Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56675 |
| ensemblid | ENSG00000175352.12 |
| hgncid | 1167 |
| symbol | NRIP3 |
| name | nuclear receptor interacting protein 3 |
| refseq_nuc | NM_020645.3 |
| refseq_prot | NP_065696.1 |
| ensembl_nuc | ENST00000309166.8 |
| ensembl_prot | ENSP00000310205.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 8980576 |
| end | 9004001 |
| strand | - |
| ver | v1.2 |
| region | chr11:8980576-9004001 |
| region5000 | chr11:8975576-9009001 |
| regionname0 | NRIP3_chr11_8980576_9004001 |
| regionname5000 | NRIP3_chr11_8975576_9009001 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 241 | 392 | 89 | 61 | 184 | 12 | 44 | 143 | NRIP3_chr11_8975576_9009001 | NRIP3 | MFYSG others(236): Show |
chr11 | 8975576 | 9009001 |
| a0002 | 0/0 | 241 | 6 | 0 | 0 | 6 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | MFYSG others(236): Show |
chr11 | 8975576 | 9009001 |
| a0003 | 0/0 | 241 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | MFYSG others(236): Show |
chr11 | 8975576 | 9009001 |
| a0004 | 0/0 | 241 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NRIP3_chr11_8975576_9009001 | NRIP3 | MFYSG others(236): Show |
chr11 | 8975576 | 9009001 |
| a0005 | 0/0 | 241 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | MFYSG others(236): Show |
chr11 | 8975576 | 9009001 |
| a0006 | 0/0 | 241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | MFYSG others(236): Show |
chr11 | 8975576 | 9009001 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 723 | 378 | 89 | 61 | 170 | 12 | 44 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 | ||
| a0001c0002 | 0/0 | 723 | 14 | 0 | 0 | 14 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 | ||
| a0002c0003 | 0/0 | 723 | 6 | 0 | 0 | 6 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 | ||
| a0003c0004 | 0/0 | 723 | 4 | 4 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 | ||
| a0004c0005 | 0/0 | 723 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 | ||
| a0005c0007 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 | ||
| a0006c0006 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | ATGTT others(718): Show |
chr11 | 8975576 | 9009001 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3762 | 94 | 16 | 6 | 63 | 0 | 9 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0002 | 0/0 | 3763 | 77 | 7 | 17 | 41 | 4 | 8 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0003 | 0/0 | 3760 | 21 | 1 | 2 | 9 | 2 | 7 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0004 | 0/0 | 3760 | 30 | 3 | 15 | 0 | 3 | 9 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0005 | 0/0 | 3762 | 23 | 9 | 0 | 14 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0006 | 1/0 | 3761 | 20 | 16 | 3 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0007 | 0/1 | 3764 | 10 | 1 | 4 | 4 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3759): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0008 | 0/0 | 3763 | 9 | 0 | 2 | 7 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0009 | 0/0 | 3762 | 8 | 8 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0010 | 0/0 | 3764 | 5 | 1 | 0 | 4 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3759): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0011 | 0/0 | 3762 | 5 | 0 | 1 | 3 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0012 | 0/0 | 3758 | 5 | 4 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3753): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0013 | 0/0 | 3763 | 5 | 0 | 2 | 0 | 0 | 3 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0014 | 0/0 | 3762 | 5 | 0 | 0 | 4 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0015 | 0/0 | 3761 | 4 | 1 | 0 | 2 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0016 | 0/0 | 3763 | 4 | 0 | 0 | 3 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0017 | 0/0 | 3763 | 4 | 1 | 0 | 2 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0018 | 0/0 | 3761 | 4 | 0 | 0 | 3 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0019 | 0/0 | 3759 | 3 | 2 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3754): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0020 | 0/0 | 3763 | 3 | 1 | 2 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0021 | 0/0 | 3761 | 3 | 3 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0022 | 0/0 | 3761 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0023 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0024 | 0/0 | 3762 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0025 | 0/0 | 3762 | 2 | 1 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0026 | 0/0 | 3759 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3754): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0029 | 0/0 | 3763 | 1 | 0 | 0 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0030 | 0/0 | 3761 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0031 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0032 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0033 | 0/0 | 3763 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0034 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3759): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0035 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0036 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3759): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0037 | 0/0 | 3761 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0038 | 0/0 | 3763 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0039 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0040 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0041 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0042 | 0/0 | 3776 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3771): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0043 | 0/0 | 3762 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0045 | 0/0 | 3761 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0046 | 0/0 | 3762 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0047 | 0/0 | 3762 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0048 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0049 | 0/0 | 3761 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0050 | 0/0 | 3761 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0051 | 0/0 | 3760 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0052 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0053 | 0/0 | 3761 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0054 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(4090): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0055 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0001c0001t0056 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3758): Show |
chr11 | 8975576 | 9009001 |
| a0001c0002t0003 | 0/0 | 3760 | 11 | 0 | 0 | 11 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0001c0002t0015 | 0/0 | 3761 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0001c0002t0026 | 0/0 | 3759 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3754): Show |
chr11 | 8975576 | 9009001 |
| a0001c0002t0044 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0002c0003t0003 | 0/0 | 3760 | 6 | 0 | 0 | 6 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0003c0004t0027 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3755): Show |
chr11 | 8975576 | 9009001 |
| a0003c0004t0028 | 0/0 | 3761 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| a0004c0005t0010 | 0/0 | 3764 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3759): Show |
chr11 | 8975576 | 9009001 |
| a0004c0005t0011 | 0/0 | 3762 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0005c0007t0001 | 0/0 | 3762 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3757): Show |
chr11 | 8975576 | 9009001 |
| a0006c0006t0006 | 0/0 | 3761 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | GCTGG others(3756): Show |
chr11 | 8975576 | 9009001 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0001 | 0/0 | 18 | 1 | 4 | 13 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 0 | 1 | 2 | 4 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0006 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0012 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0049 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0003 | 0/0 | 7 | 6 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0044 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0008 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0009g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0009g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0010g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0010g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0011g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0012g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0013g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0013g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0013g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0014g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0014g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0015g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0015g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0016g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0016g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0016g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0017g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0017g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0017g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0018g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0018g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0019g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0019g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0019g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0020g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0020g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0020g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0021g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0021g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0022g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0022g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0023g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0023g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0024g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0024g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0025g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0025g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0026g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0029g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0030g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0031g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0032g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0033g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0034g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0035g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0036g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0037g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0038g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0039g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0040g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0041g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0042g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0043g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0045g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0046g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0047g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0048g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0049g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0050g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0051g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0052g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0053g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0054g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0055g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0001t0056g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0003g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0015g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0026g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0001c0002t0044g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0002c0003t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0002c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0002c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0003c0004t0027g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0003c0004t0027g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0003c0004t0028g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0004c0005t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0004c0005t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0005c0007t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| a0006c0006t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00140 | hp2 | a0001 | c0001 | t0029 | g0254 | EUR | GBR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0020 | EUR | FIN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0043 | EUR | FIN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00323 | hp1 | a0001 | c0001 | t0018 | g0162 | EUR | FIN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | FIN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0146 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00408 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00544 | hp1 | a0001 | c0001 | t0041 | g0108 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0263 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00639 | hp2 | a0001 | c0001 | t0051 | g0127 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0047 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00673 | hp2 | a0002 | c0003 | t0003 | g0262 | EAS | CHS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0207 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01070 | hp1 | a0001 | c0001 | t0026 | g0274 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01099 | hp2 | a0005 | c0007 | t0001 | g0154 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01106 | hp2 | a0001 | c0001 | t0053 | g0246 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0060 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01168 | hp1 | a0001 | c0001 | t0013 | g0228 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0148 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01192 | hp1 | a0001 | c0001 | t0045 | g0272 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01243 | hp1 | a0001 | c0001 | t0030 | g0066 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0204 | AMR | PUR | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01257 | hp2 | a0001 | c0001 | t0011 | g0197 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0091 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01346 | hp2 | a0001 | c0001 | t0020 | g0210 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0111 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | IBS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0076 | EUR | IBS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01884 | hp2 | a0001 | c0001 | t0021 | g0245 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0079 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01943 | hp2 | a0001 | c0001 | t0019 | g0223 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01978 | hp1 | a0001 | c0001 | t0008 | g0161 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02056 | hp1 | a0001 | c0001 | t0035 | g0138 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02080 | hp1 | a0001 | c0001 | t0015 | g0052 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02083 | hp1 | a0001 | c0001 | t0056 | g0109 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02083 | hp2 | a0001 | c0002 | t0015 | g0267 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0014 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | PEL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02155 | hp1 | a0001 | c0001 | t0008 | g0033 | EAS | CDX | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02155 | hp2 | a0001 | c0001 | t0015 | g0052 | EAS | CDX | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | CDX | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02257 | hp2 | a0003 | c0004 | t0027 | g0285 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0059 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02280 | hp2 | a0003 | c0004 | t0028 | g0053 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02451 | hp1 | a0001 | c0001 | t0040 | g0061 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | KHV | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0225 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02615 | hp2 | a0001 | c0001 | t0048 | g0248 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0073 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02698 | hp1 | a0001 | c0001 | t0014 | g0099 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0256 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02723 | hp1 | a0003 | c0004 | t0027 | g0286 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02723 | hp2 | a0001 | c0001 | t0022 | g0281 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02738 | hp2 | a0001 | c0001 | t0015 | g0266 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0255 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02895 | hp1 | a0001 | c0001 | t0031 | g0071 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02965 | hp2 | a0006 | c0006 | t0006 | g0054 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02976 | hp1 | a0001 | c0001 | t0024 | g0283 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03017 | hp2 | a0001 | c0001 | t0025 | g0153 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03041 | hp1 | a0003 | c0004 | t0028 | g0053 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03098 | hp1 | a0001 | c0001 | t0023 | g0259 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03098 | hp2 | a0001 | c0001 | t0021 | g0236 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0226 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03139 | hp1 | a0001 | c0001 | t0022 | g0282 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0229 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0212 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0192 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03486 | hp2 | a0001 | c0001 | t0054 | g0257 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03490 | hp1 | a0001 | c0001 | t0052 | g0232 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03490 | hp2 | a0001 | c0001 | t0013 | g0227 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03491 | hp1 | a0001 | c0001 | t0013 | g0047 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03491 | hp2 | a0001 | c0001 | t0037 | g0213 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03516 | hp2 | a0001 | c0001 | t0038 | g0056 | AFR | ESN | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0074 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0206 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03688 | hp1 | a0001 | c0001 | t0013 | g0224 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0237 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03831 | hp1 | a0001 | c0001 | t0016 | g0150 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03927 | hp1 | a0001 | c0001 | t0050 | g0215 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0049 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0234 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0050 | SAS | BEB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0174 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18522 | hp1 | a0001 | c0001 | t0055 | g0155 | AFR | YRI | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | YRI | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | CHB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18939 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18940 | hp2 | a0001 | c0002 | t0026 | g0277 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18946 | hp1 | a0001 | c0001 | t0018 | g0176 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0084 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18954 | hp1 | a0001 | c0001 | t0014 | g0080 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18956 | hp2 | a0004 | c0005 | t0010 | g0122 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18957 | hp1 | a0001 | c0001 | t0018 | g0136 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18963 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18964 | hp1 | a0001 | c0001 | t0046 | g0165 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18966 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18969 | hp1 | a0001 | c0001 | t0011 | g0116 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18977 | hp1 | a0001 | c0001 | t0010 | g0112 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18979 | hp1 | a0001 | c0001 | t0017 | g0169 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0264 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18987 | hp1 | a0001 | c0001 | t0018 | g0160 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18987 | hp2 | a0001 | c0001 | t0014 | g0097 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18988 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18992 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18992 | hp2 | a0001 | c0001 | t0014 | g0102 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18993 | hp1 | a0001 | c0001 | t0034 | g0173 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19001 | hp2 | a0001 | c0001 | t0016 | g0177 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0151 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19004 | hp1 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19006 | hp1 | a0001 | c0001 | t0011 | g0107 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19009 | hp1 | a0001 | c0001 | t0047 | g0280 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | LWK | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | LWK | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19062 | hp2 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19063 | hp1 | a0001 | c0001 | t0014 | g0115 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19065 | hp2 | a0001 | c0001 | t0043 | g0152 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19066 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0168 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19067 | hp2 | a0001 | c0001 | t0039 | g0088 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19068 | hp2 | a0001 | c0001 | t0032 | g0221 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19075 | hp2 | a0001 | c0002 | t0044 | g0275 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19077 | hp1 | a0004 | c0005 | t0011 | g0082 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19081 | hp2 | a0001 | c0001 | t0042 | g0095 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0278 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19091 | hp1 | a0001 | c0001 | t0036 | g0145 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ASW | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA20129 | hp2 | a0001 | c0001 | t0033 | g0055 | AFR | ASW | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | TSI | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | TSI | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0065 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0260 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02109 | hp2 | a0001 | c0001 | t0012 | g0042 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02486 | hp1 | a0001 | c0001 | t0049 | g0242 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0042 | AFR | ACB | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03471 | hp1 | a0001 | c0001 | t0024 | g0284 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | USA | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA18955 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | USA | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | USA | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA21309 | hp1 | a0001 | c0001 | t0025 | g0157 | AFR | LWK | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | LWK | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0121 | REF | REF | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0008 | REF | REF | NRIP3_chr11_8975576_9009001 | NRIP3 | chr11 | 8975576 | 9009001 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8983922 | G | C | 1 | a0003 | 4 | HG02257.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
missense_variant | MODERATE | c.663C>G | p.Asp221Glu | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 6/7 | 729/3761 | 663/726 | 221/241 | chr11 | 8983922 | |||
| chr11:8983944 | C | T | 1 | a0002 | 6 | HG00408.hp2 HG00673.hp2 HG02040.hp2 others(3): Show |
missense_variant | MODERATE | c.641G>A | p.Arg214Gln | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 6/7 | 707/3761 | 641/726 | 214/241 | chr11 | 8983944 | |||
| chr11:8985728 | C | G | 1 | a0004 | 2 | NA18956.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.545G>C | p.Cys182Ser | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/7 | 611/3761 | 545/726 | 182/241 | chr11 | 8985728 | |||
| chr11:8985795 | G | A | 1 | a0005 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.478C>T | p.Arg160Trp | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/7 | 544/3761 | 478/726 | 160/241 | chr11 | 8985795 | |||
| chr11:9003803 | G | T | 1 | a0006 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.133C>A | p.Pro45Thr | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/7 | 199/3761 | 133/726 | 45/241 | chr11 | 9003803 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8985727 | G | A | 1 | a0004c0005 | 2 | NA18956.hp2 NA19077.hp1 |
synonymous_variant | LOW | c.546C>T | p.Cys182Cys | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/7 | 612/3761 | 546/726 | 182/241 | chr11 | 8985727 | |||
| chr11:8987628 | A | G | 1 | a0001c0002 | 14 | HG00544.hp2 HG02083.hp2 HG02129.hp1 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.342T>C | p.Cys114Cys | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/7 | 408/3761 | 342/726 | 114/241 | chr11 | 8987628 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8980600 | G | A | 5 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0049 others(2): Show |
36 | HG00280.hp1 HG00733.hp2 HG01069.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2945C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2945 | chr11 | 8980600 | ||||||
| chr11:8980642 | C | G | 1 | a0001c0001t0002 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2903G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2903 | chr11 | 8980642 | ||||||
| chr11:8980854 | G | A | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*2691C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2691 | chr11 | 8980854 | ||||||
| chr11:8980930 | T | C | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(26): Show |
196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*2615A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2615 | chr11 | 8980930 | ||||||
| chr11:8981020 | A | C | 1 | a0001c0001t0039 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2525T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2525 | chr11 | 8981020 | ||||||
| chr11:8981195 | T | C | 1 | a0001c0001t0022 | 2 | HG02723.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2350A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2350 | chr11 | 8981195 | ||||||
| chr11:8981245 | G | A | 3 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0046 |
9 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2300C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2300 | chr11 | 8981245 | ||||||
| chr11:8981277 | A | G | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0015 others(14): Show |
87 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2268T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2268 | chr11 | 8981277 | ||||||
| chr11:8981292 | A | AC | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(8): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2252dupG | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2252 | chr11 | 8981292 | ||||||
| chr11:8981296 | G | A | 1 | a0001c0001t0009 | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2249C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2249 | chr11 | 8981296 | ||||||
| chr11:8981318 | A | G | 1 | a0001c0001t0052 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2227T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2227 | chr11 | 8981318 | ||||||
| chr11:8981385 | A | G | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(8): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2160T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2160 | chr11 | 8981385 | ||||||
| chr11:8981408 | C | T | 1 | a0001c0001t0022 | 2 | HG02723.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2137G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2137 | chr11 | 8981408 | ||||||
| chr11:8981422 | C | T | 1 | a0001c0001t0013 | 5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2123G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2123 | chr11 | 8981422 | ||||||
| chr11:8981466 | T | TA | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(27): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*2078dupT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2078 | chr11 | 8981466 | ||||||
| chr11:8981466 | T | TAA | 8 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0017 others(5): Show |
30 | HG00408.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2077_*2078dupTT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2078 | chr11 | 8981466 | ||||||
| chr11:8981466 | TA | T | 3 | a0001c0001t0012 a0001c0001t0048 a0001c0002t0044 |
7 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2078delT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2078 | chr11 | 8981466 | ||||||
| chr11:8981486 | G | A | 1 | a0001c0001t0042 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2059C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2059 | chr11 | 8981486 | ||||||
| chr11:8981489 | T | C | 1 | a0001c0001t0041 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2056A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2056 | chr11 | 8981489 | ||||||
| chr11:8981526 | T | TAAGAGTC others(328): Show |
1 | a0001c0001t0054 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2018_*2019insTTTT others(331): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 2018 | chr11 | 8981526 | ||||||
| chr11:8981636 | G | A | 4 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0035 others(1): Show |
13 | HG00408.hp1 HG01175.hp1 HG01978.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1909C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1909 | chr11 | 8981636 | ||||||
| chr11:8981759 | A | G | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(35): Show |
229 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1786T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1786 | chr11 | 8981759 | ||||||
| chr11:8981910 | T | C | 1 | a0001c0001t0047 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1635A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1635 | chr11 | 8981910 | ||||||
| chr11:8981930 | C | T | 1 | a0001c0001t0024 | 2 | HG02976.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1615G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1615 | chr11 | 8981930 | ||||||
| chr11:8982073 | T | C | 2 | a0001c0001t0033 a0001c0001t0038 |
2 | HG03516.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1472A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1472 | chr11 | 8982073 | ||||||
| chr11:8982313 | G | A | 2 | a0001c0001t0048 a0001c0001t0049 |
2 | HG02486.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1232C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1232 | chr11 | 8982313 | ||||||
| chr11:8982395 | C | T | 1 | a0001c0001t0043 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1150G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1150 | chr11 | 8982395 | ||||||
| chr11:8982406 | C | T | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
265 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*1139G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1139 | chr11 | 8982406 | ||||||
| chr11:8982428 | C | T | 1 | a0001c0001t0022 | 2 | HG02723.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1117G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1117 | chr11 | 8982428 | ||||||
| chr11:8982455 | C | T | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(35): Show |
228 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*1090G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1090 | chr11 | 8982455 | ||||||
| chr11:8982470 | T | TACTCCTG others(7): Show |
1 | a0001c0001t0042 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061_*1074dupTGGA others(10): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1074 | chr11 | 8982470 | ||||||
| chr11:8982513 | T | C | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(31): Show |
217 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1032A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1032 | chr11 | 8982513 | ||||||
| chr11:8982535 | C | T | 1 | a0001c0001t0030 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1010G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 1010 | chr11 | 8982535 | ||||||
| chr11:8982597 | A | G | 1 | a0001c0001t0009 | 8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*948T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 948 | chr11 | 8982597 | ||||||
| chr11:8982829 | C | CT | 10 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0016 others(7): Show |
21 | HG00140.hp2 HG00642.hp1 HG01168.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*715dupA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 715 | chr11 | 8982829 | ||||||
| chr11:8982829 | CT | C | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(14): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*715delA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 715 | chr11 | 8982829 | ||||||
| chr11:8982829 | CTT | C | 5 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0022 others(2): Show |
12 | HG01070.hp1 HG01109.hp2 HG01943.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*714_*715delAA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 714 | chr11 | 8982829 | ||||||
| chr11:8983040 | G | T | 1 | a0001c0001t0023 | 2 | HG02109.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*505C>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 505 | chr11 | 8983040 | ||||||
| chr11:8983176 | T | A | 1 | a0001c0001t0055 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*369A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 369 | chr11 | 8983176 | ||||||
| chr11:8983331 | A | G | 3 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0022 |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*214T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 214 | chr11 | 8983331 | ||||||
| chr11:8983426 | T | C | 1 | a0001c0001t0056 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 119 | chr11 | 8983426 | ||||||
| chr11:8983489 | T | A | 60 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(57): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 56 | chr11 | 8983489 | ||||||
| chr11:8983518 | C | T | 1 | a0001c0001t0029 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*27G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 7/7 | 27 | chr11 | 8983518 | ||||||
| chr11:9003975 | G | C | 2 | a0003c0004t0027 a0003c0004t0028 |
4 | HG02257.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-40C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/7 | 40 | chr11 | 9003975 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8983629 | A | C | 2 | a0001c0001t0002g0106 a0001c0001t0014g0115 |
2 | NA18970.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.711-69T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 6/6 | chr11 | 8983629 | |||||||
| chr11:8983750 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0250 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.710+125T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 6/6 | chr11 | 8983750 | |||||||
| chr11:8983753 | TGTA | T | 9 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(6): Show |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.710+119_710+121del others(3): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 6/6 | chr11 | 8983753 | |||||||
| chr11:8984002 | A | G | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.616-33T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 5/6 | chr11 | 8984002 | |||||||
| chr11:8984067 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG01993.hp2 | splice_region_variant&intron_variant | LOW | c.615+5G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 5/6 | chr11 | 8984067 | |||||||
| chr11:8984158 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0250 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.563-34G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984158 | |||||||
| chr11:8984248 | GTTATTTT others(4): Show |
G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
150 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.563-135_563-125del others(11): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984248 | |||||||
| chr11:8984250 | TA | T | 3 | a0003c0004t0027g0285 a0003c0004t0027g0286 a0003c0004t0028g0053 |
4 | HG02257.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-127delT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984250 | |||||||
| chr11:8984250 | TATTTTTT others(5): Show |
T | 1 | a0001c0001t0055g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.563-138_563-127del others(12): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984250 | |||||||
| chr11:8984266 | T | A | 4 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0100 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-142A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984266 | |||||||
| chr11:8984328 | T | C | 2 | a0001c0001t0006g0022 a0001c0001t0006g0072 |
3 | HG02809.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.563-204A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984328 | |||||||
| chr11:8984398 | G | A | 5 | a0001c0001t0005g0045 a0001c0001t0005g0208 a0001c0001t0005g0216 others(2): Show |
6 | NA18947.hp2 NA18981.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.563-274C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984398 | |||||||
| chr11:8984510 | G | A | 2 | a0001c0001t0024g0283 a0001c0001t0024g0284 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.563-386C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984510 | |||||||
| chr11:8984553 | G | A | 9 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(6): Show |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.563-429C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984553 | |||||||
| chr11:8984772 | CTCTCTG | C | 7 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(4): Show |
8 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.563-654_563-649del others(6): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984772 | |||||||
| chr11:8984881 | C | T | 1 | a0001c0002t0003g0278 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.563-757G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984881 | |||||||
| chr11:8984884 | T | G | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.563-760A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984884 | |||||||
| chr11:8984890 | T | C | 1 | a0001c0001t0042g0095 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.563-766A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984890 | |||||||
| chr11:8984940 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.562+771G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984940 | |||||||
| chr11:8984976 | C | G | 1 | a0001c0001t0002g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.562+735G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984976 | |||||||
| chr11:8984979 | G | A | 3 | a0001c0001t0004g0244 a0001c0001t0004g0251 a0001c0001t0052g0232 |
3 | HG02602.hp2 HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.562+732C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984979 | |||||||
| chr11:8984992 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.562+719T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984992 | |||||||
| chr11:8984994 | G | A | 1 | a0001c0001t0003g0269 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.562+717C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8984994 | |||||||
| chr11:8985149 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.562+562G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985149 | |||||||
| chr11:8985164 | A | AT | 14 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0002g0029 others(11): Show |
15 | HG00642.hp2 HG01361.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.562+546dupA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985164 | |||||||
| chr11:8985164 | AT | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(148): Show |
215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.562+546delA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985164 | |||||||
| chr11:8985164 | ATT | A | 8 | a0001c0001t0001g0134 a0001c0002t0003g0007 a0001c0002t0003g0030 others(5): Show |
14 | HG00544.hp2 HG02083.hp2 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.562+545_562+546del others(2): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985164 | |||||||
| chr11:8985164 | ATTT | A | 10 | a0001c0001t0002g0078 a0001c0001t0012g0042 a0001c0001t0012g0059 others(7): Show |
11 | HG01109.hp2 HG01168.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.562+544_562+546del others(3): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985164 | |||||||
| chr11:8985198 | C | A | 1 | a0001c0001t0002g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.562+513G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985198 | |||||||
| chr11:8985255 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.562+456G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985255 | |||||||
| chr11:8985286 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.562+425A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985286 | |||||||
| chr11:8985295 | G | A | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+416C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985295 | |||||||
| chr11:8985330 | T | C | 1 | a0001c0001t0004g0230 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.562+381A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985330 | |||||||
| chr11:8985336 | A | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
119 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.562+375T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985336 | |||||||
| chr11:8985379 | T | C | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0032g0221 |
3 | HG02683.hp1 HG03669.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.562+332A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985379 | |||||||
| chr11:8985391 | G | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(17): Show |
30 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.562+320C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985391 | |||||||
| chr11:8985404 | T | C | 1 | a0001c0002t0003g0030 | 2 | NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.562+307A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985404 | |||||||
| chr11:8985411 | C | T | 1 | a0001c0001t0020g0210 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.562+300G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985411 | |||||||
| chr11:8985412 | G | A | 1 | a0001c0001t0025g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.562+299C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985412 | |||||||
| chr11:8985453 | C | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
260 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.562+258G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985453 | |||||||
| chr11:8985460 | C | T | 2 | a0004c0005t0010g0122 a0004c0005t0011g0082 |
2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.562+251G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985460 | |||||||
| chr11:8985461 | A | G | 1 | a0001c0002t0003g0030 | 2 | NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.562+250T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985461 | |||||||
| chr11:8985464 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.562+247G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985464 | |||||||
| chr11:8985469 | G | A | 1 | a0001c0001t0012g0042 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.562+242C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985469 | |||||||
| chr11:8985487 | A | ACCT | 190 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(187): Show |
265 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.562+223_562+224ins others(3): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985487 | |||||||
| chr11:8985594 | A | T | 1 | a0003c0004t0027g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.562+117T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 4/6 | chr11 | 8985594 | |||||||
| chr11:8986064 | CA | C | 7 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(4): Show |
8 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.423-215delT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986064 | |||||||
| chr11:8986075 | C | T | 2 | a0001c0001t0023g0259 a0001c0001t0023g0260 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.423-225G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986075 | |||||||
| chr11:8986103 | G | A | 9 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(6): Show |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.423-253C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986103 | |||||||
| chr11:8986104 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(265): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.423-254T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986104 | |||||||
| chr11:8986122 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
121 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.423-272C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986122 | |||||||
| chr11:8986350 | T | C | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.423-500A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986350 | |||||||
| chr11:8986427 | G | A | 1 | a0001c0001t0051g0127 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.423-577C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986427 | |||||||
| chr11:8986654 | T | G | 2 | a0001c0001t0022g0281 a0001c0001t0022g0282 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.423-804A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986654 | |||||||
| chr11:8986665 | C | G | 2 | a0001c0001t0006g0065 a0001c0001t0006g0069 |
2 | HG01123.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.423-815G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986665 | |||||||
| chr11:8986687 | G | T | 1 | a0001c0001t0010g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.423-837C>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986687 | |||||||
| chr11:8986790 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0002g0009 a0001c0001t0002g0081 others(4): Show |
11 | HG00597.hp2 HG00738.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.422+758C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8986790 | |||||||
| chr11:8987076 | G | C | 1 | a0001c0001t0033g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422+472C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8987076 | |||||||
| chr11:8987127 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
129 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.422+421T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8987127 | |||||||
| chr11:8987186 | A | T | 1 | a0001c0001t0013g0227 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.422+362T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8987186 | |||||||
| chr11:8987373 | C | T | 1 | a0001c0001t0055g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.422+175G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8987373 | |||||||
| chr11:8987454 | G | A | 3 | a0003c0004t0027g0285 a0003c0004t0027g0286 a0003c0004t0028g0053 |
4 | HG02257.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+94C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 3/6 | chr11 | 8987454 | |||||||
| chr11:8987751 | G | C | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-121C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 2/6 | chr11 | 8987751 | |||||||
| chr11:8987820 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.340-190C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 2/6 | chr11 | 8987820 | |||||||
| chr11:8987869 | C | A | 1 | a0001c0001t0001g0040 | 2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.340-239G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 2/6 | chr11 | 8987869 | |||||||
| chr11:8987927 | G | A | 12 | a0001c0001t0008g0033 a0001c0001t0008g0036 a0001c0001t0008g0143 others(9): Show |
14 | HG00408.hp1 HG01099.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.339+191C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 2/6 | chr11 | 8987927 | |||||||
| chr11:8988398 | C | A | 4 | a0001c0001t0004g0012 a0001c0001t0004g0020 a0001c0001t0004g0243 others(1): Show |
9 | HG00280.hp1 HG01074.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-116G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988398 | |||||||
| chr11:8988459 | A | C | 62 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(59): Show |
95 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.175-177T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988459 | |||||||
| chr11:8988587 | G | T | 31 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(28): Show |
51 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.175-305C>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988587 | |||||||
| chr11:8988810 | G | A | 1 | a0001c0001t0038g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.175-528C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988810 | |||||||
| chr11:8988845 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.175-563G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988845 | |||||||
| chr11:8988927 | C | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(184): Show |
261 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.175-645G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988927 | |||||||
| chr11:8988950 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.175-668G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988950 | |||||||
| chr11:8988963 | G | A | 1 | a0001c0001t0009g0048 | 2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.175-681C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8988963 | |||||||
| chr11:8989112 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(67): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.175-830C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989112 | |||||||
| chr11:8989185 | T | C | 2 | a0001c0001t0033g0055 a0001c0001t0038g0056 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.175-903A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989185 | |||||||
| chr11:8989190 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.175-908A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989190 | |||||||
| chr11:8989272 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.175-990A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989272 | |||||||
| chr11:8989512 | C | A | 1 | a0001c0001t0019g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.175-1230G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989512 | |||||||
| chr11:8989561 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1279T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989561 | |||||||
| chr11:8989845 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.175-1563A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989845 | |||||||
| chr11:8989849 | T | G | 2 | a0001c0001t0023g0259 a0001c0001t0023g0260 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.175-1567A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989849 | |||||||
| chr11:8989906 | G | C | 1 | a0001c0001t0040g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.175-1624C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8989906 | |||||||
| chr11:8990145 | T | G | 1 | a0001c0001t0020g0212 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175-1863A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990145 | |||||||
| chr11:8990560 | C | G | 3 | a0003c0004t0027g0285 a0003c0004t0027g0286 a0003c0004t0028g0053 |
4 | HG02257.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-2278G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990560 | |||||||
| chr11:8990677 | A | G | 1 | a0001c0001t0035g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175-2395T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990677 | |||||||
| chr11:8990684 | A | G | 2 | a0001c0001t0019g0073 a0001c0001t0019g0074 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.175-2402T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990684 | |||||||
| chr11:8990727 | G | A | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-2445C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990727 | |||||||
| chr11:8990823 | T | A | 1 | a0001c0002t0044g0275 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.175-2541A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990823 | |||||||
| chr11:8990824 | A | T | 1 | a0001c0002t0044g0275 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.175-2542T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990824 | |||||||
| chr11:8990995 | C | A | 1 | a0001c0001t0033g0055 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175-2713G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8990995 | |||||||
| chr11:8991030 | G | A | 7 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(4): Show |
8 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-2748C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991030 | |||||||
| chr11:8991031 | G | A | 1 | a0001c0001t0024g0284 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.175-2749C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991031 | |||||||
| chr11:8991114 | A | G | 2 | a0001c0001t0022g0281 a0001c0001t0022g0282 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.175-2832T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991114 | |||||||
| chr11:8991157 | C | T | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-2875G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991157 | |||||||
| chr11:8991249 | C | T | 46 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(43): Show |
75 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.175-2967G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991249 | |||||||
| chr11:8991363 | A | C | 7 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(4): Show |
8 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-3081T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991363 | |||||||
| chr11:8991455 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(189): Show |
267 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.175-3173T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8991455 | |||||||
| chr11:8992037 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.175-3755A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992037 | |||||||
| chr11:8992050 | T | C | 9 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(6): Show |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-3768A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992050 | |||||||
| chr11:8992092 | T | C | 75 | a0001c0001t0001g0018 a0001c0001t0001g0201 a0001c0001t0001g0202 others(72): Show |
113 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.175-3810A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992092 | |||||||
| chr11:8992113 | T | C | 20 | a0001c0001t0005g0003 a0001c0001t0005g0044 a0001c0001t0005g0045 others(17): Show |
29 | HG00741.hp2 HG01346.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.175-3831A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992113 | |||||||
| chr11:8992213 | A | T | 2 | a0001c0001t0022g0281 a0001c0001t0022g0282 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.175-3931T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992213 | |||||||
| chr11:8992249 | C | T | 2 | a0001c0001t0019g0073 a0001c0001t0019g0074 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.175-3967G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992249 | |||||||
| chr11:8992307 | T | C | 1 | a0001c0001t0004g0237 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.175-4025A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992307 | |||||||
| chr11:8992478 | T | G | 4 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-4196A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992478 | |||||||
| chr11:8992557 | G | A | 9 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(6): Show |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-4275C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992557 | |||||||
| chr11:8992580 | G | A | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-4298C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992580 | |||||||
| chr11:8992625 | C | T | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-4343G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992625 | |||||||
| chr11:8992633 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(67): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.175-4351C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992633 | |||||||
| chr11:8992671 | G | A | 1 | a0001c0001t0015g0052 | 2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.175-4389C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992671 | |||||||
| chr11:8992686 | G | A | 3 | a0003c0004t0027g0285 a0003c0004t0027g0286 a0003c0004t0028g0053 |
4 | HG02257.hp2 HG02280.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-4404C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992686 | |||||||
| chr11:8992842 | G | A | 1 | a0001c0001t0012g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175-4560C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992842 | |||||||
| chr11:8992911 | C | CA | 117 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
157 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.175-4630dupT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992911 | |||||||
| chr11:8992938 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.175-4656A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992938 | |||||||
| chr11:8992986 | T | C | 1 | a0001c0001t0020g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.175-4704A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8992986 | |||||||
| chr11:8993193 | A | T | 1 | a0001c0002t0044g0275 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.175-4911T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993193 | |||||||
| chr11:8993301 | T | C | 1 | a0003c0004t0027g0285 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.175-5019A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993301 | |||||||
| chr11:8993380 | A | G | 2 | a0001c0001t0033g0055 a0001c0001t0038g0056 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.175-5098T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993380 | |||||||
| chr11:8993395 | A | T | 1 | a0001c0001t0003g0270 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.175-5113T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993395 | |||||||
| chr11:8993579 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(189): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.175-5297G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993579 | |||||||
| chr11:8993729 | A | G | 1 | a0001c0001t0008g0151 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.175-5447T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993729 | |||||||
| chr11:8993808 | CA | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(150): Show |
217 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.175-5527delT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993808 | |||||||
| chr11:8993808 | CAA | C | 69 | a0001c0001t0001g0051 a0001c0001t0001g0180 a0001c0001t0001g0239 others(66): Show |
106 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.175-5528_175-5527d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993808 | |||||||
| chr11:8993839 | G | A | 2 | a0001c0001t0033g0055 a0001c0001t0038g0056 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.175-5557C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993839 | |||||||
| chr11:8993855 | A | G | 74 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(71): Show |
109 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.175-5573T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8993855 | |||||||
| chr11:8994031 | C | T | 1 | a0001c0001t0011g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.175-5749G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8994031 | |||||||
| chr11:8994032 | G | A | 1 | a0001c0001t0010g0112 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.175-5750C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8994032 | |||||||
| chr11:8994087 | C | T | 4 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-5805G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8994087 | |||||||
| chr11:8994930 | A | G | 1 | a0001c0001t0035g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175-6648T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8994930 | |||||||
| chr11:8995025 | T | A | 1 | a0001c0001t0025g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175-6743A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995025 | |||||||
| chr11:8995028 | A | G | 4 | a0001c0001t0004g0244 a0003c0004t0027g0285 a0003c0004t0027g0286 others(1): Show |
5 | HG02257.hp2 HG02280.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-6746T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995028 | |||||||
| chr11:8995114 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.175-6832G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995114 | |||||||
| chr11:8995199 | C | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.175-6917G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995199 | |||||||
| chr11:8995388 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.175-7106T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995388 | |||||||
| chr11:8995761 | C | A | 1 | a0001c0001t0003g0271 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175-7479G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995761 | |||||||
| chr11:8995820 | A | T | 2 | a0001c0001t0022g0281 a0001c0001t0022g0282 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.175-7538T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995820 | |||||||
| chr11:8995916 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(196): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.175-7634A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8995916 | |||||||
| chr11:8996020 | T | G | 58 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(55): Show |
91 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.175-7738A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996020 | |||||||
| chr11:8996077 | C | T | 1 | a0001c0001t0006g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.174+7685G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996077 | |||||||
| chr11:8996275 | C | CT | 55 | a0001c0001t0001g0131 a0001c0001t0001g0180 a0001c0001t0002g0001 others(52): Show |
91 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.174+7486dupA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996275 | |||||||
| chr11:8996275 | C | CTT | 118 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(115): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.174+7485_174+7486d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996275 | |||||||
| chr11:8996275 | C | CTTT | 23 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0128 others(20): Show |
25 | HG00597.hp1 HG00741.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+7484_174+7486d others(5): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996275 | |||||||
| chr11:8996275 | CT | C | 8 | a0001c0001t0003g0137 a0001c0001t0004g0050 a0001c0001t0004g0233 others(5): Show |
9 | HG01070.hp1 HG01258.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+7486delA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996275 | |||||||
| chr11:8996275 | CTT | C | 47 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(44): Show |
78 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.174+7485_174+7486d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996275 | |||||||
| chr11:8996275 | CTTT | C | 10 | a0001c0001t0003g0258 a0001c0001t0012g0042 a0001c0001t0012g0059 others(7): Show |
12 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+7484_174+7486d others(5): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996275 | |||||||
| chr11:8996331 | G | A | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+7431C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996331 | |||||||
| chr11:8996437 | C | T | 67 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(64): Show |
101 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.174+7325G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996437 | |||||||
| chr11:8996445 | T | C | 1 | a0001c0001t0008g0161 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.174+7317A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996445 | |||||||
| chr11:8996468 | A | G | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+7294T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996468 | |||||||
| chr11:8996652 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.174+7110T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996652 | |||||||
| chr11:8996745 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.174+7017G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996745 | |||||||
| chr11:8996830 | C | A | 67 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(64): Show |
101 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.174+6932G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996830 | |||||||
| chr11:8996857 | AC | A | 4 | a0001c0001t0013g0047 a0001c0001t0013g0224 a0001c0001t0013g0227 others(1): Show |
5 | HG00642.hp1 HG01168.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+6904delG | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8996857 | |||||||
| chr11:8997034 | C | T | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+6728G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997034 | |||||||
| chr11:8997155 | G | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.174+6607C>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997155 | |||||||
| chr11:8997230 | C | T | 1 | a0002c0003t0003g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.174+6532G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997230 | |||||||
| chr11:8997280 | CAGG | C | 67 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(64): Show |
101 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.174+6479_174+6481d others(5): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997280 | |||||||
| chr11:8997290 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+6472C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997290 | |||||||
| chr11:8997299 | C | T | 2 | a0001c0001t0004g0231 a0001c0001t0006g0068 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.174+6463G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997299 | |||||||
| chr11:8997339 | G | C | 1 | a0001c0001t0038g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.174+6423C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997339 | |||||||
| chr11:8997355 | C | CA | 93 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(90): Show |
131 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.174+6406dupT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997355 | |||||||
| chr11:8997355 | C | CAA | 33 | a0001c0001t0001g0011 a0001c0001t0001g0135 a0001c0001t0001g0158 others(30): Show |
39 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.174+6405_174+6406d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997355 | |||||||
| chr11:8997355 | CA | C | 57 | a0001c0001t0002g0276 a0001c0001t0003g0004 a0001c0001t0003g0013 others(54): Show |
91 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.174+6406delT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997355 | |||||||
| chr11:8997375 | A | AG | 62 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(59): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.174+6386_174+6387i others(3): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997375 | |||||||
| chr11:8997375 | A | G | 3 | a0001c0001t0033g0055 a0001c0001t0038g0056 a0001c0001t0042g0095 |
3 | HG03516.hp2 NA19081.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.174+6387T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997375 | |||||||
| chr11:8997379 | G | A | 1 | a0001c0001t0040g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.174+6383C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997379 | |||||||
| chr11:8997433 | T | A | 1 | a0001c0001t0019g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.174+6329A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997433 | |||||||
| chr11:8997501 | A | C | 4 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(1): Show |
5 | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+6261T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997501 | |||||||
| chr11:8997636 | GAACA | G | 79 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(76): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.174+6122_174+6125d others(6): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997636 | |||||||
| chr11:8997639 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174+6123G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997639 | |||||||
| chr11:8997643 | A | T | 79 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(76): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.174+6119T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997643 | |||||||
| chr11:8997773 | G | T | 9 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(6): Show |
10 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+5989C>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8997773 | |||||||
| chr11:8998165 | C | G | 1 | a0001c0001t0002g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.174+5597G>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998165 | |||||||
| chr11:8998231 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG00558.hp2 HG02056.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.174+5531C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998231 | |||||||
| chr11:8998784 | A | AT | 114 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(111): Show |
167 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.174+4977dupA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998784 | |||||||
| chr11:8998784 | A | ATT | 49 | a0001c0001t0001g0017 a0001c0001t0001g0032 a0001c0001t0001g0038 others(46): Show |
66 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.174+4976_174+4977d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998784 | |||||||
| chr11:8998784 | A | ATTT | 13 | a0001c0001t0005g0044 a0001c0001t0005g0214 a0001c0001t0005g0216 others(10): Show |
16 | HG00642.hp1 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.174+4975_174+4977d others(5): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998784 | |||||||
| chr11:8998784 | A | T | 1 | a0001c0001t0013g0224 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.174+4978T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998784 | |||||||
| chr11:8998784 | AT | A | 9 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
9 | HG02027.hp1 HG02027.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+4977delA | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998784 | |||||||
| chr11:8998784 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.174+4967_174+4977d others(13): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998784 | |||||||
| chr11:8998815 | A | G | 1 | a0001c0001t0019g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.174+4947T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8998815 | |||||||
| chr11:8999092 | C | T | 74 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(71): Show |
109 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.174+4670G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999092 | |||||||
| chr11:8999117 | T | TCTTATTT others(15): Show |
1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+4623_174+4644d others(24): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999117 | |||||||
| chr11:8999350 | A | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(182): Show |
259 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.174+4412T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999350 | |||||||
| chr11:8999440 | C | T | 67 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(64): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.174+4322G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999440 | |||||||
| chr11:8999467 | C | T | 74 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(71): Show |
109 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.174+4295G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999467 | |||||||
| chr11:8999522 | G | A | 2 | a0001c0001t0023g0259 a0001c0001t0023g0260 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.174+4240C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999522 | |||||||
| chr11:8999585 | A | T | 1 | a0001c0001t0003g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.174+4177T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999585 | |||||||
| chr11:8999698 | T | A | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+4064A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999698 | |||||||
| chr11:8999721 | C | A | 7 | a0001c0001t0012g0042 a0001c0001t0012g0059 a0001c0001t0012g0060 others(4): Show |
8 | HG01109.hp2 HG01943.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.174+4041G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999721 | |||||||
| chr11:8999932 | A | G | 1 | a0001c0001t0004g0233 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.174+3830T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999932 | |||||||
| chr11:8999963 | T | A | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+3799A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999963 | |||||||
| chr11:8999964 | A | T | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+3798T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999964 | |||||||
| chr11:8999982 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0132 a0001c0001t0001g0166 |
4 | NA18942.hp1 NA19002.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+3780G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 8999982 | |||||||
| chr11:9000018 | G | A | 1 | a0001c0001t0002g0028 | 2 | HG01952.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.174+3744C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000018 | |||||||
| chr11:9000031 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(37): Show |
57 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.174+3731C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000031 | |||||||
| chr11:9000043 | A | G | 2 | a0001c0001t0022g0281 a0001c0001t0022g0282 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.174+3719T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000043 | |||||||
| chr11:9000319 | C | T | 74 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(71): Show |
109 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.174+3443G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000319 | |||||||
| chr11:9000771 | T | TA | 74 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(71): Show |
109 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.174+2990dupT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000771 | |||||||
| chr11:9000838 | G | T | 1 | a0001c0001t0035g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.174+2924C>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000838 | |||||||
| chr11:9000880 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.174+2882C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000880 | |||||||
| chr11:9000931 | T | G | 1 | a0001c0001t0002g0276 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.174+2831A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9000931 | |||||||
| chr11:9001048 | T | C | 1 | a0001c0001t0012g0060 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.174+2714A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001048 | |||||||
| chr11:9001360 | T | A | 1 | a0001c0001t0006g0022 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.174+2402A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001360 | |||||||
| chr11:9001533 | C | T | 3 | a0001c0001t0007g0015 a0001c0001t0007g0083 a0001c0001t0011g0084 |
5 | NA18950.hp1 NA19001.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+2229G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001533 | |||||||
| chr11:9001712 | C | T | 62 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(59): Show |
95 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.174+2050G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001712 | |||||||
| chr11:9001722 | AAGAGAGT others(55): Show |
A | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1978_174+2039d others(64): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001722 | |||||||
| chr11:9001741 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.174+2021C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001741 | |||||||
| chr11:9001790 | G | A | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1972C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001790 | |||||||
| chr11:9001791 | GTTTC | G | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1967_174+1970d others(6): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001791 | |||||||
| chr11:9001798 | T | G | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1964A>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001798 | |||||||
| chr11:9001800 | ACCTGG | A | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1957_174+1961d others(7): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001800 | |||||||
| chr11:9001810 | TCTGTGCA others(63): Show |
T | 5 | a0001c0001t0009g0019 a0001c0001t0009g0048 a0001c0001t0009g0206 others(2): Show |
8 | HG01884.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+1882_174+1951d others(72): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001810 | |||||||
| chr11:9001861 | T | C | 1 | a0001c0002t0003g0030 | 2 | NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.174+1901A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001861 | |||||||
| chr11:9001874 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0009 others(67): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.174+1888C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001874 | |||||||
| chr11:9001901 | A | G | 1 | a0001c0001t0006g0021 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.174+1861T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001901 | |||||||
| chr11:9001958 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.174+1804C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9001958 | |||||||
| chr11:9002147 | G | A | 2 | a0004c0005t0010g0122 a0004c0005t0011g0082 |
2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.174+1615C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002147 | |||||||
| chr11:9002161 | T | C | 2 | a0001c0001t0024g0283 a0001c0001t0024g0284 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.174+1601A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002161 | |||||||
| chr11:9002232 | C | T | 1 | a0001c0001t0006g0057 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.174+1530G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002232 | |||||||
| chr11:9002268 | G | A | 1 | a0001c0001t0004g0252 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.174+1494C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002268 | |||||||
| chr11:9002335 | A | G | 1 | a0001c0001t0006g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.174+1427T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002335 | |||||||
| chr11:9002354 | C | A | 2 | a0001c0001t0033g0055 a0001c0001t0038g0056 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.174+1408G>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002354 | |||||||
| chr11:9002528 | A | AAATTATA others(8): Show |
1 | a0001c0001t0019g0223 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.174+1233_174+1234i others(17): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002528 | |||||||
| chr11:9002528 | A | AAATTATA others(8): Show |
267 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(264): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.174+1233_174+1234i others(17): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002528 | |||||||
| chr11:9002530 | A | T | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+1232T>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002530 | |||||||
| chr11:9002596 | T | TA | 148 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(145): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.174+1165dupT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002596 | |||||||
| chr11:9002596 | T | TAA | 13 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(10): Show |
15 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.174+1164_174+1165d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002596 | |||||||
| chr11:9002596 | TA | T | 34 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(31): Show |
50 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.174+1165delT | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002596 | |||||||
| chr11:9002596 | TAA | T | 6 | a0001c0001t0004g0230 a0001c0001t0004g0231 a0001c0001t0013g0047 others(3): Show |
7 | HG00642.hp1 HG00733.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+1164_174+1165d others(4): Show |
NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002596 | |||||||
| chr11:9002643 | C | T | 1 | a0001c0001t0012g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.174+1119G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002643 | |||||||
| chr11:9002695 | C | T | 2 | a0001c0001t0012g0059 a0001c0001t0012g0060 |
2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.174+1067G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002695 | |||||||
| chr11:9002717 | T | A | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+1045A>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002717 | |||||||
| chr11:9002749 | A | C | 1 | a0001c0001t0010g0255 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.174+1013T>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002749 | |||||||
| chr11:9002913 | T | C | 73 | a0001c0001t0001g0018 a0001c0001t0001g0201 a0001c0001t0001g0202 others(70): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.174+849A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002913 | |||||||
| chr11:9002991 | T | C | 1 | a0001c0001t0051g0127 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.174+771A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9002991 | |||||||
| chr11:9003050 | C | T | 1 | a0001c0001t0021g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.174+712G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003050 | |||||||
| chr11:9003083 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(166): Show |
238 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.174+679C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003083 | |||||||
| chr11:9003108 | G | C | 45 | a0001c0001t0001g0051 a0001c0001t0001g0205 a0001c0001t0001g0239 others(42): Show |
60 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.174+654C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003108 | |||||||
| chr11:9003170 | T | C | 1 | a0001c0001t0002g0043 | 2 | HG00280.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.174+592A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003170 | |||||||
| chr11:9003305 | G | A | 76 | a0001c0001t0001g0051 a0001c0001t0001g0239 a0001c0001t0001g0240 others(73): Show |
112 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.174+457C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003305 | |||||||
| chr11:9003320 | T | C | 100 | a0001c0001t0001g0051 a0001c0001t0001g0222 a0001c0001t0001g0239 others(97): Show |
145 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.174+442A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003320 | |||||||
| chr11:9003349 | T | C | 33 | a0001c0001t0001g0279 a0001c0001t0002g0276 a0001c0001t0003g0004 others(30): Show |
51 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.174+413A>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003349 | |||||||
| chr11:9003368 | A | G | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+394T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003368 | |||||||
| chr11:9003369 | G | A | 1 | a0006c0006t0006g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+393C>T | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003369 | |||||||
| chr11:9003446 | C | T | 2 | a0001c0001t0006g0057 a0001c0001t0006g0058 |
2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.174+316G>A | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003446 | |||||||
| chr11:9003465 | A | G | 2 | a0001c0001t0033g0055 a0001c0001t0038g0056 |
2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.174+297T>C | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003465 | |||||||
| chr11:9003480 | G | C | 2 | a0001c0001t0024g0283 a0001c0001t0024g0284 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.174+282C>G | NRIP3 | ENSG00000175352.12 | transcript | ENST00000309166.8 | protein_coding | 1/6 | chr11 | 9003480 |