 | 14879740 | |||||
| chr16:14879767
|
A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-248A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879767 | ||||||
| chr16:14879893
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2758-122C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879893 | ||||||
| chr16:14880012
|
T | C | 3 | a0001c0001t0005g0131a0001c0020t0002g0179a0002c0018t0001g0298 | 3 | HG03669.hp1 HG03710.hp2 NA18999.hp2 |
splice_region_variant&intron_variant | LOW | c.2758-3T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14880012 | ||||||
| chr16:14880398
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2885+256T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880398 | ||||||
| chr16:14880405
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2885+263T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880405 | ||||||
| chr16:14880416
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2885+274G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880416 | ||||||
| chr16:14880484
|
T | C | 13 | a0001c0001t0001g0126a0001c0020t0002g0179a0002c0018t0001g0298others(10): Show | 13 | HG02145.hp1 HG02257.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.2885+342T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880484 | ||||||
| chr16:14880484
|
T | G | 4 | a0001c0001t0003g0060a0001c0001t0003g0087a0001c0001t0003g0117others(1): Show | 4 | NA18961.hp1 NA18968.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2885+342T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880484 | ||||||
| chr16:14880671
|
C | T | 9 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(6): Show | 9 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2885+529C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880671 | ||||||
| chr16:14880718
|
A | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2885+576A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880718 | ||||||
| chr16:14880721
|
T | C | 3 | a0001c0010t0001g0207a0001c0020t0002g0179a0002c0018t0001g0298 | 3 | HG03579.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2885+579T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880721 | ||||||
| chr16:14880734
|
A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2885+592A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880734 | ||||||
| chr16:14880807
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2885+665C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880807 | ||||||
| chr16:14880903
|
G | T | 1 | a0001c0013t0001g0148 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2886-641G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880903 | ||||||
| chr16:14881013
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0168 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2886-531G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881013 | ||||||
| chr16:14881147
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2886-397T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881147 | ||||||
| chr16:14881173
|
G | C | 3 | a0001c0008t0001g0039a0001c0008t0001g0040a0001c0008t0001g0268 | 3 | NA18982.hp1 NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2886-371G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881173 | ||||||
| chr16:14881213
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-331G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881213 | ||||||
| chr16:14881259
|
T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2886-285T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881259 | ||||||
| chr16:14881324
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2886-220C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881324 | ||||||
| chr16:14881381
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2886-163G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881381 | ||||||
| chr16:14881392
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-152G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881392 | ||||||
| chr16:14881410
|
T | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-134T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881410 | ||||||
| chr16:14881435
|
A | G | 217 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2886-109A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881435 | ||||||
| chr16:14881439
|
A | C | 3 | a0001c0020t0002g0179a0002c0018t0001g0298a0004c0004t0001g0265 | 3 | HG03453.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-105A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881439 | ||||||
| chr16:14881439
|
A | G | 1 | a0006c0009t0001g0293 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2886-105A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881439 | ||||||
| chr16:14881504
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0078 | 2 | HG01192.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2886-40C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881504 | ||||||
| chr16:14881505
|
A | G | 1 | a0002c0002t0001g0308 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2886-39A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881505 | ||||||
| chr16:14881701
|
G | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3027+16G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14881701 | ||||||
| chr16:14881934
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3027+249G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14881934 | ||||||
| chr16:14881974
|
A | G | 10 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3027+289A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14881974 | ||||||
| chr16:14882025
|
T | C | 46 | a0001c0001t0001g0014a0001c0001t0001g0025a0001c0001t0001g0026others(43): Show | 46 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3027+340T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882025 | ||||||
| chr16:14882282
|
A | G | 254 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(251): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.3028-312A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882282 | ||||||
| chr16:14882370
|
G | A | 1 | a0004c0004t0001g0163 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3028-224G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882370 | ||||||
| chr16:14882570
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3028-24G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882570 | ||||||
| chr16:14882684
|
C | T | 1 | a0002c0002t0001g0313 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.3111+7C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882684 | ||||||
| chr16:14882725
|
G | A | 3 | a0001c0001t0001g0037a0001c0020t0002g0179a0002c0018t0001g0298 | 3 | HG00733.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+48G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882725 | ||||||
| chr16:14882731
|
A | C | 5 | a0001c0001t0002g0038a0001c0001t0002g0185a0001c0001t0002g0190others(2): Show | 5 | NA18962.hp2 NA18985.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.3111+54A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882731 | ||||||
| chr16:14882781
|
A | G | 1 | a0002c0002t0001g0243 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3111+104A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882781 | ||||||
| chr16:14882833
|
C | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+156C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882833 | ||||||
| chr16:14882852
|
A | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+175A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882852 | ||||||
| chr16:14882888
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3111+211T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882888 | ||||||
| chr16:14882909
|
C | T | 1 | a0004c0004t0001g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3111+232C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882909 | ||||||
| chr16:14882945
|
A | G | 6 | a0001c0010t0001g0011a0001c0010t0001g0164a0001c0010t0001g0207others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3111+268A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882945 | ||||||
| chr16:14882998
|
A | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+321A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882998 | ||||||
| chr16:14883231
|
T | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+554T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883231 | ||||||
| chr16:14883333
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+656C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883333 | ||||||
| chr16:14883339
|
CT | C | 6 | a0001c0001t0001g0096a0001c0001t0008g0195a0001c0020t0002g0179others(3): Show | 6 | HG03669.hp1 HG03704.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.3111+677delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr16 | 14883339 | |||||
| chr16:14883359
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+682C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883359 | ||||||
| chr16:14883478
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+801C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883478 | ||||||
| chr16:14883494
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+817G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883494 | ||||||
| chr16:14883521
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3111+844G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883521 | ||||||
| chr16:14883565
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3112-807C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883565 | ||||||
| chr16:14883626
|
T | C | 10 | a0001c0020t0002g0179a0002c0018t0001g0298a0003c0003t0001g0016others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.3112-746T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883626 | ||||||
| chr16:14884026
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3112-346C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884026 | ||||||
| chr16:14884145
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3112-227G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884145 | ||||||
| chr16:14884168
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0177 | 2 | HG02129.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3112-204C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884168 | ||||||
| chr16:14884212
|
A | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3112-160A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884212 | ||||||
| chr16:14884252
|
C | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3112-120C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884252 | ||||||
| chr16:14884292
|
C | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0015t0001g0263 | 3 | HG01074.hp1 HG01167.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3112-80C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884292 | ||||||
| chr16:14884350
|
T | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(256): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.3112-22T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884350 | ||||||
| chr16:14884556
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3222+74G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884556 | ||||||
| chr16:14884558
|
G | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+76G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884558 | ||||||
| chr16:14884608
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+126C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884608 | ||||||
| chr16:14884759
|
C | T | 3 | a0007c0007t0001g0010a0007c0007t0001g0296a0007c0007t0001g0297 | 4 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3222+277C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884759 | ||||||
| chr16:14884771
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3222+289C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884771 | ||||||
| chr16:14884776
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3222+294C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884776 | ||||||
| chr16:14884806
|
T | C | 6 | a0001c0020t0002g0179a0002c0018t0001g0298a0003c0003t0001g0003others(3): Show | 8 | HG03669.hp1 NA18973.hp2 NA18995.hp1 others(5): Show |
intron_variant | MODIFIER | c.3222+324T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884806 | ||||||
| chr16:14884861
|
T | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+379T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884861 | ||||||
| chr16:14884942
|
G | T | 1 | a0016c0016t0001g0273 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3222+460G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884942 | ||||||
| chr16:14884963
|
T | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+481T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884963 | ||||||
| chr16:14884996
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0059a0001c0001t0001g0061others(9): Show | 13 | HG00735.hp2 HG01123.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.3222+514A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884996 | ||||||
| chr16:14885105
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+623G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885105 | ||||||
| chr16:14885166
|
C | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+684C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885166 | ||||||
| chr16:14885169
|
C | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+687C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885169 | ||||||
| chr16:14885189
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3222+707G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885189 | ||||||
| chr16:14885281
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3222+799G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885281 | ||||||
| chr16:14885365
|
CA | C | 4 | a0001c0001t0002g0181a0001c0001t0002g0188a0001c0001t0002g0194others(1): Show | 4 | HG00733.hp1 HG02735.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.3222+887delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr16 | 14885365 | |||||
| chr16:14885476
|
A | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+994A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885476 | ||||||
| chr16:14885519
|
A | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+1037A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885519 | ||||||
| chr16:14885591
|
T | C | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+1109T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885591 | ||||||
| chr16:14885632
|
A | T | 1 | a0002c0002t0001g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3223-1129A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885632 | ||||||
| chr16:14885663
|
G | T | 1 | a0006c0009t0001g0293 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3223-1098G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885663 | ||||||
| chr16:14885700
|
T | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-1061T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885700 | ||||||
| chr16:14885707
|
G | A | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-1054G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885707 | ||||||
| chr16:14885811
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3223-950C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885811 | ||||||
| chr16:14885827
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3223-934T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885827 | ||||||
| chr16:14885976
|
T | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-785T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885976 | ||||||
| chr16:14886111
|
G | C | 3 | a0001c0001t0001g0206a0001c0020t0002g0179a0002c0018t0001g0298 | 3 | HG01884.hp1 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-650G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886111 | ||||||
| chr16:14886136
|
G | C | 3 | a0001c0001t0001g0206a0001c0020t0002g0179a0002c0018t0001g0298 | 3 | HG01884.hp1 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-625G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886136 | ||||||
| chr16:14886438
|
G | A | 52 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(49): Show | 53 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.3223-323G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886438 | ||||||
| chr16:14886669
|
C | T | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-92C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886669 | ||||||
| chr16:14886677
|
A | G | 2 | a0001c0020t0002g0179a0002c0018t0001g0298 | 2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-84A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886677 | ||||||
| chr16:14886894
|
C | T | 2 | a0001c0001t0003g0117a0001c0021t0003g0088 | 2 | NA18961.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3324+32C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14886894 | ||||||
| chr16:14886974
|
A | G | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+112A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14886974 | ||||||
| chr16:14887118
|
T | C | 2 | a0008c0012t0001g0128a0008c0012t0001g0129 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3324+256T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887118 | ||||||
| chr16:14887244
|
G | A | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+382G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887244 | ||||||
| chr16:14887320
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0284 | 2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3324+458G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887320 | ||||||
| chr16:14887442
|
T | C | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+580T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887442 | ||||||
| chr16:14887463
|
C | T | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+601C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887463 | ||||||
| chr16:14887472
|
T | G | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+610T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887472 | ||||||
| chr16:14887474
|
T | G | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+612T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887474 | ||||||
| chr16:14887490
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3324+628C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887490 | ||||||
| chr16:14887653
|
C | G | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+791C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887653 | ||||||
| chr16:14887805
|
A | G | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+943A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887805 | ||||||
| chr16:14888018
|
C | T | 2 | a0001c0001t0002g0185a0001c0001t0002g0197 | 2 | NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3325-1078C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888018 | ||||||
| chr16:14888243
|
A | G | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3325-853A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888243 | ||||||
| chr16:14888265
|
C | T | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3325-831C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888265 | ||||||
| chr16:14888319
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3325-777C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888319 | ||||||
| chr16:14888398
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0202 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3325-698G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888398 | ||||||
| chr16:14888425
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3325-671T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888425 | ||||||
| chr16:14888571
|
T | C | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3325-525T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888571 | ||||||
| chr16:14888575
|
T | C | 1 | a0002c0018t0001g0298 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3325-521T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888575 | ||||||
| chr16:14888609
|
C | T | 10 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0121others(7): Show | 10 | HG02027.hp2 HG02040.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.3325-487C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888609 | ||||||
| chr16:14888614
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3325-482C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888614 | ||||||
| chr16:14888703
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3325-393G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888703 | ||||||
| chr16:14888723
|
G | A | 169 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0024others(166): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.3325-373G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888723 | ||||||
| chr16:14888812
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3325-284G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888812 | ||||||
| chr16:14888901
|
A | G | 1 | a0001c0011t0002g0187 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3325-195A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888901 | ||||||
| chr16:14888944
|
T | C | 1 | a0002c0002t0001g0223 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3325-152T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888944 | ||||||
| chr16:14889065
|
G | A | 1 | a0001c0010t0001g0210 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3325-31G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14889065 | ||||||
| chr16:14889093
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp1 | splice_region_variant&intron_variant | LOW | c.3325-3C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14889093 | ||||||
| chr16:14889248
|
T | C | 1 | a0001c0001t0002g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3444+33T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889248 | ||||||
| chr16:14889276
|
A | T | 1 | a0003c0003t0001g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3444+61A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889276 | ||||||
| chr16:14889311
|
C | G | 74 | a0002c0002t0001g0089a0002c0002t0001g0092a0002c0002t0001g0141others(71): Show | 75 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.3444+96C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889311 | ||||||
| chr16:14889322
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3444+107A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889322 | ||||||
| chr16:14889562
|
C | A | 2 | a0001c0001t0002g0288a0001c0001t0006g0184 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3444+347C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889562 | ||||||
| chr16:14889582
|
G | A | 1 | a0001c0001t0006g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3444+367G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889582 | ||||||
| chr16:14889616
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0100others(21): Show | 30 | HG01109.hp2 HG01993.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.3444+401A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889616 | ||||||
| chr16:14889861
|
A | G | 1 | a0006c0009t0001g0293 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3444+646A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889861 | ||||||
| chr16:14890104
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3444+889A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890104 | ||||||
| chr16:14890110
|
G | A | 51 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0027others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.3444+895G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890110 | ||||||
| chr16:14890321
|
C | T | 1 | a0001c0010t0001g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3444+1106C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890321 | ||||||
| chr16:14890667
|
G | A | 233 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(230): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.3444+1452G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890667 | ||||||
| chr16:14890988
|
T | C | 3 | a0002c0002t0004g0143a0002c0002t0004g0144a0002c0002t0004g0248 | 3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3444+1773T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890988 | ||||||
| chr16:14891057
|
G | A | 1 | a0004c0004t0001g0136 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3444+1842G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891057 | ||||||
| chr16:14891120
|
G | A | 1 | a0009c0026t0001g0322 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3444+1905G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891120 | ||||||
| chr16:14891212
|
G | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03834.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3444+1997G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891212 | ||||||
| chr16:14891437
|
T | G | 1 | a0002c0002t0001g0312 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3444+2222T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891437 | ||||||
| chr16:14891904
|
A | C | 1 | a0001c0001t0001g0062 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3444+2689A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891904 | ||||||
| chr16:14891952
|
C | T | 2 | a0001c0001t0001g0114a0002c0005t0001g0236 | 2 | HG02486.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.3444+2737C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891952 | ||||||
| chr16:14892223
|
C | T | 1 | a0002c0002t0001g0314 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3445-2775C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892223 | ||||||
| chr16:14892242
|
C | CA | 6 | a0001c0001t0003g0060a0001c0001t0003g0087a0001c0001t0003g0117others(3): Show | 6 | HG01257.hp1 HG01258.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3445-2744dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 14892242 | |||||
| chr16:14892253
|
A | G | 8 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3445-2745A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892253 | ||||||
| chr16:14892328
|
T | C | 3 | a0007c0007t0001g0010a0007c0007t0001g0296a0007c0007t0001g0297 | 4 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3445-2670T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892328 | ||||||
| chr16:14892351
|
G | A | 1 | a0002c0005t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3445-2647G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892351 | ||||||
| chr16:14892609
|
TA | T | 18 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(15): Show | 18 | HG00140.hp1 HG01257.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3445-2370delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 14892609 | |||||
| chr16:14892683
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3445-2315A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892683 | ||||||
| chr16:14892686
|
G | A | 4 | a0003c0003t0001g0016a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3445-2312G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892686 | ||||||
| chr16:14892836
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3445-2162G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892836 | ||||||
| chr16:14892898
|
T | A | 229 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(226): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.3445-2100T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892898 | ||||||
| chr16:14892904
|
C | T | 230 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(227): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.3445-2094C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892904 | ||||||
| chr16:14892912
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3445-2086G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892912 | ||||||
| chr16:14893156
|
T | A | 1 | a0001c0001t0002g0191 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3445-1842T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893156 | ||||||
| chr16:14893161
|
C | CT | 3 | a0001c0001t0001g0048a0001c0001t0001g0054a0001c0001t0001g0055 | 3 | HG01243.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3445-1836dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 14893161 | |||||
| chr16:14893284
|
T | C | 2 | a0008c0012t0001g0128a0008c0012t0001g0129 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3445-1714T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893284 | ||||||
| chr16:14893289
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3445-1709G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893289 | ||||||
| chr16:14893552
|
A | G | 1 | a0001c0001t0007g0269 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3445-1446A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893552 | ||||||
| chr16:14893638
|
G | C | 9 | a0001c0008t0001g0108a0003c0003t0001g0016a0003c0003t0001g0017others(6): Show | 9 | HG02071.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3445-1360G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893638 | ||||||
| chr16:14893669
|
C | T | 3 | a0008c0012t0001g0128a0008c0012t0001g0129a0011c0027t0001g0127 | 3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3445-1329C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893669 | ||||||
| chr16:14893923
|
C | G | 2 | a0001c0001t0001g0111a0001c0001t0007g0269 | 2 | HG01433.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3445-1075C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893923 | ||||||
| chr16:14894024
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3445-974T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894024 | ||||||
| chr16:14894064
|
G | A | 1 | a0002c0002t0001g0292 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3445-934G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894064 | ||||||
| chr16:14894096
|
A | T | 1 | a0001c0001t0001g0078 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3445-902A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894096 | ||||||
| chr16:14894324
|
C | A | 1 | a0002c0002t0001g0244 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3445-674C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894324 | ||||||
| chr16:14894391
|
C | G | 4 | a0003c0003t0001g0003a0003c0003t0001g0105a0003c0003t0001g0106others(1): Show | 6 | NA18973.hp2 NA18995.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.3445-607C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894391 | ||||||
| chr16:14894413
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3445-585G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894413 | ||||||
| chr16:14894414
|
G | A | 1 | a0018c0025t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3445-584G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894414 | ||||||
| chr16:14894441
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3445-557C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894441 | ||||||
| chr16:14894511
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3445-487G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894511 | ||||||
| chr16:14894824
|
T | C | 1 | a0001c0001t0008g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3445-174T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894824 | ||||||
| chr16:14894837
|
T | C | 4 | a0002c0002t0001g0092a0002c0002t0001g0240a0002c0002t0001g0243others(1): Show | 4 | NA18985.hp1 NA19004.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.3445-161T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894837 | ||||||
| chr16:14894948
|
G | C | 1 | a0003c0003t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3445-50G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894948 | ||||||
| chr16:14894953
|
T | G | 3 | a0001c0001t0008g0195a0002c0005t0001g0236a0002c0005t0001g0253 | 3 | HG03704.hp2 NA18963.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3445-45T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894953 | ||||||
| chr16:14894955
|
G | T | 3 | a0001c0001t0008g0195a0002c0005t0001g0236a0002c0005t0001g0253 | 3 | HG03704.hp2 NA18963.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3445-43G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894955 | ||||||
| chr16:14895108
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3537+18C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 30/30 | chr16 | 14895108 |