Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 121441 |
|---|---|
| ensemblid | ENSG00000139350.12 |
| hgncid | 7723 |
| symbol | NEDD1 |
| name | NEDD1 gamma-tubulin ring complex targeting factor |
| refseq_nuc | NM_152905.4 |
| refseq_prot | NP_690869.1 |
| ensembl_nuc | ENST00000266742.9 |
| ensembl_prot | ENSP00000266742.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 96907257 |
| end | 96953780 |
| strand | + |
| ver | v1.2 |
| region | chr12:96907257-96953780 |
| region5000 | chr12:96902257-96958780 |
| regionname0 | NEDD1_chr12_96907257_96953780 |
| regionname5000 | NEDD1_chr12_96902257_96958780 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 660 | 394 | 88 | 72 | 183 | 14 | 35 | 143 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0002 | 0/0 | 660 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0003 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0004 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0005 | 0/0 | 660 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0006 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1983 | 387 | 81 | 72 | 183 | 14 | 35 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0002 | 0/0 | 1983 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0003 | 0/0 | 1983 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0004 | 0/0 | 1983 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0005 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0006 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0007 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| c0008 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2033 | 133 | 28 | 22 | 67 | 0 | 15 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0002 | 0/0 | 2033 | 99 | 8 | 26 | 46 | 10 | 9 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0003 | 1/0 | 2033 | 56 | 1 | 11 | 39 | 0 | 4 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0004 | 0/0 | 2034 | 27 | 1 | 5 | 21 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0005 | 0/0 | 2033 | 22 | 5 | 5 | 5 | 4 | 3 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0006 | 0/0 | 2033 | 14 | 12 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0007 | 0/0 | 2034 | 8 | 8 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0008 | 0/0 | 2033 | 6 | 1 | 0 | 0 | 0 | 5 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0009 | 0/0 | 2033 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0010 | 0/0 | 2033 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0011 | 0/0 | 2034 | 5 | 5 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0012 | 0/0 | 2033 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0013 | 0/0 | 2033 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0014 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0015 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0016 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0017 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0018 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0019 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0020 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0021 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0022 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0023 | 0/0 | 2033 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0024 | 0/0 | 2033 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| t0025 | 0/0 | 2033 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0353 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1983 | 387 | 81 | 72 | 183 | 14 | 35 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0002 | 0/0 | 1983 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0006 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0002c0003 | 0/0 | 1983 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0003c0005 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0004c0008 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0005c0004 | 0/0 | 1983 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0006c0007 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4015 | 132 | 28 | 22 | 66 | 0 | 15 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0002 | 0/0 | 4015 | 99 | 8 | 26 | 46 | 10 | 9 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0003 | 1/0 | 4015 | 54 | 1 | 11 | 37 | 0 | 4 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0004 | 0/0 | 4016 | 27 | 1 | 5 | 21 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0005 | 0/0 | 4015 | 22 | 5 | 5 | 5 | 4 | 3 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0006 | 0/0 | 4015 | 13 | 11 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0007 | 0/0 | 4016 | 7 | 7 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0008 | 0/0 | 4015 | 5 | 1 | 0 | 0 | 0 | 4 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0009 | 0/0 | 4015 | 5 | 5 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0011 | 0/0 | 4016 | 5 | 5 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0012 | 0/0 | 4015 | 3 | 0 | 0 | 3 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0013 | 0/0 | 4015 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0014 | 0/0 | 4342 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0015 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0016 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0017 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0018 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0019 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0020 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0021 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0022 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0023 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0024 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0001t0025 | 0/0 | 4015 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0002t0010 | 0/0 | 4015 | 6 | 6 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0001c0006t0006 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0002c0003t0003 | 0/0 | 4015 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0003c0005t0009 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0004c0008t0007 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0005c0004t0008 | 0/0 | 4015 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| a0006c0007t0001 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | copy fasta | chr12 | 96902257 | 96958780 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0002g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0003g0353 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0005g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0006g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0007g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0008g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0009g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0012g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0016g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0017g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0018g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0019g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0020g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0021g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0023g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0024g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0001t0025g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0002t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0001c0006t0006g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0002c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0002c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0003c0005t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0004c0008t0007g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0005c0004t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| a0006c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0362 | EUR | GBR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | GBR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0091 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0355 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0089 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0146 | EUR | FIN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0365 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0318 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0330 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0364 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0319 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01255 | hp1 | a0001 | c0001 | t0025 | g0141 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0357 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | IBS | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01884 | hp1 | a0001 | c0006 | t0006 | g0334 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0169 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0161 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0331 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0329 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0351 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0352 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0252 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CDX | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CDX | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0339 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0048 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0335 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0390 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0317 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02451 | hp2 | a0001 | c0002 | t0010 | g0323 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0332 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0166 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0328 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02622 | hp2 | a0001 | c0001 | t0023 | g0379 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0249 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02895 | hp2 | a0001 | c0002 | t0010 | g0053 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0367 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02897 | hp1 | a0001 | c0002 | t0010 | g0052 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0369 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02922 | hp2 | a0004 | c0008 | t0007 | g0372 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02965 | hp2 | a0001 | c0001 | t0014 | g0017 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0370 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0387 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02976 | hp1 | a0003 | c0005 | t0009 | g0248 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0378 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0368 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0375 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0049 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0380 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0385 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0250 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0383 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03239 | hp2 | a0005 | c0004 | t0008 | g0228 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03453 | hp1 | a0001 | c0002 | t0010 | g0324 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0327 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0251 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0225 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0371 | AFR | ESN | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0333 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03579 | hp1 | a0001 | c0002 | t0010 | g0051 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0057 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03654 | hp1 | a0001 | c0001 | t0008 | g0233 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0366 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0356 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0247 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0299 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | BEB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | STU | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0321 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0384 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0016 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18946 | hp2 | a0001 | c0001 | t0016 | g0042 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0188 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18963 | hp2 | a0001 | c0001 | t0017 | g0306 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18971 | hp1 | a0002 | c0003 | t0003 | g0189 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18974 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0363 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0354 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19064 | hp1 | a0001 | c0001 | t0018 | g0133 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0361 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19067 | hp2 | a0001 | c0001 | t0012 | g0087 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19081 | hp2 | a0001 | c0001 | t0015 | g0063 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19086 | hp2 | a0006 | c0007 | t0001 | g0258 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19089 | hp1 | a0001 | c0001 | t0024 | g0056 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0373 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0382 | AFR | YRI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0386 | AFR | ASW | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20129 | hp2 | a0001 | c0001 | t0022 | g0212 | AFR | ASW | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0358 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0359 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0113 | EUR | TSI | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | GIH | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0360 | SAS | GIH | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02109 | hp1 | a0001 | c0002 | t0010 | g0050 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0381 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0374 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0389 | AFR | ACB | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0388 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0269 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA18955 | hp2 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| NA21309 | hp2 | a0001 | c0001 | t0019 | g0350 | AFR | LWK | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0240 | REF | REF | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0353 | REF | REF | NEDD1_chr12_96902257_96958780 | NEDD1 | chr12 | 96902257 | 96958780 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96920078
|
G | A | 1 | a0003 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.442G>A | p.Val148Ile | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/16 | 747/4015 | 442/1983 | 148/660 | chr12 | 96920078 | ||
| chr12:96943694
|
C | A | 1 | a0006 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.1429C>A | p.Arg477Ser | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/16 | 1734/4015 | 1429/1983 | 477/660 | chr12 | 96943694 | ||
| chr12:96944701
|
C | A | 1 | a0002 | 2 | NA18959.hp2 NA18971.hp1 |
missense_variant | MODERATE | c.1560C>A | p.Asn520Lys | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/16 | 1865/4015 | 1560/1983 | 520/660 | chr12 | 96944701 | ||
| chr12:96945695
|
C | G | 1 | a0004 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.1657C>G | p.Pro553Ala | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/16 | 1962/4015 | 1657/1983 | 553/660 | chr12 | 96945695 | ||
| chr12:96945828
|
A | G | 1 | a0005 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1790A>G | p.Gln597Arg | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/16 | 2095/4015 | 1790/1983 | 597/660 | chr12 | 96945828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96912817
|
G | A | 1 | a0005c0004 | 1 | HG03239.hp2 | splice_region_variant&synonymous_variant | LOW | c.231G>A | p.Gly77Gly | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/16 | 536/4015 | 231/1983 | 77/660 | chr12 | 96912817 | ||
| chr12:96940443
|
T | C | 1 | a0001c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1152T>C | p.Ser384Ser | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/16 | 1457/4015 | 1152/1983 | 384/660 | chr12 | 96940443 | ||
| chr12:96943708
|
T | C | 1 | a0001c0002 | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
synonymous_variant | LOW | c.1443T>C | p.Ala481Ala | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/16 | 1748/4015 | 1443/1983 | 481/660 | chr12 | 96943708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96907296
|
G | T | 1 | a0001c0001t0011 | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-266G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/16 | 2464 | chr12 | 96907296 | |||||
| chr12:96907648
|
C | T | 1 | a0001c0001t0025 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/16 | 2112 | chr12 | 96907648 | |||||
| chr12:96952083
|
A | T | 1 | a0001c0001t0024 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 30 | chr12 | 96952083 | |||||
| chr12:96952177
|
A | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*124A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 124 | chr12 | 96952177 | |||||
| chr12:96952347
|
A | G | 1 | a0001c0002t0010 | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*294A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 294 | chr12 | 96952347 | |||||
| chr12:96952352
|
A | T | 1 | a0001c0001t0023 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 299 | chr12 | 96952352 | |||||
| chr12:96952429
|
G | A | 1 | a0001c0001t0015 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*376G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 376 | chr12 | 96952429 | |||||
| chr12:96952445
|
A | C | 1 | a0001c0001t0022 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*392A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 392 | chr12 | 96952445 | |||||
| chr12:96952501
|
T | C | 2 | a0001c0001t0008a0005c0004t0008 | 6 | HG03239.hp2 HG03490.hp1 HG03654.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 448 | chr12 | 96952501 | |||||
| chr12:96952538
|
C | T | 1 | a0001c0001t0021 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 485 | chr12 | 96952538 | |||||
| chr12:96952642
|
T | C | 1 | a0001c0001t0016 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*589T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 589 | chr12 | 96952642 | |||||
| chr12:96952727
|
A | G | 5 | a0001c0001t0005a0001c0001t0011a0001c0001t0019others(2): Show | 35 | HG00140.hp1 HG00280.hp2 HG01074.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*674A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 674 | chr12 | 96952727 | |||||
| chr12:96952822
|
A | G | 2 | a0001c0001t0009a0003c0005t0009 | 6 | HG01891.hp2 HG02145.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*769A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 769 | chr12 | 96952822 | |||||
| chr12:96952882
|
C | CT | 3 | a0001c0001t0007a0001c0001t0014a0004c0008t0007 | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*834dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 835 | INFO_REALIGN_3_PRIME | chr12 | 96952882 | ||||
| chr12:96953013
|
A | G | 1 | a0001c0001t0018 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*960A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 960 | chr12 | 96953013 | |||||
| chr12:96953146
|
G | A | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(16): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*1093G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1093 | chr12 | 96953146 | |||||
| chr12:96953209
|
T | TA | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0016others(2): Show | 35 | HG01123.hp2 HG01358.hp1 HG01891.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1169dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1170 | INFO_REALIGN_3_PRIME | chr12 | 96953209 | ||||
| chr12:96953216
|
A | C | 2 | a0001c0001t0006a0001c0006t0006 | 14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1163A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1163 | chr12 | 96953216 | |||||
| chr12:96953343
|
T | C | 1 | a0001c0001t0019 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1290 | chr12 | 96953343 | |||||
| chr12:96953407
|
A | G | 1 | a0001c0002t0010 | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1354A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1354 | chr12 | 96953407 | |||||
| chr12:96953524
|
C | A | 1 | a0001c0001t0012 | 3 | NA18955.hp2 NA18974.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1471C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1471 | chr12 | 96953524 | |||||
| chr12:96953536
|
T | TCCTGTTG others(319): Show |
1 | a0001c0001t0014 | 2 | HG02965.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1497_*1498insTTTT others(322): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1498 | INFO_REALIGN_3_PRIME | chr12 | 96953536 | ||||
| chr12:96953583
|
G | T | 1 | a0001c0001t0020 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1530 | chr12 | 96953583 | |||||
| chr12:96953727
|
A | G | 1 | a0001c0001t0013 | 2 | HG02647.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1674A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 16/16 | 1674 | chr12 | 96953727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:96907335
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-262+35C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/15 | chr12 | 96907335 | ||||||
| chr12:96907362
|
G | T | 1 | a0001c0001t0001g0375 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-262+62G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/15 | chr12 | 96907362 | ||||||
| chr12:96907456
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-261-148G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 1/15 | chr12 | 96907456 | ||||||
| chr12:96908203
|
A | G | 1 | a0001c0001t0001g0374 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-9+347A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908203 | ||||||
| chr12:96908255
|
A | G | 1 | a0001c0001t0002g0373 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-9+399A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908255 | ||||||
| chr12:96908420
|
AG | A | 6 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0007g0369others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+566delG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96908420 | |||||
| chr12:96908535
|
T | C | 373 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(370): Show | 383 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(380): Show |
intron_variant | MODIFIER | c.-9+679T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908535 | ||||||
| chr12:96908595
|
T | G | 1 | a0001c0001t0001g0011 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-9+739T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908595 | ||||||
| chr12:96908616
|
G | A | 7 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(4): Show | 7 | HG02965.hp2 HG03098.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+760G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908616 | ||||||
| chr12:96908704
|
T | G | 1 | a0001c0001t0006g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-9+848T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908704 | ||||||
| chr12:96908810
|
G | T | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-8-942G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908810 | ||||||
| chr12:96908849
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-8-903T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908849 | ||||||
| chr12:96908871
|
G | T | 1 | a0001c0001t0002g0347 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-8-881G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908871 | ||||||
| chr12:96908897
|
C | T | 1 | a0001c0001t0001g0346 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-8-855C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908897 | ||||||
| chr12:96908905
|
G | A | 141 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(138): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-8-847G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908905 | ||||||
| chr12:96908947
|
C | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-805C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908947 | ||||||
| chr12:96908966
|
C | T | 1 | a0001c0001t0001g0345 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-786C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96908966 | ||||||
| chr12:96909021
|
A | G | 1 | a0004c0008t0007g0372 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-731A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909021 | ||||||
| chr12:96909142
|
C | T | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG00642.hp2 HG01109.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-610C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909142 | ||||||
| chr12:96909176
|
C | CA | 208 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(205): Show | 213 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.-8-558dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909176 | |||||
| chr12:96909176
|
C | CAA | 9 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0340others(6): Show | 9 | HG00642.hp2 HG01891.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-559_-8-558dupAA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909176 | |||||
| chr12:96909176
|
CA | C | 10 | a0001c0001t0001g0390a0001c0001t0002g0152a0001c0001t0002g0153others(7): Show | 10 | HG01243.hp2 HG01257.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-558delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909176 | |||||
| chr12:96909187
|
A | T | 3 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014 | 3 | HG03098.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-8-565A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909187 | ||||||
| chr12:96909197
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8-555C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909197 | ||||||
| chr12:96909468
|
A | G | 6 | a0001c0001t0005g0316a0001c0001t0005g0317a0001c0001t0005g0318others(3): Show | 6 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-284A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909468 | ||||||
| chr12:96909501
|
A | AG | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-249dupG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 96909501 | |||||
| chr12:96909639
|
T | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18944.hp2 NA18965.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-113T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909639 | ||||||
| chr12:96909744
|
A | G | 138 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 141 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
splice_region_variant&intron_variant | LOW | c.-8-8A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 2/15 | chr12 | 96909744 | ||||||
| chr12:96909904
|
T | TA | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0011g0002others(3): Show | 7 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+21dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96909904 | |||||
| chr12:96909904
|
TA | T | 110 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0002g0001others(107): Show | 113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.136+21delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96909904 | |||||
| chr12:96909913
|
A | C | 5 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(2): Show | 5 | HG00323.hp2 HG01192.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+18A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909913 | ||||||
| chr12:96909915
|
A | C | 12 | a0001c0001t0002g0001a0001c0001t0002g0140a0001c0001t0002g0142others(9): Show | 14 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+20A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909915 | ||||||
| chr12:96909917
|
C | A | 1 | a0001c0001t0006g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.136+22C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909917 | ||||||
| chr12:96909966
|
A | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0338a0001c0001t0001g0376others(14): Show | 18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.136+71A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909966 | ||||||
| chr12:96909970
|
A | C | 1 | a0001c0001t0001g0313 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.136+75A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96909970 | ||||||
| chr12:96910150
|
A | C | 1 | a0001c0001t0002g0139 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.136+255A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910150 | ||||||
| chr12:96910230
|
AAAT | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(209): Show | 218 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.136+339_136+341del others(3): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96910230 | |||||
| chr12:96910241
|
A | G | 7 | a0001c0001t0006g0328a0001c0001t0006g0329a0001c0001t0006g0330others(4): Show | 7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+346A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910241 | ||||||
| chr12:96910353
|
C | T | 248 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 254 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.136+458C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910353 | ||||||
| chr12:96910659
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.136+764G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910659 | ||||||
| chr12:96910686
|
A | G | 106 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(103): Show | 109 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.136+791A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910686 | ||||||
| chr12:96910826
|
C | T | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.136+931C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910826 | ||||||
| chr12:96910934
|
G | A | 4 | a0001c0001t0001g0156a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18944.hp2 NA18965.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1039G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96910934 | ||||||
| chr12:96911273
|
CTT | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.136+1381_136+1382d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96911273 | |||||
| chr12:96911345
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-1378G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911345 | ||||||
| chr12:96911560
|
C | T | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.137-1163C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911560 | ||||||
| chr12:96911776
|
G | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-947G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911776 | ||||||
| chr12:96911802
|
A | G | 4 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0136others(1): Show | 4 | HG00597.hp1 NA18983.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-921A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96911802 | ||||||
| chr12:96912108
|
TTACATTT others(2): Show |
T | 16 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.137-613_137-605del others(9): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 96912108 | |||||
| chr12:96912188
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.137-535G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912188 | ||||||
| chr12:96912247
|
A | G | 2 | a0001c0001t0004g0045a0001c0001t0004g0046 | 2 | NA18954.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.137-476A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912247 | ||||||
| chr12:96912475
|
C | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-248C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912475 | ||||||
| chr12:96912661
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.137-62T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 3/15 | chr12 | 96912661 | ||||||
| chr12:96912825
|
AT | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0376a0001c0001t0001g0377others(4): Show | 7 | HG02976.hp2 HG03041.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+22delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96912825 | |||||
| chr12:96912840
|
A | T | 1 | a0001c0001t0004g0044 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.231+23A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96912840 | ||||||
| chr12:96912848
|
A | T | 7 | a0001c0001t0005g0160a0001c0001t0005g0316a0001c0001t0005g0317others(4): Show | 7 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+31A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96912848 | ||||||
| chr12:96913257
|
A | T | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 140 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.231+440A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913257 | ||||||
| chr12:96913357
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.231+540C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913357 | ||||||
| chr12:96913374
|
C | CT | 27 | a0001c0001t0001g0008a0001c0001t0001g0156a0001c0001t0001g0162others(24): Show | 28 | HG00558.hp2 HG02015.hp1 HG02027.hp2 others(25): Show |
intron_variant | MODIFIER | c.231+569dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96913374 | |||||
| chr12:96913404
|
C | G | 1 | a0001c0001t0005g0366 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.231+587C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913404 | ||||||
| chr12:96913404
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03669.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.231+587C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913404 | ||||||
| chr12:96913452
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.231+635C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913452 | ||||||
| chr12:96913484
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.231+667C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913484 | ||||||
| chr12:96913574
|
A | G | 2 | a0001c0001t0004g0043a0001c0001t0006g0327 | 2 | HG03453.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.231+757A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913574 | ||||||
| chr12:96913589
|
G | A | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.231+772G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913589 | ||||||
| chr12:96913643
|
A | T | 3 | a0001c0001t0007g0015a0001c0001t0014g0016a0001c0001t0014g0017 | 3 | HG02965.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.231+826A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913643 | ||||||
| chr12:96913726
|
C | T | 1 | a0001c0001t0016g0042 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.231+909C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913726 | ||||||
| chr12:96913755
|
ATTTC | A | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.231+942_231+945del others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96913755 | |||||
| chr12:96913808
|
C | CT | 27 | a0001c0001t0001g0290a0001c0001t0004g0021a0001c0001t0004g0024others(24): Show | 27 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.231+1001dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96913808 | |||||
| chr12:96913866
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0310a0001c0001t0001g0311 | 4 | NA18942.hp1 NA19054.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+1049A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913866 | ||||||
| chr12:96913877
|
C | T | 1 | a0001c0001t0005g0366 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.231+1060C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96913877 | ||||||
| chr12:96914204
|
G | T | 1 | a0001c0001t0002g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.231+1387G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914204 | ||||||
| chr12:96914411
|
A | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+1594A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914411 | ||||||
| chr12:96914470
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.231+1653A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914470 | ||||||
| chr12:96914785
|
T | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.231+1968T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914785 | ||||||
| chr12:96914893
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.231+2076T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914893 | ||||||
| chr12:96914957
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.231+2140A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96914957 | ||||||
| chr12:96915113
|
A | C | 2 | a0001c0001t0003g0006a0001c0001t0003g0213 | 3 | NA18968.hp1 NA19064.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.231+2296A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915113 | ||||||
| chr12:96915235
|
C | T | 1 | a0001c0001t0001g0375 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.232-2386C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915235 | ||||||
| chr12:96915273
|
C | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.232-2348C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915273 | ||||||
| chr12:96915901
|
T | C | 1 | a0001c0001t0004g0059 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.232-1720T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96915901 | ||||||
| chr12:96916084
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.232-1537T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916084 | ||||||
| chr12:96916127
|
G | A | 1 | a0001c0001t0021g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.232-1494G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916127 | ||||||
| chr12:96916170
|
C | G | 1 | a0001c0001t0001g0313 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.232-1451C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916170 | ||||||
| chr12:96916230
|
T | TTTA | 95 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(92): Show | 96 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.232-1361_232-1359d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | |||||
| chr12:96916230
|
T | TTTATTA | 74 | a0001c0001t0001g0008a0001c0001t0001g0156a0001c0001t0001g0163others(71): Show | 76 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.232-1364_232-1359d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | |||||
| chr12:96916230
|
T | TTTATTAT others(2): Show |
30 | a0001c0001t0001g0162a0001c0001t0001g0183a0001c0001t0001g0184others(27): Show | 32 | HG00621.hp1 HG01952.hp2 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.232-1367_232-1359d others(11): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | |||||
| chr12:96916230
|
T | TTTATTAT others(5): Show |
6 | a0001c0001t0001g0340a0001c0001t0001g0343a0001c0001t0001g0344others(3): Show | 6 | HG00642.hp2 HG01261.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-1370_232-1359d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | |||||
| chr12:96916230
|
TTTA | T | 14 | a0001c0001t0002g0054a0001c0001t0002g0129a0001c0001t0002g0130others(11): Show | 14 | HG01106.hp1 HG01515.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.232-1361_232-1359d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916230 | |||||
| chr12:96916262
|
T | TATTATTA others(3): Show |
1 | a0001c0001t0001g0342 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.232-1359_232-1358i others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916262 | ||||||
| chr12:96916263
|
T | A | 1 | a0001c0001t0023g0379 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.232-1358T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916263 | ||||||
| chr12:96916302
|
T | C | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.232-1319T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916302 | ||||||
| chr12:96916321
|
C | T | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.232-1300C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916321 | ||||||
| chr12:96916322
|
G | A | 1 | a0001c0001t0008g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.232-1299G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916322 | ||||||
| chr12:96916389
|
A | G | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.232-1232A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916389 | ||||||
| chr12:96916476
|
A | G | 2 | a0002c0003t0003g0188a0002c0003t0003g0189 | 2 | NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.232-1145A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916476 | ||||||
| chr12:96916492
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.232-1129G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916492 | ||||||
| chr12:96916534
|
C | T | 1 | a0004c0008t0007g0372 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.232-1087C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916534 | ||||||
| chr12:96916582
|
A | G | 2 | a0001c0002t0010g0052a0001c0002t0010g0053 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.232-1039A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916582 | ||||||
| chr12:96916613
|
C | G | 3 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0315 | 3 | HG00423.hp1 NA18971.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.232-1008C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916613 | ||||||
| chr12:96916705
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.232-916G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916705 | ||||||
| chr12:96916774
|
CATG | C | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-844_232-842del others(3): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96916774 | |||||
| chr12:96916975
|
G | T | 1 | a0001c0001t0007g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.232-646G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96916975 | ||||||
| chr12:96917053
|
A | T | 3 | a0001c0001t0003g0185a0001c0001t0003g0186a0001c0001t0003g0187 | 3 | NA18950.hp2 NA18995.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.232-568A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96917053 | ||||||
| chr12:96917380
|
T | C | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.232-241T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96917380 | ||||||
| chr12:96917485
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.232-136T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | chr12 | 96917485 | ||||||
| chr12:96917598
|
CT | C | 244 | a0001c0001t0001g0009a0001c0001t0001g0162a0001c0001t0001g0163others(241): Show | 252 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(249): Show |
splice_region_variant&intron_variant | LOW | c.232-7delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 96917598 | |||||
| chr12:96917763
|
T | C | 237 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(234): Show | 243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.348+26T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917763 | ||||||
| chr12:96917781
|
A | G | 2 | a0001c0001t0002g0137a0001c0001t0002g0138 | 2 | HG01433.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.348+44A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917781 | ||||||
| chr12:96917806
|
T | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+69T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917806 | ||||||
| chr12:96917837
|
G | C | 1 | a0001c0001t0004g0024 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.348+100G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917837 | ||||||
| chr12:96917863
|
G | A | 25 | a0001c0001t0003g0004a0001c0001t0003g0005a0001c0001t0003g0157others(22): Show | 27 | HG00621.hp1 HG01952.hp2 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.348+126G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96917863 | ||||||
| chr12:96918043
|
C | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.348+306C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918043 | ||||||
| chr12:96918177
|
T | G | 27 | a0001c0001t0001g0227a0001c0001t0004g0021a0001c0001t0004g0024others(24): Show | 27 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.348+440T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918177 | ||||||
| chr12:96918179
|
G | T | 1 | a0001c0001t0006g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.348+442G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918179 | ||||||
| chr12:96918203
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.348+466C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918203 | ||||||
| chr12:96918401
|
TAATATGA others(2): Show |
T | 210 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(207): Show | 216 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.348+670_348+678del others(9): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 96918401 | |||||
| chr12:96918500
|
G | A | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.348+763G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918500 | ||||||
| chr12:96918512
|
T | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.348+775T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918512 | ||||||
| chr12:96918556
|
G | A | 1 | a0005c0004t0008g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.348+819G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918556 | ||||||
| chr12:96918699
|
A | G | 24 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0027others(21): Show | 24 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.348+962A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918699 | ||||||
| chr12:96918786
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.348+1049T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918786 | ||||||
| chr12:96918805
|
T | C | 6 | a0001c0002t0010g0050a0001c0002t0010g0051a0001c0002t0010g0052others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+1068T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918805 | ||||||
| chr12:96918851
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(13): Show | 17 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1114C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96918851 | ||||||
| chr12:96919169
|
C | T | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-816C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919169 | ||||||
| chr12:96919266
|
G | T | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-719G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919266 | ||||||
| chr12:96919310
|
T | TA | 8 | a0001c0001t0005g0160a0001c0001t0005g0316a0001c0001t0005g0317others(5): Show | 8 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-674dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr12 | 96919310 | |||||
| chr12:96919473
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.349-512C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919473 | ||||||
| chr12:96919557
|
T | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0338a0001c0001t0001g0376others(14): Show | 18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-428T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919557 | ||||||
| chr12:96919753
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.349-232T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919753 | ||||||
| chr12:96919808
|
C | T | 2 | a0001c0001t0001g0378a0001c0001t0001g0389 | 2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.349-177C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919808 | ||||||
| chr12:96919809
|
G | A | 1 | a0001c0001t0015g0063 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.349-176G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 5/15 | chr12 | 96919809 | ||||||
| chr12:96920191
|
C | T | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0007g0369others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+66C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920191 | ||||||
| chr12:96920223
|
A | G | 98 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0003others(95): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.489+98A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920223 | ||||||
| chr12:96920306
|
A | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+181A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920306 | ||||||
| chr12:96920395
|
A | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+270A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920395 | ||||||
| chr12:96920571
|
A | G | 237 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(234): Show | 243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.489+446A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920571 | ||||||
| chr12:96920636
|
T | C | 1 | a0001c0001t0006g0329 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.489+511T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920636 | ||||||
| chr12:96920855
|
A | G | 1 | a0001c0001t0003g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.489+730A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96920855 | ||||||
| chr12:96920924
|
CTT | C | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+804_489+805del others(2): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96920924 | |||||
| chr12:96921047
|
T | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0338a0001c0001t0001g0376others(14): Show | 18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+922T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921047 | ||||||
| chr12:96921467
|
C | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+1342C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921467 | ||||||
| chr12:96921533
|
C | G | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.489+1408C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921533 | ||||||
| chr12:96921662
|
A | ATT | 198 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 204 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.489+1547_489+1548d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921662 | |||||
| chr12:96921662
|
A | ATTT | 13 | a0001c0001t0001g0010a0001c0001t0001g0217a0001c0001t0006g0012others(10): Show | 13 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+1546_489+1548d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921662 | |||||
| chr12:96921775
|
A | AT | 118 | a0001c0001t0001g0167a0001c0001t0001g0283a0001c0001t0001g0313others(115): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.489+1667dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921775 | |||||
| chr12:96921775
|
AT | A | 60 | a0001c0001t0001g0164a0001c0001t0001g0183a0001c0001t0001g0184others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.489+1667delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96921775 | |||||
| chr12:96921873
|
C | G | 13 | a0001c0001t0003g0006a0001c0001t0003g0168a0001c0001t0003g0202others(10): Show | 14 | HG00423.hp2 HG00558.hp1 NA18946.hp1 others(11): Show |
intron_variant | MODIFIER | c.489+1748C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96921873 | ||||||
| chr12:96922079
|
G | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.489+1954G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922079 | ||||||
| chr12:96922308
|
A | AG | 237 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(234): Show | 243 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.489+2184dupG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96922308 | |||||
| chr12:96922315
|
C | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.489+2190C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922315 | ||||||
| chr12:96922384
|
A | C | 1 | a0001c0001t0021g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.489+2259A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922384 | ||||||
| chr12:96922396
|
T | A | 1 | a0001c0001t0007g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489+2271T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922396 | ||||||
| chr12:96922503
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+2378A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922503 | ||||||
| chr12:96922681
|
C | G | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.489+2556C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922681 | ||||||
| chr12:96922730
|
G | A | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.489+2605G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922730 | ||||||
| chr12:96922845
|
C | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0126 | 2 | NA18960.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.489+2720C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96922845 | ||||||
| chr12:96923121
|
GA | G | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.489+3006delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923121 | |||||
| chr12:96923134
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489+3009A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923134 | ||||||
| chr12:96923186
|
G | A | 3 | a0001c0001t0007g0015a0001c0001t0014g0016a0001c0001t0014g0017 | 3 | HG02965.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+3061G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923186 | ||||||
| chr12:96923214
|
A | C | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+3089A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923214 | ||||||
| chr12:96923214
|
A | G | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18942.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.489+3089A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923214 | ||||||
| chr12:96923314
|
T | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.489+3189T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923314 | ||||||
| chr12:96923315
|
G | A | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+3190G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923315 | ||||||
| chr12:96923349
|
CAT | C | 61 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(58): Show | 64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.489+3225_489+3226d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923349 | ||||||
| chr12:96923358
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3233A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923358 | ||||||
| chr12:96923552
|
G | T | 4 | a0001c0001t0001g0162a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | NA18963.hp2 NA18983.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+3427G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923552 | ||||||
| chr12:96923594
|
T | A | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.489+3469T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923594 | ||||||
| chr12:96923657
|
G | T | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+3532G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923657 | ||||||
| chr12:96923663
|
T | C | 1 | a0001c0001t0001g0390 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+3538T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923663 | ||||||
| chr12:96923669
|
G | A | 62 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0227others(59): Show | 65 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.489+3544G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923669 | ||||||
| chr12:96923699
|
T | C | 1 | a0001c0001t0006g0012 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+3574T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923699 | ||||||
| chr12:96923780
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3655A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923780 | ||||||
| chr12:96923784
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0002g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.489+3662_489+3663i others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923784 | |||||
| chr12:96923787
|
TTTGTGTG others(4): Show |
T | 1 | a0001c0001t0001g0322 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.489+3664_489+3674d others(13): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923787 | |||||
| chr12:96923788
|
T | G | 1 | a0001c0001t0002g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.489+3663T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923788 | ||||||
| chr12:96923788
|
T | TGTGTGTG others(6): Show |
2 | a0001c0001t0002g0065a0001c0001t0002g0088 | 2 | NA18949.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.489+3663_489+3664i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923788 | ||||||
| chr12:96923788
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0002g0022 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.489+3663_489+3664i others(17): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923788 | ||||||
| chr12:96923788
|
T | TTG | 13 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0037others(10): Show | 13 | HG00140.hp1 HG01074.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+3704_489+3705d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTG | 7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0137others(4): Show | 7 | HG00280.hp1 HG01433.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+3702_489+3705d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTGTG | 20 | a0001c0001t0002g0003a0001c0001t0002g0066a0001c0001t0002g0067others(17): Show | 21 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.489+3700_489+3705d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTGTGT others(1): Show |
13 | a0001c0001t0002g0054a0001c0001t0002g0068a0001c0001t0002g0069others(10): Show | 13 | HG00408.hp1 HG00438.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+3698_489+3705d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTGTGT others(3): Show |
26 | a0001c0001t0002g0020a0001c0001t0002g0055a0001c0001t0002g0062others(23): Show | 26 | HG00323.hp2 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+3696_489+3705d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTGTGT others(5): Show |
23 | a0001c0001t0002g0023a0001c0001t0002g0061a0001c0001t0002g0075others(20): Show | 23 | HG00621.hp2 HG00673.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.489+3694_489+3705d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTGTGT others(7): Show |
10 | a0001c0001t0002g0001a0001c0001t0002g0082a0001c0001t0002g0083others(7): Show | 12 | HG00140.hp2 HG01123.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+3692_489+3705d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0002g0136a0001c0001t0012g0087 | 2 | HG00597.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.489+3690_489+3705d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTG | T | 10 | a0001c0001t0002g0152a0001c0001t0004g0027a0001c0001t0004g0028others(7): Show | 10 | HG01123.hp2 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+3704_489+3705d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTG | T | 8 | a0001c0001t0004g0043a0001c0001t0004g0045a0001c0001t0014g0017others(5): Show | 8 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3702_489+3705d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTGTG | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0007g0015 | 3 | HG02723.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.489+3700_489+3705d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTGTGT others(1): Show |
T | 9 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0279others(6): Show | 9 | HG00408.hp2 HG02698.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+3698_489+3705d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTGTGT others(3): Show |
T | 97 | a0001c0001t0001g0010a0001c0001t0001g0165a0001c0001t0001g0223others(94): Show | 100 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.489+3696_489+3705d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTGTGT others(5): Show |
T | 88 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(85): Show | 91 | HG00558.hp2 HG01070.hp1 HG01099.hp2 others(88): Show |
intron_variant | MODIFIER | c.489+3694_489+3705d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTGTGT others(7): Show |
T | 5 | a0001c0001t0001g0007a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 6 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+3692_489+3705d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923788
|
TTGTGTGT others(9): Show |
T | 13 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(10): Show | 13 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.489+3690_489+3705d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96923788 | |||||
| chr12:96923850
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.489+3725G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923850 | ||||||
| chr12:96923995
|
C | A | 5 | a0001c0001t0001g0377a0001c0001t0001g0381a0001c0001t0001g0382others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3870C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96923995 | ||||||
| chr12:96924207
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0075 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.489+4082G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924207 | ||||||
| chr12:96924334
|
T | G | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0007g0369others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+4209T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924334 | ||||||
| chr12:96924607
|
T | A | 1 | a0001c0001t0004g0045 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.489+4482T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924607 | ||||||
| chr12:96924874
|
A | G | 2 | a0001c0001t0001g0376a0001c0001t0001g0380 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.489+4749A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924874 | ||||||
| chr12:96924924
|
G | A | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+4799G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924924 | ||||||
| chr12:96924942
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489+4817G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96924942 | ||||||
| chr12:96925136
|
G | A | 6 | a0001c0001t0001g0340a0001c0001t0001g0343a0001c0001t0011g0002others(3): Show | 7 | HG00642.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5011G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925136 | ||||||
| chr12:96925462
|
C | T | 1 | a0001c0001t0009g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+5337C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925462 | ||||||
| chr12:96925505
|
C | G | 18 | a0001c0001t0002g0003a0001c0001t0002g0090a0001c0001t0002g0092others(15): Show | 19 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.489+5380C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925505 | ||||||
| chr12:96925546
|
A | G | 2 | a0001c0002t0010g0052a0001c0002t0010g0053 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+5421A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925546 | ||||||
| chr12:96925658
|
C | T | 1 | a0001c0001t0005g0316 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.489+5533C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925658 | ||||||
| chr12:96925660
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0234 | 3 | HG01257.hp1 HG01258.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.489+5535A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925660 | ||||||
| chr12:96925909
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+5784A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96925909 | ||||||
| chr12:96926031
|
A | AT | 7 | a0001c0001t0002g0373a0001c0001t0007g0367a0001c0001t0007g0368others(4): Show | 7 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5917dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926031 | |||||
| chr12:96926031
|
A | ATT | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+5916_489+5917d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926031 | |||||
| chr12:96926353
|
A | G | 201 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(198): Show | 207 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.489+6228A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926353 | ||||||
| chr12:96926385
|
C | A | 1 | a0001c0001t0002g0068 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.489+6260C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926385 | ||||||
| chr12:96926550
|
AT | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+6439delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926550 | |||||
| chr12:96926604
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+6479T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926604 | ||||||
| chr12:96926709
|
G | A | 1 | a0001c0001t0005g0360 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.489+6584G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926709 | ||||||
| chr12:96926960
|
C | A | 1 | a0001c0001t0004g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.489+6835C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926960 | ||||||
| chr12:96926987
|
A | AATT | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+6862_489+6863i others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926987 | ||||||
| chr12:96926988
|
T | A | 4 | a0001c0001t0002g0076a0001c0001t0002g0145a0001c0001t0003g0193others(1): Show | 4 | HG01168.hp1 HG01884.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6863T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926988 | ||||||
| chr12:96926988
|
T | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+6863T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926988 | ||||||
| chr12:96926988
|
TTG | T | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(313): Show | 326 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.489+6883_489+6884d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96926988 | |||||
| chr12:96926989
|
TG | T | 4 | a0001c0001t0002g0076a0001c0001t0002g0145a0001c0001t0003g0193others(1): Show | 4 | HG01168.hp1 HG01884.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+6865delG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926989 | ||||||
| chr12:96926994
|
G | A | 15 | a0001c0001t0001g0226a0001c0001t0001g0229a0001c0001t0001g0232others(12): Show | 15 | HG01070.hp1 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+6869G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96926994 | ||||||
| chr12:96927101
|
C | G | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+6976C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927101 | ||||||
| chr12:96927143
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.489+7018A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927143 | ||||||
| chr12:96927293
|
G | A | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.489+7168G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927293 | ||||||
| chr12:96927405
|
A | G | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0007g0369others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+7280A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927405 | ||||||
| chr12:96927433
|
C | T | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.489+7308C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927433 | ||||||
| chr12:96927908
|
G | A | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.490-7068G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96927908 | ||||||
| chr12:96928129
|
A | T | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 217 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.490-6847A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928129 | ||||||
| chr12:96928141
|
A | G | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-6835A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928141 | ||||||
| chr12:96928179
|
T | C | 5 | a0001c0001t0002g0001a0001c0001t0002g0109a0001c0001t0002g0110others(2): Show | 7 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-6797T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928179 | ||||||
| chr12:96928281
|
T | C | 1 | a0001c0001t0008g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490-6695T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928281 | ||||||
| chr12:96928292
|
A | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-6684A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928292 | ||||||
| chr12:96928305
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-6671A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928305 | ||||||
| chr12:96928402
|
C | G | 1 | a0001c0001t0004g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.490-6574C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928402 | ||||||
| chr12:96928612
|
G | A | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-6364G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928612 | ||||||
| chr12:96928681
|
C | CT | 22 | a0001c0001t0001g0341a0001c0001t0002g0022a0001c0001t0002g0055others(19): Show | 22 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.490-6272dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96928681 | |||||
| chr12:96928681
|
C | CTT | 21 | a0001c0001t0004g0021a0001c0001t0004g0025a0001c0001t0004g0026others(18): Show | 21 | HG01934.hp1 HG01975.hp2 NA18612.hp2 others(18): Show |
intron_variant | MODIFIER | c.490-6273_490-6272d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96928681 | |||||
| chr12:96928681
|
CT | C | 143 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 146 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.490-6272delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96928681 | |||||
| chr12:96928776
|
T | A | 1 | a0001c0001t0021g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-6200T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928776 | ||||||
| chr12:96928926
|
G | A | 93 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(90): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.490-6050G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928926 | ||||||
| chr12:96928969
|
C | T | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(116): Show | 121 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.490-6007C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96928969 | ||||||
| chr12:96929341
|
T | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-5635T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929341 | ||||||
| chr12:96929341
|
TCTTAATG others(18): Show |
T | 233 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(230): Show | 239 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.490-5609_490-5585d others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929341 | |||||
| chr12:96929356
|
TTTTTTTT others(17): Show |
T | 14 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.490-5610_490-5587d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929356 | |||||
| chr12:96929465
|
T | C | 4 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196others(1): Show | 4 | HG00642.hp1 HG01255.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5511T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929465 | ||||||
| chr12:96929556
|
T | TAC | 47 | a0001c0001t0002g0020a0001c0001t0002g0023a0001c0001t0002g0062others(44): Show | 47 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.490-5376_490-5375d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
T | TACAC | 15 | a0001c0001t0002g0001a0001c0001t0002g0055a0001c0001t0002g0065others(12): Show | 17 | HG01123.hp1 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-5378_490-5375d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TAC | T | 17 | a0001c0001t0001g0167a0001c0001t0001g0390a0001c0001t0002g0085others(14): Show | 17 | HG00438.hp1 HG01069.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.490-5376_490-5375d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACAC | T | 11 | a0001c0001t0001g0389a0001c0001t0002g0066a0001c0001t0002g0086others(8): Show | 11 | HG01261.hp2 HG02004.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-5378_490-5375d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACAC | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(15): Show | 20 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-5380_490-5375d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACACA others(1): Show |
T | 17 | a0001c0001t0001g0386a0001c0001t0003g0198a0001c0001t0003g0215others(14): Show | 17 | HG00741.hp1 HG01081.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-5382_490-5375d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACACA others(3): Show |
T | 18 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(15): Show | 18 | HG00642.hp2 HG01106.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.490-5384_490-5375d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACACA others(5): Show |
T | 4 | a0001c0001t0001g0338a0001c0001t0006g0014a0001c0001t0007g0015others(1): Show | 4 | HG03195.hp2 HG03239.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-5386_490-5375d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACACA others(7): Show |
T | 190 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(187): Show | 195 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.490-5388_490-5375d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACACA others(9): Show |
T | 14 | a0001c0001t0001g0217a0001c0001t0001g0224a0001c0001t0001g0227others(11): Show | 14 | HG02258.hp1 HG02622.hp2 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.490-5390_490-5375d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929556
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.490-5392_490-5375d others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929556 | |||||
| chr12:96929594
|
C | T | 1 | a0001c0001t0001g0390 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-5382C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929594 | ||||||
| chr12:96929596
|
C | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(14): Show | 18 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-5380C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929596 | ||||||
| chr12:96929597
|
A | G | 1 | a0001c0001t0001g0390 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-5379A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929597 | ||||||
| chr12:96929598
|
C | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0183a0001c0001t0001g0184others(16): Show | 20 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.490-5378C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929598 | ||||||
| chr12:96929599
|
A | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(14): Show | 18 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-5377A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929599 | ||||||
| chr12:96929600
|
C | T | 163 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(160): Show | 167 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.490-5376C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929600 | ||||||
| chr12:96929601
|
A | G | 18 | a0001c0001t0001g0009a0001c0001t0001g0183a0001c0001t0001g0184others(15): Show | 19 | HG00741.hp1 HG02109.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-5375A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929601 | ||||||
| chr12:96929603
|
A | G | 150 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(147): Show | 153 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.490-5373A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929603 | ||||||
| chr12:96929605
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0377others(14): Show | 18 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-5371G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929605 | ||||||
| chr12:96929607
|
G | A | 141 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(138): Show | 145 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.490-5369G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929607 | ||||||
| chr12:96929607
|
G | GTA | 85 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0022others(82): Show | 86 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.490-5353_490-5352d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929607 | |||||
| chr12:96929607
|
G | GTATA | 59 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0340others(56): Show | 64 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.490-5355_490-5352d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929607 | |||||
| chr12:96929622
|
TA | T | 7 | a0001c0001t0005g0160a0001c0001t0005g0316a0001c0001t0005g0317others(4): Show | 7 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-5353delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929622 | ||||||
| chr12:96929623
|
A | AT | 6 | a0001c0001t0007g0018a0001c0001t0007g0367a0001c0001t0007g0368others(3): Show | 6 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-5343dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | |||||
| chr12:96929623
|
A | ATATTT | 7 | a0001c0001t0006g0328a0001c0001t0006g0329a0001c0001t0006g0330others(4): Show | 7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-5352_490-5351i others(7): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | |||||
| chr12:96929623
|
A | ATT | 6 | a0001c0001t0001g0217a0001c0001t0002g0054a0001c0001t0002g0145others(3): Show | 6 | HG00323.hp2 HG01192.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-5344_490-5343d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | |||||
| chr12:96929623
|
A | T | 2 | a0001c0001t0014g0016a0001c0001t0014g0017 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-5353A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929623 | ||||||
| chr12:96929623
|
AT | A | 25 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0026others(22): Show | 25 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-5343delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96929623 | |||||
| chr12:96929624
|
T | TA | 6 | a0001c0001t0001g0224a0001c0001t0001g0274a0001c0001t0004g0021others(3): Show | 6 | HG02738.hp1 HG02922.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-5352_490-5351i others(3): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929624 | ||||||
| chr12:96929625
|
T | A | 171 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(168): Show | 176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.490-5351T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929625 | ||||||
| chr12:96929626
|
T | A | 2 | a0001c0001t0001g0293a0001c0001t0004g0025 | 2 | HG03669.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.490-5350T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929626 | ||||||
| chr12:96929627
|
T | A | 9 | a0001c0001t0001g0167a0001c0001t0002g0001a0001c0001t0002g0109others(6): Show | 11 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-5349T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929627 | ||||||
| chr12:96929647
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-5329T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929647 | ||||||
| chr12:96929723
|
G | A | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-5253G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929723 | ||||||
| chr12:96929771
|
GGACACAC | G | 11 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(8): Show | 11 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-5204_490-5198d others(9): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929771 | ||||||
| chr12:96929781
|
TGGC | T | 11 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(8): Show | 11 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-5194_490-5192d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929781 | ||||||
| chr12:96929946
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0235a0001c0001t0001g0236others(8): Show | 11 | HG01109.hp1 HG01167.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-5030C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96929946 | ||||||
| chr12:96930156
|
AAC | A | 7 | a0001c0001t0001g0167a0001c0001t0005g0316a0001c0001t0005g0317others(4): Show | 7 | HG00140.hp1 HG00280.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-4765_490-4764d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACAC | A | 4 | a0001c0001t0002g0145a0001c0001t0005g0318a0001c0001t0005g0319others(1): Show | 4 | HG01081.hp2 HG01192.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4767_490-4764d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACAC | A | 4 | a0001c0001t0002g0144a0001c0001t0005g0160a0001c0001t0011g0049others(1): Show | 4 | HG01515.hp2 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4769_490-4764d others(8): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(1): Show |
A | 8 | a0001c0001t0002g0065a0001c0001t0002g0095a0001c0001t0002g0104others(5): Show | 8 | HG02148.hp1 HG02922.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-4771_490-4764d others(10): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(3): Show |
A | 31 | a0001c0001t0001g0338a0001c0001t0002g0003a0001c0001t0002g0066others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-4773_490-4764d others(12): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(5): Show |
A | 32 | a0001c0001t0001g0278a0001c0001t0002g0020a0001c0001t0002g0023others(29): Show | 32 | HG00323.hp1 HG00673.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-4775_490-4764d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(7): Show |
A | 39 | a0001c0001t0001g0162a0001c0001t0001g0237a0001c0001t0001g0257others(36): Show | 41 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.490-4777_490-4764d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(9): Show |
A | 19 | a0001c0001t0001g0011a0001c0001t0001g0230a0001c0001t0001g0235others(16): Show | 19 | HG01069.hp2 HG01167.hp1 HG02004.hp1 others(16): Show |
intron_variant | MODIFIER | c.490-4779_490-4764d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(11): Show |
A | 28 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0216others(25): Show | 29 | HG00408.hp2 HG00738.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.490-4781_490-4764d others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(13): Show |
A | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(59): Show | 64 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.490-4783_490-4764d others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(15): Show |
A | 13 | a0001c0001t0001g0217a0001c0001t0001g0234a0001c0001t0001g0239others(10): Show | 13 | HG01975.hp1 HG01978.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.490-4785_490-4764d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930156
|
AACACACA others(17): Show |
A | 58 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0253others(55): Show | 60 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.490-4787_490-4764d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930156 | |||||
| chr12:96930179
|
ACACACAC others(33): Show |
A | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-4795_490-4756d others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930179 | |||||
| chr12:96930183
|
ACACACAC others(23): Show |
A | 1 | a0001c0001t0023g0379 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.490-4791_490-4762d others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930183 | |||||
| chr12:96930185
|
ACACACAC others(33): Show |
A | 25 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(22): Show | 25 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-4789_490-4750d others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930185 | |||||
| chr12:96930186
|
CACACACA others(12): Show |
C | 1 | a0001c0001t0001g0260 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-4789_490-4771d others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930186 | ||||||
| chr12:96930187
|
ACACACAC others(19): Show |
A | 3 | a0001c0001t0001g0377a0001c0001t0001g0381a0001c0001t0001g0382 | 3 | HG02109.hp2 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-4787_490-4762d others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930187 | |||||
| chr12:96930187
|
ACACACAC others(21): Show |
A | 2 | a0001c0001t0006g0332a0002c0003t0003g0188 | 2 | HG02572.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.490-4787_490-4760d others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930187 | |||||
| chr12:96930187
|
ACACACAC others(31): Show |
A | 1 | a0001c0001t0004g0041 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.490-4787_490-4750d others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930187 | |||||
| chr12:96930189
|
ACACACAC others(17): Show |
A | 7 | a0001c0001t0001g0009a0001c0001t0001g0376a0001c0001t0001g0378others(4): Show | 8 | HG00741.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-4785_490-4762d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930189 | |||||
| chr12:96930189
|
ACACACAC others(19): Show |
A | 4 | a0001c0001t0001g0388a0001c0001t0006g0330a0001c0001t0006g0331others(1): Show | 4 | HG01106.hp1 HG01928.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-4785_490-4760d others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930189 | |||||
| chr12:96930189
|
ACACACAC others(21): Show |
A | 1 | a0001c0001t0006g0329 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-4785_490-4758d others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930189 | |||||
| chr12:96930191
|
ACACACAC others(15): Show |
A | 1 | a0001c0001t0006g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.490-4783_490-4762d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930191 | |||||
| chr12:96930191
|
ACACACAC others(19): Show |
A | 4 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(1): Show | 4 | HG02280.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-4783_490-4758d others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930191 | |||||
| chr12:96930191
|
ACACACAC others(21): Show |
A | 1 | a0001c0006t0006g0334 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-4783_490-4756d others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930191 | |||||
| chr12:96930193
|
A | T | 2 | a0001c0001t0002g0074a0001c0001t0007g0018 | 2 | NA18747.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.490-4783A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930193 | ||||||
| chr12:96930193
|
ACACACAC others(15): Show |
A | 1 | a0001c0001t0006g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.490-4781_490-4760d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930193 | |||||
| chr12:96930195
|
A | T | 1 | a0001c0001t0007g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-4781A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930195 | ||||||
| chr12:96930195
|
ACACACAC others(13): Show |
A | 1 | a0001c0001t0006g0328 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.490-4779_490-4760d others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930195 | |||||
| chr12:96930195
|
ACACACAC others(15): Show |
A | 2 | a0001c0001t0007g0370a0001c0001t0007g0371 | 2 | HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.490-4779_490-4758d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930195 | |||||
| chr12:96930197
|
A | T | 2 | a0001c0001t0014g0016a0001c0001t0014g0017 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-4779A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930197 | ||||||
| chr12:96930197
|
ACACACAC others(9): Show |
A | 2 | a0001c0001t0002g0153a0001c0002t0010g0051 | 2 | HG01257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-4777_490-4762d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930197 | |||||
| chr12:96930197
|
ACACACAC others(11): Show |
A | 1 | a0001c0001t0002g0115 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.490-4777_490-4760d others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930197 | |||||
| chr12:96930197
|
ACACACAC others(17): Show |
A | 1 | a0001c0001t0007g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-4777_490-4754d others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930197 | |||||
| chr12:96930199
|
A | T | 3 | a0001c0001t0001g0278a0001c0001t0008g0233a0001c0001t0009g0161 | 3 | HG01891.hp2 HG03654.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.490-4777A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930199 | ||||||
| chr12:96930199
|
ACACACAC others(9): Show |
A | 1 | a0001c0001t0002g0083 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.490-4775_490-4760d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930199 | |||||
| chr12:96930199
|
ACACACAC others(15): Show |
A | 2 | a0001c0001t0007g0015a0001c0002t0010g0323 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.490-4775_490-4754d others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930199 | |||||
| chr12:96930201
|
A | T | 10 | a0001c0001t0001g0162a0001c0001t0001g0237a0001c0001t0001g0257others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-4775A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930201 | ||||||
| chr12:96930201
|
ACACACAC others(5): Show |
A | 1 | a0001c0001t0002g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.490-4773_490-4762d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | |||||
| chr12:96930201
|
ACACACAC others(7): Show |
A | 1 | a0001c0001t0007g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-4773_490-4760d others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | |||||
| chr12:96930201
|
ACACACAC others(9): Show |
A | 2 | a0001c0001t0007g0367a0001c0001t0007g0369 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.490-4773_490-4758d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | |||||
| chr12:96930201
|
ACACACAC others(13): Show |
A | 2 | a0001c0001t0014g0016a0001c0001t0014g0017 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-4773_490-4754d others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930201 | |||||
| chr12:96930203
|
A | T | 25 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0230others(22): Show | 25 | HG01099.hp2 HG01109.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.490-4773A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930203 | ||||||
| chr12:96930205
|
A | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0165others(38): Show | 41 | HG00408.hp2 HG01099.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.490-4771A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930205 | ||||||
| chr12:96930207
|
A | T | 114 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(111): Show | 117 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.490-4769A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930207 | ||||||
| chr12:96930209
|
A | ACT | 3 | a0001c0001t0011g0047a0001c0001t0011g0048a0001c0001t0020g0166 | 3 | HG01891.hp1 HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.490-4766_490-4765i others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930209 | |||||
| chr12:96930209
|
A | T | 131 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(128): Show | 134 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.490-4767A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930209 | ||||||
| chr12:96930209
|
ACACTCTC others(5): Show |
A | 1 | a0001c0002t0010g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.490-4765_490-4754d others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96930209 | |||||
| chr12:96930211
|
A | T | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(175): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.490-4765A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930211 | ||||||
| chr12:96930243
|
T | A | 28 | a0001c0001t0001g0235a0001c0001t0004g0021a0001c0001t0004g0024others(25): Show | 28 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.490-4733T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930243 | ||||||
| chr12:96930245
|
A | T | 1 | a0001c0001t0001g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.490-4731A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930245 | ||||||
| chr12:96930557
|
G | A | 2 | a0001c0002t0010g0050a0001c0002t0010g0051 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.490-4419G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930557 | ||||||
| chr12:96930557
|
G | C | 1 | a0001c0001t0003g0186 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.490-4419G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930557 | ||||||
| chr12:96930633
|
C | T | 1 | a0001c0001t0008g0233 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.490-4343C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930633 | ||||||
| chr12:96930700
|
G | A | 93 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(90): Show | 96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.490-4276G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930700 | ||||||
| chr12:96930784
|
A | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-4192A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930784 | ||||||
| chr12:96930848
|
A | G | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(244): Show | 253 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(250): Show |
intron_variant | MODIFIER | c.490-4128A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930848 | ||||||
| chr12:96930960
|
A | G | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.490-4016A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930960 | ||||||
| chr12:96930981
|
T | C | 2 | a0001c0001t0001g0342a0001c0001t0001g0344 | 2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.490-3995T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96930981 | ||||||
| chr12:96931355
|
A | G | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-3621A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931355 | ||||||
| chr12:96931414
|
A | T | 1 | a0001c0001t0008g0225 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.490-3562A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931414 | ||||||
| chr12:96931449
|
T | A | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.490-3527T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931449 | ||||||
| chr12:96931755
|
A | AGTAT | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-3219_490-3216d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96931755 | |||||
| chr12:96931786
|
A | G | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.490-3190A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931786 | ||||||
| chr12:96931894
|
C | G | 1 | a0001c0001t0012g0087 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.490-3082C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931894 | ||||||
| chr12:96931911
|
T | A | 7 | a0001c0001t0001g0219a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 7 | HG02004.hp2 HG02129.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-3065T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96931911 | ||||||
| chr12:96932145
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.490-2831A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932145 | ||||||
| chr12:96932166
|
G | A | 97 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(94): Show | 100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.490-2810G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932166 | ||||||
| chr12:96932190
|
T | C | 1 | a0001c0001t0002g0373 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.490-2786T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932190 | ||||||
| chr12:96932440
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01109.hp1 HG01167.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2536C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932440 | ||||||
| chr12:96932442
|
T | TA | 6 | a0001c0001t0005g0160a0001c0001t0005g0316a0001c0001t0005g0320others(3): Show | 6 | HG02071.hp1 HG02896.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2512dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932442 | |||||
| chr12:96932443
|
A | C | 1 | a0001c0001t0001g0272 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.490-2533A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932443 | ||||||
| chr12:96932444
|
A | C | 2 | a0001c0002t0010g0323a0001c0002t0010g0324 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.490-2532A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932444 | ||||||
| chr12:96932455
|
A | AATATATA others(11): Show |
1 | a0001c0001t0002g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.490-2520_490-2519i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | |||||
| chr12:96932455
|
A | AATATATA others(17): Show |
1 | a0001c0001t0002g0123 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.490-2520_490-2519i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | |||||
| chr12:96932455
|
A | AATATATA others(19): Show |
1 | a0001c0001t0002g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-2520_490-2519i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | |||||
| chr12:96932455
|
A | AATATATA others(27): Show |
1 | a0001c0001t0018g0133 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.490-2520_490-2519i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | |||||
| chr12:96932455
|
AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155 | 3 | HG01257.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.490-2519_490-2504d others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932455 | |||||
| chr12:96932457
|
A | AATATATA others(7): Show |
1 | a0001c0001t0002g0094 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.490-2518_490-2517i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(9): Show |
5 | a0001c0001t0002g0054a0001c0001t0002g0096a0001c0001t0002g0105others(2): Show | 5 | HG02818.hp2 NA18959.hp1 NA19078.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(11): Show |
4 | a0001c0001t0002g0097a0001c0001t0002g0107a0001c0001t0002g0114others(1): Show | 4 | HG00438.hp1 HG01167.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(13): Show |
6 | a0001c0001t0002g0003a0001c0001t0002g0061a0001c0001t0002g0085others(3): Show | 7 | HG00673.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(15): Show |
7 | a0001c0001t0002g0023a0001c0001t0002g0092a0001c0001t0002g0103others(4): Show | 7 | HG01433.hp1 HG01433.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(17): Show |
8 | a0001c0001t0002g0076a0001c0001t0002g0079a0001c0001t0002g0084others(5): Show | 8 | HG01069.hp1 HG01243.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(19): Show |
7 | a0001c0001t0002g0020a0001c0001t0002g0022a0001c0001t0002g0090others(4): Show | 7 | HG00597.hp1 HG01516.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(21): Show |
6 | a0001c0001t0002g0083a0001c0001t0002g0091a0001c0001t0002g0101others(3): Show | 6 | HG00280.hp1 HG01123.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2518_490-2517i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(25): Show |
3 | a0001c0001t0002g0104a0001c0001t0002g0129a0001c0001t0004g0060 | 3 | HG02148.hp1 NA18947.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.490-2518_490-2517i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | AATATATA others(31): Show |
1 | a0001c0001t0002g0062 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.490-2518_490-2517i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932457 | |||||
| chr12:96932457
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.490-2519_490-2518i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0002g0077a0001c0001t0002g0086 | 2 | NA18998.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.490-2519_490-2518i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0002g0068a0001c0001t0002g0075a0001c0001t0024g0056 | 3 | HG02615.hp1 NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.490-2519_490-2518i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0055 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.490-2519_490-2518i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0002g0065 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.490-2519_490-2518i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0002g0071a0001c0001t0002g0082 | 2 | NA19084.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.490-2519_490-2518i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0012g0073 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.490-2519_490-2518i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932457
|
A | T | 5 | a0001c0001t0002g0081a0001c0001t0002g0120a0001c0001t0002g0123others(2): Show | 5 | HG00621.hp2 HG01106.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2519A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932457 | ||||||
| chr12:96932459
|
A | AATATATA others(7): Show |
1 | a0001c0001t0006g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.490-2516_490-2515i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(9): Show |
1 | a0001c0001t0002g0121 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(13): Show |
1 | a0001c0001t0002g0126 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(15): Show |
2 | a0001c0001t0002g0067a0001c0001t0002g0127 | 2 | HG02723.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.490-2516_490-2515i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(19): Show |
1 | a0001c0001t0002g0112 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(21): Show |
3 | a0001c0001t0002g0066a0001c0001t0002g0078a0001c0001t0002g0115 | 3 | HG02004.hp2 NA18984.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.490-2516_490-2515i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(23): Show |
1 | a0001c0001t0002g0119 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(25): Show |
2 | a0001c0001t0002g0125a0001c0001t0015g0063 | 2 | NA19081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.490-2516_490-2515i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | AATATATA others(27): Show |
1 | a0001c0001t0002g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.490-2516_490-2515i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932459 | |||||
| chr12:96932459
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0347 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.490-2517_490-2516i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | ||||||
| chr12:96932459
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0088 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.490-2517_490-2516i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | ||||||
| chr12:96932459
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0002g0001 | 3 | HG01256.hp1 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.490-2517_490-2516i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | ||||||
| chr12:96932459
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0002g0124a0001c0001t0002g0139 | 2 | HG00140.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.490-2517_490-2516i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | ||||||
| chr12:96932459
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.490-2517_490-2516i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | ||||||
| chr12:96932459
|
A | T | 68 | a0001c0001t0002g0003a0001c0001t0002g0020a0001c0001t0002g0022others(65): Show | 69 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.490-2517A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932459 | ||||||
| chr12:96932461
|
A | AATATATA others(15): Show |
1 | a0001c0001t0002g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.490-2514_490-2513i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932461 | |||||
| chr12:96932461
|
A | AATATATA others(21): Show |
1 | a0001c0001t0002g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.490-2514_490-2513i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932461 | |||||
| chr12:96932461
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0013g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.490-2515_490-2514i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | ||||||
| chr12:96932461
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.490-2515_490-2514i others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | ||||||
| chr12:96932461
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0002g0089 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.490-2515_490-2514i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | ||||||
| chr12:96932461
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0064 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.490-2515_490-2514i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | ||||||
| chr12:96932461
|
A | T | 87 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(84): Show | 90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.490-2515A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932461 | ||||||
| chr12:96932463
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0006g0332 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0006g0330 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0001g0236 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(24): Show |
2 | a0001c0001t0001g0275a0001c0001t0001g0348 | 2 | HG02135.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0003g0170 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0002g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0387 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0276 | 2 | HG02056.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0006g0333 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0009g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0007a0001c0001t0006g0012 | 3 | HG01257.hp1 HG01258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(22): Show |
3 | a0001c0001t0001g0011a0001c0001t0001g0296a0001c0001t0001g0304 | 3 | HG01167.hp1 HG02027.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0288 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(26): Show |
2 | a0001c0001t0001g0226a0001c0001t0001g0243 | 2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(28): Show |
5 | a0001c0001t0001g0239a0001c0001t0001g0254a0001c0001t0001g0303others(2): Show | 5 | HG01255.hp1 HG01975.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0004g0027 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(32): Show |
2 | a0001c0001t0004g0030a0001c0001t0004g0151 | 2 | HG02148.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(34): Show |
1 | a0001c0001t0001g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(43): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0307 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(11): Show |
1 | a0001c0002t0010g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0006g0329 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(15): Show |
4 | a0001c0001t0001g0381a0001c0001t0001g0384a0001c0001t0001g0385others(1): Show | 4 | HG02109.hp2 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(17): Show |
3 | a0001c0001t0001g0390a0001c0001t0002g0144a0001c0001t0009g0251 | 3 | HG01515.hp2 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(21): Show |
4 | a0001c0001t0001g0163a0001c0001t0001g0234a0001c0001t0001g0272others(1): Show | 4 | HG00438.hp2 HG01978.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0302 | 2 | NA18955.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(25): Show |
7 | a0001c0001t0001g0224a0001c0001t0001g0255a0001c0001t0001g0274others(4): Show | 7 | HG00408.hp2 HG01975.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(27): Show |
5 | a0001c0001t0001g0240a0001c0001t0001g0314a0001c0001t0003g0157others(2): Show | 5 | HG00621.hp1 NA18946.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(29): Show |
5 | a0001c0001t0001g0246a0001c0001t0001g0265a0001c0001t0001g0287others(2): Show | 5 | HG00673.hp2 HG01099.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0315a0001c0001t0001g0336 | 2 | HG01070.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(33): Show |
4 | a0001c0001t0001g0286a0001c0001t0002g0145a0001c0001t0003g0203others(1): Show | 4 | HG00558.hp1 HG00738.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0001g0291 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(46): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0376a0001c0001t0006g0331 | 2 | HG01928.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0388 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0297 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(22): Show |
2 | a0001c0001t0001g0310a0001c0001t0003g0174 | 2 | NA19054.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(24): Show |
8 | a0001c0001t0001g0220a0001c0001t0001g0227a0001c0001t0001g0231others(5): Show | 9 | HG02809.hp1 NA18945.hp1 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(26): Show |
4 | a0001c0001t0001g0221a0001c0001t0001g0244a0001c0001t0002g0142others(1): Show | 4 | HG01069.hp2 HG03017.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(28): Show |
4 | a0001c0001t0001g0184a0001c0001t0001g0259a0001c0001t0003g0159others(1): Show | 4 | HG01952.hp2 HG02300.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(30): Show |
3 | a0001c0001t0001g0245a0001c0001t0002g0148a0001c0001t0004g0024 | 3 | HG01192.hp1 HG02293.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(32): Show |
4 | a0001c0001t0001g0232a0001c0001t0001g0282a0001c0001t0001g0285others(1): Show | 4 | HG00423.hp1 HG01081.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(34): Show |
2 | a0001c0001t0003g0158a0001c0001t0003g0177 | 2 | NA19076.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(43): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(48): Show |
1 | a0001c0001t0001g0262 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(57): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0261a0001c0001t0014g0017 | 2 | HG02965.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0377a0001c0001t0001g0382 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(15): Show |
6 | a0001c0001t0001g0273a0001c0001t0001g0308a0001c0001t0001g0383others(3): Show | 6 | HG02080.hp2 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(19): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0311a0001c0001t0006g0014 | 3 | HG03195.hp2 NA18942.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0008a0001c0001t0001g0257 | 3 | NA18999.hp2 NA19068.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(23): Show |
6 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0222others(3): Show | 6 | HG02083.hp2 NA19001.hp1 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(25): Show |
4 | a0001c0001t0001g0263a0001c0001t0001g0305a0001c0001t0003g0005others(1): Show | 5 | HG00738.hp1 HG02083.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(27): Show |
6 | a0001c0001t0001g0294a0001c0001t0003g0178a0001c0001t0003g0204others(3): Show | 6 | HG01358.hp1 NA18959.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(29): Show |
5 | a0001c0001t0001g0340a0001c0001t0003g0210a0001c0001t0003g0213others(2): Show | 5 | HG00423.hp2 HG00642.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(31): Show |
10 | a0001c0001t0001g0266a0001c0001t0001g0284a0001c0001t0001g0341others(7): Show | 11 | HG01109.hp2 HG03540.hp2 HG04204.hp2 others(8): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(33): Show |
2 | a0001c0001t0003g0199a0001c0001t0004g0025 | 2 | HG00741.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(35): Show |
1 | a0001c0001t0008g0247 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(44): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(37): Show |
1 | a0001c0001t0003g0194 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(46): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(39): Show |
1 | a0001c0001t0009g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(48): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0349 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0007g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0001g0267a0001c0001t0001g0322a0001c0001t0004g0040 | 3 | HG01934.hp1 HG02523.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0289a0001c0001t0007g0370 | 2 | HG00609.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0380 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(20): Show |
4 | a0001c0001t0001g0165a0001c0001t0001g0223a0001c0001t0004g0044others(1): Show | 4 | HG00609.hp1 HG02896.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(22): Show |
4 | a0001c0001t0001g0278a0001c0001t0001g0312a0001c0001t0004g0032others(1): Show | 4 | HG03098.hp1 NA18957.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(24): Show |
3 | a0001c0001t0003g0195a0001c0001t0004g0038a0001c0001t0008g0225 | 3 | HG01496.hp1 HG03490.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(26): Show |
2 | a0001c0001t0001g0229a0001c0001t0001g0264 | 2 | HG01175.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(35): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(28): Show |
6 | a0001c0001t0001g0268a0001c0001t0001g0279a0001c0001t0003g0179others(3): Show | 6 | HG02080.hp1 HG02698.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(30): Show |
1 | a0001c0001t0001g0283 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(32): Show |
3 | a0001c0001t0001g0313a0001c0001t0003g0196a0001c0001t0004g0046 | 3 | HG01255.hp2 HG02602.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0014g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(18): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0230 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(20): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0009 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0003g0201a0001c0001t0007g0369 | 2 | HG02897.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(21): Show |
3 | a0001c0001t0002g0149a0001c0001t0004g0039a0001c0001t0008g0269 | 3 | HG02735.hp2 HG06807.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0343 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(25): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0216a0001c0001t0001g0277others(5): Show | 8 | HG01168.hp1 HG02698.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(27): Show |
7 | a0001c0001t0001g0219a0001c0001t0001g0309a0001c0001t0002g0152others(4): Show | 7 | HG01243.hp2 HG02015.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(29): Show |
3 | a0001c0001t0001g0260a0001c0001t0001g0337a0001c0001t0003g0206 | 3 | HG00597.hp2 HG02071.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(38): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(31): Show |
3 | a0001c0001t0001g0300a0001c0001t0004g0035a0001c0001t0004g0045 | 3 | HG00558.hp2 NA18954.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0004g0036 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(6): Show |
1 | a0004c0008t0007g0372 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(17): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0007g0371 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(23): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0007g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(25): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0185 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(27): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0007g0368 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(29): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(31): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(28): Show |
4 | a0001c0001t0001g0342a0001c0001t0001g0344a0001c0001t0002g0146others(1): Show | 4 | HG00323.hp2 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(30): Show |
4 | a0001c0001t0003g0197a0001c0002t0010g0050a0001c0002t0010g0052others(1): Show | 4 | HG01361.hp1 HG02109.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-2512_490-2511i others(39): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(32): Show |
1 | a0001c0001t0001g0270 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0238 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(25): Show |
1 | a0001c0001t0004g0037 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(27): Show |
3 | a0001c0001t0001g0280a0001c0001t0001g0374a0001c0001t0004g0021 | 3 | HG02486.hp1 NA18975.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(36): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0003g0180 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(40): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAA others(33): Show |
1 | a0001c0001t0004g0028 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(42): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAT others(24): Show |
1 | a0001c0001t0001g0271 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(33): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAAAT others(32): Show |
1 | a0001c0001t0001g0301 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(41): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0022g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAATA others(7): Show |
1 | a0001c0001t0021g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(16): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAATA others(15): Show |
1 | a0001c0001t0006g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(24): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAAATA others(23): Show |
1 | a0005c0004t0008g0228 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(32): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0378 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(19): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAAATAT others(28): Show |
1 | a0001c0002t0010g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(37): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAATATA others(21): Show |
3 | a0001c0001t0003g0191a0001c0001t0003g0200a0001c0001t0003g0208 | 3 | HG01099.hp1 HG01256.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAATATA others(25): Show |
1 | a0001c0001t0003g0198 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0346 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(22): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAATATA others(19): Show |
1 | a0001c0001t0001g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(28): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAAATATA others(21): Show |
1 | a0001c0001t0001g0292 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.490-2512_490-2511i others(30): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0013g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.490-2512_490-2511i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | AATATATA others(25): Show |
1 | a0001c0001t0001g0218 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.490-2488_490-2487i others(34): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932463 | |||||
| chr12:96932463
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0074 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.490-2513_490-2512i others(15): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932463 | ||||||
| chr12:96932463
|
A | T | 94 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(91): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.490-2513A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932463 | ||||||
| chr12:96932464
|
AT | A | 3 | a0001c0001t0005g0357a0001c0001t0005g0364a0001c0001t0020g0166 | 3 | HG01175.hp2 HG01261.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.490-2511delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932464 | ||||||
| chr12:96932465
|
T | A | 6 | a0001c0001t0005g0160a0001c0001t0005g0318a0001c0001t0005g0319others(3): Show | 6 | HG01081.hp2 HG01192.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2511T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932465 | ||||||
| chr12:96932467
|
T | A | 2 | a0001c0001t0005g0358a0001c0001t0020g0166 | 2 | HG02572.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.490-2509T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932467 | ||||||
| chr12:96932471
|
T | A | 1 | a0001c0006t0006g0334 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-2505T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932471 | ||||||
| chr12:96932473
|
T | A | 1 | a0001c0006t0006g0334 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.490-2503T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932473 | ||||||
| chr12:96932480
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.490-2488_490-2487i others(21): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932480 | |||||
| chr12:96932487
|
T | A | 2 | a0001c0001t0002g0139a0001c0006t0006g0334 | 2 | HG01884.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.490-2489T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932487 | ||||||
| chr12:96932487
|
T | TATATATA others(17): Show |
2 | a0001c0001t0002g0069a0001c0001t0004g0059 | 2 | HG01515.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.490-2488_490-2487i others(26): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932487 | |||||
| chr12:96932489
|
A | G | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-2487A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932489 | ||||||
| chr12:96932489
|
A | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0289 | 2 | HG00609.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.490-2487A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932489 | ||||||
| chr12:96932491
|
A | T | 1 | a0001c0001t0001g0289 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.490-2485A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932491 | ||||||
| chr12:96932529
|
T | A | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2447T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932529 | ||||||
| chr12:96932546
|
G | A | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.490-2430G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932546 | ||||||
| chr12:96932566
|
T | TC | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.490-2408dupC | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932566 | |||||
| chr12:96932587
|
C | T | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2389C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932587 | ||||||
| chr12:96932588
|
T | C | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2388T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932588 | ||||||
| chr12:96932599
|
C | A | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2377C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932599 | ||||||
| chr12:96932733
|
T | G | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-2243T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932733 | ||||||
| chr12:96932883
|
G | A | 373 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(370): Show | 383 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(380): Show |
intron_variant | MODIFIER | c.490-2093G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932883 | ||||||
| chr12:96932947
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.490-2029C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96932947 | ||||||
| chr12:96932999
|
C | CT | 29 | a0001c0001t0001g0254a0001c0001t0002g0123a0001c0001t0003g0182others(26): Show | 29 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.490-1960dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932999 | |||||
| chr12:96932999
|
CT | C | 7 | a0001c0001t0001g0345a0001c0001t0002g0085a0001c0001t0002g0110others(4): Show | 7 | HG01069.hp1 HG01099.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1960delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96932999 | |||||
| chr12:96933016
|
TA | T | 5 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(2): Show | 6 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-1957delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96933016 | |||||
| chr12:96933109
|
A | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-1867A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933109 | ||||||
| chr12:96933136
|
CTTG | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-1834_490-1832d others(5): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96933136 | |||||
| chr12:96933190
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0234 | 3 | HG01257.hp1 HG01258.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.490-1786G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933190 | ||||||
| chr12:96933214
|
A | T | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-1762A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933214 | ||||||
| chr12:96933236
|
C | A | 1 | a0001c0001t0001g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-1740C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933236 | ||||||
| chr12:96933336
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0274 | 2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.490-1640C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933336 | ||||||
| chr12:96933367
|
A | T | 1 | a0006c0007t0001g0258 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.490-1609A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933367 | ||||||
| chr12:96933475
|
T | G | 3 | a0001c0001t0005g0319a0001c0001t0005g0320a0001c0001t0005g0321 | 3 | HG01192.hp2 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.490-1501T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933475 | ||||||
| chr12:96933816
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0083 | 2 | NA18963.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.490-1160G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933816 | ||||||
| chr12:96933829
|
C | T | 5 | a0001c0001t0002g0023a0001c0001t0002g0055a0001c0001t0002g0083others(2): Show | 5 | NA18950.hp1 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-1147C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933829 | ||||||
| chr12:96933849
|
C | T | 1 | a0001c0001t0006g0169 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-1127C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933849 | ||||||
| chr12:96933985
|
G | T | 1 | a0001c0001t0003g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.490-991G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96933985 | ||||||
| chr12:96934191
|
A | G | 2 | a0001c0001t0005g0356a0001c0001t0005g0360 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.490-785A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934191 | ||||||
| chr12:96934207
|
C | CT | 236 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(233): Show | 242 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.490-758dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96934207 | |||||
| chr12:96934387
|
T | C | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.490-589T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934387 | ||||||
| chr12:96934499
|
T | C | 1 | a0004c0008t0007g0372 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.490-477T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934499 | ||||||
| chr12:96934501
|
C | CT | 16 | a0001c0001t0001g0314a0001c0001t0001g0375a0001c0001t0006g0012others(13): Show | 16 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.490-463dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 96934501 | |||||
| chr12:96934518
|
C | A | 2 | a0001c0001t0014g0016a0001c0001t0014g0017 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-458C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934518 | ||||||
| chr12:96934576
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.490-400C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934576 | ||||||
| chr12:96934592
|
C | A | 212 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(209): Show | 218 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.490-384C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934592 | ||||||
| chr12:96934593
|
A | T | 2 | a0001c0001t0014g0016a0001c0001t0014g0017 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.490-383A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934593 | ||||||
| chr12:96934671
|
G | A | 4 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0035others(1): Show | 4 | NA18970.hp1 NA19003.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-305G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934671 | ||||||
| chr12:96934936
|
TGCTTATA others(1): Show |
T | 198 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 204 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.490-39_490-32delGC others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 6/15 | chr12 | 96934936 | ||||||
| chr12:96935321
|
A | G | 14 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+116A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935321 | ||||||
| chr12:96935437
|
G | A | 1 | a0001c0001t0019g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.719+232G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935437 | ||||||
| chr12:96935461
|
C | A | 1 | a0001c0001t0022g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.719+256C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935461 | ||||||
| chr12:96935619
|
A | T | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.719+414A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935619 | ||||||
| chr12:96935732
|
A | T | 1 | a0001c0001t0002g0095 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.719+527A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935732 | ||||||
| chr12:96935755
|
A | C | 1 | a0001c0001t0002g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.719+550A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935755 | ||||||
| chr12:96935761
|
C | T | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.719+556C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935761 | ||||||
| chr12:96935834
|
C | CAA | 17 | a0001c0001t0001g0009a0001c0001t0001g0338a0001c0001t0001g0376others(14): Show | 18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.719+633_719+634dup others(2): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 96935834 | |||||
| chr12:96935905
|
G | GT | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.719+701dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr12 | 96935905 | |||||
| chr12:96935935
|
C | T | 1 | a0001c0001t0003g0197 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.720-676C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935935 | ||||||
| chr12:96935941
|
G | C | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.720-670G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96935941 | ||||||
| chr12:96936168
|
A | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.720-443A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936168 | ||||||
| chr12:96936218
|
A | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0200 | 2 | HG01099.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.720-393A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936218 | ||||||
| chr12:96936290
|
G | A | 1 | a0001c0001t0001g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.720-321G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936290 | ||||||
| chr12:96936357
|
G | C | 4 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0014g0016others(1): Show | 4 | HG02965.hp2 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-254G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936357 | ||||||
| chr12:96936391
|
AG | A | 198 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(195): Show | 204 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.720-219delG | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936391 | ||||||
| chr12:96936525
|
C | G | 1 | a0001c0001t0002g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.720-86C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 7/15 | chr12 | 96936525 | ||||||
| chr12:96936887
|
C | CA | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+77dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 96936887 | |||||
| chr12:96937023
|
T | A | 1 | a0001c0001t0003g0213 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.922-175T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937023 | ||||||
| chr12:96937037
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.922-161A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937037 | ||||||
| chr12:96937047
|
T | G | 9 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0027others(6): Show | 9 | HG01123.hp2 HG01358.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.922-151T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937047 | ||||||
| chr12:96937065
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.922-133C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937065 | ||||||
| chr12:96937072
|
G | T | 1 | a0001c0001t0001g0216 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.922-126G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937072 | ||||||
| chr12:96937137
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.922-61T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | chr12 | 96937137 | ||||||
| chr12:96937157
|
CATT | C | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.922-39_922-37delTT others(1): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 96937157 | |||||
| chr12:96937441
|
GT | G | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1117+55delT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 96937441 | |||||
| chr12:96937571
|
A | G | 1 | a0001c0001t0020g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1117+178A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937571 | ||||||
| chr12:96937587
|
A | T | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1117+194A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937587 | ||||||
| chr12:96937650
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1117+257G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937650 | ||||||
| chr12:96937882
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+489A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937882 | ||||||
| chr12:96937926
|
T | A | 95 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1117+533T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96937926 | ||||||
| chr12:96938157
|
C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(102): Show | 108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1117+764C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938157 | ||||||
| chr12:96938544
|
G | A | 12 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(9): Show | 12 | HG01106.hp1 HG01884.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1117+1151G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938544 | ||||||
| chr12:96938827
|
TCTCTCTC others(3): Show |
T | 200 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(197): Show | 206 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.1117+1436_1117+144 others(14): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 96938827 | |||||
| chr12:96938835
|
T | TCA | 3 | a0001c0001t0005g0357a0001c0001t0005g0358a0001c0001t0005g0364 | 3 | HG01175.hp2 HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1117+1455_1117+145 others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 96938835 | |||||
| chr12:96938847
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1117+1454A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938847 | ||||||
| chr12:96938858
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1117+1465T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938858 | ||||||
| chr12:96938924
|
A | G | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1118-1485A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938924 | ||||||
| chr12:96938978
|
T | A | 3 | a0001c0001t0004g0027a0001c0001t0004g0031a0001c0001t0004g0150 | 3 | HG01123.hp2 HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1118-1431T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96938978 | ||||||
| chr12:96939071
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1118-1338T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939071 | ||||||
| chr12:96939190
|
G | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0070 | 2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1118-1219G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939190 | ||||||
| chr12:96939213
|
G | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1118-1196G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939213 | ||||||
| chr12:96939270
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1118-1139T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939270 | ||||||
| chr12:96939548
|
T | A | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1118-861T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939548 | ||||||
| chr12:96939629
|
A | T | 2 | a0001c0001t0002g0109a0001c0001t0002g0110 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1118-780A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939629 | ||||||
| chr12:96939651
|
T | A | 1 | a0001c0001t0021g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1118-758T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939651 | ||||||
| chr12:96939835
|
A | G | 1 | a0001c0001t0009g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1118-574A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939835 | ||||||
| chr12:96939871
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1118-538T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939871 | ||||||
| chr12:96939947
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1118-462G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96939947 | ||||||
| chr12:96940036
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1118-373T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96940036 | ||||||
| chr12:96940381
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1118-28A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 9/15 | chr12 | 96940381 | ||||||
| chr12:96940667
|
G | C | 2 | a0002c0003t0003g0188a0002c0003t0003g0189 | 2 | NA18959.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1246+130G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940667 | ||||||
| chr12:96940671
|
T | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0164 | 2 | NA18965.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1246+134T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940671 | ||||||
| chr12:96940742
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1246+205A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940742 | ||||||
| chr12:96940826
|
C | T | 1 | a0001c0001t0023g0379 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1246+289C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940826 | ||||||
| chr12:96940847
|
A | G | 14 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1246+310A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940847 | ||||||
| chr12:96940874
|
G | A | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1246+337G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940874 | ||||||
| chr12:96940949
|
T | G | 1 | a0001c0001t0001g0280 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1246+412T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940949 | ||||||
| chr12:96940953
|
C | T | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1246+416C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940953 | ||||||
| chr12:96940994
|
T | A | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1246+457T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96940994 | ||||||
| chr12:96941453
|
T | G | 17 | a0001c0001t0001g0009a0001c0001t0001g0338a0001c0001t0001g0376others(14): Show | 18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1246+916T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941453 | ||||||
| chr12:96941459
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246+922G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941459 | ||||||
| chr12:96941572
|
A | C | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(117): Show | 122 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1247-1005A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941572 | ||||||
| chr12:96941747
|
C | CT | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1247-824dupT | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr12 | 96941747 | |||||
| chr12:96941804
|
C | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1247-773C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941804 | ||||||
| chr12:96941935
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1247-642T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 10/15 | chr12 | 96941935 | ||||||
| chr12:96942649
|
C | T | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0007g0369others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1294+25C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942649 | ||||||
| chr12:96942667
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0292a0001c0001t0001g0293 | 3 | HG03669.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1294+43A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942667 | ||||||
| chr12:96942735
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1294+111G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942735 | ||||||
| chr12:96942905
|
T | TA | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1294+282dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 96942905 | |||||
| chr12:96942942
|
G | A | 7 | a0001c0001t0006g0328a0001c0001t0006g0329a0001c0001t0006g0330others(4): Show | 7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1294+318G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942942 | ||||||
| chr12:96942978
|
C | T | 8 | a0001c0001t0005g0160a0001c0001t0005g0316a0001c0001t0005g0317others(5): Show | 8 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+354C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96942978 | ||||||
| chr12:96943305
|
T | C | 1 | a0001c0006t0006g0334 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1295-255T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943305 | ||||||
| chr12:96943339
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1295-221A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943339 | ||||||
| chr12:96943404
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1295-156C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943404 | ||||||
| chr12:96943421
|
G | A | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1295-139G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943421 | ||||||
| chr12:96943499
|
T | C | 2 | a0001c0001t0001g0348a0001c0001t0001g0349 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1295-61T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 11/15 | chr12 | 96943499 | ||||||
| chr12:96943818
|
G | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1497+56G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943818 | ||||||
| chr12:96943832
|
C | T | 248 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 254 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.1497+70C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943832 | ||||||
| chr12:96943918
|
C | T | 60 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0340others(57): Show | 63 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1497+156C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943918 | ||||||
| chr12:96943956
|
T | G | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1497+194T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96943956 | ||||||
| chr12:96944057
|
A | G | 1 | a0001c0001t0006g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1497+295A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944057 | ||||||
| chr12:96944129
|
C | G | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1497+367C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944129 | ||||||
| chr12:96944194
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1497+432A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944194 | ||||||
| chr12:96944227
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1498-412A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944227 | ||||||
| chr12:96944301
|
T | A | 8 | a0001c0001t0001g0218a0001c0001t0001g0292a0001c0001t0001g0293others(5): Show | 8 | HG03239.hp2 HG03490.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-338T>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944301 | ||||||
| chr12:96944330
|
G | A | 248 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 254 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.1498-309G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944330 | ||||||
| chr12:96944492
|
C | T | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 244 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1498-147C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944492 | ||||||
| chr12:96944564
|
A | G | 5 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(2): Show | 5 | NA18959.hp1 NA18964.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-75A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 12/15 | chr12 | 96944564 | ||||||
| chr12:96944818
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1654+23T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944818 | ||||||
| chr12:96944829
|
G | A | 6 | a0001c0002t0010g0050a0001c0002t0010g0051a0001c0002t0010g0052others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654+34G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944829 | ||||||
| chr12:96944904
|
A | C | 1 | a0001c0001t0006g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1654+109A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944904 | ||||||
| chr12:96944918
|
G | A | 235 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 241 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1654+123G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96944918 | ||||||
| chr12:96945052
|
T | G | 1 | a0001c0001t0020g0166 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1654+257T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945052 | ||||||
| chr12:96945061
|
TA | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0338a0001c0001t0001g0376others(14): Show | 18 | HG02109.hp2 HG02258.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1654+267delA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945061 | ||||||
| chr12:96945081
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1654+286G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945081 | ||||||
| chr12:96945084
|
T | G | 235 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 241 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(238): Show |
intron_variant | MODIFIER | c.1654+289T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945084 | ||||||
| chr12:96945142
|
T | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1654+347T>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945142 | ||||||
| chr12:96945150
|
G | A | 373 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(370): Show | 383 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(380): Show |
intron_variant | MODIFIER | c.1654+355G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945150 | ||||||
| chr12:96945168
|
C | G | 2 | a0001c0001t0014g0016a0001c0001t0014g0017 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1654+373C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945168 | ||||||
| chr12:96945236
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1654+441A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945236 | ||||||
| chr12:96945265
|
G | A | 248 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 254 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.1655-428G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945265 | ||||||
| chr12:96945458
|
A | T | 35 | a0001c0001t0001g0010a0001c0001t0001g0216a0001c0001t0001g0219others(32): Show | 35 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1655-235A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945458 | ||||||
| chr12:96945487
|
T | TTA | 10 | a0001c0001t0003g0004a0001c0001t0003g0157a0001c0001t0003g0159others(7): Show | 11 | HG02027.hp1 HG02080.hp1 HG04184.hp2 others(8): Show |
intron_variant | MODIFIER | c.1655-197_1655-196d others(4): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 96945487 | |||||
| chr12:96945610
|
G | C | 365 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(362): Show | 375 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(372): Show |
intron_variant | MODIFIER | c.1655-83G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 13/15 | chr12 | 96945610 | ||||||
| chr12:96945908
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1811+59A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96945908 | ||||||
| chr12:96945950
|
G | A | 1 | a0001c0001t0008g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1811+101G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96945950 | ||||||
| chr12:96945950
|
G | T | 1 | a0001c0001t0002g0373 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1811+101G>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96945950 | ||||||
| chr12:96946142
|
A | C | 1 | a0001c0001t0003g0178 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1811+293A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946142 | ||||||
| chr12:96946191
|
A | G | 7 | a0001c0001t0006g0328a0001c0001t0006g0329a0001c0001t0006g0330others(4): Show | 7 | HG01106.hp1 HG01928.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1811+342A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946191 | ||||||
| chr12:96946253
|
A | G | 1 | a0001c0001t0003g0186 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1811+404A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946253 | ||||||
| chr12:96946273
|
ATACT | A | 5 | a0001c0001t0007g0367a0001c0001t0007g0368a0001c0001t0007g0369others(2): Show | 5 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1811+427_1811+430d others(6): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 96946273 | |||||
| chr12:96946283
|
T | TA | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+442dupA | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 96946283 | |||||
| chr12:96946300
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1811+451C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946300 | ||||||
| chr12:96946308
|
T | C | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1811+459T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946308 | ||||||
| chr12:96946420
|
T | C | 10 | a0001c0001t0001g0260a0001c0001t0001g0266a0001c0001t0001g0267others(7): Show | 10 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+571T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946420 | ||||||
| chr12:96946740
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1811+891A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946740 | ||||||
| chr12:96946754
|
G | A | 365 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(362): Show | 375 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(372): Show |
intron_variant | MODIFIER | c.1811+905G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946754 | ||||||
| chr12:96946772
|
A | G | 2 | a0001c0001t0013g0057a0001c0001t0013g0058 | 2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1811+923A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946772 | ||||||
| chr12:96946807
|
G | A | 1 | a0001c0001t0003g0192 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1811+958G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946807 | ||||||
| chr12:96946826
|
C | A | 1 | a0001c0001t0002g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1811+977C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96946826 | ||||||
| chr12:96947356
|
A | G | 1 | a0001c0001t0021g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1811+1507A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947356 | ||||||
| chr12:96947385
|
G | A | 1 | a0001c0002t0010g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1811+1536G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947385 | ||||||
| chr12:96947422
|
A | G | 1 | a0001c0001t0006g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1811+1573A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947422 | ||||||
| chr12:96947676
|
A | G | 8 | a0001c0001t0001g0226a0001c0001t0001g0241a0001c0001t0001g0242others(5): Show | 8 | HG01070.hp1 HG01099.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1811+1827A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947676 | ||||||
| chr12:96947686
|
C | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1811+1837C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947686 | ||||||
| chr12:96947702
|
C | A | 1 | a0001c0001t0012g0087 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1811+1853C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947702 | ||||||
| chr12:96947704
|
T | C | 248 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(245): Show | 254 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(251): Show |
intron_variant | MODIFIER | c.1811+1855T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947704 | ||||||
| chr12:96947765
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0047a0001c0001t0011g0048others(1): Show | 5 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1811+1916C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947765 | ||||||
| chr12:96947941
|
G | A | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+2092G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947941 | ||||||
| chr12:96947955
|
C | T | 2 | a0001c0001t0001g0376a0001c0001t0001g0380 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1811+2106C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947955 | ||||||
| chr12:96947956
|
G | A | 1 | a0001c0001t0008g0299 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1811+2107G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96947956 | ||||||
| chr12:96948055
|
A | G | 10 | a0001c0001t0007g0015a0001c0001t0007g0018a0001c0001t0007g0367others(7): Show | 10 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1811+2206A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948055 | ||||||
| chr12:96948418
|
C | T | 9 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1811+2569C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948418 | ||||||
| chr12:96948578
|
A | G | 177 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(174): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1811+2729A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948578 | ||||||
| chr12:96948581
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1811+2732A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948581 | ||||||
| chr12:96948649
|
G | A | 16 | a0001c0001t0005g0351a0001c0001t0005g0352a0001c0001t0005g0354others(13): Show | 16 | HG00140.hp1 HG00280.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1812-2783G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948649 | ||||||
| chr12:96948714
|
G | A | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-2718G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948714 | ||||||
| chr12:96948811
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1812-2621G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948811 | ||||||
| chr12:96948941
|
G | A | 1 | a0001c0001t0005g0352 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1812-2491G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96948941 | ||||||
| chr12:96949228
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1812-2204C>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949228 | ||||||
| chr12:96949261
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1812-2171A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949261 | ||||||
| chr12:96949400
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1812-2032G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949400 | ||||||
| chr12:96949417
|
A | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1812-2015A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949417 | ||||||
| chr12:96949731
|
A | G | 1 | a0001c0001t0001g0383 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1812-1701A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949731 | ||||||
| chr12:96949736
|
C | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0075 | 2 | HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1812-1696C>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949736 | ||||||
| chr12:96949951
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1812-1481C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96949951 | ||||||
| chr12:96950055
|
G | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-1377G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950055 | ||||||
| chr12:96950104
|
A | C | 1 | a0001c0001t0004g0035 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1812-1328A>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950104 | ||||||
| chr12:96950281
|
C | T | 151 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(148): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1812-1151C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950281 | ||||||
| chr12:96950352
|
T | C | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-1080T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950352 | ||||||
| chr12:96950371
|
GTATACAC others(6): Show |
G | 2 | a0001c0002t0010g0323a0001c0002t0010g0324 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1812-1058_1812-104 others(17): Show |
NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr12 | 96950371 | |||||
| chr12:96950540
|
T | C | 1 | a0001c0001t0001g0375 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1812-892T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950540 | ||||||
| chr12:96950733
|
G | A | 12 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(9): Show | 12 | HG01106.hp1 HG01884.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1812-699G>A | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96950733 | ||||||
| chr12:96951013
|
T | C | 14 | a0001c0001t0006g0012a0001c0001t0006g0013a0001c0001t0006g0014others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1812-419T>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951013 | ||||||
| chr12:96951080
|
C | T | 151 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0020others(148): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1812-352C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951080 | ||||||
| chr12:96951145
|
C | T | 26 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0025others(23): Show | 26 | HG01123.hp2 HG01358.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1812-287C>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951145 | ||||||
| chr12:96951206
|
A | G | 1 | a0001c0001t0005g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1812-226A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951206 | ||||||
| chr12:96951328
|
A | G | 1 | a0001c0001t0005g0319 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1812-104A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 14/15 | chr12 | 96951328 | ||||||
| chr12:96951594
|
G | C | 1 | a0001c0001t0006g0019 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1878+96G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951594 | ||||||
| chr12:96951636
|
A | G | 7 | a0001c0001t0004g0021a0001c0001t0004g0024a0001c0001t0004g0030others(4): Show | 7 | HG02148.hp2 NA18612.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1878+138A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951636 | ||||||
| chr12:96951639
|
A | T | 1 | a0001c0001t0001g0387 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1878+141A>T | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951639 | ||||||
| chr12:96951702
|
A | G | 2 | a0001c0001t0012g0080a0001c0001t0012g0087 | 2 | NA18974.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1878+204A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951702 | ||||||
| chr12:96951763
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1879-186A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951763 | ||||||
| chr12:96951826
|
A | G | 3 | a0001c0001t0002g0153a0001c0001t0002g0154a0001c0001t0002g0155 | 3 | HG01257.hp2 HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1879-123A>G | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951826 | ||||||
| chr12:96951873
|
G | C | 8 | a0001c0001t0005g0160a0001c0001t0005g0316a0001c0001t0005g0317others(5): Show | 8 | HG01081.hp2 HG01192.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1879-76G>C | NEDD1 | ENSG00000139350.12 | transcript | ENST00000266742.9 | protein_coding | 15/15 | chr12 | 96951873 |