Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4898 |
| ensemblid | ENSG00000078618.23 |
| hgncid | 7995 |
| symbol | NRDC |
| name | nardilysin convertase |
| refseq_nuc | NM_001101662.2 |
| refseq_prot | NP_001095132.1 |
| ensembl_nuc | ENST00000352171.12 |
| ensembl_prot | ENSP00000262679.8 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 51789210 |
| end | 51878727 |
| strand | - |
| ver | v1.2 |
| region | chr1:51789210-51878727 |
| region5000 | chr1:51784210-51883727 |
| regionname0 | NRDC_chr1_51789210_51878727 |
| regionname5000 | NRDC_chr1_51784210_51883727 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1151 | 136 | 73 | 18 | 18 | 5 | 20 | 16 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002 | 0/0 | 1150 | 101 | 18 | 25 | 41 | 1 | 16 | 32 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0003 | 0/0 | 1151 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0004 | 0/0 | 1150 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0005 | 0/0 | 1150 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0006 | 0/0 | 1151 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3453 | 68 | 12 | 14 | 27 | 1 | 14 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0002 | 0/0 | 3456 | 67 | 50 | 8 | 2 | 3 | 4 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0003 | 1/1 | 3456 | 41 | 12 | 9 | 9 | 2 | 7 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0004 | 0/0 | 3453 | 15 | 2 | 2 | 10 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0005 | 0/0 | 3456 | 12 | 3 | 0 | 4 | 0 | 5 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0006 | 0/0 | 3456 | 8 | 2 | 1 | 3 | 0 | 2 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0007 | 0/0 | 3453 | 7 | 1 | 2 | 4 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0008 | 0/0 | 3456 | 3 | 2 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0009 | 0/0 | 3453 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0010 | 0/0 | 3453 | 3 | 0 | 3 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0011 | 0/0 | 3456 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0012 | 0/0 | 3456 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0013 | 0/0 | 3453 | 2 | 0 | 0 | 2 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0014 | 0/0 | 3453 | 2 | 0 | 2 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0015 | 0/0 | 3453 | 2 | 0 | 2 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0016 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0017 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0018 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0019 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| c0020 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 139 | 239 | 89 | 44 | 62 | 6 | 36 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| t0002 | 0/0 | 135 | 4 | 4 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| t0003 | 0/0 | 139 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3456 | 67 | 50 | 8 | 2 | 3 | 4 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0003 | 1/1 | 3456 | 41 | 12 | 9 | 9 | 2 | 7 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0005 | 0/0 | 3456 | 12 | 3 | 0 | 4 | 0 | 5 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0006 | 0/0 | 3456 | 8 | 2 | 1 | 3 | 0 | 2 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0008 | 0/0 | 3456 | 3 | 2 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0011 | 0/0 | 3456 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0016 | 0/0 | 3456 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0001c0017 | 0/0 | 3456 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0001 | 0/0 | 3453 | 68 | 12 | 14 | 27 | 1 | 14 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0004 | 0/0 | 3453 | 15 | 2 | 2 | 10 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0007 | 0/0 | 3453 | 7 | 1 | 2 | 4 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0009 | 0/0 | 3453 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0010 | 0/0 | 3453 | 3 | 0 | 3 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0014 | 0/0 | 3453 | 2 | 0 | 2 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0015 | 0/0 | 3453 | 2 | 0 | 2 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0002c0019 | 0/0 | 3453 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0003c0012 | 0/0 | 3456 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0004c0013 | 0/0 | 3453 | 2 | 0 | 0 | 2 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0005c0020 | 0/0 | 3453 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 | |
| a0006c0018 | 0/0 | 3456 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 3594 | 66 | 49 | 8 | 2 | 3 | 4 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0002t0003 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0003t0001 | 1/1 | 3594 | 41 | 12 | 9 | 9 | 2 | 7 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0005t0001 | 0/0 | 3594 | 12 | 3 | 0 | 4 | 0 | 5 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0006t0001 | 0/0 | 3594 | 8 | 2 | 1 | 3 | 0 | 2 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0008t0001 | 0/0 | 3594 | 3 | 2 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0011t0002 | 0/0 | 3590 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0016t0001 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0001c0017t0001 | 0/0 | 3594 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0001t0001 | 0/0 | 3591 | 68 | 12 | 14 | 27 | 1 | 14 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0004t0001 | 0/0 | 3591 | 14 | 1 | 2 | 10 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0004t0002 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0007t0001 | 0/0 | 3591 | 7 | 1 | 2 | 4 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0009t0001 | 0/0 | 3591 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0010t0001 | 0/0 | 3591 | 3 | 0 | 3 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0014t0001 | 0/0 | 3591 | 2 | 0 | 2 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0015t0001 | 0/0 | 3591 | 2 | 0 | 2 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0002c0019t0001 | 0/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0003c0012t0001 | 0/0 | 3594 | 3 | 3 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0004c0013t0001 | 0/0 | 3591 | 2 | 0 | 0 | 2 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0005c0020t0001 | 0/0 | 3591 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| a0006c0018t0001 | 0/0 | 3594 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | copy fasta | chr1 | 51784210 | 51883727 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0002t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0038 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0008t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0011t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0011t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0011t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0016t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0001c0017t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0004t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0009t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0009t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0009t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0010t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0010t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0010t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0014t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0014t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0015t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0015t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0002c0019t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0003c0012t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0003c0012t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0003c0012t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0004c0013t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0004c0013t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0005c0020t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| a0006c0018t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0001 | EUR | GBR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0057 | EUR | GBR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0116 | EAS | CHS | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00544 | hp2 | a0001 | c0005 | t0001 | g0223 | EAS | CHS | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | CHS | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00558 | hp2 | a0001 | c0005 | t0001 | g0227 | EAS | CHS | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0133 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00673 | hp1 | a0002 | c0004 | t0001 | g0190 | EAS | CHS | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0148 | EAS | CHS | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0183 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00738 | hp2 | a0002 | c0015 | t0001 | g0166 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0188 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG00741 | hp2 | a0002 | c0010 | t0001 | g0153 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01069 | hp2 | a0002 | c0007 | t0001 | g0160 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01071 | hp1 | a0002 | c0007 | t0001 | g0182 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01071 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0157 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01081 | hp2 | a0002 | c0001 | t0001 | g0110 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0172 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0156 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0124 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0129 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01168 | hp2 | a0006 | c0018 | t0001 | g0019 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01175 | hp1 | a0002 | c0014 | t0001 | g0196 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0030 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01257 | hp1 | a0002 | c0014 | t0001 | g0152 | AMR | CLM | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01346 | hp1 | a0002 | c0015 | t0001 | g0167 | AMR | CLM | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | CLM | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01884 | hp2 | a0002 | c0009 | t0001 | g0125 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0077 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0170 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01928 | hp2 | a0002 | c0004 | t0001 | g0180 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0162 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01943 | hp2 | a0001 | c0006 | t0001 | g0239 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01981 | hp1 | a0002 | c0010 | t0001 | g0150 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0120 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01993 | hp1 | a0002 | c0010 | t0001 | g0149 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0199 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | KHV | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0178 | EAS | KHV | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0209 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02055 | hp2 | a0001 | c0011 | t0002 | g0218 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0140 | EAS | KHV | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02071 | hp2 | a0005 | c0020 | t0001 | g0139 | EAS | KHV | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02145 | hp2 | a0002 | c0009 | t0001 | g0126 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02257 | hp1 | a0003 | c0012 | t0001 | g0221 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0127 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0163 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0181 | AMR | PEL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02451 | hp2 | a0001 | c0016 | t0001 | g0005 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02572 | hp1 | a0001 | c0008 | t0001 | g0055 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02602 | hp1 | a0001 | c0005 | t0001 | g0226 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0137 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02615 | hp1 | a0002 | c0001 | t0001 | g0198 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02615 | hp2 | a0002 | c0001 | t0001 | g0211 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0238 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02698 | hp1 | a0001 | c0005 | t0001 | g0229 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02723 | hp1 | a0002 | c0004 | t0002 | g0123 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0210 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02735 | hp1 | a0001 | c0017 | t0001 | g0215 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0168 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0114 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0115 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0082 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0242 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02970 | hp2 | a0003 | c0012 | t0001 | g0219 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0036 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0131 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03098 | hp2 | a0001 | c0011 | t0002 | g0216 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0237 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0097 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03195 | hp2 | a0002 | c0004 | t0001 | g0122 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0132 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03453 | hp2 | a0002 | c0009 | t0001 | g0128 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0021 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0158 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03492 | hp1 | a0001 | c0008 | t0001 | g0032 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0165 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0119 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0206 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0169 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03710 | hp2 | a0001 | c0005 | t0001 | g0222 | SAS | PJL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0143 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0146 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0184 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0135 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0028 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0187 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03942 | hp1 | a0002 | c0019 | t0001 | g0204 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0029 | SAS | BEB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04115 | hp1 | a0001 | c0005 | t0001 | g0228 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04115 | hp2 | a0002 | c0001 | t0001 | g0213 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04199 | hp2 | a0001 | c0005 | t0001 | g0231 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04204 | hp1 | a0001 | c0006 | t0001 | g0235 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0034 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0155 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | STU | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0208 | AFR | YRI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | YRI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18612 | hp1 | a0002 | c0007 | t0001 | g0197 | EAS | CHB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18612 | hp2 | a0002 | c0004 | t0001 | g0193 | EAS | CHB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18906 | hp1 | a0001 | c0011 | t0002 | g0217 | AFR | YRI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0241 | AFR | YRI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18948 | hp2 | a0002 | c0004 | t0001 | g0192 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18959 | hp1 | a0002 | c0004 | t0001 | g0177 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18963 | hp1 | a0002 | c0007 | t0001 | g0121 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18963 | hp2 | a0001 | c0006 | t0001 | g0232 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0195 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18969 | hp2 | a0001 | c0006 | t0001 | g0233 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18981 | hp1 | a0004 | c0013 | t0001 | g0004 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18982 | hp1 | a0002 | c0004 | t0001 | g0189 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18982 | hp2 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18983 | hp1 | a0002 | c0004 | t0001 | g0191 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0142 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18988 | hp1 | a0002 | c0007 | t0001 | g0186 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18988 | hp2 | a0001 | c0005 | t0001 | g0225 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0159 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0234 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18990 | hp2 | a0002 | c0007 | t0001 | g0185 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0118 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18994 | hp1 | a0002 | c0004 | t0001 | g0151 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18995 | hp1 | a0002 | c0001 | t0001 | g0171 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18997 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19000 | hp1 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0202 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19004 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19004 | hp2 | a0004 | c0013 | t0001 | g0003 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0141 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19010 | hp2 | a0002 | c0004 | t0001 | g0175 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0212 | AFR | LWK | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | LWK | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0236 | AFR | LWK | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | LWK | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0194 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19063 | hp1 | a0001 | c0005 | t0001 | g0224 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19074 | hp1 | a0002 | c0004 | t0001 | g0173 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0174 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19083 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19240 | hp1 | a0002 | c0007 | t0001 | g0207 | AFR | YRI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0240 | AFR | YRI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ASW | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | ASW | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0020 | EUR | TSI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0083 | EUR | TSI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0161 | EUR | TSI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | TSI | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | GIH | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20905 | hp2 | a0001 | c0006 | t0001 | g0230 | SAS | GIH | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0130 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0113 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | MSL | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20300 | hp1 | a0003 | c0012 | t0001 | g0220 | AFR | USA | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0084 | AFR | USA | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | LWK | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | LWK | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0038 | REF | REF | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0088 | REF | REF | NRDC_chr1_51784210_51883727 | NRDC | chr1 | 51784210 | 51883727 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:51794846 | C | T | 1 | a0005 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2613G>A | p.Met871Ile | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 23/31 | 2725/3594 | 2613/3456 | 871/1151 | chr1 | 51794846 | ||
| chr1:51810367 | T | G | 1 | a0006 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.1817A>C | p.Lys606Thr | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 16/31 | 1929/3594 | 1817/3456 | 606/1151 | chr1 | 51810367 | ||
| chr1:51840391 | ATCT | A | 3 | a0002a0004a0005 | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
disruptive_inframe_deletion | MODERATE | c.462_464delAGA | p.Glu154del | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/31 | 576/3594 | 462/3456 | 154/1151 | chr1 | 51840391 | ||
| chr1:51878485 | G | A | 1 | a0003 | 3 | HG02257.hp1 HG02970.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.131C>T | p.Pro44Leu | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/31 | 243/3594 | 131/3456 | 44/1151 | chr1 | 51878485 | ||
| chr1:51878555 | C | T | 1 | a0004 | 2 | NA18981.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.61G>A | p.Gly21Arg | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/31 | 173/3594 | 61/3456 | 21/1151 | chr1 | 51878555 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:51798392 | A | G | 11 | a0001c0002a0001c0006a0001c0011others(8): Show | 113 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(110): Show |
synonymous_variant | LOW | c.2461T>C | p.Leu821Leu | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/31 | 2573/3594 | 2461/3456 | 821/1151 | chr1 | 51798392 | ||
| chr1:51800570 | G | A | 6 | a0001c0008a0002c0001a0002c0007others(3): Show | 83 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(80): Show |
synonymous_variant | LOW | c.2427C>T | p.Pro809Pro | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/31 | 2539/3594 | 2427/3456 | 809/1151 | chr1 | 51800570 | ||
| chr1:51800678 | C | T | 3 | a0002c0004a0002c0010a0002c0019 | 19 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(16): Show |
synonymous_variant | LOW | c.2319G>A | p.Leu773Leu | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/31 | 2431/3594 | 2319/3456 | 773/1151 | chr1 | 51800678 | ||
| chr1:51825312 | T | G | 6 | a0002c0001a0002c0007a0002c0009others(3): Show | 83 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(80): Show |
synonymous_variant | LOW | c.1011A>C | p.Gly337Gly | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/31 | 1123/3594 | 1011/3456 | 337/1151 | chr1 | 51825312 | ||
| chr1:51825345 | C | T | 1 | a0001c0017 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.978G>A | p.Lys326Lys | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/31 | 1090/3594 | 978/3456 | 326/1151 | chr1 | 51825345 | ||
| chr1:51836177 | G | A | 1 | a0002c0010 | 3 | HG00741.hp2 HG01981.hp1 HG01993.hp1 |
synonymous_variant | LOW | c.666C>T | p.Phe222Phe | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/31 | 778/3594 | 666/3456 | 222/1151 | chr1 | 51836177 | ||
| chr1:51840355 | G | A | 1 | a0002c0015 | 2 | HG00738.hp2 HG01346.hp1 |
synonymous_variant | LOW | c.501C>T | p.Asp167Asp | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/31 | 613/3594 | 501/3456 | 167/1151 | chr1 | 51840355 | ||
| chr1:51878337 | C | T | 1 | a0001c0016 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.279G>A | p.Gly93Gly | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/31 | 391/3594 | 279/3456 | 93/1151 | chr1 | 51878337 | ||
| chr1:51878439 | G | A | 1 | a0001c0011 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.177C>T | p.Thr59Thr | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/31 | 289/3594 | 177/3456 | 59/1151 | chr1 | 51878439 | ||
| chr1:51878573 | T | G | 2 | a0001c0005a0001c0006 | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
synonymous_variant | LOW | c.43A>C | p.Arg15Arg | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/31 | 155/3594 | 43/3456 | 15/1151 | chr1 | 51878573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:51789230 | GTTTA | G | 2 | a0001c0011t0002a0002c0004t0002 | 4 | HG02055.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2_*5delTAAA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 31/31 | 2 | chr1 | 51789230 | |||||
| chr1:51878704 | G | A | 1 | a0001c0002t0003 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/31 | 89 | chr1 | 51878704 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:51789811 | C | T | 4 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218others(1): Show | 4 | HG02055.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3169-154G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51789811 | ||||||
| chr1:51789899 | A | G | 1 | a0001c0011t0002g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3169-242T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51789899 | ||||||
| chr1:51789900 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3169-243T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51789900 | ||||||
| chr1:51789933 | C | G | 2 | a0002c0001t0001g0127a0002c0014t0001g0196 | 2 | HG01175.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3169-276G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51789933 | ||||||
| chr1:51789965 | C | T | 4 | a0001c0002t0001g0048a0001c0002t0001g0051a0001c0002t0001g0052others(1): Show | 4 | HG02622.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3169-308G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51789965 | ||||||
| chr1:51789972 | C | T | 3 | a0002c0001t0001g0113a0002c0001t0001g0114a0002c0001t0001g0115 | 3 | HG02559.hp1 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3169-315G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51789972 | ||||||
| chr1:51790068 | A | G | 1 | a0002c0001t0001g0171 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3169-411T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790068 | ||||||
| chr1:51790084 | C | T | 1 | a0001c0002t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3169-427G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790084 | ||||||
| chr1:51790215 | CAA | C | 4 | a0001c0002t0001g0048a0001c0002t0001g0051a0001c0002t0001g0052others(1): Show | 4 | HG02622.hp1 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3168+316_3168+317d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790215 | ||||||
| chr1:51790252 | T | C | 1 | a0001c0003t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3168+281A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790252 | ||||||
| chr1:51790271 | T | C | 1 | a0002c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3168+262A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790271 | ||||||
| chr1:51790403 | C | T | 14 | a0001c0002t0001g0059a0001c0002t0001g0063a0001c0006t0001g0232others(11): Show | 14 | HG00673.hp1 HG01928.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.3168+130G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790403 | ||||||
| chr1:51790457 | G | A | 3 | a0002c0001t0001g0143a0002c0007t0001g0160a0002c0007t0001g0182 | 3 | HG01069.hp2 HG01071.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3168+76C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 29/30 | chr1 | 51790457 | ||||||
| chr1:51790671 | A | T | 1 | a0001c0002t0001g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3052-22T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 28/30 | chr1 | 51790671 | ||||||
| chr1:51790687 | A | G | 15 | a0001c0002t0001g0060a0001c0006t0001g0230a0002c0001t0001g0131others(12): Show | 15 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.3052-38T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 28/30 | chr1 | 51790687 | ||||||
| chr1:51791041 | G | A | 5 | a0001c0002t0001g0079a0001c0011t0002g0216a0001c0011t0002g0217others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2961-51C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 27/30 | chr1 | 51791041 | ||||||
| chr1:51791402 | A | G | 1 | a0002c0001t0001g0161 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2960+176T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 27/30 | chr1 | 51791402 | ||||||
| chr1:51791414 | T | C | 1 | a0001c0005t0001g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2960+164A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 27/30 | chr1 | 51791414 | ||||||
| chr1:51791927 | T | C | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2876+119A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 26/30 | chr1 | 51791927 | ||||||
| chr1:51792628 | G | C | 1 | a0002c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2776-204C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51792628 | ||||||
| chr1:51792717 | C | G | 1 | a0001c0003t0001g0009 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2776-293G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51792717 | ||||||
| chr1:51792731 | T | C | 2 | a0001c0002t0001g0068a0002c0014t0001g0152 | 2 | HG01257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2776-307A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51792731 | ||||||
| chr1:51792815 | AAATG | A | 22 | a0001c0002t0001g0041a0001c0002t0001g0042a0001c0002t0001g0045others(19): Show | 22 | HG00639.hp1 HG01069.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2776-395_2776-392d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51792815 | ||||||
| chr1:51792926 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2776-502C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51792926 | ||||||
| chr1:51793053 | T | C | 17 | a0001c0002t0001g0065a0001c0002t0001g0073a0001c0002t0001g0074others(14): Show | 17 | HG00639.hp1 HG01069.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2776-629A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51793053 | ||||||
| chr1:51793053 | T | G | 4 | a0001c0002t0001g0057a0001c0002t0001g0061a0001c0017t0001g0215others(1): Show | 4 | HG00099.hp2 HG01175.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.2776-629A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51793053 | ||||||
| chr1:51793572 | G | A | 1 | a0001c0002t0001g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2775+900C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51793572 | ||||||
| chr1:51793897 | T | C | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2775+575A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51793897 | ||||||
| chr1:51793930 | C | T | 1 | a0001c0006t0001g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2775+542G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 24/30 | chr1 | 51793930 | ||||||
| chr1:51795008 | T | G | 1 | a0001c0002t0001g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2605-154A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795008 | ||||||
| chr1:51795178 | T | C | 2 | a0001c0006t0001g0235a0002c0001t0001g0168 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2605-324A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795178 | ||||||
| chr1:51795258 | T | C | 3 | a0002c0001t0001g0113a0002c0001t0001g0114a0002c0001t0001g0115 | 3 | HG02559.hp1 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2605-404A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795258 | ||||||
| chr1:51795406 | C | G | 1 | a0001c0002t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2605-552G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795406 | ||||||
| chr1:51795458 | G | A | 58 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(55): Show | 58 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.2605-604C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795458 | ||||||
| chr1:51795474 | A | G | 1 | a0001c0003t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2605-620T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795474 | ||||||
| chr1:51795757 | T | C | 1 | a0001c0002t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2605-903A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795757 | ||||||
| chr1:51795790 | C | T | 3 | a0001c0002t0001g0085a0001c0006t0001g0235a0002c0001t0001g0168 | 3 | HG02717.hp1 HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2605-936G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795790 | ||||||
| chr1:51795926 | G | A | 2 | a0002c0001t0001g0194a0002c0001t0001g0200 | 2 | NA19056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2605-1072C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795926 | ||||||
| chr1:51795976 | G | A | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2605-1122C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51795976 | ||||||
| chr1:51796055 | A | T | 5 | a0001c0002t0001g0079a0001c0011t0002g0216a0001c0011t0002g0217others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2605-1201T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796055 | ||||||
| chr1:51796069 | T | C | 6 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0104others(3): Show | 6 | HG00639.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2605-1215A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796069 | ||||||
| chr1:51796192 | T | C | 1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2605-1338A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796192 | ||||||
| chr1:51796591 | CT | C | 184 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.2604+1657delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796591 | ||||||
| chr1:51796761 | T | C | 5 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0101others(2): Show | 5 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2604+1488A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796761 | ||||||
| chr1:51796770 | C | T | 241 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(240): Show |
intron_variant | MODIFIER | c.2604+1479G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796770 | ||||||
| chr1:51796833 | A | C | 56 | a0001c0002t0001g0039a0001c0002t0001g0044a0001c0002t0001g0047others(53): Show | 56 | HG00642.hp1 HG00673.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.2604+1416T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796833 | ||||||
| chr1:51796967 | G | A | 2 | a0002c0001t0001g0130a0002c0001t0001g0133 | 2 | HG00642.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2604+1282C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51796967 | ||||||
| chr1:51797117 | G | A | 3 | a0002c0001t0001g0142a0002c0001t0001g0145a0002c0001t0001g0147 | 3 | HG02040.hp1 NA18983.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2604+1132C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51797117 | ||||||
| chr1:51797369 | G | A | 5 | a0001c0006t0001g0230a0001c0006t0001g0232a0001c0006t0001g0233others(2): Show | 5 | HG04204.hp1 NA18963.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.2604+880C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51797369 | ||||||
| chr1:51797410 | G | A | 95 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(92): Show | 95 | HG00639.hp1 HG00642.hp1 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.2604+839C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51797410 | ||||||
| chr1:51797593 | G | A | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2604+656C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51797593 | ||||||
| chr1:51797631 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2604+618G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51797631 | ||||||
| chr1:51798210 | C | T | 22 | a0001c0002t0001g0039a0001c0002t0001g0044a0001c0002t0001g0047others(19): Show | 22 | HG01175.hp1 HG01257.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2604+39G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 22/30 | chr1 | 51798210 | ||||||
| chr1:51798519 | G | C | 10 | a0001c0005t0001g0222a0001c0005t0001g0226a0001c0005t0001g0228others(7): Show | 10 | HG02602.hp1 HG02698.hp1 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.2442-108C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51798519 | ||||||
| chr1:51798554 | A | G | 31 | a0001c0002t0001g0065a0001c0002t0001g0067a0001c0002t0001g0069others(28): Show | 31 | HG00639.hp1 HG01069.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.2442-143T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51798554 | ||||||
| chr1:51798797 | A | G | 1 | a0002c0004t0001g0192 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2442-386T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51798797 | ||||||
| chr1:51798800 | G | A | 1 | a0001c0003t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2442-389C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51798800 | ||||||
| chr1:51798925 | A | G | 3 | a0001c0006t0001g0239a0002c0004t0001g0122a0002c0004t0001g0184 | 3 | HG01943.hp2 HG03195.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2442-514T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51798925 | ||||||
| chr1:51799124 | TATAA | T | 3 | a0002c0007t0001g0121a0002c0007t0001g0185a0002c0007t0001g0197 | 3 | NA18612.hp1 NA18963.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2442-717_2442-714d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799124 | ||||||
| chr1:51799172 | C | T | 191 | a0001c0002t0001g0007a0001c0002t0001g0047a0001c0002t0001g0048others(188): Show | 192 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(189): Show |
intron_variant | MODIFIER | c.2442-761G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799172 | ||||||
| chr1:51799221 | A | G | 25 | a0001c0003t0001g0103a0001c0003t0001g0109a0002c0004t0001g0122others(22): Show | 25 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.2442-810T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799221 | ||||||
| chr1:51799321 | T | A | 16 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(13): Show | 16 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.2442-910A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799321 | ||||||
| chr1:51799347 | G | T | 4 | a0001c0002t0001g0007a0001c0002t0001g0075a0001c0002t0001g0076others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-936C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799347 | ||||||
| chr1:51799348 | CA | C | 4 | a0001c0002t0001g0007a0001c0002t0001g0075a0001c0002t0001g0076others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2442-938delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799348 | ||||||
| chr1:51799349 | A | C | 2 | a0001c0005t0001g0222a0001c0005t0001g0226 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2442-938T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799349 | ||||||
| chr1:51799362 | A | G | 1 | a0001c0003t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2442-951T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799362 | ||||||
| chr1:51799527 | T | C | 1 | a0001c0003t0001g0033 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2441+1029A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799527 | ||||||
| chr1:51799711 | G | T | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.2441+845C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799711 | ||||||
| chr1:51799851 | T | C | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2441+705A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799851 | ||||||
| chr1:51799978 | T | C | 1 | a0002c0001t0001g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2441+578A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51799978 | ||||||
| chr1:51800030 | G | A | 3 | a0002c0001t0001g0156a0002c0015t0001g0166a0002c0015t0001g0167 | 3 | HG00738.hp2 HG01109.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2441+526C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51800030 | ||||||
| chr1:51800066 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2441+490G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51800066 | ||||||
| chr1:51800297 | C | T | 46 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(43): Show | 47 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(44): Show |
intron_variant | MODIFIER | c.2441+259G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51800297 | ||||||
| chr1:51800371 | A | G | 1 | a0002c0001t0001g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2441+185T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51800371 | ||||||
| chr1:51800448 | C | T | 13 | a0001c0002t0001g0065a0001c0002t0001g0080a0001c0002t0001g0081others(10): Show | 13 | HG01069.hp1 HG01074.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.2441+108G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 21/30 | chr1 | 51800448 | ||||||
| chr1:51801011 | AT | A | 9 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2314-329delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801011 | ||||||
| chr1:51801159 | T | C | 1 | a0002c0001t0001g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2314-476A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801159 | ||||||
| chr1:51801261 | CT | C | 196 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(193): Show | 197 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.2314-579delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801261 | ||||||
| chr1:51801301 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2314-618G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801301 | ||||||
| chr1:51801383 | C | T | 1 | a0002c0004t0001g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2314-700G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801383 | ||||||
| chr1:51801486 | TG | T | 4 | a0001c0002t0001g0007a0001c0002t0001g0075a0001c0002t0001g0076others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2314-804delC | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801486 | ||||||
| chr1:51801591 | C | A | 11 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(8): Show | 11 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2314-908G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801591 | ||||||
| chr1:51801690 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.2314-1007A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801690 | ||||||
| chr1:51801699 | T | C | 24 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(21): Show | 25 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2314-1016A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801699 | ||||||
| chr1:51801765 | G | A | 24 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(21): Show | 25 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.2314-1082C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801765 | ||||||
| chr1:51801794 | A | AT | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2314-1112dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801794 | ||||||
| chr1:51801822 | C | G | 1 | a0001c0003t0001g0024 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2314-1139G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801822 | ||||||
| chr1:51801850 | C | T | 5 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0069others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2314-1167G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801850 | ||||||
| chr1:51801851 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2314-1168C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801851 | ||||||
| chr1:51801980 | G | T | 1 | a0001c0005t0001g0225 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2314-1297C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51801980 | ||||||
| chr1:51802079 | G | A | 4 | a0002c0007t0001g0121a0002c0007t0001g0185a0002c0007t0001g0186others(1): Show | 4 | NA18612.hp1 NA18963.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2314-1396C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802079 | ||||||
| chr1:51802099 | C | A | 1 | a0001c0006t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2314-1416G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802099 | ||||||
| chr1:51802354 | T | TATAC | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.2313+1456_2313+145 others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802354 | ||||||
| chr1:51802384 | A | C | 215 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(212): Show | 216 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.2313+1430T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802384 | ||||||
| chr1:51802592 | T | C | 1 | a0002c0001t0001g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2313+1222A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802592 | ||||||
| chr1:51802662 | C | T | 16 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(13): Show | 16 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2313+1152G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802662 | ||||||
| chr1:51802688 | T | C | 1 | a0001c0002t0001g0108 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2313+1126A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802688 | ||||||
| chr1:51802967 | C | T | 1 | a0002c0001t0001g0168 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2313+847G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51802967 | ||||||
| chr1:51803054 | C | T | 16 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(13): Show | 16 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2313+760G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803054 | ||||||
| chr1:51803197 | C | T | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.2313+617G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803197 | ||||||
| chr1:51803212 | C | T | 1 | a0001c0005t0001g0238 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2313+602G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803212 | ||||||
| chr1:51803308 | C | G | 13 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(10): Show | 13 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2313+506G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803308 | ||||||
| chr1:51803354 | A | G | 4 | a0002c0001t0001g0116a0002c0001t0001g0142a0002c0001t0001g0145others(1): Show | 4 | HG00544.hp1 HG02040.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2313+460T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803354 | ||||||
| chr1:51803374 | C | A | 105 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0008t0001g0032others(102): Show | 105 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.2313+440G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803374 | ||||||
| chr1:51803474 | C | CA | 13 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(10): Show | 13 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.2313+339dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803474 | ||||||
| chr1:51803474 | CA | C | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2313+339delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803474 | ||||||
| chr1:51803474 | CAA | C | 171 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(168): Show | 172 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.2313+338_2313+339d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803474 | ||||||
| chr1:51803474 | CAAAA | C | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2313+336_2313+339d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803474 | ||||||
| chr1:51803573 | G | A | 6 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(3): Show | 6 | HG02630.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2313+241C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803573 | ||||||
| chr1:51803601 | C | T | 1 | a0002c0004t0001g0175 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2313+213G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 20/30 | chr1 | 51803601 | ||||||
| chr1:51804040 | G | A | 9 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(6): Show | 9 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2163-76C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804040 | ||||||
| chr1:51804373 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.2163-409A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804373 | ||||||
| chr1:51804384 | C | A | 196 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(193): Show | 197 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.2163-420G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804384 | ||||||
| chr1:51804489 | G | GCTACGTT others(23): Show |
16 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(13): Show | 16 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2163-555_2163-526d others(32): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804489 | ||||||
| chr1:51804489 | G | GCTACGTT others(83): Show |
161 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0077others(158): Show | 162 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.2163-526_2163-525i others(92): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804489 | ||||||
| chr1:51804489 | G | GCTACGTT others(173): Show |
1 | a0001c0003t0001g0078 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2163-526_2163-525i others(182): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804489 | ||||||
| chr1:51804494 | G | GTTCAGAC others(83): Show |
1 | a0002c0001t0001g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2163-531_2163-530i others(92): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804494 | ||||||
| chr1:51804529 | G | GATACATT others(83): Show |
10 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2163-566_2163-565i others(92): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804529 | ||||||
| chr1:51804579 | G | C | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163-615C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804579 | ||||||
| chr1:51804583 | T | C | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163-619A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804583 | ||||||
| chr1:51804613 | G | C | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163-649C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804613 | ||||||
| chr1:51804621 | C | T | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163-657G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804621 | ||||||
| chr1:51804638 | T | C | 189 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(186): Show | 190 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.2163-674A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804638 | ||||||
| chr1:51804639 | G | C | 7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163-675C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804639 | ||||||
| chr1:51804653 | C | CATTTCCC others(143): Show |
7 | a0001c0002t0001g0039a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2163-690_2163-689i others(152): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804653 | ||||||
| chr1:51804667 | C | G | 1 | a0002c0001t0001g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2163-703G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804667 | ||||||
| chr1:51804794 | A | ATTCAGAC others(23): Show |
4 | a0001c0002t0001g0007a0001c0002t0001g0075a0001c0002t0001g0076others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2162+686_2162+715d others(32): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804794 | ||||||
| chr1:51804853 | C | G | 1 | a0001c0003t0001g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2162+657G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804853 | ||||||
| chr1:51804854 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2162+656C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804854 | ||||||
| chr1:51804872 | A | C | 1 | a0001c0002t0001g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2162+638T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804872 | ||||||
| chr1:51804939 | A | G | 3 | a0002c0010t0001g0149a0002c0010t0001g0150a0002c0010t0001g0153 | 3 | HG00741.hp2 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.2162+571T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804939 | ||||||
| chr1:51804944 | G | A | 21 | a0002c0004t0001g0122a0002c0004t0001g0151a0002c0004t0001g0173others(18): Show | 21 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.2162+566C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51804944 | ||||||
| chr1:51805067 | C | T | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2162+443G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51805067 | ||||||
| chr1:51805080 | G | A | 21 | a0002c0004t0001g0122a0002c0004t0001g0151a0002c0004t0001g0173others(18): Show | 21 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.2162+430C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51805080 | ||||||
| chr1:51805163 | T | C | 3 | a0001c0003t0001g0013a0001c0003t0001g0014a0001c0003t0001g0016 | 3 | NA18948.hp1 NA19005.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2162+347A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51805163 | ||||||
| chr1:51805184 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2162+326T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51805184 | ||||||
| chr1:51805303 | A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0031 | 2 | HG00738.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2162+207T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 19/30 | chr1 | 51805303 | ||||||
| chr1:51806218 | G | GA | 19 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(16): Show | 19 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.2110+575dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 18/30 | chr1 | 51806218 | ||||||
| chr1:51806291 | T | C | 1 | a0001c0005t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2110+503A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 18/30 | chr1 | 51806291 | ||||||
| chr1:51806352 | G | C | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2110+442C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 18/30 | chr1 | 51806352 | ||||||
| chr1:51806400 | G | GAA | 17 | a0001c0002t0001g0007a0001c0002t0001g0057a0001c0002t0001g0058others(14): Show | 17 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2110+392_2110+393d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 18/30 | chr1 | 51806400 | ||||||
| chr1:51806446 | C | T | 1 | a0001c0003t0001g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2110+348G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 18/30 | chr1 | 51806446 | ||||||
| chr1:51806511 | A | G | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2110+283T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 18/30 | chr1 | 51806511 | ||||||
| chr1:51807033 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1991-120A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51807033 | ||||||
| chr1:51807050 | TTAG | T | 196 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(193): Show | 197 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.1991-140_1991-138d others(5): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51807050 | ||||||
| chr1:51807221 | C | A | 1 | a0001c0003t0001g0016 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1991-308G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51807221 | ||||||
| chr1:51807796 | CT | C | 63 | a0001c0002t0001g0039a0001c0002t0001g0047a0001c0002t0001g0048others(60): Show | 64 | HG00639.hp1 HG00642.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.1991-884delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51807796 | ||||||
| chr1:51807985 | T | C | 164 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(161): Show | 165 | HG00544.hp1 HG00558.hp1 HG00642.hp1 others(162): Show |
intron_variant | MODIFIER | c.1991-1072A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51807985 | ||||||
| chr1:51808047 | G | A | 3 | a0001c0003t0001g0022a0001c0003t0001g0028a0001c0003t0001g0029 | 3 | HG03927.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1991-1134C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51808047 | ||||||
| chr1:51808159 | T | C | 19 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(16): Show | 19 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1990+1156A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51808159 | ||||||
| chr1:51808406 | T | G | 103 | a0001c0008t0001g0032a0001c0008t0001g0055a0002c0001t0001g0110others(100): Show | 103 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1990+909A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51808406 | ||||||
| chr1:51809008 | C | G | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1990+307G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 17/30 | chr1 | 51809008 | ||||||
| chr1:51809483 | C | T | 27 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(24): Show | 27 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1904-82G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 16/30 | chr1 | 51809483 | ||||||
| chr1:51809619 | A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1904-218T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 16/30 | chr1 | 51809619 | ||||||
| chr1:51809905 | C | CA | 18 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(15): Show | 18 | HG00099.hp2 HG00642.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1903+375dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 16/30 | chr1 | 51809905 | ||||||
| chr1:51810593 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1780-189C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51810593 | ||||||
| chr1:51810833 | T | G | 3 | a0002c0001t0001g0116a0002c0001t0001g0145a0002c0001t0001g0147 | 3 | HG00544.hp1 HG02040.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1780-429A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51810833 | ||||||
| chr1:51810896 | A | G | 3 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0203 | 3 | NA18982.hp2 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1780-492T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51810896 | ||||||
| chr1:51810982 | A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1780-578T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51810982 | ||||||
| chr1:51811205 | T | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1779+789A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811205 | ||||||
| chr1:51811226 | C | T | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1779+768G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811226 | ||||||
| chr1:51811433 | A | G | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1779+561T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811433 | ||||||
| chr1:51811468 | C | T | 1 | a0002c0001t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1779+526G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811468 | ||||||
| chr1:51811548 | T | C | 1 | a0001c0016t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1779+446A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811548 | ||||||
| chr1:51811580 | C | T | 2 | a0001c0003t0001g0103a0001c0003t0001g0109 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1779+414G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811580 | ||||||
| chr1:51811663 | A | G | 1 | a0002c0001t0001g0163 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1779+331T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811663 | ||||||
| chr1:51811783 | G | T | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.1779+211C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 15/30 | chr1 | 51811783 | ||||||
| chr1:51812158 | C | T | 1 | a0001c0006t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1675-60G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812158 | ||||||
| chr1:51812223 | C | T | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1675-125G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812223 | ||||||
| chr1:51812294 | G | A | 7 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675-196C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812294 | ||||||
| chr1:51812387 | G | T | 1 | a0001c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1675-289C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812387 | ||||||
| chr1:51812760 | T | C | 1 | a0002c0001t0001g0179 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1675-662A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812760 | ||||||
| chr1:51812819 | G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1675-721C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812819 | ||||||
| chr1:51812934 | C | T | 1 | a0002c0007t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1675-836G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812934 | ||||||
| chr1:51812961 | C | CA | 81 | a0001c0002t0001g0067a0001c0008t0001g0055a0002c0001t0001g0110others(78): Show | 81 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1675-864dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812961 | ||||||
| chr1:51812961 | C | CAA | 8 | a0002c0001t0001g0116a0002c0001t0001g0136a0002c0001t0001g0141others(5): Show | 8 | HG00544.hp1 HG02055.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1675-865_1675-864d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812961 | ||||||
| chr1:51812961 | CA | C | 108 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(105): Show | 110 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.1675-864delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812961 | ||||||
| chr1:51812961 | CAA | C | 16 | a0001c0002t0001g0074a0001c0003t0001g0027a0001c0005t0001g0222others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.1675-865_1675-864d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51812961 | ||||||
| chr1:51813050 | A | C | 213 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(210): Show | 214 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(211): Show |
intron_variant | MODIFIER | c.1675-952T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51813050 | ||||||
| chr1:51813094 | C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1674+941G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51813094 | ||||||
| chr1:51813284 | C | T | 1 | a0002c0001t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1674+751G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51813284 | ||||||
| chr1:51813558 | A | C | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1674+477T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51813558 | ||||||
| chr1:51813670 | A | G | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1674+365T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51813670 | ||||||
| chr1:51813978 | T | G | 203 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(200): Show | 203 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.1674+57A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 14/30 | chr1 | 51813978 | ||||||
| chr1:51814154 | C | T | 1 | a0001c0002t0001g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1620-65G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 13/30 | chr1 | 51814154 | ||||||
| chr1:51814326 | C | T | 2 | a0002c0015t0001g0166a0002c0015t0001g0167 | 2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1619+225G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 13/30 | chr1 | 51814326 | ||||||
| chr1:51814344 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1619+207C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 13/30 | chr1 | 51814344 | ||||||
| chr1:51814393 | C | G | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1619+158G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 13/30 | chr1 | 51814393 | ||||||
| chr1:51814839 | A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1440-26T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51814839 | ||||||
| chr1:51815174 | CTTTT | C | 103 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(100): Show | 103 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1440-365_1440-362d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815174 | ||||||
| chr1:51815177 | TTTTTC | T | 20 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(17): Show | 20 | HG01069.hp1 HG01168.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1440-369_1440-365d others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815177 | ||||||
| chr1:51815182 | C | CT | 30 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0060others(27): Show | 31 | HG00544.hp2 HG01074.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1440-370dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815182 | ||||||
| chr1:51815182 | C | CTT | 6 | a0001c0005t0001g0228a0001c0005t0001g0237a0001c0005t0001g0238others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440-371_1440-370d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815182 | ||||||
| chr1:51815182 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1440-369G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815182 | ||||||
| chr1:51815183 | T | C | 20 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(17): Show | 20 | HG01069.hp1 HG01168.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1440-370A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815183 | ||||||
| chr1:51815187 | T | C | 103 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(100): Show | 103 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.1440-374A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815187 | ||||||
| chr1:51815188 | T | C | 20 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(17): Show | 20 | HG01069.hp1 HG01168.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1440-375A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815188 | ||||||
| chr1:51815192 | T | C | 1 | a0002c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1440-379A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815192 | ||||||
| chr1:51815410 | T | A | 19 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(16): Show | 19 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1440-597A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815410 | ||||||
| chr1:51815450 | G | C | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440-637C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815450 | ||||||
| chr1:51815483 | G | GA | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1440-671dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815483 | ||||||
| chr1:51815602 | C | T | 1 | a0002c0001t0001g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1439+710G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815602 | ||||||
| chr1:51815680 | T | TC | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1439+631dupG | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815680 | ||||||
| chr1:51815812 | T | C | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.1439+500A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815812 | ||||||
| chr1:51815815 | G | A | 1 | a0002c0001t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1439+497C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815815 | ||||||
| chr1:51815873 | C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1439+439G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815873 | ||||||
| chr1:51815978 | T | A | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1439+334A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 11/30 | chr1 | 51815978 | ||||||
| chr1:51816644 | A | T | 3 | a0002c0010t0001g0149a0002c0010t0001g0150a0002c0010t0001g0153 | 3 | HG00741.hp2 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1362-255T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51816644 | ||||||
| chr1:51816718 | A | C | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1362-329T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51816718 | ||||||
| chr1:51816777 | T | C | 5 | a0001c0005t0001g0222a0001c0005t0001g0226a0001c0005t0001g0228others(2): Show | 5 | HG02602.hp1 HG02698.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1362-388A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51816777 | ||||||
| chr1:51816790 | A | G | 1 | a0001c0016t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1362-401T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51816790 | ||||||
| chr1:51816920 | A | G | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.1362-531T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51816920 | ||||||
| chr1:51817186 | T | C | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1362-797A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817186 | ||||||
| chr1:51817188 | G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1362-799C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817188 | ||||||
| chr1:51817312 | CT | C | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361+753delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817312 | ||||||
| chr1:51817407 | C | A | 1 | a0002c0004t0001g0175 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1361+659G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817407 | ||||||
| chr1:51817602 | C | T | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.1361+464G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817602 | ||||||
| chr1:51817698 | C | T | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1361+368G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817698 | ||||||
| chr1:51817797 | C | A | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1361+269G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817797 | ||||||
| chr1:51817798 | G | A | 1 | a0002c0001t0001g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1361+268C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 10/30 | chr1 | 51817798 | ||||||
| chr1:51818332 | G | A | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292-197C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51818332 | ||||||
| chr1:51818346 | A | C | 123 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(120): Show | 123 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.1292-211T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51818346 | ||||||
| chr1:51818364 | A | G | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1292-229T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51818364 | ||||||
| chr1:51818438 | G | A | 19 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(16): Show | 19 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1292-303C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51818438 | ||||||
| chr1:51818545 | T | G | 213 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(210): Show | 214 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(211): Show |
intron_variant | MODIFIER | c.1292-410A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51818545 | ||||||
| chr1:51818784 | G | C | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1292-649C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51818784 | ||||||
| chr1:51819160 | G | C | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1291+640C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819160 | ||||||
| chr1:51819246 | T | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1291+554A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819246 | ||||||
| chr1:51819272 | T | C | 1 | a0001c0002t0001g0079 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1291+528A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819272 | ||||||
| chr1:51819281 | G | A | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1291+519C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819281 | ||||||
| chr1:51819317 | T | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291+483A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819317 | ||||||
| chr1:51819384 | T | C | 2 | a0002c0014t0001g0152a0002c0014t0001g0196 | 2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1291+416A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819384 | ||||||
| chr1:51819620 | A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1291+180T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 9/30 | chr1 | 51819620 | ||||||
| chr1:51820151 | T | A | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1218-278A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51820151 | ||||||
| chr1:51820273 | A | G | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1218-400T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51820273 | ||||||
| chr1:51820514 | C | T | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1218-641G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51820514 | ||||||
| chr1:51820723 | G | T | 2 | a0001c0002t0001g0059a0001c0002t0001g0063 | 2 | NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1217+775C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51820723 | ||||||
| chr1:51820832 | G | C | 1 | a0002c0015t0001g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1217+666C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51820832 | ||||||
| chr1:51820953 | A | C | 10 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1217+545T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51820953 | ||||||
| chr1:51821133 | T | A | 13 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(10): Show | 13 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1217+365A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51821133 | ||||||
| chr1:51821154 | C | T | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1217+344G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51821154 | ||||||
| chr1:51821297 | A | T | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1217+201T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51821297 | ||||||
| chr1:51821435 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1217+63A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 8/30 | chr1 | 51821435 | ||||||
| chr1:51821761 | G | A | 1 | a0002c0004t0001g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1160-206C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51821761 | ||||||
| chr1:51821880 | G | A | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1160-325C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51821880 | ||||||
| chr1:51822128 | A | G | 6 | a0002c0001t0001g0208a0002c0001t0001g0209a0002c0001t0001g0210others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-573T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51822128 | ||||||
| chr1:51822149 | C | T | 14 | a0001c0002t0001g0072a0001c0002t0001g0073a0001c0002t0001g0074others(11): Show | 14 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1160-594G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51822149 | ||||||
| chr1:51822294 | T | A | 1 | a0001c0002t0001g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1160-739A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51822294 | ||||||
| chr1:51822373 | A | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1160-818T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51822373 | ||||||
| chr1:51822651 | G | C | 1 | a0002c0001t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1159+1013C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51822651 | ||||||
| chr1:51822694 | A | G | 13 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(10): Show | 13 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1159+970T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51822694 | ||||||
| chr1:51823144 | T | A | 1 | a0001c0003t0001g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1159+520A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51823144 | ||||||
| chr1:51823206 | T | C | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1159+458A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51823206 | ||||||
| chr1:51823548 | TGTATTAA others(6): Show |
T | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.1159+103_1159+115d others(15): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51823548 | ||||||
| chr1:51823623 | G | A | 1 | a0002c0015t0001g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1159+41C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 7/30 | chr1 | 51823623 | ||||||
| chr1:51824122 | C | CT | 18 | a0001c0003t0001g0010a0001c0005t0001g0222a0001c0005t0001g0223others(15): Show | 18 | HG00544.hp2 HG00558.hp2 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1037-337dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824122 | ||||||
| chr1:51824122 | CT | C | 20 | a0001c0002t0001g0072a0001c0002t0001g0075a0001c0002t0001g0076others(17): Show | 20 | HG01168.hp1 HG02055.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1037-337delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824122 | ||||||
| chr1:51824200 | A | G | 1 | a0002c0001t0001g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1037-414T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824200 | ||||||
| chr1:51824311 | A | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1037-525T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824311 | ||||||
| chr1:51824370 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1037-584G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824370 | ||||||
| chr1:51824404 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1037-618C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824404 | ||||||
| chr1:51824440 | T | C | 1 | a0001c0003t0001g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1037-654A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824440 | ||||||
| chr1:51824593 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1036+694G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824593 | ||||||
| chr1:51824666 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1036+621C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824666 | ||||||
| chr1:51824701 | T | A | 2 | a0001c0003t0001g0103a0001c0003t0001g0109 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1036+586A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824701 | ||||||
| chr1:51824730 | G | A | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036+557C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824730 | ||||||
| chr1:51824961 | T | C | 4 | a0002c0001t0001g0117a0002c0001t0001g0118a0004c0013t0001g0003others(1): Show | 4 | NA18981.hp1 NA18991.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+326A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824961 | ||||||
| chr1:51824985 | T | C | 1 | a0002c0007t0001g0207 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1036+302A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51824985 | ||||||
| chr1:51825145 | G | A | 7 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0069others(4): Show | 7 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1036+142C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51825145 | ||||||
| chr1:51825196 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.1036+91A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 6/30 | chr1 | 51825196 | ||||||
| chr1:51825409 | A | G | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.941-27T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51825409 | ||||||
| chr1:51825783 | G | A | 1 | a0001c0003t0001g0078 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.941-401C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51825783 | ||||||
| chr1:51826252 | G | A | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.941-870C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826252 | ||||||
| chr1:51826455 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.941-1073C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826455 | ||||||
| chr1:51826458 | G | A | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.941-1076C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826458 | ||||||
| chr1:51826521 | G | A | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.941-1139C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826521 | ||||||
| chr1:51826629 | A | C | 213 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(210): Show | 214 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(211): Show |
intron_variant | MODIFIER | c.940+1167T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826629 | ||||||
| chr1:51826632 | A | G | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.940+1164T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826632 | ||||||
| chr1:51826635 | C | T | 2 | a0002c0007t0001g0160a0002c0007t0001g0182 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.940+1161G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826635 | ||||||
| chr1:51826748 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.940+1048T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826748 | ||||||
| chr1:51826904 | C | T | 1 | a0002c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.940+892G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51826904 | ||||||
| chr1:51827244 | C | T | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.940+552G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827244 | ||||||
| chr1:51827284 | G | A | 30 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0002t0001g0077others(27): Show | 30 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.940+512C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827284 | ||||||
| chr1:51827344 | C | T | 2 | a0002c0001t0001g0134a0002c0001t0001g0144 | 2 | NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.940+452G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827344 | ||||||
| chr1:51827422 | C | A | 13 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(10): Show | 13 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.940+374G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827422 | ||||||
| chr1:51827472 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.940+324C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827472 | ||||||
| chr1:51827508 | C | A | 1 | a0004c0013t0001g0004 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.940+288G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827508 | ||||||
| chr1:51827510 | T | C | 3 | a0001c0003t0001g0022a0001c0003t0001g0028a0001c0003t0001g0029 | 3 | HG03927.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.940+286A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827510 | ||||||
| chr1:51827577 | A | G | 1 | a0001c0003t0001g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.940+219T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 5/30 | chr1 | 51827577 | ||||||
| chr1:51827898 | G | A | 123 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(120): Show | 123 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.867-29C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51827898 | ||||||
| chr1:51828032 | T | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.867-163A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828032 | ||||||
| chr1:51828130 | C | T | 6 | a0002c0001t0001g0208a0002c0001t0001g0209a0002c0001t0001g0210others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.867-261G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828130 | ||||||
| chr1:51828183 | T | C | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.867-314A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828183 | ||||||
| chr1:51828212 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.867-343G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828212 | ||||||
| chr1:51828444 | T | G | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.867-575A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828444 | ||||||
| chr1:51828468 | A | G | 3 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0203 | 3 | NA18982.hp2 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.867-599T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828468 | ||||||
| chr1:51828718 | C | CT | 177 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(174): Show | 178 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.867-850dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828718 | ||||||
| chr1:51828741 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.867-872A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828741 | ||||||
| chr1:51828811 | C | T | 2 | a0001c0002t0001g0079a0001c0008t0001g0097 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.867-942G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828811 | ||||||
| chr1:51828816 | T | G | 19 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(16): Show | 19 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.867-947A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828816 | ||||||
| chr1:51828843 | G | A | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.867-974C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828843 | ||||||
| chr1:51828862 | G | A | 213 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(210): Show | 214 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(211): Show |
intron_variant | MODIFIER | c.867-993C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828862 | ||||||
| chr1:51828883 | T | A | 19 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0080others(16): Show | 19 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.867-1014A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51828883 | ||||||
| chr1:51829257 | A | G | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.867-1388T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829257 | ||||||
| chr1:51829430 | C | T | 2 | a0001c0002t0001g0079a0001c0008t0001g0097 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.867-1561G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829430 | ||||||
| chr1:51829657 | T | C | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.867-1788A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829657 | ||||||
| chr1:51829778 | T | C | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.867-1909A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829778 | ||||||
| chr1:51829852 | AT | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0077a0001c0002t0001g0099others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.867-1984delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829852 | ||||||
| chr1:51829965 | C | CT | 27 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(24): Show | 27 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.867-2097dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829965 | ||||||
| chr1:51829965 | C | CTT | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.867-2098_867-2097d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829965 | ||||||
| chr1:51829965 | CT | C | 17 | a0001c0002t0001g0072a0001c0002t0001g0077a0001c0002t0001g0099others(14): Show | 17 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-2097delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51829965 | ||||||
| chr1:51830031 | C | T | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.867-2162G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51830031 | ||||||
| chr1:51830087 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.867-2218G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51830087 | ||||||
| chr1:51830251 | C | A | 1 | a0002c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.867-2382G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51830251 | ||||||
| chr1:51830252 | T | G | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.867-2383A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51830252 | ||||||
| chr1:51830784 | G | A | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.867-2915C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51830784 | ||||||
| chr1:51831105 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.866+2912A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831105 | ||||||
| chr1:51831201 | CA | C | 7 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0069others(4): Show | 7 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.866+2815delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831201 | ||||||
| chr1:51831243 | T | A | 1 | a0001c0011t0002g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.866+2774A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831243 | ||||||
| chr1:51831387 | T | A | 12 | a0002c0001t0001g0124a0002c0001t0001g0129a0002c0001t0001g0130others(9): Show | 12 | HG00642.hp2 HG01109.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.866+2630A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831387 | ||||||
| chr1:51831582 | C | CT | 9 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(6): Show | 9 | HG01943.hp2 HG02071.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.866+2434dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831582 | ||||||
| chr1:51831582 | C | CTT | 13 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(10): Show | 13 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.866+2433_866+2434d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831582 | ||||||
| chr1:51831582 | CT | C | 5 | a0001c0002t0001g0072a0001c0002t0001g0102a0001c0003t0001g0006others(2): Show | 5 | HG01167.hp1 HG02735.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.866+2434delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831582 | ||||||
| chr1:51831610 | G | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0077a0001c0002t0001g0099others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.866+2407C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831610 | ||||||
| chr1:51831655 | T | C | 3 | a0001c0002t0001g0100a0001c0002t0001g0101a0001c0002t0001g0102 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.866+2362A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831655 | ||||||
| chr1:51831689 | G | C | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.866+2328C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831689 | ||||||
| chr1:51831703 | C | T | 3 | a0002c0009t0001g0125a0002c0009t0001g0126a0002c0009t0001g0128 | 3 | HG01884.hp2 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.866+2314G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831703 | ||||||
| chr1:51831804 | C | T | 3 | a0001c0003t0001g0082a0001c0003t0001g0084a0001c0003t0001g0098 | 3 | HG02896.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.866+2213G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831804 | ||||||
| chr1:51831877 | G | A | 1 | a0001c0002t0001g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.866+2140C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831877 | ||||||
| chr1:51831886 | T | C | 213 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(210): Show | 214 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(211): Show |
intron_variant | MODIFIER | c.866+2131A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831886 | ||||||
| chr1:51831956 | G | A | 7 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.866+2061C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831956 | ||||||
| chr1:51831994 | A | G | 30 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0002t0001g0077others(27): Show | 30 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.866+2023T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51831994 | ||||||
| chr1:51832133 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.866+1884C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832133 | ||||||
| chr1:51832267 | G | A | 4 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(1): Show | 4 | HG02647.hp1 HG03130.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+1750C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832267 | ||||||
| chr1:51832289 | C | T | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.866+1728G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832289 | ||||||
| chr1:51832293 | C | A | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.866+1724G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832293 | ||||||
| chr1:51832354 | A | T | 15 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(12): Show | 15 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.866+1663T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832354 | ||||||
| chr1:51832479 | C | T | 83 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(80): Show | 83 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.866+1538G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832479 | ||||||
| chr1:51832486 | T | C | 1 | a0001c0006t0001g0239 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.866+1531A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832486 | ||||||
| chr1:51832512 | A | T | 3 | a0002c0001t0001g0116a0002c0001t0001g0145a0002c0001t0001g0147 | 3 | HG00544.hp1 HG02040.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.866+1505T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832512 | ||||||
| chr1:51832645 | C | T | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.866+1372G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832645 | ||||||
| chr1:51832797 | G | T | 30 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0002t0001g0077others(27): Show | 30 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.866+1220C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51832797 | ||||||
| chr1:51833440 | T | TA | 11 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(8): Show | 12 | HG00741.hp2 HG01981.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.866+576dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833440 | ||||||
| chr1:51833440 | TA | T | 5 | a0001c0003t0001g0027a0001c0006t0001g0236a0001c0017t0001g0215others(2): Show | 5 | HG01069.hp2 HG01943.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.866+576delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833440 | ||||||
| chr1:51833575 | G | T | 2 | a0001c0002t0001g0041a0001c0002t0001g0042 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.866+442C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833575 | ||||||
| chr1:51833576 | T | C | 2 | a0001c0002t0001g0041a0001c0002t0001g0042 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.866+441A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833576 | ||||||
| chr1:51833599 | T | C | 1 | a0001c0002t0001g0023 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.866+418A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833599 | ||||||
| chr1:51833738 | G | A | 237 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(236): Show |
intron_variant | MODIFIER | c.866+279C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833738 | ||||||
| chr1:51833762 | T | A | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.866+255A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 4/30 | chr1 | 51833762 | ||||||
| chr1:51834191 | G | A | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.713-21C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51834191 | ||||||
| chr1:51834385 | G | GCCTCCTG others(19): Show |
1 | a0001c0002t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.713-241_713-216dup others(26): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51834385 | ||||||
| chr1:51834498 | T | G | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.713-328A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51834498 | ||||||
| chr1:51834526 | G | A | 3 | a0002c0001t0001g0120a0002c0001t0001g0163a0002c0001t0001g0170 | 3 | HG01928.hp1 HG01981.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.713-356C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51834526 | ||||||
| chr1:51834565 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.713-395G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51834565 | ||||||
| chr1:51834976 | C | T | 1 | a0001c0005t0001g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.713-806G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51834976 | ||||||
| chr1:51835009 | G | T | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.713-839C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835009 | ||||||
| chr1:51835123 | G | A | 1 | a0002c0001t0001g0129 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.713-953C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835123 | ||||||
| chr1:51835136 | A | G | 2 | a0001c0002t0001g0081a0001c0002t0001g0089 | 2 | HG01069.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.713-966T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835136 | ||||||
| chr1:51835139 | G | A | 12 | a0002c0001t0001g0124a0002c0001t0001g0129a0002c0001t0001g0130others(9): Show | 12 | HG00642.hp2 HG01109.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.713-969C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835139 | ||||||
| chr1:51835364 | T | C | 3 | a0001c0003t0001g0013a0001c0003t0001g0014a0001c0003t0001g0016 | 3 | NA18948.hp1 NA19005.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.712+767A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835364 | ||||||
| chr1:51835383 | C | T | 1 | a0002c0001t0001g0208 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.712+748G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835383 | ||||||
| chr1:51835444 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.712+687A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835444 | ||||||
| chr1:51835467 | G | GT | 31 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(28): Show | 31 | HG01071.hp2 HG01891.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.712+663dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835467 | ||||||
| chr1:51835467 | G | GTT | 11 | a0001c0002t0001g0007a0001c0002t0001g0067a0001c0002t0001g0068others(8): Show | 11 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.712+662_712+663dup others(2): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835467 | ||||||
| chr1:51835467 | GT | G | 15 | a0001c0002t0001g0101a0001c0003t0001g0002a0001c0003t0001g0009others(12): Show | 16 | HG01943.hp2 HG02486.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.712+663delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835467 | ||||||
| chr1:51835492 | A | T | 1 | a0002c0004t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.712+639T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835492 | ||||||
| chr1:51835623 | C | T | 47 | a0002c0001t0001g0110a0002c0001t0001g0117a0002c0001t0001g0118others(44): Show | 47 | HG00735.hp1 HG00738.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.712+508G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835623 | ||||||
| chr1:51835880 | T | A | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.712+251A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51835880 | ||||||
| chr1:51836021 | C | G | 9 | a0001c0002t0001g0007a0001c0002t0001g0077a0001c0002t0001g0099others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.712+110G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51836021 | ||||||
| chr1:51836085 | A | C | 1 | a0002c0001t0001g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.712+46T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51836085 | ||||||
| chr1:51836087 | G | C | 5 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(2): Show | 5 | HG02647.hp1 HG03130.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.712+44C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51836087 | ||||||
| chr1:51836092 | A | G | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.712+39T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 3/30 | chr1 | 51836092 | ||||||
| chr1:51836253 | T | C | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.631-41A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51836253 | ||||||
| chr1:51836944 | C | CT | 24 | a0001c0002t0001g0007a0001c0002t0001g0057a0001c0002t0001g0058others(21): Show | 24 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.631-733dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51836944 | ||||||
| chr1:51836944 | C | CTT | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.631-734_631-733dup others(2): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51836944 | ||||||
| chr1:51836944 | CT | C | 63 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0073others(60): Show | 64 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.631-733delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51836944 | ||||||
| chr1:51837231 | AT | A | 10 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.631-1020delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51837231 | ||||||
| chr1:51837333 | G | A | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.631-1121C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51837333 | ||||||
| chr1:51837733 | A | G | 1 | a0001c0016t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.631-1521T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51837733 | ||||||
| chr1:51837809 | C | T | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-1597G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51837809 | ||||||
| chr1:51837880 | G | A | 1 | a0001c0002t0001g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.631-1668C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51837880 | ||||||
| chr1:51837896 | TCTC | T | 5 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(2): Show | 5 | HG02647.hp1 HG03130.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-1687_631-1685d others(5): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51837896 | ||||||
| chr1:51838018 | C | T | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.631-1806G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838018 | ||||||
| chr1:51838046 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.631-1834A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838046 | ||||||
| chr1:51838154 | G | A | 1 | a0001c0006t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.631-1942C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838154 | ||||||
| chr1:51838373 | C | A | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630+1853G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838373 | ||||||
| chr1:51838459 | T | C | 1 | a0001c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630+1767A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838459 | ||||||
| chr1:51838547 | A | T | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.630+1679T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838547 | ||||||
| chr1:51838597 | T | C | 5 | a0001c0002t0001g0100a0001c0002t0001g0101a0001c0002t0001g0102others(2): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1629A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838597 | ||||||
| chr1:51838761 | T | G | 1 | a0001c0003t0001g0009 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.630+1465A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838761 | ||||||
| chr1:51838986 | T | TAAACAGG | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.630+1233_630+1239d others(9): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51838986 | ||||||
| chr1:51839018 | C | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.630+1208G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839018 | ||||||
| chr1:51839060 | T | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.630+1166A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839060 | ||||||
| chr1:51839061 | A | T | 1 | a0001c0002t0001g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.630+1165T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839061 | ||||||
| chr1:51839130 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.630+1096G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839130 | ||||||
| chr1:51839160 | C | CT | 113 | a0001c0002t0001g0059a0001c0002t0001g0072a0001c0005t0001g0222others(110): Show | 113 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.630+1065dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839160 | ||||||
| chr1:51839160 | C | CTT | 12 | a0001c0005t0001g0231a0001c0005t0001g0237a0001c0005t0001g0238others(9): Show | 12 | HG01109.hp2 HG01993.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+1064_630+1065d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839160 | ||||||
| chr1:51839166 | T | C | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.630+1060A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839166 | ||||||
| chr1:51839171 | TTTTTTTG others(3): Show |
T | 1 | a0001c0003t0001g0016 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.630+1045_630+1054d others(12): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839171 | ||||||
| chr1:51839233 | C | CACTGCAA others(5): Show |
1 | a0001c0002t0001g0101 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.630+981_630+992dup others(12): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839233 | ||||||
| chr1:51839680 | T | G | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+546A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839680 | ||||||
| chr1:51839787 | A | G | 6 | a0001c0002t0001g0048a0001c0002t0001g0050a0001c0002t0001g0051others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+439T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839787 | ||||||
| chr1:51839809 | C | T | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.630+417G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839809 | ||||||
| chr1:51839890 | C | T | 1 | a0002c0001t0001g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.630+336G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839890 | ||||||
| chr1:51839992 | G | A | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.630+234C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51839992 | ||||||
| chr1:51840222 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | splice_region_variant&intron_variant | LOW | c.630+4C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 2/30 | chr1 | 51840222 | ||||||
| chr1:51840524 | G | GA | 26 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(23): Show | 26 | HG00544.hp2 HG00558.hp2 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.342-11dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51840524 | ||||||
| chr1:51840838 | A | G | 7 | a0001c0002t0001g0072a0001c0005t0001g0237a0001c0005t0001g0238others(4): Show | 7 | HG01943.hp2 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.342-324T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51840838 | ||||||
| chr1:51841371 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-857C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51841371 | ||||||
| chr1:51841719 | T | C | 237 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(236): Show |
intron_variant | MODIFIER | c.342-1205A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51841719 | ||||||
| chr1:51841986 | C | T | 1 | a0001c0003t0001g0020 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.342-1472G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51841986 | ||||||
| chr1:51842029 | T | C | 3 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0030 | 3 | HG00735.hp2 HG01192.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.342-1515A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842029 | ||||||
| chr1:51842032 | C | A | 1 | a0001c0003t0001g0015 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.342-1518G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842032 | ||||||
| chr1:51842044 | C | T | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-1530G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842044 | ||||||
| chr1:51842089 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-1575A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842089 | ||||||
| chr1:51842231 | G | GT | 14 | a0001c0002t0001g0040a0001c0002t0001g0041a0001c0002t0001g0042others(11): Show | 14 | HG01175.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.342-1718dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842231 | ||||||
| chr1:51842231 | GT | G | 8 | a0001c0002t0001g0007a0001c0002t0001g0090a0001c0002t0001g0091others(5): Show | 8 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-1718delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842231 | ||||||
| chr1:51842233 | T | G | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.342-1719A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842233 | ||||||
| chr1:51842245 | G | T | 1 | a0001c0002t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.342-1731C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842245 | ||||||
| chr1:51842353 | G | GGAGAAAA others(5): Show |
1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-1840_342-1839i others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842353 | ||||||
| chr1:51842480 | G | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-1966C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842480 | ||||||
| chr1:51842525 | CTG | C | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-2013_342-2012d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842525 | ||||||
| chr1:51842544 | T | A | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-2030A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842544 | ||||||
| chr1:51842905 | A | G | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-2391T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842905 | ||||||
| chr1:51842933 | G | C | 7 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.342-2419C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842933 | ||||||
| chr1:51842936 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-2422A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51842936 | ||||||
| chr1:51843063 | C | CA | 89 | a0001c0006t0001g0235a0002c0001t0001g0113a0002c0001t0001g0114others(86): Show | 89 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.342-2550dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843063 | ||||||
| chr1:51843063 | C | CAA | 12 | a0002c0001t0001g0115a0002c0001t0001g0129a0002c0001t0001g0130others(9): Show | 12 | HG00642.hp2 HG01109.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.342-2551_342-2550d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843063 | ||||||
| chr1:51843063 | CA | C | 92 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0039others(89): Show | 94 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.342-2550delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843063 | ||||||
| chr1:51843063 | CAA | C | 9 | a0001c0002t0001g0043a0001c0002t0001g0048a0001c0003t0001g0006others(6): Show | 9 | HG01167.hp1 HG02647.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-2551_342-2550d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843063 | ||||||
| chr1:51843169 | C | T | 6 | a0002c0001t0001g0110a0002c0001t0001g0157a0002c0001t0001g0162others(3): Show | 6 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-2655G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843169 | ||||||
| chr1:51843260 | A | C | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-2746T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843260 | ||||||
| chr1:51843311 | TA | T | 184 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(181): Show | 186 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.342-2798delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843311 | ||||||
| chr1:51843311 | TAA | T | 22 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.342-2799_342-2798d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843311 | ||||||
| chr1:51843323 | A | C | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.342-2809T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843323 | ||||||
| chr1:51843325 | A | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-2811T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843325 | ||||||
| chr1:51843606 | T | C | 2 | a0001c0005t0001g0225a0001c0005t0001g0227 | 2 | HG00558.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.342-3092A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843606 | ||||||
| chr1:51843742 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-3228A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843742 | ||||||
| chr1:51843851 | C | T | 222 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.342-3337G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843851 | ||||||
| chr1:51843854 | A | G | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-3340T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843854 | ||||||
| chr1:51843867 | G | GA | 6 | a0001c0002t0001g0031a0001c0002t0001g0094a0001c0005t0001g0225others(3): Show | 6 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-3354dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843867 | ||||||
| chr1:51843868 | A | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-3354T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51843868 | ||||||
| chr1:51844051 | A | G | 1 | a0002c0001t0001g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.342-3537T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844051 | ||||||
| chr1:51844109 | C | T | 1 | a0001c0008t0001g0032 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.342-3595G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844109 | ||||||
| chr1:51844113 | C | T | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-3599G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844113 | ||||||
| chr1:51844127 | C | G | 1 | a0001c0002t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.342-3613G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844127 | ||||||
| chr1:51844260 | T | C | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-3746A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844260 | ||||||
| chr1:51844486 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-3972G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844486 | ||||||
| chr1:51844620 | G | A | 2 | a0002c0001t0001g0164a0002c0001t0001g0171 | 2 | NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.342-4106C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844620 | ||||||
| chr1:51844633 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-4119C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844633 | ||||||
| chr1:51844726 | A | G | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-4212T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844726 | ||||||
| chr1:51844753 | C | G | 1 | a0001c0003t0001g0012 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.342-4239G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844753 | ||||||
| chr1:51844772 | G | T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-4258C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844772 | ||||||
| chr1:51844781 | A | AG | 23 | a0001c0002t0001g0072a0001c0002t0001g0087a0001c0003t0001g0017others(20): Show | 23 | HG00544.hp2 HG00558.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.342-4268dupC | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844781 | ||||||
| chr1:51844799 | G | T | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.342-4285C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844799 | ||||||
| chr1:51844813 | G | C | 1 | a0001c0002t0001g0031 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.342-4299C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844813 | ||||||
| chr1:51844817 | A | AGAAG | 4 | a0001c0003t0001g0084a0001c0003t0001g0098a0002c0001t0001g0116others(1): Show | 4 | HG00544.hp1 HG03516.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-4307_342-4304d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | A | AGAAGGAA others(5): Show |
1 | a0002c0001t0001g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.342-4315_342-4304d others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAG | A | 19 | a0001c0002t0001g0077a0001c0002t0001g0083a0001c0002t0001g0099others(16): Show | 19 | HG00558.hp1 HG00735.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.342-4307_342-4304d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(1): Show |
A | 37 | a0001c0002t0001g0079a0001c0002t0001g0085a0001c0002t0001g0086others(34): Show | 37 | HG00741.hp1 HG01106.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.342-4311_342-4304d others(10): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(5): Show |
A | 52 | a0001c0002t0001g0007a0001c0002t0001g0075a0001c0002t0001g0076others(49): Show | 52 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.342-4315_342-4304d others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(9): Show |
A | 40 | a0001c0002t0001g0023a0001c0002t0001g0039a0001c0002t0001g0064others(37): Show | 41 | HG00741.hp2 HG01069.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.342-4319_342-4304d others(18): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(13): Show |
A | 44 | a0001c0002t0001g0031a0001c0002t0001g0041a0001c0002t0001g0042others(41): Show | 45 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.342-4323_342-4304d others(22): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(17): Show |
A | 12 | a0001c0002t0001g0040a0001c0002t0001g0044a0001c0002t0001g0046others(9): Show | 12 | HG00639.hp1 HG01071.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.342-4327_342-4304d others(26): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(21): Show |
A | 3 | a0001c0002t0001g0054a0001c0002t0001g0072a0001c0003t0001g0066 | 3 | HG00642.hp1 HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.342-4331_342-4304d others(30): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(25): Show |
A | 15 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(12): Show | 15 | HG01167.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.342-4335_342-4304d others(34): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844817 | AGAAGGAA others(33): Show |
A | 1 | a0001c0003t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342-4343_342-4304d others(42): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844817 | ||||||
| chr1:51844844 | A | G | 1 | a0001c0003t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.342-4330T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844844 | ||||||
| chr1:51844933 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-4419C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51844933 | ||||||
| chr1:51845021 | C | A | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-4507G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845021 | ||||||
| chr1:51845033 | A | G | 2 | a0001c0002t0001g0079a0001c0008t0001g0097 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.342-4519T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845033 | ||||||
| chr1:51845084 | A | G | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.342-4570T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845084 | ||||||
| chr1:51845210 | C | T | 146 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0002t0001g0075others(143): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.342-4696G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845210 | ||||||
| chr1:51845305 | C | G | 1 | a0002c0001t0001g0174 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.342-4791G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845305 | ||||||
| chr1:51845383 | G | A | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-4869C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845383 | ||||||
| chr1:51845443 | T | C | 38 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0111others(35): Show | 40 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.342-4929A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845443 | ||||||
| chr1:51845596 | A | AAAAAG | 8 | a0001c0002t0001g0007a0001c0003t0001g0002a0001c0003t0001g0035others(5): Show | 9 | HG02486.hp1 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-5087_342-5083d others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845596 | ||||||
| chr1:51845620 | T | C | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.342-5106A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845620 | ||||||
| chr1:51845626 | G | C | 1 | a0001c0006t0001g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342-5112C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845626 | ||||||
| chr1:51845693 | T | C | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.342-5179A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845693 | ||||||
| chr1:51845860 | T | C | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-5346A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845860 | ||||||
| chr1:51845878 | C | T | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.342-5364G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845878 | ||||||
| chr1:51845886 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.342-5372C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845886 | ||||||
| chr1:51845889 | G | A | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-5375C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845889 | ||||||
| chr1:51845959 | T | TA | 9 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(6): Show | 9 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.342-5446dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845959 | ||||||
| chr1:51845960 | A | T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-5446T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51845960 | ||||||
| chr1:51846105 | T | C | 2 | a0001c0002t0001g0059a0001c0002t0001g0063 | 2 | NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.342-5591A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846105 | ||||||
| chr1:51846116 | A | AT | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.342-5603dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846116 | ||||||
| chr1:51846116 | AT | A | 22 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(19): Show | 22 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.342-5603delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846116 | ||||||
| chr1:51846152 | C | G | 1 | a0001c0005t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.342-5638G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846152 | ||||||
| chr1:51846170 | G | A | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-5656C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846170 | ||||||
| chr1:51846258 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-5744C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846258 | ||||||
| chr1:51846376 | A | C | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-5862T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846376 | ||||||
| chr1:51846414 | G | A | 1 | a0001c0003t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342-5900C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846414 | ||||||
| chr1:51846490 | A | G | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-5976T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846490 | ||||||
| chr1:51846495 | G | A | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.342-5981C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846495 | ||||||
| chr1:51846513 | G | A | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.342-5999C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846513 | ||||||
| chr1:51846568 | T | C | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.342-6054A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846568 | ||||||
| chr1:51846613 | G | A | 1 | a0001c0003t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.342-6099C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846613 | ||||||
| chr1:51846647 | G | A | 1 | a0002c0007t0001g0186 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.342-6133C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846647 | ||||||
| chr1:51846659 | G | A | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-6145C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846659 | ||||||
| chr1:51846718 | G | T | 1 | a0002c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.342-6204C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846718 | ||||||
| chr1:51846721 | G | C | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.342-6207C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846721 | ||||||
| chr1:51846762 | C | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.342-6248G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846762 | ||||||
| chr1:51846951 | TGATTGGT others(153): Show |
T | 1 | a0002c0001t0001g0141 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.342-6597_342-6438d others(2): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846951 | ||||||
| chr1:51846992 | TGATTGGT others(34): Show |
T | 2 | a0002c0007t0001g0160a0002c0007t0001g0182 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.342-6519_342-6479d others(43): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51846992 | ||||||
| chr1:51847042 | C | A | 1 | a0001c0006t0001g0239 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.342-6528G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847042 | ||||||
| chr1:51847093 | CAGCTAGA others(34): Show |
C | 1 | a0001c0003t0001g0009 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.342-6620_342-6580d others(43): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847093 | ||||||
| chr1:51847095 | G | A | 1 | a0002c0001t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.342-6581C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847095 | ||||||
| chr1:51847257 | C | A | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-6743G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847257 | ||||||
| chr1:51847337 | C | T | 3 | a0001c0002t0001g0057a0001c0002t0001g0061a0001c0017t0001g0215 | 3 | HG00099.hp2 HG01175.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.342-6823G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847337 | ||||||
| chr1:51847352 | G | T | 3 | a0001c0002t0001g0057a0001c0002t0001g0061a0001c0017t0001g0215 | 3 | HG00099.hp2 HG01175.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.342-6838C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847352 | ||||||
| chr1:51847374 | G | A | 2 | a0002c0014t0001g0152a0002c0014t0001g0196 | 2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.342-6860C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847374 | ||||||
| chr1:51847380 | A | G | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-6866T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847380 | ||||||
| chr1:51847398 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-6884C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847398 | ||||||
| chr1:51847426 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-6912C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847426 | ||||||
| chr1:51847473 | C | T | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.342-6959G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847473 | ||||||
| chr1:51847555 | G | C | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.342-7041C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847555 | ||||||
| chr1:51847574 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-7060A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847574 | ||||||
| chr1:51847611 | G | T | 1 | a0001c0003t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342-7097C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847611 | ||||||
| chr1:51847651 | G | A | 2 | a0001c0002t0001g0007a0001c0006t0001g0240 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.342-7137C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847651 | ||||||
| chr1:51847893 | C | G | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.342-7379G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51847893 | ||||||
| chr1:51848114 | G | A | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-7600C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848114 | ||||||
| chr1:51848174 | T | C | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-7660A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848174 | ||||||
| chr1:51848272 | AAGACCAT others(904): Show |
A | 1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-8669_342-7759d others(2): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848272 | ||||||
| chr1:51848302 | C | G | 3 | a0001c0002t0001g0104a0001c0002t0001g0106a0001c0002t0001g0107 | 3 | HG00639.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.342-7788G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848302 | ||||||
| chr1:51848302 | C | T | 1 | a0002c0001t0001g0146 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.342-7788G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848302 | ||||||
| chr1:51848366 | A | T | 2 | a0002c0001t0001g0145a0002c0001t0001g0147 | 2 | HG02040.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.342-7852T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848366 | ||||||
| chr1:51848484 | A | AAATAATA others(5): Show |
1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-7982_342-7971d others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848484 | ||||||
| chr1:51848484 | A | T | 6 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0083others(3): Show | 6 | HG01069.hp1 HG01192.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-7970T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848484 | ||||||
| chr1:51848558 | A | G | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-8044T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848558 | ||||||
| chr1:51848686 | T | A | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-8172A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848686 | ||||||
| chr1:51848731 | T | A | 2 | a0002c0004t0001g0122a0002c0004t0002g0123 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.342-8217A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51848731 | ||||||
| chr1:51849162 | G | A | 6 | a0001c0002t0001g0077a0001c0002t0001g0104a0001c0002t0001g0105others(3): Show | 6 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-8648C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849162 | ||||||
| chr1:51849296 | G | T | 7 | a0001c0002t0001g0077a0001c0002t0001g0104a0001c0002t0001g0105others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.342-8782C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849296 | ||||||
| chr1:51849441 | C | A | 1 | a0001c0002t0001g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.342-8927G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849441 | ||||||
| chr1:51849554 | C | A | 1 | a0002c0001t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.342-9040G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849554 | ||||||
| chr1:51849617 | C | A | 1 | a0002c0004t0001g0189 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.342-9103G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849617 | ||||||
| chr1:51849647 | TCTACTAA others(356): Show |
T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-9496_342-9134d others(2): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849647 | ||||||
| chr1:51849945 | A | G | 29 | a0001c0002t0001g0072a0001c0002t0001g0077a0001c0002t0001g0099others(26): Show | 29 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.342-9431T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849945 | ||||||
| chr1:51849996 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-9482A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51849996 | ||||||
| chr1:51850057 | A | C | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-9543T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850057 | ||||||
| chr1:51850111 | A | C | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-9597T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850111 | ||||||
| chr1:51850183 | A | T | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.342-9669T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850183 | ||||||
| chr1:51850186 | T | A | 39 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0075others(36): Show | 40 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.342-9672A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850186 | ||||||
| chr1:51850188 | A | T | 4 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(1): Show | 4 | HG02976.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-9674T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850188 | ||||||
| chr1:51850189 | T | A | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.342-9675A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850189 | ||||||
| chr1:51850192 | T | A | 1 | a0001c0002t0001g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342-9678A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850192 | ||||||
| chr1:51850245 | T | G | 16 | a0002c0004t0001g0151a0002c0004t0001g0173a0002c0004t0001g0175others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.342-9731A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850245 | ||||||
| chr1:51850262 | A | G | 1 | a0001c0003t0001g0103 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.342-9748T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850262 | ||||||
| chr1:51850332 | TACC | T | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-9821_342-9819d others(5): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850332 | ||||||
| chr1:51850338 | A | T | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-9824T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850338 | ||||||
| chr1:51850430 | AT | A | 38 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0111others(35): Show | 40 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.342-9917delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850430 | ||||||
| chr1:51850463 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-9949A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850463 | ||||||
| chr1:51850478 | G | T | 1 | a0002c0001t0001g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.342-9964C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850478 | ||||||
| chr1:51850509 | A | G | 30 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0002t0001g0077others(27): Show | 30 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.342-9995T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850509 | ||||||
| chr1:51850512 | T | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0077a0001c0002t0001g0099others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-9998A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850512 | ||||||
| chr1:51850609 | C | T | 21 | a0001c0002t0001g0072a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-10095G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850609 | ||||||
| chr1:51850759 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-10245C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51850759 | ||||||
| chr1:51851113 | T | C | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.342-10599A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851113 | ||||||
| chr1:51851121 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-10607G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851121 | ||||||
| chr1:51851227 | C | T | 1 | a0002c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.342-10713G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851227 | ||||||
| chr1:51851424 | C | T | 2 | a0001c0002t0001g0058a0002c0001t0001g0155 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.342-10910G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851424 | ||||||
| chr1:51851484 | T | G | 1 | a0001c0002t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342-10970A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851484 | ||||||
| chr1:51851546 | G | GA | 41 | a0001c0002t0001g0007a0001c0002t0001g0057a0001c0002t0001g0058others(38): Show | 41 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.342-11033dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851546 | ||||||
| chr1:51851546 | GA | G | 22 | a0001c0002t0001g0080a0001c0002t0001g0081a0001c0002t0001g0083others(19): Show | 22 | HG00673.hp1 HG00741.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.342-11033delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851546 | ||||||
| chr1:51851559 | T | A | 106 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(103): Show | 108 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.342-11045A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851559 | ||||||
| chr1:51851650 | C | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-11136G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851650 | ||||||
| chr1:51851690 | G | C | 1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-11176C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851690 | ||||||
| chr1:51851716 | A | T | 1 | a0001c0016t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.342-11202T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851716 | ||||||
| chr1:51851728 | C | A | 1 | a0001c0002t0001g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.342-11214G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851728 | ||||||
| chr1:51851815 | A | G | 1 | a0002c0001t0001g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.342-11301T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851815 | ||||||
| chr1:51851847 | G | A | 2 | a0002c0001t0001g0164a0002c0001t0001g0171 | 2 | NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.342-11333C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51851847 | ||||||
| chr1:51852015 | G | A | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.342-11501C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852015 | ||||||
| chr1:51852053 | G | A | 1 | a0002c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.342-11539C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852053 | ||||||
| chr1:51852258 | TCTTAGTT others(3): Show |
T | 2 | a0002c0001t0001g0210a0002c0001t0001g0212 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.342-11754_342-1174 others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852258 | ||||||
| chr1:51852327 | T | G | 1 | a0001c0005t0001g0225 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.342-11813A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852327 | ||||||
| chr1:51852336 | A | T | 1 | a0001c0005t0001g0225 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.342-11822T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852336 | ||||||
| chr1:51852436 | T | C | 21 | a0002c0004t0001g0122a0002c0004t0001g0151a0002c0004t0001g0173others(18): Show | 21 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.342-11922A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852436 | ||||||
| chr1:51852457 | ATATAAC | A | 16 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.342-11949_342-1194 others(10): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852457 | ||||||
| chr1:51852543 | A | ATAATATA others(552): Show |
2 | a0002c0004t0001g0173a0002c0004t0001g0189 | 2 | NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.342-12030_342-1202 others(563): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852543 | ||||||
| chr1:51852549 | A | AAACTATA others(518): Show |
2 | a0001c0002t0001g0104a0001c0002t0001g0107 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.342-12036_342-1203 others(529): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852549 | ||||||
| chr1:51852549 | A | ATAGTTTT others(545): Show |
2 | a0001c0002t0001g0079a0001c0008t0001g0097 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.342-12036_342-1203 others(556): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852549 | ||||||
| chr1:51852549 | A | ATAGTTTT others(623): Show |
7 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(4): Show | 7 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.342-12036_342-1203 others(634): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852549 | ||||||
| chr1:51852550 | G | GTTTTAAA others(463): Show |
1 | a0001c0002t0001g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(474): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(463): Show |
1 | a0001c0002t0001g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(474): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(633): Show |
1 | a0001c0006t0001g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(644): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(535): Show |
1 | a0001c0002t0001g0099 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(546): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(497): Show |
1 | a0001c0016t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(508): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(526): Show |
1 | a0001c0002t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(537): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(525): Show |
2 | a0001c0002t0001g0105a0001c0002t0001g0108 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(536): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(525): Show |
1 | a0001c0002t0001g0106 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(536): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(548): Show |
1 | a0002c0004t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(559): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(528): Show |
2 | a0002c0004t0001g0175a0002c0004t0001g0192 | 2 | NA18948.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(539): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(504): Show |
1 | a0002c0004t0001g0151 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(515): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(528): Show |
1 | a0002c0004t0001g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(539): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(548): Show |
1 | a0002c0004t0001g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(559): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(622): Show |
6 | a0002c0001t0001g0208a0002c0001t0001g0209a0002c0001t0001g0210others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(633): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(546): Show |
4 | a0002c0001t0001g0116a0002c0001t0001g0129a0002c0001t0001g0145others(1): Show | 4 | HG00544.hp1 HG01168.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(557): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(552): Show |
21 | a0002c0001t0001g0119a0002c0001t0001g0127a0002c0001t0001g0131others(18): Show | 21 | HG00558.hp1 HG00673.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(563): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(551): Show |
1 | a0002c0009t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(562): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(552): Show |
1 | a0002c0001t0001g0132 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(563): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(582): Show |
2 | a0002c0004t0001g0122a0002c0004t0002g0123 | 2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(593): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(526): Show |
1 | a0002c0004t0001g0180 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(537): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(528): Show |
2 | a0002c0001t0001g0143a0002c0004t0001g0181 | 2 | HG02293.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(539): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(547): Show |
2 | a0002c0001t0001g0124a0002c0001t0001g0135 | 2 | HG01167.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(558): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(646): Show |
3 | a0002c0001t0001g0113a0002c0001t0001g0114a0002c0001t0001g0115 | 3 | HG02559.hp1 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(657): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(576): Show |
3 | a0002c0001t0001g0134a0002c0014t0001g0152a0002c0014t0001g0196 | 3 | HG01175.hp1 HG01257.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(587): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(598): Show |
1 | a0002c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(609): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(507): Show |
1 | a0001c0003t0001g0015 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(518): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(483): Show |
23 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(20): Show | 24 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(494): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(469): Show |
1 | a0001c0003t0001g0013 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(480): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(484): Show |
1 | a0001c0003t0001g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(495): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(482): Show |
1 | a0001c0008t0001g0032 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(493): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(435): Show |
1 | a0001c0003t0001g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(446): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(588): Show |
1 | a0001c0002t0001g0070 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(599): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(564): Show |
16 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(13): Show | 16 | HG00642.hp1 HG01167.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(575): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(649): Show |
1 | a0001c0005t0001g0225 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(660): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(487): Show |
5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(498): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(647): Show |
3 | a0001c0005t0001g0223a0001c0005t0001g0224a0001c0005t0001g0227 | 3 | HG00544.hp2 HG00558.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(658): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(707): Show |
1 | a0001c0005t0001g0231 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(718): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(737): Show |
2 | a0001c0005t0001g0222a0001c0005t0001g0226 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(748): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(767): Show |
3 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234 | 3 | NA18963.hp2 NA18969.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(778): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(827): Show |
1 | a0001c0006t0001g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(838): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(767): Show |
1 | a0001c0005t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(778): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(567): Show |
3 | a0001c0003t0001g0078a0001c0003t0001g0084a0001c0003t0001g0098 | 3 | HG02280.hp2 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(578): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(597): Show |
1 | a0001c0003t0001g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(608): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(829): Show |
1 | a0001c0005t0001g0229 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(840): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(567): Show |
6 | a0001c0002t0001g0073a0001c0002t0001g0074a0001c0002t0001g0083others(3): Show | 6 | HG01192.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(578): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(597): Show |
2 | a0001c0002t0001g0080a0001c0002t0003g0242 | 2 | HG01346.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(608): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(542): Show |
2 | a0001c0002t0001g0081a0001c0002t0001g0089 | 2 | HG01069.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(553): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(573): Show |
2 | a0001c0003t0001g0103a0001c0003t0001g0109 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(584): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(543): Show |
3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(554): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(525): Show |
3 | a0001c0002t0001g0100a0001c0002t0001g0101a0001c0002t0001g0102 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(536): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(639): Show |
1 | a0001c0006t0001g0239 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(650): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(596): Show |
1 | a0001c0002t0001g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(607): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(600): Show |
2 | a0001c0002t0001g0059a0001c0002t0001g0063 | 2 | NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(611): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(630): Show |
2 | a0001c0002t0001g0060a0001c0002t0001g0064 | 2 | HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(641): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(606): Show |
1 | a0001c0002t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(617): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(600): Show |
2 | a0001c0002t0001g0057a0001c0002t0001g0061 | 2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(611): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(600): Show |
1 | a0001c0017t0001g0215 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(611): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(606): Show |
1 | a0001c0006t0001g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(617): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(635): Show |
1 | a0001c0005t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(646): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(635): Show |
1 | a0001c0005t0001g0238 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(646): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(605): Show |
1 | a0001c0005t0001g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(616): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(1024): Show |
1 | a0001c0006t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(1035): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(626): Show |
1 | a0001c0002t0001g0058 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(637): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(568): Show |
10 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(7): Show | 10 | HG02257.hp1 HG02280.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(579): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(585): Show |
1 | a0002c0007t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(596): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(611): Show |
1 | a0002c0001t0001g0159 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(622): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(627): Show |
2 | a0002c0007t0001g0121a0002c0007t0001g0185 | 2 | NA18963.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(638): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(559): Show |
1 | a0002c0001t0001g0179 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(570): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(589): Show |
37 | a0002c0001t0001g0117a0002c0001t0001g0118a0002c0001t0001g0120others(34): Show | 37 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.342-12037_342-1203 others(600): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(619): Show |
1 | a0002c0001t0001g0195 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(630): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(565): Show |
1 | a0002c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(576): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(613): Show |
3 | a0002c0001t0001g0158a0002c0001t0001g0165a0002c0001t0001g0198 | 3 | HG02615.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(624): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(567): Show |
2 | a0002c0001t0001g0157a0002c0001t0001g0188 | 2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(578): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(857): Show |
1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(868): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(778): Show |
1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.342-12037_342-1203 others(789): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(491): Show |
3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.342-12037_342-1203 others(502): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | GTTTTAAA others(572): Show |
1 | a0001c0002t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.342-12037_342-1203 others(583): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852550 | G | T | 11 | a0001c0002t0001g0079a0001c0002t0001g0090a0001c0002t0001g0091others(8): Show | 11 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.342-12036C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852550 | ||||||
| chr1:51852594 | A | G | 1 | a0001c0003t0001g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.342-12080T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852594 | ||||||
| chr1:51852594 | ATATAGTT others(3): Show |
A | 2 | a0002c0015t0001g0166a0002c0015t0001g0167 | 2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.342-12090_342-1208 others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852594 | ||||||
| chr1:51852714 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-12200C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852714 | ||||||
| chr1:51852994 | C | T | 1 | a0002c0001t0001g0201 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.342-12480G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51852994 | ||||||
| chr1:51853074 | A | T | 1 | a0002c0001t0001g0131 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.342-12560T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853074 | ||||||
| chr1:51853214 | T | C | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-12700A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853214 | ||||||
| chr1:51853222 | A | AAT | 10 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(7): Show | 10 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.342-12709_342-1270 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853222 | ||||||
| chr1:51853222 | A | T | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.342-12708T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853222 | ||||||
| chr1:51853224 | A | T | 141 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(138): Show | 141 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.342-12710T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853224 | ||||||
| chr1:51853226 | T | A | 42 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0057others(39): Show | 43 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.342-12712A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853226 | ||||||
| chr1:51853228 | T | A | 2 | a0001c0002t0001g0064a0001c0003t0001g0027 | 2 | HG02698.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.342-12714A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853228 | ||||||
| chr1:51853229 | A | G | 1 | a0002c0010t0001g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.342-12715T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853229 | ||||||
| chr1:51853241 | T | A | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342-12727A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853241 | ||||||
| chr1:51853398 | T | TG | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-12885_342-1288 others(5): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853398 | ||||||
| chr1:51853400 | A | T | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.342-12886T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853400 | ||||||
| chr1:51853585 | T | G | 1 | a0001c0003t0001g0028 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.342-13071A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853585 | ||||||
| chr1:51853675 | T | C | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-13161A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51853675 | ||||||
| chr1:51854059 | G | T | 2 | a0001c0002t0001g0105a0001c0002t0001g0108 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.342-13545C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854059 | ||||||
| chr1:51854098 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.342-13584C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854098 | ||||||
| chr1:51854140 | C | T | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.342-13626G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854140 | ||||||
| chr1:51854228 | C | T | 1 | a0002c0001t0001g0144 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.342-13714G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854228 | ||||||
| chr1:51854294 | G | A | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.342-13780C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854294 | ||||||
| chr1:51854510 | C | T | 2 | a0001c0002t0001g0079a0001c0008t0001g0097 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.342-13996G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854510 | ||||||
| chr1:51854887 | T | C | 83 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(80): Show | 83 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.342-14373A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854887 | ||||||
| chr1:51854909 | A | G | 1 | a0002c0001t0001g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.342-14395T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854909 | ||||||
| chr1:51854981 | G | A | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.342-14467C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51854981 | ||||||
| chr1:51855044 | T | C | 1 | a0002c0004t0001g0205 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.342-14530A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855044 | ||||||
| chr1:51855099 | C | T | 2 | a0001c0002t0001g0059a0001c0002t0001g0063 | 2 | NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.342-14585G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855099 | ||||||
| chr1:51855401 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.342-14887T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855401 | ||||||
| chr1:51855468 | T | TA | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.342-14955dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855468 | ||||||
| chr1:51855491 | G | GA | 17 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(14): Show | 17 | HG00099.hp2 HG00673.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.342-14978dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855491 | ||||||
| chr1:51855561 | T | G | 1 | a0001c0011t0002g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.342-15047A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855561 | ||||||
| chr1:51855854 | CAGAT | C | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-15344_342-1534 others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855854 | ||||||
| chr1:51855902 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.342-15388A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855902 | ||||||
| chr1:51855911 | C | A | 3 | a0002c0001t0001g0131a0002c0001t0001g0132a0002c0001t0001g0137 | 3 | HG02602.hp2 HG03017.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.342-15397G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51855911 | ||||||
| chr1:51856139 | G | T | 222 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.342-15625C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856139 | ||||||
| chr1:51856230 | C | G | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.342-15716G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856230 | ||||||
| chr1:51856457 | G | A | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.342-15943C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856457 | ||||||
| chr1:51856586 | G | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.342-16072C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856586 | ||||||
| chr1:51856629 | C | T | 1 | a0002c0001t0001g0136 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.342-16115G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856629 | ||||||
| chr1:51856837 | A | G | 98 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.342-16323T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856837 | ||||||
| chr1:51856917 | G | A | 1 | a0002c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.342-16403C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856917 | ||||||
| chr1:51856989 | C | T | 33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.342-16475G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51856989 | ||||||
| chr1:51857035 | A | G | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.342-16521T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857035 | ||||||
| chr1:51857086 | T | TAA | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.342-16574_342-1657 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857086 | ||||||
| chr1:51857206 | C | G | 1 | a0002c0001t0001g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.342-16692G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857206 | ||||||
| chr1:51857541 | G | A | 1 | a0001c0002t0001g0058 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.342-17027C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857541 | ||||||
| chr1:51857545 | T | C | 1 | a0002c0001t0001g0176 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.342-17031A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857545 | ||||||
| chr1:51857681 | A | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.342-17167T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857681 | ||||||
| chr1:51857702 | G | C | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-17188C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857702 | ||||||
| chr1:51857705 | C | G | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-17191G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857705 | ||||||
| chr1:51857766 | C | G | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-17252G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857766 | ||||||
| chr1:51857910 | A | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.342-17396T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857910 | ||||||
| chr1:51857951 | G | A | 21 | a0002c0004t0001g0122a0002c0004t0001g0151a0002c0004t0001g0173others(18): Show | 21 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.342-17437C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51857951 | ||||||
| chr1:51858053 | T | C | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.342-17539A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858053 | ||||||
| chr1:51858095 | G | C | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.342-17581C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858095 | ||||||
| chr1:51858100 | G | C | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.342-17586C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858100 | ||||||
| chr1:51858208 | G | T | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.342-17694C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858208 | ||||||
| chr1:51858471 | T | C | 1 | a0002c0019t0001g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.342-17957A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858471 | ||||||
| chr1:51858471 | T | TA | 24 | a0001c0002t0001g0058a0001c0003t0001g0056a0001c0005t0001g0222others(21): Show | 24 | HG00544.hp2 HG00558.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.342-17958dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858471 | ||||||
| chr1:51858471 | TA | T | 9 | a0001c0002t0001g0040a0001c0002t0001g0090a0001c0002t0001g0102others(6): Show | 9 | HG00639.hp1 HG01167.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.342-17958delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858471 | ||||||
| chr1:51858556 | C | T | 222 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.342-18042G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858556 | ||||||
| chr1:51858795 | C | T | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.342-18281G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858795 | ||||||
| chr1:51858873 | G | C | 1 | a0001c0003t0001g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.342-18359C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51858873 | ||||||
| chr1:51859177 | T | C | 3 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0203 | 3 | NA18982.hp2 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.342-18663A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51859177 | ||||||
| chr1:51859804 | G | A | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+18471C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51859804 | ||||||
| chr1:51859928 | G | A | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+18347C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51859928 | ||||||
| chr1:51859986 | A | G | 2 | a0002c0001t0001g0124a0002c0001t0001g0135 | 2 | HG01167.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.341+18289T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51859986 | ||||||
| chr1:51860353 | T | C | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.341+17922A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860353 | ||||||
| chr1:51860787 | T | C | 1 | a0002c0001t0001g0199 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.341+17488A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860787 | ||||||
| chr1:51860819 | A | G | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+17456T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860819 | ||||||
| chr1:51860951 | C | CT | 19 | a0001c0002t0001g0067a0001c0011t0002g0216a0002c0001t0001g0144others(16): Show | 19 | HG00673.hp1 HG00741.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.341+17323dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860951 | ||||||
| chr1:51860951 | C | CTT | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.341+17322_341+1732 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860951 | ||||||
| chr1:51860951 | CT | C | 21 | a0001c0002t0001g0007a0001c0005t0001g0222a0001c0005t0001g0223others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+17323delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860951 | ||||||
| chr1:51860996 | C | G | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.341+17279G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51860996 | ||||||
| chr1:51861011 | A | G | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+17264T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861011 | ||||||
| chr1:51861012 | T | C | 222 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.341+17263A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861012 | ||||||
| chr1:51861159 | A | C | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+17116T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861159 | ||||||
| chr1:51861213 | G | A | 1 | a0002c0004t0001g0192 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.341+17062C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861213 | ||||||
| chr1:51861229 | CGTGA | C | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+17042_341+1704 others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861229 | ||||||
| chr1:51861230 | G | A | 2 | a0002c0001t0001g0124a0002c0001t0001g0135 | 2 | HG01167.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.341+17045C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861230 | ||||||
| chr1:51861238 | C | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+17037G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861238 | ||||||
| chr1:51861239 | TGCACCC | T | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+17030_341+1703 others(10): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861239 | ||||||
| chr1:51861265 | C | CT | 52 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(49): Show | 53 | HG00673.hp1 HG00741.hp2 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.341+17009dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861265 | ||||||
| chr1:51861265 | C | CTT | 80 | a0001c0002t0001g0111a0002c0001t0001g0110a0002c0001t0001g0113others(77): Show | 80 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.341+17008_341+1700 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861265 | ||||||
| chr1:51861265 | C | CTTTT | 12 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(9): Show | 12 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.341+17006_341+1700 others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861265 | ||||||
| chr1:51861280 | T | TC | 7 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0069others(4): Show | 7 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+16994_341+1699 others(5): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861280 | ||||||
| chr1:51861330 | C | CT | 45 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(42): Show | 45 | HG00099.hp2 HG00558.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.341+16944dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861330 | ||||||
| chr1:51861330 | C | CTT | 14 | a0001c0002t0001g0049a0001c0005t0001g0222a0001c0005t0001g0223others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+16943_341+1694 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861330 | ||||||
| chr1:51861330 | C | CTTT | 7 | a0001c0005t0001g0225a0001c0005t0001g0238a0001c0005t0001g0241others(4): Show | 7 | HG01943.hp2 HG02647.hp1 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.341+16944_341+1694 others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861330 | ||||||
| chr1:51861333 | C | T | 217 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0039others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.341+16942G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861333 | ||||||
| chr1:51861419 | T | C | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+16856A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861419 | ||||||
| chr1:51861511 | ATTT | A | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.341+16761_341+1676 others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861511 | ||||||
| chr1:51861514 | T | A | 183 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(180): Show | 185 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.341+16761A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51861514 | ||||||
| chr1:51862232 | T | C | 1 | a0002c0001t0001g0124 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.341+16043A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862232 | ||||||
| chr1:51862255 | C | T | 1 | a0002c0001t0001g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.341+16020G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862255 | ||||||
| chr1:51862328 | G | A | 1 | a0001c0006t0001g0230 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.341+15947C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862328 | ||||||
| chr1:51862481 | G | T | 2 | a0001c0003t0001g0022a0001c0003t0001g0028 | 2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.341+15794C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862481 | ||||||
| chr1:51862643 | G | C | 3 | a0003c0012t0001g0219a0003c0012t0001g0220a0003c0012t0001g0221 | 3 | HG02257.hp1 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.341+15632C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862643 | ||||||
| chr1:51862668 | A | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+15607T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862668 | ||||||
| chr1:51862743 | C | T | 1 | a0001c0002t0001g0058 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.341+15532G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862743 | ||||||
| chr1:51862905 | G | T | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+15370C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862905 | ||||||
| chr1:51862953 | C | T | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.341+15322G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862953 | ||||||
| chr1:51862964 | C | A | 1 | a0001c0006t0001g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.341+15311G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51862964 | ||||||
| chr1:51863005 | G | A | 1 | a0001c0005t0001g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.341+15270C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863005 | ||||||
| chr1:51863013 | G | GA | 45 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0039others(42): Show | 46 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.341+15261dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | G | GAA | 66 | a0001c0002t0001g0031a0001c0002t0001g0052a0001c0002t0001g0053others(63): Show | 66 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.341+15260_341+1526 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | G | GAAA | 61 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0075others(58): Show | 61 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.341+15259_341+1526 others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | G | GAAAA | 16 | a0001c0002t0001g0090a0001c0002t0001g0091a0001c0002t0001g0092others(13): Show | 16 | HG00673.hp1 HG00741.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.341+15258_341+1526 others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | G | GAAAAA | 5 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096others(2): Show | 5 | HG01928.hp2 HG02572.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+15257_341+1526 others(9): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | G | GGAAAAAA | 2 | a0001c0003t0001g0002a0001c0003t0001g0038 | 3 | HG02486.hp1 HG02970.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.341+15261_341+1526 others(11): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | GAA | G | 20 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(17): Show | 20 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.341+15260_341+1526 others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863013 | GAAAAAAA others(3): Show |
G | 1 | a0002c0001t0001g0136 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.341+15252_341+1526 others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863013 | ||||||
| chr1:51863229 | T | C | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+15046A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863229 | ||||||
| chr1:51863327 | G | A | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+14948C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863327 | ||||||
| chr1:51863416 | T | A | 1 | a0001c0006t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.341+14859A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863416 | ||||||
| chr1:51863420 | C | G | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+14855G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863420 | ||||||
| chr1:51863906 | A | C | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.341+14369T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51863906 | ||||||
| chr1:51864131 | A | C | 1 | a0001c0003t0001g0033 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.341+14144T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864131 | ||||||
| chr1:51864166 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341+14109G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864166 | ||||||
| chr1:51864243 | C | T | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+14032G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864243 | ||||||
| chr1:51864244 | G | A | 1 | a0002c0001t0001g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.341+14031C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864244 | ||||||
| chr1:51864330 | T | A | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+13945A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864330 | ||||||
| chr1:51864491 | T | C | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.341+13784A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864491 | ||||||
| chr1:51864728 | G | T | 1 | a0001c0003t0001g0109 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.341+13547C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864728 | ||||||
| chr1:51864829 | G | A | 38 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.341+13446C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864829 | ||||||
| chr1:51864949 | T | TA | 16 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(13): Show | 17 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.341+13325dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864949 | ||||||
| chr1:51864949 | TA | T | 21 | a0001c0002t0001g0048a0001c0002t0001g0060a0001c0002t0003g0242others(18): Show | 21 | HG00544.hp2 HG00558.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.341+13325delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51864949 | ||||||
| chr1:51865042 | A | G | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341+13233T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865042 | ||||||
| chr1:51865067 | T | C | 1 | a0002c0007t0001g0197 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.341+13208A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865067 | ||||||
| chr1:51865076 | A | G | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+13199T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865076 | ||||||
| chr1:51865310 | G | GT | 6 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0006t0001g0235others(3): Show | 6 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+12964dupA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865310 | ||||||
| chr1:51865354 | G | C | 1 | a0002c0001t0001g0145 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.341+12921C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865354 | ||||||
| chr1:51865366 | G | A | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.341+12909C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865366 | ||||||
| chr1:51865601 | C | A | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.341+12674G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865601 | ||||||
| chr1:51865651 | G | A | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+12624C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865651 | ||||||
| chr1:51865663 | T | G | 5 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(2): Show | 5 | HG02647.hp1 HG03130.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+12612A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865663 | ||||||
| chr1:51865847 | C | T | 1 | a0001c0003t0001g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.341+12428G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865847 | ||||||
| chr1:51865895 | C | CA | 17 | a0001c0002t0001g0072a0001c0002t0001g0075a0001c0002t0001g0076others(14): Show | 17 | HG02257.hp2 HG02293.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.341+12379dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51865895 | ||||||
| chr1:51866023 | C | A | 33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+12252G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866023 | ||||||
| chr1:51866034 | C | T | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+12241G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866034 | ||||||
| chr1:51866055 | C | CA | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+12219dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866055 | ||||||
| chr1:51866065 | A | G | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+12210T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866065 | ||||||
| chr1:51866174 | A | G | 2 | a0002c0004t0001g0180a0002c0004t0001g0181 | 2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.341+12101T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866174 | ||||||
| chr1:51866324 | A | G | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+11951T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866324 | ||||||
| chr1:51866349 | A | C | 1 | a0001c0002t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.341+11926T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866349 | ||||||
| chr1:51866351 | T | C | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+11924A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866351 | ||||||
| chr1:51866413 | C | T | 3 | a0001c0003t0001g0020a0001c0003t0001g0021a0001c0008t0001g0032 | 3 | HG03490.hp1 HG03492.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.341+11862G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866413 | ||||||
| chr1:51866483 | T | C | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+11792A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866483 | ||||||
| chr1:51866579 | A | G | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+11696T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866579 | ||||||
| chr1:51866601 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+11674A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866601 | ||||||
| chr1:51866648 | A | T | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+11627T>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866648 | ||||||
| chr1:51866650 | T | C | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+11625A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866650 | ||||||
| chr1:51866666 | G | T | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+11609C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866666 | ||||||
| chr1:51866693 | C | CA | 14 | a0001c0002t0001g0007a0001c0002t0001g0039a0001c0002t0001g0040others(11): Show | 14 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+11581dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866693 | ||||||
| chr1:51866705 | A | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+11570T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866705 | ||||||
| chr1:51866853 | GA | G | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+11421delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51866853 | ||||||
| chr1:51867214 | C | T | 5 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(2): Show | 5 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+11061G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51867214 | ||||||
| chr1:51867276 | A | C | 1 | a0002c0001t0001g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.341+10999T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51867276 | ||||||
| chr1:51867295 | G | A | 2 | a0002c0001t0001g0178a0002c0001t0001g0179 | 2 | HG02040.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.341+10980C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51867295 | ||||||
| chr1:51867350 | G | C | 1 | a0002c0001t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.341+10925C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51867350 | ||||||
| chr1:51867642 | CAAG | C | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+10630_341+1063 others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51867642 | ||||||
| chr1:51868174 | T | C | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341+10101A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868174 | ||||||
| chr1:51868375 | A | G | 98 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.341+9900T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868375 | ||||||
| chr1:51868612 | G | A | 12 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0079others(9): Show | 12 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+9663C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868612 | ||||||
| chr1:51868616 | G | A | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+9659C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868616 | ||||||
| chr1:51868628 | C | G | 1 | a0002c0001t0001g0157 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.341+9647G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868628 | ||||||
| chr1:51868652 | T | C | 1 | a0001c0005t0001g0238 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.341+9623A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868652 | ||||||
| chr1:51868806 | G | A | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.341+9469C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868806 | ||||||
| chr1:51868976 | G | A | 2 | a0001c0002t0001g0054a0001c0008t0001g0055 | 2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.341+9299C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51868976 | ||||||
| chr1:51869033 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+9242C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869033 | ||||||
| chr1:51869151 | T | G | 3 | a0001c0002t0001g0104a0001c0002t0001g0106a0001c0002t0001g0107 | 3 | HG00639.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.341+9124A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869151 | ||||||
| chr1:51869186 | G | A | 222 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.341+9089C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869186 | ||||||
| chr1:51869288 | G | A | 55 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(52): Show | 57 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.341+8987C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869288 | ||||||
| chr1:51869358 | A | C | 13 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(10): Show | 13 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.341+8917T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869358 | ||||||
| chr1:51869424 | G | A | 33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+8851C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869424 | ||||||
| chr1:51869560 | ATCTC | A | 3 | a0001c0002t0001g0086a0001c0002t0001g0087a0001c0008t0001g0097 | 3 | HG01192.hp2 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.341+8711_341+8714d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869560 | ||||||
| chr1:51869711 | C | A | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+8564G>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51869711 | ||||||
| chr1:51870249 | A | G | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+8026T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51870249 | ||||||
| chr1:51870382 | A | AACTACTG others(335): Show |
1 | a0001c0002t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.341+7892_341+7893i others(344): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51870382 | ||||||
| chr1:51870465 | C | T | 6 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(3): Show | 7 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+7810G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51870465 | ||||||
| chr1:51870767 | TGAATACA others(14): Show |
T | 10 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+7487_341+7507d others(23): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51870767 | ||||||
| chr1:51870828 | TAATACA | T | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.341+7441_341+7446d others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51870828 | ||||||
| chr1:51871007 | A | G | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.341+7268T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871007 | ||||||
| chr1:51871012 | A | C | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.341+7263T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871012 | ||||||
| chr1:51871037 | C | T | 1 | a0002c0001t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.341+7238G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871037 | ||||||
| chr1:51871324 | C | T | 8 | a0001c0002t0001g0077a0001c0002t0001g0099a0001c0002t0001g0104others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.341+6951G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871324 | ||||||
| chr1:51871367 | T | C | 104 | a0002c0001t0001g0110a0002c0001t0001g0113a0002c0001t0001g0114others(101): Show | 104 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.341+6908A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871367 | ||||||
| chr1:51871515 | T | TA | 13 | a0001c0002t0001g0105a0001c0002t0001g0106a0001c0002t0001g0107others(10): Show | 13 | HG00639.hp1 HG01109.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.341+6759dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | T | TAAAAAAA | 5 | a0001c0005t0001g0226a0001c0005t0001g0231a0001c0006t0001g0232others(2): Show | 5 | HG02602.hp1 HG04199.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+6753_341+6759d others(9): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | T | TAAAAAAA others(3): Show |
2 | a0001c0005t0001g0224a0001c0005t0001g0227 | 2 | HG00558.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.341+6750_341+6759d others(12): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | T | TAAAAAAA others(4): Show |
1 | a0001c0005t0001g0223 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.341+6749_341+6759d others(13): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TA | T | 95 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0060others(92): Show | 96 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.341+6759delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TAA | T | 30 | a0001c0002t0001g0058a0001c0002t0001g0059a0001c0002t0001g0064others(27): Show | 30 | HG00642.hp2 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.341+6758_341+6759d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TAAA | T | 20 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(17): Show | 21 | HG00099.hp2 HG01167.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+6757_341+6759d others(5): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TAAAAAA | T | 5 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(2): Show | 5 | HG02647.hp1 HG03130.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+6754_341+6759d others(8): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TAAAAAAA others(5): Show |
T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341+6748_341+6759d others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TAAAAAAA others(6): Show |
T | 1 | a0001c0002t0001g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.341+6747_341+6759d others(15): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871515 | TAAAAAAA others(7): Show |
T | 1 | a0001c0005t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.341+6746_341+6759d others(16): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871515 | ||||||
| chr1:51871637 | T | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.341+6638A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871637 | ||||||
| chr1:51871961 | T | TC | 7 | a0001c0002t0001g0067a0001c0002t0001g0068a0001c0002t0001g0069others(4): Show | 7 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.341+6313dupG | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871961 | ||||||
| chr1:51871964 | C | T | 1 | a0002c0019t0001g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.341+6311G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51871964 | ||||||
| chr1:51872208 | T | G | 1 | a0002c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.341+6067A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872208 | ||||||
| chr1:51872337 | T | TAC | 5 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0011t0002g0216others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+5936_341+5937d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872337 | ||||||
| chr1:51872485 | T | C | 17 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(14): Show | 17 | HG00642.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.341+5790A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872485 | ||||||
| chr1:51872510 | C | T | 20 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(17): Show | 20 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.341+5765G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872510 | ||||||
| chr1:51872578 | A | G | 5 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(2): Show | 5 | HG02647.hp1 HG03130.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+5697T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872578 | ||||||
| chr1:51872868 | CCTTTA | C | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.341+5402_341+5406d others(7): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872868 | ||||||
| chr1:51872893 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.341+5382C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872893 | ||||||
| chr1:51872943 | A | G | 1 | a0002c0001t0001g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.341+5332T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872943 | ||||||
| chr1:51872984 | A | ATAATGAT others(91): Show |
2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.341+5290_341+5291i others(100): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51872984 | ||||||
| chr1:51873152 | G | A | 10 | a0001c0002t0001g0057a0001c0002t0001g0058a0001c0002t0001g0059others(7): Show | 10 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.341+5123C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873152 | ||||||
| chr1:51873479 | T | A | 3 | a0002c0001t0001g0201a0002c0001t0001g0202a0002c0001t0001g0203 | 3 | NA18982.hp2 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.341+4796A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873479 | T | TTTTA | 87 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0002t0001g0046others(84): Show | 88 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.341+4792_341+4795d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873479 | T | TTTTATTT others(1): Show |
5 | a0001c0003t0001g0033a0001c0003t0001g0034a0002c0001t0001g0198others(2): Show | 5 | HG01071.hp2 HG01993.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+4788_341+4795d others(10): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873479 | T | TTTTATTT others(5): Show |
1 | a0001c0003t0001g0016 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.341+4784_341+4795d others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873479 | TTTTA | T | 46 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(43): Show | 47 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.341+4792_341+4795d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873479 | TTTTATTT others(1): Show |
T | 5 | a0001c0002t0001g0064a0001c0002t0001g0075a0001c0002t0001g0076others(2): Show | 5 | HG00544.hp2 HG02622.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.341+4788_341+4795d others(10): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873479 | TTTTATTT others(5): Show |
T | 12 | a0001c0002t0001g0007a0001c0002t0001g0057a0001c0002t0001g0058others(9): Show | 12 | HG00099.hp2 HG01074.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.341+4784_341+4795d others(14): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873479 | ||||||
| chr1:51873486 | T | C | 1 | a0002c0019t0001g0204 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.341+4789A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873486 | ||||||
| chr1:51873515 | AT | A | 4 | a0001c0002t0001g0100a0001c0002t0001g0101a0001c0002t0001g0102others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.341+4759delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873515 | ||||||
| chr1:51873663 | A | G | 2 | a0001c0002t0001g0111a0001c0002t0001g0112 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.341+4612T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873663 | ||||||
| chr1:51873697 | G | A | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341+4578C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873697 | ||||||
| chr1:51873764 | G | A | 1 | a0001c0006t0001g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.341+4511C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873764 | ||||||
| chr1:51873888 | G | T | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.341+4387C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873888 | ||||||
| chr1:51873913 | G | T | 1 | a0001c0005t0001g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.341+4362C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51873913 | ||||||
| chr1:51874087 | T | C | 106 | a0001c0002t0001g0111a0001c0002t0001g0112a0002c0001t0001g0110others(103): Show | 106 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.341+4188A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874087 | ||||||
| chr1:51874145 | T | TA | 20 | a0001c0002t0001g0007a0001c0002t0001g0048a0001c0002t0001g0049others(17): Show | 20 | HG00642.hp1 HG01074.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.341+4129dupT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874145 | ||||||
| chr1:51874266 | C | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.341+4009G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874266 | ||||||
| chr1:51874280 | G | A | 6 | a0002c0001t0001g0208a0002c0001t0001g0209a0002c0001t0001g0210others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+3995C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874280 | ||||||
| chr1:51874312 | T | A | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+3963A>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874312 | ||||||
| chr1:51874422 | G | C | 1 | a0001c0006t0001g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.341+3853C>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874422 | ||||||
| chr1:51874524 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.341+3751T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874524 | ||||||
| chr1:51874605 | C | T | 96 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(93): Show | 98 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.341+3670G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874605 | ||||||
| chr1:51874662 | C | T | 5 | a0001c0003t0001g0002a0001c0003t0001g0035a0001c0003t0001g0036others(2): Show | 6 | HG02486.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+3613G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874662 | ||||||
| chr1:51874683 | C | T | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+3592G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874683 | ||||||
| chr1:51874833 | G | T | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+3442C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874833 | ||||||
| chr1:51874999 | C | T | 1 | a0002c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.341+3276G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51874999 | ||||||
| chr1:51875000 | G | A | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+3275C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875000 | ||||||
| chr1:51875003 | C | T | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+3272G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875003 | ||||||
| chr1:51875004 | A | G | 2 | a0001c0002t0001g0007a0001c0002t0001g0072 | 2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.341+3271T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875004 | ||||||
| chr1:51875308 | T | C | 2 | a0001c0003t0001g0103a0001c0003t0001g0109 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.341+2967A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875308 | ||||||
| chr1:51875370 | GA | G | 33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+2904delT | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875370 | ||||||
| chr1:51875594 | T | C | 6 | a0001c0005t0001g0237a0001c0005t0001g0238a0001c0005t0001g0241others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.341+2681A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875594 | ||||||
| chr1:51875594 | T | G | 1 | a0001c0016t0001g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.341+2681A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875594 | ||||||
| chr1:51875716 | C | T | 10 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.341+2559G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875716 | ||||||
| chr1:51875719 | G | A | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+2556C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875719 | ||||||
| chr1:51875747 | GCTCA | G | 33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+2524_341+2527d others(6): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875747 | ||||||
| chr1:51875835 | G | A | 33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+2440C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875835 | ||||||
| chr1:51875856 | AT | A | 22 | a0001c0002t0001g0104a0001c0002t0001g0105a0001c0002t0001g0106others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.341+2418delA | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51875856 | ||||||
| chr1:51876252 | T | C | 3 | a0001c0011t0002g0216a0001c0011t0002g0217a0001c0011t0002g0218 | 3 | HG02055.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.341+2023A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876252 | ||||||
| chr1:51876294 | C | G | 9 | a0001c0003t0001g0008a0001c0003t0001g0009a0001c0003t0001g0010others(6): Show | 9 | NA18944.hp1 NA18948.hp1 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.341+1981G>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876294 | ||||||
| chr1:51876694 | A | AAT | 28 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(25): Show | 29 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.341+1579_341+1580d others(4): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876694 | ||||||
| chr1:51876730 | T | C | 22 | a0001c0002t0001g0007a0001c0002t0001g0072a0001c0005t0001g0222others(19): Show | 22 | HG00544.hp2 HG00558.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.341+1545A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876730 | ||||||
| chr1:51876755 | T | C | 106 | a0001c0002t0001g0111a0001c0002t0001g0112a0002c0001t0001g0110others(103): Show | 106 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.341+1520A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876755 | ||||||
| chr1:51876814 | C | T | 11 | a0001c0002t0001g0039a0001c0002t0001g0040a0001c0002t0001g0041others(8): Show | 11 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.341+1461G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876814 | ||||||
| chr1:51876821 | G | A | 1 | a0001c0003t0001g0109 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.341+1454C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876821 | ||||||
| chr1:51876841 | A | C | 3 | a0001c0002t0001g0075a0001c0002t0001g0076a0001c0002t0001g0214 | 3 | HG02622.hp2 HG03225.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.341+1434T>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876841 | ||||||
| chr1:51876988 | A | G | 2 | a0001c0002t0001g0073a0001c0002t0001g0074 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.341+1287T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51876988 | ||||||
| chr1:51877046 | G | T | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+1229C>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877046 | ||||||
| chr1:51877146 | C | CCACTGCA others(6): Show |
33 | a0001c0002t0001g0023a0001c0002t0001g0031a0001c0003t0001g0001others(30): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.341+1116_341+1128d others(15): Show |
NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877146 | ||||||
| chr1:51877510 | C | T | 1 | a0001c0002t0001g0007 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341+765G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877510 | ||||||
| chr1:51877517 | A | G | 14 | a0001c0005t0001g0222a0001c0005t0001g0223a0001c0005t0001g0224others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.341+758T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877517 | ||||||
| chr1:51877565 | AC | A | 106 | a0001c0002t0001g0111a0001c0002t0001g0112a0002c0001t0001g0110others(103): Show | 106 | HG00544.hp1 HG00558.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.341+709delG | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877565 | ||||||
| chr1:51877588 | T | C | 1 | a0001c0005t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.341+687A>G | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877588 | ||||||
| chr1:51877625 | A | G | 96 | a0001c0002t0001g0007a0001c0002t0001g0023a0001c0002t0001g0031others(93): Show | 98 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.341+650T>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877625 | ||||||
| chr1:51877742 | G | A | 1 | a0002c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.341+533C>T | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877742 | ||||||
| chr1:51877754 | C | T | 1 | a0001c0003t0001g0006 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.341+521G>A | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877754 | ||||||
| chr1:51877868 | T | G | 1 | a0001c0002t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.341+407A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51877868 | ||||||
| chr1:51878157 | T | G | 1 | a0001c0017t0001g0215 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.341+118A>C | NRDC | ENSG00000078618.23 | transcript | ENST00000352171.12 | protein_coding | 1/30 | chr1 | 51878157 |