Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54904 |
|---|---|
| ensemblid | ENSG00000147548.17 |
| hgncid | 12767 |
| symbol | NSD3 |
| name | nuclear receptor binding SET domain protein 3 |
| refseq_nuc | NM_023034.2 |
| refseq_prot | NP_075447.1 |
| ensembl_nuc | ENST00000317025.13 |
| ensembl_prot | ENSP00000313983.7 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 38269704 |
| end | 38382271 |
| strand | - |
| ver | v1.2 |
| region | chr8:38269704-38382271 |
| region5000 | chr8:38264704-38387271 |
| regionname0 | NSD3_chr8_38269704_38382271 |
| regionname5000 | NSD3_chr8_38264704_38387271 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1437 | 217 | 39 | 42 | 106 | 13 | 15 | 82 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0002 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0003 | 0/0 | 1437 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0004 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0005 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0006 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0007 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0008 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4314 | 211 | 38 | 41 | 104 | 13 | 13 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0002 | 0/0 | 4314 | 2 | 2 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0003 | 0/0 | 4314 | 2 | 2 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0004 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0005 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0006 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0007 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0008 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0009 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0010 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0011 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0012 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0013 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| c0014 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 6455 | 117 | 31 | 20 | 47 | 8 | 9 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0002 | 0/0 | 6455 | 76 | 7 | 15 | 46 | 6 | 2 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0003 | 0/0 | 6455 | 3 | 0 | 0 | 3 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0004 | 0/0 | 6456 | 3 | 0 | 0 | 3 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0005 | 0/0 | 6455 | 3 | 0 | 3 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0006 | 0/0 | 6455 | 3 | 0 | 0 | 2 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0007 | 0/0 | 6455 | 2 | 0 | 0 | 2 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0008 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0009 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0010 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0011 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0012 | 0/0 | 6455 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0013 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0014 | 0/0 | 6455 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0015 | 0/0 | 6455 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0016 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0017 | 0/0 | 6455 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0018 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0019 | 0/0 | 6455 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0020 | 0/0 | 6455 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0021 | 0/0 | 6455 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0022 | 0/0 | 6455 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0023 | 0/0 | 6455 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0024 | 0/0 | 6455 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0025 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| t0026 | 0/0 | 6455 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4314 | 211 | 38 | 41 | 104 | 13 | 13 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0004 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0006 | 0/0 | 4314 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0008 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0009 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0011 | 0/0 | 4314 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0013 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0002c0003 | 0/0 | 4314 | 2 | 2 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0003c0002 | 0/0 | 4314 | 2 | 2 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0004c0005 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0005c0014 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0006c0012 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0007c0007 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0008c0010 | 0/0 | 4314 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 10768 | 105 | 24 | 19 | 47 | 7 | 6 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0002 | 0/0 | 10768 | 74 | 7 | 15 | 44 | 6 | 2 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0003 | 0/0 | 10768 | 3 | 0 | 0 | 3 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0004 | 0/0 | 10769 | 3 | 0 | 0 | 3 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0005 | 0/0 | 10768 | 3 | 0 | 3 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0006 | 0/0 | 10768 | 3 | 0 | 0 | 2 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0007 | 0/0 | 10768 | 2 | 0 | 0 | 2 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0008 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0010 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0011 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0012 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0013 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0014 | 0/0 | 10768 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0015 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0016 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0017 | 0/0 | 10768 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0018 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0019 | 0/0 | 10768 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0020 | 0/0 | 10768 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0021 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0022 | 0/0 | 10768 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0023 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0024 | 0/0 | 10768 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0025 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0001t0026 | 0/0 | 10768 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0004t0002 | 0/0 | 10768 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0006t0001 | 0/0 | 10768 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0008t0001 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0009t0009 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0011t0002 | 0/0 | 10768 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0001c0013t0001 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0002c0003t0001 | 0/0 | 10768 | 2 | 2 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0003c0002t0001 | 0/0 | 10768 | 2 | 2 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0004c0005t0001 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0005c0014t0001 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0006c0012t0001 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0007c0007t0001 | 0/0 | 10768 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| a0008c0010t0001 | 0/0 | 10768 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | copy fasta | chr8 | 38264704 | 38387271 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0015g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0016g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0017g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0018g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0019g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0020g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0021g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0022g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0023g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0024g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0025g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0001t0026g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0006t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0009t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0011t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0001c0013t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0002c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0002c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0003c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0003c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0004c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0005c0014t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0006c0012t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0007c0007t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| a0008c0010t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0006 | c0012 | t0001 | g0172 | EUR | GBR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00673 | hp1 | a0001 | c0001 | t0026 | g0137 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00673 | hp2 | a0001 | c0001 | t0014 | g0035 | EAS | CHS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00738 | hp2 | a0001 | c0006 | t0001 | g0161 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01168 | hp1 | a0001 | c0001 | t0024 | g0057 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0110 | AMR | PUR | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0112 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01258 | hp2 | a0001 | c0001 | t0022 | g0213 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01358 | hp2 | a0001 | c0001 | t0017 | g0140 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01433 | hp1 | a0001 | c0001 | t0020 | g0162 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0169 | EUR | IBS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0076 | EUR | IBS | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CDX | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0113 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02630 | hp2 | a0003 | c0002 | t0001 | g0122 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02647 | hp1 | a0003 | c0002 | t0001 | g0125 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02647 | hp2 | a0001 | c0001 | t0025 | g0225 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02683 | hp1 | a0001 | c0013 | t0001 | g0088 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02698 | hp2 | a0001 | c0008 | t0001 | g0085 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0108 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0093 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02738 | hp1 | a0001 | c0001 | t0023 | g0109 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02738 | hp2 | a0001 | c0001 | t0015 | g0223 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02809 | hp2 | a0005 | c0014 | t0001 | g0083 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02965 | hp2 | a0007 | c0007 | t0001 | g0153 | AFR | ESN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0151 | AFR | ESN | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03225 | hp1 | a0004 | c0005 | t0001 | g0091 | AFR | MSL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0132 | AFR | MSL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0089 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0131 | AFR | GWD | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03688 | hp1 | a0008 | c0010 | t0001 | g0210 | SAS | STU | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0170 | AFR | YRI | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18747 | hp1 | a0001 | c0001 | t0019 | g0101 | EAS | CHB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHB | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18962 | hp1 | a0001 | c0004 | t0002 | g0046 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18999 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0069 | AFR | LWK | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19065 | hp1 | a0001 | c0011 | t0002 | g0016 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0207 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ASW | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0017 | SAS | GIH | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03471 | hp1 | a0001 | c0009 | t0009 | g0090 | AFR | MSL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG06807 | hp1 | a0001 | c0001 | t0018 | g0221 | AFR | USA | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | USA | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0175 | REF | REF | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0114 | REF | REF | NSD3_chr8_38264704_38387271 | NSD3 | chr8 | 38264704 | 38387271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38279678
|
G | A | 1 | a0008 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.3622C>T | p.Arg1208Cys | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 21/24 | 4139/10768 | 3622/4314 | 1208/1437 | chr8 | 38279678 | ||
| chr8:38281562
|
C | T | 1 | a0007 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.3523G>A | p.Val1175Ile | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/24 | 4040/10768 | 3523/4314 | 1175/1437 | chr8 | 38281562 | ||
| chr8:38305427
|
G | A | 1 | a0006 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.2261C>T | p.Ser754Leu | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 13/24 | 2778/10768 | 2261/4314 | 754/1437 | chr8 | 38305427 | ||
| chr8:38326771
|
G | A | 1 | a0005 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1667C>T | p.Thr556Met | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/24 | 2184/10768 | 1667/4314 | 556/1437 | chr8 | 38326771 | ||
| chr8:38329811
|
C | G | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.1148G>C | p.Arg383Pro | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/24 | 1665/10768 | 1148/4314 | 383/1437 | chr8 | 38329811 | ||
| chr8:38347615
|
G | A | 1 | a0002 | 2 | HG03225.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.557C>T | p.Thr186Met | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/24 | 1074/10768 | 557/4314 | 186/1437 | chr8 | 38347615 | ||
| chr8:38348051
|
C | T | 1 | a0003 | 2 | HG02630.hp2 HG02647.hp1 |
missense_variant | MODERATE | c.121G>A | p.Ala41Thr | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/24 | 638/10768 | 121/4314 | 41/1437 | chr8 | 38348051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38275779
|
C | A | 1 | a0001c0008 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.4176G>T | p.Gly1392Gly | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 4693/10768 | 4176/4314 | 1392/1437 | chr8 | 38275779 | ||
| chr8:38279664
|
G | A | 1 | a0001c0009 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.3636C>T | p.Ala1212Ala | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 21/24 | 4153/10768 | 3636/4314 | 1212/1437 | chr8 | 38279664 | ||
| chr8:38290488
|
C | T | 1 | a0001c0006 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.3105G>A | p.Lys1035Lys | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/24 | 3622/10768 | 3105/4314 | 1035/1437 | chr8 | 38290488 | ||
| chr8:38290632
|
G | A | 1 | a0001c0011 | 1 | NA19065.hp1 | synonymous_variant | LOW | c.2961C>T | p.Asn987Asn | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/24 | 3478/10768 | 2961/4314 | 987/1437 | chr8 | 38290632 | ||
| chr8:38318917
|
T | G | 1 | a0001c0013 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1833A>C | p.Thr611Thr | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/24 | 2350/10768 | 1833/4314 | 611/1437 | chr8 | 38318917 | ||
| chr8:38347758
|
C | T | 1 | a0001c0004 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.414G>A | p.Ser138Ser | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/24 | 931/10768 | 414/4314 | 138/1437 | chr8 | 38347758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38270195
|
A | G | 1 | a0001c0001t0019 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5446T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 5446 | chr8 | 38270195 | |||||
| chr8:38270250
|
T | C | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(11): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*5391A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 5391 | chr8 | 38270250 | |||||
| chr8:38270353
|
T | C | 1 | a0001c0001t0020 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5288A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 5288 | chr8 | 38270353 | |||||
| chr8:38270408
|
A | AT | 1 | a0001c0001t0004 | 3 | NA18944.hp2 NA18957.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5232dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 5232 | chr8 | 38270408 | |||||
| chr8:38270411
|
T | C | 2 | a0001c0001t0021a0001c0001t0023 | 2 | HG02735.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5230A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 5230 | chr8 | 38270411 | |||||
| chr8:38270417
|
C | G | 1 | a0001c0001t0018 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5224G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 5224 | chr8 | 38270417 | |||||
| chr8:38270696
|
T | C | 1 | a0001c0001t0022 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4945A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 4945 | chr8 | 38270696 | |||||
| chr8:38270838
|
A | G | 1 | a0001c0001t0011 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4803T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 4803 | chr8 | 38270838 | |||||
| chr8:38271405
|
C | T | 1 | a0001c0001t0017 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4236G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 4236 | chr8 | 38271405 | |||||
| chr8:38271610
|
T | C | 9 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(6): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*4031A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 4031 | chr8 | 38271610 | |||||
| chr8:38271620
|
C | A | 1 | a0001c0001t0013 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4021G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 4021 | chr8 | 38271620 | |||||
| chr8:38272117
|
A | G | 1 | a0001c0001t0011 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3524T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 3524 | chr8 | 38272117 | |||||
| chr8:38272297
|
G | A | 1 | a0001c0001t0011 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3344C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 3344 | chr8 | 38272297 | |||||
| chr8:38272507
|
G | A | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(8): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*3134C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 3134 | chr8 | 38272507 | |||||
| chr8:38272651
|
A | G | 1 | a0001c0001t0016 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 2990 | chr8 | 38272651 | |||||
| chr8:38272688
|
A | C | 1 | a0001c0001t0015 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2953T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 2953 | chr8 | 38272688 | |||||
| chr8:38272915
|
C | A | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(8): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2726G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 2726 | chr8 | 38272915 | |||||
| chr8:38274004
|
T | C | 1 | a0001c0001t0026 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1637A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 1637 | chr8 | 38274004 | |||||
| chr8:38274444
|
C | G | 1 | a0001c0001t0014 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1197G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 1197 | chr8 | 38274444 | |||||
| chr8:38274554
|
A | G | 1 | a0001c0001t0013 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1087T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 1087 | chr8 | 38274554 | |||||
| chr8:38274677
|
C | T | 1 | a0001c0001t0012 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*964G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 964 | chr8 | 38274677 | |||||
| chr8:38274772
|
C | T | 3 | a0001c0001t0010a0001c0001t0011a0001c0009t0009 | 3 | HG02572.hp2 HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*869G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 869 | chr8 | 38274772 | |||||
| chr8:38274877
|
A | G | 1 | a0001c0001t0008 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 764 | chr8 | 38274877 | |||||
| chr8:38274886
|
G | A | 1 | a0001c0001t0007 | 2 | NA18999.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*755C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 755 | chr8 | 38274886 | |||||
| chr8:38275468
|
A | G | 1 | a0001c0001t0003 | 3 | NA18953.hp1 NA19056.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*173T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 24/24 | 173 | chr8 | 38275468 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:38276037
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4073-155G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 23/23 | chr8 | 38276037 | ||||||
| chr8:38276094
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.4072+202G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 23/23 | chr8 | 38276094 | ||||||
| chr8:38276173
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4072+123C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 23/23 | chr8 | 38276173 | ||||||
| chr8:38276275
|
G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.4072+21C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 23/23 | chr8 | 38276275 | ||||||
| chr8:38276933
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3868-433G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38276933 | ||||||
| chr8:38277005
|
G | A | 2 | a0001c0001t0002g0044a0001c0004t0002g0046 | 2 | NA18747.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3868-505C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277005 | ||||||
| chr8:38277185
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3868-685C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277185 | ||||||
| chr8:38277262
|
G | T | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.3868-762C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277262 | ||||||
| chr8:38277341
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3868-841C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277341 | ||||||
| chr8:38277359
|
C | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.3868-859G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277359 | ||||||
| chr8:38277523
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3867+783C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277523 | ||||||
| chr8:38277556
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3867+750G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277556 | ||||||
| chr8:38277557
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 10 | HG00280.hp2 HG00597.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.3867+749C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277557 | ||||||
| chr8:38277894
|
T | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.3867+412A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277894 | ||||||
| chr8:38277991
|
T | G | 1 | a0001c0001t0002g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3867+315A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38277991 | ||||||
| chr8:38278160
|
G | A | 1 | a0001c0001t0002g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3867+146C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38278160 | ||||||
| chr8:38278228
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3867+78C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38278228 | ||||||
| chr8:38278229
|
C | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3867+77G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38278229 | ||||||
| chr8:38278260
|
A | G | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | NA18941.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3867+46T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38278260 | ||||||
| chr8:38278270
|
G | A | 1 | a0002c0003t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3867+36C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 22/23 | chr8 | 38278270 | ||||||
| chr8:38278466
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3761-54G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 21/23 | chr8 | 38278466 | ||||||
| chr8:38279439
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3760+101T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 21/23 | chr8 | 38279439 | ||||||
| chr8:38279485
|
T | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3760+55A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 21/23 | chr8 | 38279485 | ||||||
| chr8:38279537
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.3760+3A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 21/23 | chr8 | 38279537 | ||||||
| chr8:38279752
|
G | C | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3619-71C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/23 | chr8 | 38279752 | ||||||
| chr8:38280012
|
A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.3619-331T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/23 | chr8 | 38280012 | ||||||
| chr8:38280316
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3619-635C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/23 | chr8 | 38280316 | ||||||
| chr8:38280399
|
T | C | 2 | a0002c0003t0001g0131a0002c0003t0001g0132 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3619-718A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/23 | chr8 | 38280399 | ||||||
| chr8:38280618
|
G | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3618+849C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/23 | chr8 | 38280618 | ||||||
| chr8:38281410
|
A | G | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3618+57T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 20/23 | chr8 | 38281410 | ||||||
| chr8:38281771
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3502-188C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38281771 | ||||||
| chr8:38281843
|
C | G | 5 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(2): Show | 5 | NA18957.hp1 NA18961.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.3502-260G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38281843 | ||||||
| chr8:38282211
|
C | A | 2 | a0001c0001t0001g0086a0001c0013t0001g0088 | 2 | HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3502-628G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38282211 | ||||||
| chr8:38282218
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3502-635A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38282218 | ||||||
| chr8:38282396
|
C | T | 1 | a0004c0005t0001g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3502-813G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38282396 | ||||||
| chr8:38282465
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.3502-882C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38282465 | ||||||
| chr8:38282507
|
C | A | 1 | a0001c0001t0002g0024 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3502-924G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38282507 | ||||||
| chr8:38282585
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3502-1002G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38282585 | ||||||
| chr8:38283177
|
A | G | 1 | a0001c0001t0006g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3502-1594T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283177 | ||||||
| chr8:38283313
|
T | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3502-1730A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283313 | ||||||
| chr8:38283483
|
G | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3502-1900C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283483 | ||||||
| chr8:38283629
|
G | A | 1 | a0001c0011t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3502-2046C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283629 | ||||||
| chr8:38283655
|
T | C | 5 | a0001c0001t0001g0086a0001c0001t0002g0079a0001c0001t0002g0080others(2): Show | 5 | HG00323.hp2 HG01243.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.3502-2072A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283655 | ||||||
| chr8:38283669
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0117a0001c0001t0001g0206others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.3502-2086G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283669 | ||||||
| chr8:38283813
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0127 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.3502-2230T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283813 | ||||||
| chr8:38283861
|
G | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.3502-2278C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38283861 | ||||||
| chr8:38284028
|
G | A | 12 | a0001c0001t0001g0116a0001c0001t0001g0135a0001c0001t0001g0136others(9): Show | 12 | HG00673.hp1 NA18612.hp1 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.3502-2445C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38284028 | ||||||
| chr8:38284248
|
A | G | 217 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.3502-2665T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38284248 | ||||||
| chr8:38284410
|
C | T | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3502-2827G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38284410 | ||||||
| chr8:38284606
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3502-3023G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38284606 | ||||||
| chr8:38284697
|
T | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.3502-3114A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38284697 | ||||||
| chr8:38284941
|
G | A | 16 | a0001c0001t0001g0106a0001c0001t0001g0146a0001c0001t0001g0149others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3502-3358C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38284941 | ||||||
| chr8:38285015
|
A | T | 1 | a0001c0011t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3502-3432T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285015 | ||||||
| chr8:38285111
|
G | C | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3501+3376C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285111 | ||||||
| chr8:38285217
|
T | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.3501+3270A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285217 | ||||||
| chr8:38285270
|
A | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0214 | 3 | HG02723.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3501+3217T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285270 | ||||||
| chr8:38285827
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3501+2660T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285827 | ||||||
| chr8:38285839
|
T | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.3501+2648A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285839 | ||||||
| chr8:38285907
|
G | A | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3501+2580C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38285907 | ||||||
| chr8:38286019
|
C | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0010a0001c0001t0002g0011others(2): Show | 5 | NA18957.hp1 NA18961.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.3501+2468G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286019 | ||||||
| chr8:38286021
|
C | T | 1 | a0006c0012t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3501+2466G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286021 | ||||||
| chr8:38286022
|
G | T | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.3501+2465C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286022 | ||||||
| chr8:38286054
|
T | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.3501+2433A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286054 | ||||||
| chr8:38286327
|
A | G | 6 | a0001c0001t0001g0147a0001c0001t0001g0156a0001c0001t0001g0168others(3): Show | 6 | HG00408.hp2 HG01256.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.3501+2160T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286327 | ||||||
| chr8:38286389
|
C | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3501+2098G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286389 | ||||||
| chr8:38286471
|
G | A | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3501+2016C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286471 | ||||||
| chr8:38286694
|
C | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3501+1793G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286694 | ||||||
| chr8:38286726
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3501+1761G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286726 | ||||||
| chr8:38286823
|
C | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0126others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3501+1664G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38286823 | ||||||
| chr8:38287133
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3501+1354G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287133 | ||||||
| chr8:38287176
|
C | A | 2 | a0001c0001t0001g0166a0001c0001t0001g0167 | 2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3501+1311G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287176 | ||||||
| chr8:38287554
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3501+933C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287554 | ||||||
| chr8:38287799
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3501+688G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287799 | ||||||
| chr8:38287809
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3501+678G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287809 | ||||||
| chr8:38287902
|
T | C | 2 | a0001c0001t0001g0086a0001c0013t0001g0088 | 2 | HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3501+585A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287902 | ||||||
| chr8:38287906
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3501+581G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38287906 | ||||||
| chr8:38288039
|
G | T | 1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3501+448C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38288039 | ||||||
| chr8:38288040
|
C | G | 1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3501+447G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38288040 | ||||||
| chr8:38288042
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3501+445A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38288042 | ||||||
| chr8:38288236
|
T | C | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG01243.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3501+251A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38288236 | ||||||
| chr8:38288252
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0192 | 2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3501+235G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38288252 | ||||||
| chr8:38288468
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0019g0101 | 2 | HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3501+19G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 19/23 | chr8 | 38288468 | ||||||
| chr8:38289573
|
T | C | 7 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0014others(4): Show | 8 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.3119-68A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/23 | chr8 | 38289573 | ||||||
| chr8:38289917
|
T | G | 1 | a0001c0001t0002g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3119-412A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/23 | chr8 | 38289917 | ||||||
| chr8:38290142
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG00438.hp1 HG01981.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.3118+333C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/23 | chr8 | 38290142 | ||||||
| chr8:38290212
|
TA | T | 86 | a0001c0001t0001g0211a0001c0001t0002g0001a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.3118+262delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/23 | chr8 | 38290212 | ||||||
| chr8:38290285
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3118+190T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/23 | chr8 | 38290285 | ||||||
| chr8:38290322
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.3118+153G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 17/23 | chr8 | 38290322 | ||||||
| chr8:38290721
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2916-44G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38290721 | ||||||
| chr8:38291242
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0023 | 2 | HG01070.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.2916-565C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38291242 | ||||||
| chr8:38291546
|
T | C | 3 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | NA18942.hp2 NA18990.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2916-869A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38291546 | ||||||
| chr8:38291886
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2916-1209G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38291886 | ||||||
| chr8:38291917
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2916-1240C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38291917 | ||||||
| chr8:38292049
|
TAAATC | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0019g0101 | 3 | HG02165.hp2 NA18747.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2916-1377_2916-137 others(9): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38292049 | ||||||
| chr8:38292209
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2916-1532A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38292209 | ||||||
| chr8:38292896
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2916-2219G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38292896 | ||||||
| chr8:38292897
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2916-2220C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38292897 | ||||||
| chr8:38292998
|
C | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0008t0001g0085others(1): Show | 4 | HG01192.hp1 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-2321G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38292998 | ||||||
| chr8:38293135
|
C | CA | 13 | a0001c0001t0001g0084a0001c0001t0001g0102a0001c0001t0001g0103others(10): Show | 13 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.2916-2459dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293135 | ||||||
| chr8:38293535
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2915+2261G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293535 | ||||||
| chr8:38293740
|
C | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | NA18959.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2915+2056G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293740 | ||||||
| chr8:38293784
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | NA18959.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2915+2012C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293784 | ||||||
| chr8:38293855
|
G | C | 1 | a0001c0001t0006g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2915+1941C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293855 | ||||||
| chr8:38293922
|
C | CA | 9 | a0001c0001t0001g0118a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 9 | HG01952.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2915+1873dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293922
|
CA | C | 81 | a0001c0001t0001g0082a0001c0001t0001g0087a0001c0001t0001g0092others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2915+1873delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293922
|
CAA | C | 9 | a0001c0001t0001g0086a0001c0001t0001g0117a0001c0001t0001g0124others(6): Show | 9 | HG00323.hp2 HG01175.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2915+1872_2915+187 others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293922
|
CAAAA | C | 11 | a0001c0001t0002g0002a0001c0001t0002g0022a0001c0001t0002g0034others(8): Show | 11 | HG00642.hp2 HG00741.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2915+1870_2915+187 others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293922
|
CAAAAA | C | 70 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(67): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.2915+1869_2915+187 others(9): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293922
|
CAAAAAA | C | 5 | a0001c0001t0002g0009a0001c0001t0002g0018a0001c0001t0002g0032others(2): Show | 5 | HG01070.hp2 HG01516.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2915+1868_2915+187 others(10): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293922
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2915+1863_2915+187 others(15): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293922 | ||||||
| chr8:38293975
|
GA | G | 8 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG02683.hp2 HG02735.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2915+1820delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38293975 | ||||||
| chr8:38294429
|
C | T | 4 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0055others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2915+1367G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294429 | ||||||
| chr8:38294477
|
T | G | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2915+1319A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294477 | ||||||
| chr8:38294503
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2915+1293G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294503 | ||||||
| chr8:38294618
|
C | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2915+1178G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294618 | ||||||
| chr8:38294797
|
A | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2915+999T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294797 | ||||||
| chr8:38294809
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2915+987G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294809 | ||||||
| chr8:38294843
|
A | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2915+953T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294843 | ||||||
| chr8:38294926
|
A | G | 90 | a0001c0001t0001g0143a0001c0001t0002g0001a0001c0001t0002g0002others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2915+870T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294926 | ||||||
| chr8:38294929
|
G | C | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG01243.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2915+867C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38294929 | ||||||
| chr8:38295000
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2915+796G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38295000 | ||||||
| chr8:38295074
|
C | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2915+722G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38295074 | ||||||
| chr8:38295143
|
C | CA | 16 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0141others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.2915+652dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 16/23 | chr8 | 38295143 | ||||||
| chr8:38296053
|
A | T | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2759-101T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296053 | ||||||
| chr8:38296282
|
G | C | 1 | a0001c0001t0002g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2759-330C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296282 | ||||||
| chr8:38296329
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2759-377G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296329 | ||||||
| chr8:38296425
|
C | CA | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2759-474dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296425 | ||||||
| chr8:38296674
|
C | CTG | 43 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0102others(40): Show | 43 | HG00099.hp1 HG00609.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.2759-724_2759-723d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
C | CTGTG | 13 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0096others(10): Show | 13 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.2759-726_2759-723d others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
C | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0217 | 2 | HG02886.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2759-722G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
CTG | C | 8 | a0001c0001t0001g0082a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG00438.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2759-724_2759-723d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
CTGTG | C | 43 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0214others(40): Show | 43 | HG00408.hp1 HG00609.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.2759-726_2759-723d others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
CTGTGTG | C | 39 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0010others(36): Show | 40 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.2759-728_2759-723d others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
CTGTGTGT others(1): Show |
C | 22 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0148others(19): Show | 22 | HG00323.hp2 HG00438.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2759-730_2759-723d others(10): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296674
|
CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2759-732_2759-723d others(12): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296674 | ||||||
| chr8:38296833
|
G | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2759-881C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38296833 | ||||||
| chr8:38297452
|
G | A | 1 | a0001c0011t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2759-1500C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38297452 | ||||||
| chr8:38297574
|
A | G | 1 | a0001c0001t0013g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2759-1622T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38297574 | ||||||
| chr8:38297649
|
G | A | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2759-1697C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38297649 | ||||||
| chr8:38298220
|
G | A | 18 | a0001c0001t0001g0106a0001c0001t0001g0146a0001c0001t0001g0149others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.2758+1224C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38298220 | ||||||
| chr8:38298530
|
C | CTG | 11 | a0001c0001t0001g0160a0001c0001t0001g0194a0001c0001t0002g0013others(8): Show | 11 | HG00408.hp1 HG00738.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.2758+912_2758+913d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38298530 | ||||||
| chr8:38298530
|
C | CTGTG | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(1): Show | 4 | HG01168.hp2 HG01192.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2758+910_2758+913d others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38298530 | ||||||
| chr8:38298873
|
C | G | 8 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0054others(5): Show | 8 | HG00408.hp1 HG00609.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.2758+571G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38298873 | ||||||
| chr8:38299222
|
T | C | 3 | a0001c0001t0005g0110a0001c0001t0005g0111a0001c0001t0005g0112 | 3 | HG01243.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2758+222A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38299222 | ||||||
| chr8:38299390
|
GA | G | 3 | a0001c0001t0002g0054a0001c0001t0002g0073a0001c0001t0002g0224 | 3 | HG00408.hp1 HG00609.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.2758+53delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 15/23 | chr8 | 38299390 | ||||||
| chr8:38299965
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0127 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2612-375A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38299965 | ||||||
| chr8:38300158
|
TTATATTA others(2): Show |
T | 7 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG02683.hp2 HG02735.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2612-577_2612-569d others(11): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38300158 | ||||||
| chr8:38300213
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2612-623C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38300213 | ||||||
| chr8:38300377
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2612-787T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38300377 | ||||||
| chr8:38300496
|
T | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2612-906A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38300496 | ||||||
| chr8:38300573
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0189 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2612-983C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38300573 | ||||||
| chr8:38300748
|
T | C | 2 | a0001c0001t0002g0075a0001c0001t0024g0057 | 2 | HG01081.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2612-1158A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38300748 | ||||||
| chr8:38301395
|
T | C | 2 | a0001c0001t0002g0075a0001c0001t0024g0057 | 2 | HG01081.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.2612-1805A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38301395 | ||||||
| chr8:38301428
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2612-1838C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38301428 | ||||||
| chr8:38301441
|
G | A | 1 | a0001c0001t0024g0057 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2612-1851C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38301441 | ||||||
| chr8:38302517
|
T | A | 1 | a0001c0001t0002g0010 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2611+2070A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38302517 | ||||||
| chr8:38302525
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2611+2062G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38302525 | ||||||
| chr8:38302614
|
T | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2611+1973A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38302614 | ||||||
| chr8:38303335
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2611+1252T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38303335 | ||||||
| chr8:38303546
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2611+1041T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38303546 | ||||||
| chr8:38303951
|
T | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.2611+636A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38303951 | ||||||
| chr8:38304054
|
T | C | 1 | a0001c0011t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2611+533A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38304054 | ||||||
| chr8:38304068
|
C | G | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2611+519G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38304068 | ||||||
| chr8:38304388
|
C | A | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2611+199G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38304388 | ||||||
| chr8:38304457
|
G | GT | 88 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.2611+129dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 14/23 | chr8 | 38304457 | ||||||
| chr8:38304914
|
T | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0158a0001c0001t0001g0199others(2): Show | 5 | HG02074.hp1 HG02080.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.2441-157A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 13/23 | chr8 | 38304914 | ||||||
| chr8:38304946
|
C | T | 2 | a0002c0003t0001g0131a0002c0003t0001g0132 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2441-189G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 13/23 | chr8 | 38304946 | ||||||
| chr8:38304969
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2441-212T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 13/23 | chr8 | 38304969 | ||||||
| chr8:38305778
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2243-333C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38305778 | ||||||
| chr8:38305785
|
T | A | 90 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2243-340A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38305785 | ||||||
| chr8:38306037
|
C | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG00438.hp1 HG01981.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-592G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306037 | ||||||
| chr8:38306467
|
T | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2243-1022A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306467 | ||||||
| chr8:38306752
|
C | T | 2 | a0001c0001t0021g0108a0001c0001t0023g0109 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.2243-1307G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306752 | ||||||
| chr8:38306769
|
G | A | 87 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2243-1324C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306769 | ||||||
| chr8:38306785
|
G | A | 1 | a0001c0001t0006g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2243-1340C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306785 | ||||||
| chr8:38306852
|
T | C | 4 | a0001c0001t0002g0045a0001c0001t0002g0051a0001c0001t0002g0061others(1): Show | 4 | HG02080.hp1 NA18939.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.2243-1407A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306852 | ||||||
| chr8:38306918
|
T | C | 2 | a0001c0001t0002g0055a0001c0001t0002g0078 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2243-1473A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306918 | ||||||
| chr8:38306942
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2243-1497C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306942 | ||||||
| chr8:38306974
|
G | GTGTGGTG others(9): Show |
2 | a0001c0001t0002g0044a0001c0004t0002g0046 | 2 | NA18747.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2243-1545_2243-153 others(20): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38306974 | ||||||
| chr8:38307039
|
C | T | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2243-1594G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307039 | ||||||
| chr8:38307077
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2243-1632G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307077 | ||||||
| chr8:38307080
|
A | G | 2 | a0001c0001t0010g0113a0001c0001t0011g0089 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2243-1635T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307080 | ||||||
| chr8:38307102
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0002g0040 | 2 | NA18985.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2243-1657C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307102 | ||||||
| chr8:38307125
|
A | T | 8 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(5): Show | 8 | HG00280.hp1 HG00438.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.2243-1680T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307125 | ||||||
| chr8:38307127
|
A | T | 1 | a0001c0001t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2243-1682T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307127 | ||||||
| chr8:38307128
|
AT | A | 15 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0028others(12): Show | 15 | HG00323.hp1 HG00609.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.2243-1684delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307128 | ||||||
| chr8:38307129
|
T | A | 55 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0087others(52): Show | 55 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2243-1684A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307129 | ||||||
| chr8:38307130
|
A | T | 31 | a0001c0001t0001g0084a0001c0001t0001g0087a0001c0001t0001g0118others(28): Show | 31 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.2243-1685T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307130 | ||||||
| chr8:38307131
|
A | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0194a0001c0001t0001g0208 | 3 | HG00323.hp2 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2243-1686T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307131 | ||||||
| chr8:38307132
|
AAT | A | 64 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(61): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2243-1689_2243-168 others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307132 | ||||||
| chr8:38307134
|
T | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0194a0001c0001t0001g0208others(6): Show | 9 | HG00323.hp2 HG00735.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.2243-1689A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307134 | ||||||
| chr8:38307134
|
TA | T | 17 | a0001c0001t0002g0009a0001c0001t0002g0025a0001c0001t0002g0027others(14): Show | 17 | HG00323.hp1 HG00609.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.2243-1690delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307134 | ||||||
| chr8:38307135
|
A | T | 69 | a0001c0001t0001g0086a0001c0001t0001g0188a0001c0001t0001g0194others(66): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.2243-1690T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307135 | ||||||
| chr8:38307554
|
A | G | 87 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2243-2109T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307554 | ||||||
| chr8:38307641
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2243-2196A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307641 | ||||||
| chr8:38307775
|
G | A | 1 | a0001c0001t0006g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2243-2330C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38307775 | ||||||
| chr8:38308248
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | NA18959.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2243-2803T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38308248 | ||||||
| chr8:38308744
|
A | C | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2243-3299T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38308744 | ||||||
| chr8:38308883
|
G | T | 87 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2243-3438C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38308883 | ||||||
| chr8:38308889
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2243-3444A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38308889 | ||||||
| chr8:38308913
|
G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | NA18959.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2243-3468C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38308913 | ||||||
| chr8:38309136
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2243-3691C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38309136 | ||||||
| chr8:38309146
|
T | TA | 5 | a0001c0001t0001g0115a0001c0001t0001g0127a0001c0001t0001g0129others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2243-3702dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38309146 | ||||||
| chr8:38309662
|
C | G | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2243-4217G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38309662 | ||||||
| chr8:38310131
|
G | A | 87 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.2242+4516C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310131 | ||||||
| chr8:38310397
|
ATAC | A | 85 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2242+4247_2242+424 others(7): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310397 | ||||||
| chr8:38310550
|
C | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0196 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2242+4097G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310550 | ||||||
| chr8:38310622
|
C | T | 1 | a0001c0006t0001g0161 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2242+4025G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310622 | ||||||
| chr8:38310756
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2242+3891G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310756 | ||||||
| chr8:38310803
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2242+3844G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310803 | ||||||
| chr8:38310897
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2242+3750A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310897 | ||||||
| chr8:38310974
|
G | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2242+3673C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38310974 | ||||||
| chr8:38311076
|
C | CT | 83 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2242+3570dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311076 | ||||||
| chr8:38311181
|
C | T | 24 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 24 | HG00673.hp1 HG01258.hp2 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.2242+3466G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311181 | ||||||
| chr8:38311197
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2242+3450C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311197 | ||||||
| chr8:38311429
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2242+3218G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311429 | ||||||
| chr8:38311470
|
G | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0193 | 2 | HG00280.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2242+3177C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311470 | ||||||
| chr8:38311490
|
C | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2242+3157G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311490 | ||||||
| chr8:38311605
|
C | T | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2242+3042G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311605 | ||||||
| chr8:38311661
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2242+2986C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38311661 | ||||||
| chr8:38312047
|
GT | G | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(4): Show | 7 | HG00438.hp2 NA18942.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2242+2599delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38312047 | ||||||
| chr8:38312207
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2242+2440T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38312207 | ||||||
| chr8:38312216
|
A | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0076 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2242+2431T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38312216 | ||||||
| chr8:38312611
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2242+2036G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38312611 | ||||||
| chr8:38312718
|
T | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0189 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2242+1929A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38312718 | ||||||
| chr8:38313406
|
C | G | 1 | a0001c0001t0018g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2242+1241G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313406 | ||||||
| chr8:38313674
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2242+973C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313674 | ||||||
| chr8:38313742
|
T | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2242+905A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313742 | ||||||
| chr8:38313774
|
C | T | 10 | a0001c0001t0001g0115a0001c0001t0001g0127a0001c0001t0001g0128others(7): Show | 10 | HG01167.hp1 HG01433.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2242+873G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313774 | ||||||
| chr8:38313787
|
C | CA | 7 | a0001c0001t0001g0133a0001c0001t0002g0002a0001c0001t0010g0113others(4): Show | 7 | HG00099.hp1 HG00673.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242+859dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313787 | ||||||
| chr8:38313787
|
CA | C | 6 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0002g0018others(3): Show | 6 | HG01070.hp2 HG01243.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2242+859delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313787 | ||||||
| chr8:38313995
|
G | GCAAAA | 60 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.2242+647_2242+651d others(7): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38313995 | ||||||
| chr8:38314052
|
T | G | 5 | a0001c0001t0002g0063a0001c0001t0003g0062a0001c0001t0003g0068others(2): Show | 5 | HG00673.hp2 NA18612.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.2242+595A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38314052 | ||||||
| chr8:38314279
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2242+368A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 12/23 | chr8 | 38314279 | ||||||
| chr8:38314816
|
C | T | 1 | a0006c0012t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2116-43G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 11/23 | chr8 | 38314816 | ||||||
| chr8:38314893
|
G | A | 1 | a0001c0001t0013g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2116-120C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 11/23 | chr8 | 38314893 | ||||||
| chr8:38315089
|
G | A | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2116-316C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 11/23 | chr8 | 38315089 | ||||||
| chr8:38315857
|
G | C | 90 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1986+55C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 10/23 | chr8 | 38315857 | ||||||
| chr8:38316335
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1856-293A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38316335 | ||||||
| chr8:38316459
|
T | C | 1 | a0001c0001t0024g0057 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1856-417A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38316459 | ||||||
| chr8:38317219
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0002g0051a0001c0001t0002g0061others(1): Show | 4 | HG02080.hp1 NA18939.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1856-1177G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38317219 | ||||||
| chr8:38318021
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1855+874G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38318021 | ||||||
| chr8:38318300
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1855+595A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38318300 | ||||||
| chr8:38318349
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1855+546T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38318349 | ||||||
| chr8:38318669
|
T | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1855+226A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38318669 | ||||||
| chr8:38318740
|
T | TCA | 2 | a0001c0001t0001g0105a0001c0001t0001g0193 | 2 | HG00280.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1855+153_1855+154d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 9/23 | chr8 | 38318740 | ||||||
| chr8:38319247
|
A | G | 1 | a0005c0014t0001g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1810-307T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 8/23 | chr8 | 38319247 | ||||||
| chr8:38319268
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1810-328C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 8/23 | chr8 | 38319268 | ||||||
| chr8:38319862
|
A | T | 1 | a0001c0001t0001g0168 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1810-922T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 8/23 | chr8 | 38319862 | ||||||
| chr8:38320692
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1809+380T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 8/23 | chr8 | 38320692 | ||||||
| chr8:38321190
|
C | T | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157 | 3 | HG01168.hp2 HG01952.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1709-18G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38321190 | ||||||
| chr8:38321249
|
C | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1709-77G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38321249 | ||||||
| chr8:38321400
|
C | T | 26 | a0001c0001t0001g0084a0001c0001t0001g0118a0001c0001t0001g0119others(23): Show | 26 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1709-228G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38321400 | ||||||
| chr8:38321410
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0193 | 2 | HG00280.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1709-238C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38321410 | ||||||
| chr8:38321665
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1709-493C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38321665 | ||||||
| chr8:38321707
|
A | G | 1 | a0004c0005t0001g0091 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1709-535T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38321707 | ||||||
| chr8:38322179
|
C | G | 1 | a0001c0001t0002g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1709-1007G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38322179 | ||||||
| chr8:38322516
|
G | T | 2 | a0001c0001t0001g0191a0001c0001t0008g0170 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1709-1344C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38322516 | ||||||
| chr8:38322728
|
T | G | 1 | a0001c0001t0001g0097 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1709-1556A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38322728 | ||||||
| chr8:38322784
|
C | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1709-1612G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38322784 | ||||||
| chr8:38323043
|
T | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(74): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1709-1871A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323043 | ||||||
| chr8:38323056
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1709-1884G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323056 | ||||||
| chr8:38323078
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0055others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1709-1906C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323078 | ||||||
| chr8:38323117
|
C | T | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1709-1945G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323117 | ||||||
| chr8:38323131
|
T | C | 1 | a0002c0003t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1709-1959A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323131 | ||||||
| chr8:38323749
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | NA18941.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1709-2577C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323749 | ||||||
| chr8:38323821
|
C | CA | 6 | a0001c0001t0001g0097a0001c0001t0001g0147a0001c0001t0010g0113others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1709-2650dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323821 | ||||||
| chr8:38323821
|
CA | C | 87 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0126others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.1709-2650delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323821 | ||||||
| chr8:38323853
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1709-2681G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38323853 | ||||||
| chr8:38324286
|
C | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1708+2444G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38324286 | ||||||
| chr8:38325126
|
G | T | 1 | a0001c0001t0002g0004 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1708+1604C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38325126 | ||||||
| chr8:38325698
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1708+1032C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38325698 | ||||||
| chr8:38326077
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1708+653C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38326077 | ||||||
| chr8:38326430
|
T | C | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1708+300A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38326430 | ||||||
| chr8:38326502
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1708+228A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38326502 | ||||||
| chr8:38326640
|
A | G | 1 | a0001c0001t0013g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1708+90T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 7/23 | chr8 | 38326640 | ||||||
| chr8:38326979
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1582-123C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38326979 | ||||||
| chr8:38327068
|
GAGA | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | NA18966.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1582-215_1582-213d others(5): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327068 | ||||||
| chr8:38327352
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1582-496C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327352 | ||||||
| chr8:38327364
|
T | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0065 | 2 | HG02074.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1582-508A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327364 | ||||||
| chr8:38327425
|
G | A | 30 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0037others(27): Show | 30 | HG00408.hp1 HG00609.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1582-569C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327425 | ||||||
| chr8:38327446
|
G | C | 224 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1582-590C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327446 | ||||||
| chr8:38327611
|
C | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0205a0001c0001t0008g0170 | 3 | HG02622.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1582-755G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327611 | ||||||
| chr8:38327742
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1582-886C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38327742 | ||||||
| chr8:38328019
|
T | C | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1582-1163A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328019 | ||||||
| chr8:38328029
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1582-1173G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328029 | ||||||
| chr8:38328032
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1582-1176A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328032 | ||||||
| chr8:38328385
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1581+993G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328385 | ||||||
| chr8:38328519
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1581+859C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328519 | ||||||
| chr8:38328800
|
T | C | 1 | a0001c0001t0015g0223 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1581+578A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328800 | ||||||
| chr8:38328982
|
C | CAA | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(4): Show | 7 | HG00438.hp2 NA18942.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1581+395_1581+396i others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38328982 | ||||||
| chr8:38329214
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1581+164G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 6/23 | chr8 | 38329214 | ||||||
| chr8:38329995
|
T | C | 1 | a0007c0007t0001g0153 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1066-102A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 5/23 | chr8 | 38329995 | ||||||
| chr8:38330495
|
A | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.1066-602T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 5/23 | chr8 | 38330495 | ||||||
| chr8:38330716
|
G | A | 2 | a0001c0001t0010g0113a0001c0001t0011g0089 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1065+715C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 5/23 | chr8 | 38330716 | ||||||
| chr8:38330891
|
C | G | 1 | a0001c0001t0018g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1065+540G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 5/23 | chr8 | 38330891 | ||||||
| chr8:38331827
|
T | TCAAAA | 2 | a0001c0001t0002g0079a0001c0009t0009g0090 | 2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.911-247_911-243dup others(5): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38331827 | ||||||
| chr8:38331827
|
TCAAAA | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0171 | 2 | HG00408.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.911-247_911-243del others(5): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38331827 | ||||||
| chr8:38331827
|
TCAAAACA others(3): Show |
T | 6 | a0001c0001t0001g0149a0001c0001t0001g0163a0001c0001t0001g0192others(3): Show | 6 | HG00738.hp2 HG00741.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.911-252_911-243del others(10): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38331827 | ||||||
| chr8:38331827
|
TCAAAACA others(13): Show |
T | 1 | a0001c0001t0001g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.911-262_911-243del others(20): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38331827 | ||||||
| chr8:38332786
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.911-1201A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38332786 | ||||||
| chr8:38332841
|
G | C | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.911-1256C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38332841 | ||||||
| chr8:38333251
|
T | G | 8 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG02683.hp2 HG02735.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.911-1666A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333251 | ||||||
| chr8:38333292
|
C | T | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.911-1707G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333292 | ||||||
| chr8:38333393
|
A | G | 2 | a0004c0005t0001g0091a0005c0014t0001g0083 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.911-1808T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333393 | ||||||
| chr8:38333416
|
T | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.911-1831A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333416 | ||||||
| chr8:38333466
|
T | C | 1 | a0001c0001t0013g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.911-1881A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333466 | ||||||
| chr8:38333636
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.911-2051C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333636 | ||||||
| chr8:38333835
|
C | A | 5 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0014others(2): Show | 6 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(3): Show |
intron_variant | MODIFIER | c.911-2250G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333835 | ||||||
| chr8:38333857
|
G | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(77): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.911-2272C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333857 | ||||||
| chr8:38333906
|
C | T | 1 | a0001c0001t0002g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.911-2321G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333906 | ||||||
| chr8:38333916
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.911-2331T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333916 | ||||||
| chr8:38333927
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.911-2342G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38333927 | ||||||
| chr8:38334034
|
T | G | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.911-2449A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334034 | ||||||
| chr8:38334255
|
T | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.911-2670A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334255 | ||||||
| chr8:38334446
|
G | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910+2859C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334446 | ||||||
| chr8:38334492
|
C | T | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910+2813G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334492 | ||||||
| chr8:38334526
|
A | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.910+2779T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334526 | ||||||
| chr8:38334581
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.910+2724G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334581 | ||||||
| chr8:38334753
|
AAAAC | A | 36 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(33): Show | 36 | HG00673.hp1 HG01167.hp1 HG01258.hp2 others(33): Show |
intron_variant | MODIFIER | c.910+2548_910+2551d others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334753 | ||||||
| chr8:38334981
|
A | AT | 59 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0095others(56): Show | 59 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.910+2323dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334981 | ||||||
| chr8:38334981
|
AT | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0156a0001c0001t0001g0193others(2): Show | 5 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+2323delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38334981 | ||||||
| chr8:38335111
|
A | G | 1 | a0001c0011t0002g0016 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.910+2194T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335111 | ||||||
| chr8:38335321
|
T | C | 2 | a0004c0005t0001g0091a0005c0014t0001g0083 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.910+1984A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335321 | ||||||
| chr8:38335489
|
AT | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.910+1815delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335489 | ||||||
| chr8:38335493
|
A | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.910+1812T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335493 | ||||||
| chr8:38335495
|
C | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.910+1810G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335495 | ||||||
| chr8:38335544
|
T | TAAGAAAG others(1711): Show |
1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910+1760_910+1761i others(1720): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335544 | ||||||
| chr8:38335713
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0214 | 3 | HG02723.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.910+1592A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335713 | ||||||
| chr8:38335852
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.910+1453T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335852 | ||||||
| chr8:38335854
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.910+1451C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38335854 | ||||||
| chr8:38336000
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.910+1305G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38336000 | ||||||
| chr8:38336517
|
A | G | 1 | a0001c0001t0018g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.910+788T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38336517 | ||||||
| chr8:38336580
|
T | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910+725A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38336580 | ||||||
| chr8:38336690
|
T | C | 4 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0002g0056others(1): Show | 4 | HG00735.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.910+615A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38336690 | ||||||
| chr8:38336912
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.910+393G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38336912 | ||||||
| chr8:38337043
|
C | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.910+262G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38337043 | ||||||
| chr8:38337098
|
C | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0039 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.910+207G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 4/23 | chr8 | 38337098 | ||||||
| chr8:38337518
|
T | G | 1 | a0001c0001t0001g0144 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.748-51A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 3/23 | chr8 | 38337518 | ||||||
| chr8:38338105
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.747+431C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 3/23 | chr8 | 38338105 | ||||||
| chr8:38338305
|
G | GA | 88 | a0001c0001t0001g0188a0001c0001t0002g0001a0001c0001t0002g0002others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.747+230dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 3/23 | chr8 | 38338305 | ||||||
| chr8:38338787
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.676-180G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38338787 | ||||||
| chr8:38338805
|
T | C | 3 | a0001c0001t0001g0191a0001c0001t0001g0205a0001c0001t0008g0170 | 3 | HG02622.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.676-198A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38338805 | ||||||
| chr8:38339139
|
C | CA | 90 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0156others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.676-533dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38339139 | ||||||
| chr8:38339366
|
T | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.676-759A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38339366 | ||||||
| chr8:38339417
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.676-810C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38339417 | ||||||
| chr8:38339458
|
G | A | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.676-851C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38339458 | ||||||
| chr8:38339598
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.676-991G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38339598 | ||||||
| chr8:38339724
|
C | CA | 5 | a0001c0001t0002g0037a0001c0001t0002g0075a0001c0001t0015g0223others(2): Show | 5 | HG01081.hp2 HG01168.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-1118dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38339724 | ||||||
| chr8:38340182
|
T | TAAAAAGA others(196): Show |
1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.676-1576_676-1575i others(205): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38340182 | ||||||
| chr8:38340557
|
T | TG | 8 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 8 | HG02683.hp2 HG02735.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-1951dupC | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38340557 | ||||||
| chr8:38340577
|
A | T | 1 | a0001c0013t0001g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.676-1970T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38340577 | ||||||
| chr8:38340685
|
A | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.676-2078T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38340685 | ||||||
| chr8:38340987
|
G | A | 217 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.676-2380C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38340987 | ||||||
| chr8:38341075
|
G | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0118a0001c0001t0001g0119others(15): Show | 18 | HG00597.hp2 HG00609.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.676-2468C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341075 | ||||||
| chr8:38341107
|
G | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.676-2500C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341107 | ||||||
| chr8:38341117
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.676-2510G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341117 | ||||||
| chr8:38341271
|
A | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.676-2664T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341271 | ||||||
| chr8:38341279
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | NA18970.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.676-2672G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341279 | ||||||
| chr8:38341321
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.676-2714G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341321 | ||||||
| chr8:38341519
|
C | A | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.676-2912G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341519 | ||||||
| chr8:38341524
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0175 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.676-2917G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38341524 | ||||||
| chr8:38342195
|
G | T | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.676-3588C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38342195 | ||||||
| chr8:38342425
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.676-3818T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38342425 | ||||||
| chr8:38342644
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.676-4037A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38342644 | ||||||
| chr8:38342703
|
T | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.676-4096A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38342703 | ||||||
| chr8:38342776
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.676-4169A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38342776 | ||||||
| chr8:38342805
|
G | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0070 | 2 | HG02165.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.676-4198C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38342805 | ||||||
| chr8:38343021
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.676-4414C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38343021 | ||||||
| chr8:38343121
|
G | A | 11 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(8): Show | 11 | HG00280.hp2 HG00597.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.675+4376C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38343121 | ||||||
| chr8:38343270
|
A | G | 3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.675+4227T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38343270 | ||||||
| chr8:38343714
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(75): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.675+3783G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38343714 | ||||||
| chr8:38343821
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.675+3676G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38343821 | ||||||
| chr8:38343830
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.675+3667G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38343830 | ||||||
| chr8:38344003
|
G | A | 1 | a0001c0001t0016g0151 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675+3494C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344003 | ||||||
| chr8:38344075
|
T | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+3422A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344075 | ||||||
| chr8:38344429
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0192 | 2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.675+3068C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344429 | ||||||
| chr8:38344446
|
A | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.675+3051T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344446 | ||||||
| chr8:38344480
|
G | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.675+3017C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344480 | ||||||
| chr8:38344560
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.675+2937T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344560 | ||||||
| chr8:38344664
|
A | T | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.675+2833T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344664 | ||||||
| chr8:38344950
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.675+2547A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38344950 | ||||||
| chr8:38345218
|
G | GGA | 4 | a0001c0001t0002g0036a0001c0001t0002g0039a0001c0001t0002g0055others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.675+2277_675+2278d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38345218 | ||||||
| chr8:38345541
|
C | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.675+1956G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38345541 | ||||||
| chr8:38345771
|
G | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.675+1726C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38345771 | ||||||
| chr8:38345905
|
G | A | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.675+1592C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38345905 | ||||||
| chr8:38346169
|
TATATATG others(9): Show |
T | 1 | a0001c0001t0001g0169 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.675+1312_675+1327d others(18): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346169 | ||||||
| chr8:38346334
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.675+1163G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346334 | ||||||
| chr8:38346360
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.675+1137A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346360 | ||||||
| chr8:38346372
|
T | C | 1 | a0001c0001t0002g0004 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.675+1125A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346372 | ||||||
| chr8:38346377
|
A | ATGTATAT others(30): Show |
1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.675+1083_675+1119d others(39): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346377 | ||||||
| chr8:38346497
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.675+1000A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346497 | ||||||
| chr8:38346897
|
A | ATT | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.675+599_675+600ins others(2): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 2/23 | chr8 | 38346897 | ||||||
| chr8:38348297
|
A | C | 2 | a0001c0001t0003g0068a0001c0001t0003g0077 | 2 | NA18953.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-44-82T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38348297 | ||||||
| chr8:38348306
|
G | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44-91C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38348306 | ||||||
| chr8:38348363
|
C | A | 11 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(8): Show | 11 | HG00280.hp2 HG00597.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44-148G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38348363 | ||||||
| chr8:38348724
|
C | T | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-44-509G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38348724 | ||||||
| chr8:38349464
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-44-1249T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349464 | ||||||
| chr8:38349640
|
TA | T | 3 | a0001c0001t0002g0039a0001c0001t0002g0055a0001c0001t0002g0078 | 3 | HG02615.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-44-1426delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349640 | ||||||
| chr8:38349665
|
T | TTA | 29 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0001g0104others(26): Show | 29 | HG01069.hp2 HG01192.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-44-1452_-44-1451d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349665 | ||||||
| chr8:38349665
|
T | TTATA | 33 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0102others(30): Show | 33 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-44-1454_-44-1451d others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349665 | ||||||
| chr8:38349665
|
T | TTATATA | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0092others(8): Show | 11 | HG00323.hp2 HG01433.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44-1456_-44-1451d others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349665 | ||||||
| chr8:38349665
|
T | TTATATAT others(1): Show |
7 | a0001c0001t0001g0098a0001c0001t0001g0128a0001c0001t0001g0129others(4): Show | 7 | HG01167.hp1 HG01256.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44-1458_-44-1451d others(10): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349665 | ||||||
| chr8:38349665
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0127 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-44-1460_-44-1451d others(12): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349665 | ||||||
| chr8:38349665
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-44-1462_-44-1451d others(14): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349665 | ||||||
| chr8:38349683
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0011g0089a0001c0001t0025g0225 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-44-1478_-44-1469d others(12): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349683 | ||||||
| chr8:38349687
|
ATATATG | A | 11 | a0001c0001t0001g0097a0001c0001t0002g0002a0001c0001t0002g0003others(8): Show | 11 | HG00438.hp2 HG02615.hp1 HG03471.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44-1478_-44-1473d others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349687 | ||||||
| chr8:38349689
|
ATATG | A | 38 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0011others(35): Show | 39 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-44-1478_-44-1475d others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349689 | ||||||
| chr8:38349691
|
ATG | A | 38 | a0001c0001t0001g0106a0001c0001t0001g0117a0001c0001t0001g0124others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.-44-1478_-44-1477d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349691 | ||||||
| chr8:38349693
|
G | A | 127 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(124): Show | 127 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-44-1478C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349693 | ||||||
| chr8:38349697
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-44-1482A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38349697 | ||||||
| chr8:38350097
|
C | T | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-44-1882G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350097 | ||||||
| chr8:38350112
|
T | A | 11 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(8): Show | 11 | HG00280.hp2 HG00597.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44-1897A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350112 | ||||||
| chr8:38350135
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-44-1920C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350135 | ||||||
| chr8:38350172
|
A | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-44-1957T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350172 | ||||||
| chr8:38350884
|
G | T | 2 | a0001c0001t0001g0142a0001c0001t0022g0213 | 2 | HG01258.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-44-2669C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350884 | ||||||
| chr8:38350892
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-44-2677G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350892 | ||||||
| chr8:38350973
|
C | CT | 85 | a0001c0001t0001g0117a0001c0001t0001g0188a0001c0001t0002g0001others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-44-2759dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38350973 | ||||||
| chr8:38351038
|
C | G | 1 | a0001c0001t0002g0025 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-44-2823G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351038 | ||||||
| chr8:38351208
|
AC | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-44-2994delG | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351208 | ||||||
| chr8:38351611
|
A | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-44-3396T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351611 | ||||||
| chr8:38351662
|
C | CA | 5 | a0001c0001t0001g0165a0001c0001t0001g0217a0001c0001t0001g0218others(2): Show | 5 | HG01258.hp2 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-3448dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351662 | ||||||
| chr8:38351662
|
CA | C | 6 | a0001c0001t0001g0121a0001c0001t0002g0015a0001c0001t0002g0080others(3): Show | 6 | HG01069.hp1 HG01243.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-3448delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351662 | ||||||
| chr8:38351765
|
G | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44-3550C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351765 | ||||||
| chr8:38351813
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0204 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-44-3598A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351813 | ||||||
| chr8:38351971
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-3756G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38351971 | ||||||
| chr8:38352157
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0158a0001c0001t0001g0199others(2): Show | 5 | HG02074.hp1 HG02080.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-3942C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38352157 | ||||||
| chr8:38352480
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-44-4265A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38352480 | ||||||
| chr8:38352488
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-44-4273T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38352488 | ||||||
| chr8:38352757
|
G | A | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-44-4542C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38352757 | ||||||
| chr8:38353188
|
C | CA | 6 | a0001c0001t0001g0146a0001c0001t0001g0217a0001c0001t0002g0025others(3): Show | 6 | HG02074.hp1 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-4974dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38353188 | ||||||
| chr8:38353564
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-44-5349A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38353564 | ||||||
| chr8:38353609
|
C | A | 2 | a0001c0001t0002g0059a0001c0001t0002g0074 | 2 | HG00741.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-44-5394G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38353609 | ||||||
| chr8:38354003
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-5788G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38354003 | ||||||
| chr8:38354069
|
T | C | 2 | a0001c0001t0021g0108a0001c0001t0023g0109 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-44-5854A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38354069 | ||||||
| chr8:38354428
|
C | A | 1 | a0001c0001t0002g0003 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-44-6213G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38354428 | ||||||
| chr8:38354895
|
T | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-44-6680A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38354895 | ||||||
| chr8:38355049
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-44-6834G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38355049 | ||||||
| chr8:38355093
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-44-6878A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38355093 | ||||||
| chr8:38355410
|
TA | T | 96 | a0001c0001t0001g0082a0001c0001t0001g0118a0001c0001t0001g0155others(93): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-44-7196delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38355410 | ||||||
| chr8:38355464
|
T | C | 1 | a0002c0003t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-44-7249A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38355464 | ||||||
| chr8:38355683
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-44-7468G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38355683 | ||||||
| chr8:38355796
|
A | G | 2 | a0001c0001t0002g0004a0001c0001t0002g0009 | 2 | NA18952.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-44-7581T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38355796 | ||||||
| chr8:38356065
|
A | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-44-7850T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38356065 | ||||||
| chr8:38356221
|
A | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-44-8006T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38356221 | ||||||
| chr8:38356247
|
G | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-44-8032C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38356247 | ||||||
| chr8:38356419
|
A | G | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44-8204T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38356419 | ||||||
| chr8:38356835
|
T | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-8620A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38356835 | ||||||
| chr8:38356988
|
A | G | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-44-8773T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38356988 | ||||||
| chr8:38357020
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-44-8805C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357020 | ||||||
| chr8:38357038
|
G | A | 3 | a0001c0001t0002g0045a0001c0001t0002g0051a0001c0001t0002g0064 | 3 | NA18939.hp2 NA18977.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-44-8823C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357038 | ||||||
| chr8:38357118
|
C | CA | 32 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0103others(29): Show | 32 | HG00280.hp2 HG00597.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.-44-8904dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357118
|
C | CAA | 7 | a0001c0001t0001g0099a0001c0001t0001g0124a0001c0001t0002g0039others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-8905_-44-8904d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357118
|
C | CAAAAA | 40 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0008others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.-44-8908_-44-8904d others(7): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357118
|
C | CAAAAAA | 23 | a0001c0001t0002g0001a0001c0001t0002g0006a0001c0001t0002g0010others(20): Show | 24 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.-44-8909_-44-8904d others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357118
|
C | CAAAAAAA | 5 | a0001c0001t0002g0002a0001c0001t0002g0040a0001c0001t0002g0043others(2): Show | 5 | HG01168.hp1 HG02523.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-8910_-44-8904d others(9): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357118
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0034 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-44-8913_-44-8904d others(12): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357118
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0066 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-44-8914_-44-8904d others(13): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357118 | ||||||
| chr8:38357389
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-44-9174A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357389 | ||||||
| chr8:38357926
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-44-9711A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357926 | ||||||
| chr8:38357935
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0019g0101 | 3 | HG02165.hp2 NA18747.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-44-9720A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357935 | ||||||
| chr8:38357991
|
G | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | NA18965.hp2 NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-44-9776C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38357991 | ||||||
| chr8:38358676
|
T | C | 1 | a0001c0001t0002g0040 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-44-10461A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38358676 | ||||||
| chr8:38358875
|
T | C | 1 | a0001c0001t0002g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-44-10660A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38358875 | ||||||
| chr8:38358922
|
A | AT | 26 | a0001c0001t0001g0106a0001c0001t0001g0146a0001c0001t0001g0147others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.-44-10708dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38358922 | ||||||
| chr8:38358929
|
T | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44-10714A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38358929 | ||||||
| chr8:38359172
|
A | C | 1 | a0001c0001t0001g0159 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-44-10957T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38359172 | ||||||
| chr8:38359675
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-44-11460G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38359675 | ||||||
| chr8:38359999
|
A | AT | 13 | a0001c0001t0001g0175a0001c0001t0001g0199a0001c0001t0001g0209others(10): Show | 13 | HG01243.hp1 HG02572.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44-11785dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38359999 | ||||||
| chr8:38359999
|
A | ATT | 73 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(70): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.-44-11786_-44-1178 others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38359999 | ||||||
| chr8:38360094
|
C | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-44-11879G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360094 | ||||||
| chr8:38360223
|
T | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-44-12008A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360223 | ||||||
| chr8:38360262
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-44-12047C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360262 | ||||||
| chr8:38360618
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44-12403T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360618 | ||||||
| chr8:38360685
|
A | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-12470T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360685 | ||||||
| chr8:38360781
|
T | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-12566A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360781 | ||||||
| chr8:38360899
|
A | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0135 | 2 | NA18612.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-44-12684T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360899 | ||||||
| chr8:38360940
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-44-12725G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38360940 | ||||||
| chr8:38361026
|
A | G | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-12811T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361026 | ||||||
| chr8:38361191
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006 | 3 | NA18942.hp2 NA18990.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-44-12976T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361191 | ||||||
| chr8:38361330
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-44-13115C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361330 | ||||||
| chr8:38361527
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-44-13312C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361527 | ||||||
| chr8:38361583
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-44-13368C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361583 | ||||||
| chr8:38361720
|
G | A | 224 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-44-13505C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361720 | ||||||
| chr8:38361734
|
T | G | 224 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-44-13519A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361734 | ||||||
| chr8:38361754
|
C | CA | 46 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0094others(43): Show | 46 | HG00140.hp1 HG00597.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.-44-13540dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361754 | ||||||
| chr8:38361754
|
CA | C | 12 | a0001c0001t0001g0104a0001c0001t0001g0126a0001c0001t0001g0128others(9): Show | 12 | HG00099.hp1 HG01516.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44-13540delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361754 | ||||||
| chr8:38361803
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44-13588C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361803 | ||||||
| chr8:38361804
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44-13589T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38361804 | ||||||
| chr8:38362050
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-44-13835A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362050 | ||||||
| chr8:38362162
|
T | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG01981.hp1 NA19007.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-13947A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362162 | ||||||
| chr8:38362256
|
C | CG | 27 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0099others(24): Show | 28 | HG00140.hp2 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.-44-14042dupC | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | CGG | 35 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0134others(32): Show | 35 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-44-14043_-44-1404 others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | CGGG | 32 | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0119others(29): Show | 32 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-44-14044_-44-1404 others(7): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | CGGGG | 18 | a0001c0001t0001g0084a0001c0001t0001g0118a0001c0001t0001g0121others(15): Show | 18 | HG00438.hp1 HG00735.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44-14045_-44-1404 others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | CGGGGG | 17 | a0001c0001t0001g0087a0001c0001t0001g0107a0001c0001t0001g0149others(14): Show | 17 | HG01175.hp2 HG01192.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-44-14046_-44-1404 others(9): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | CGGGGGGG others(5): Show |
1 | a0001c0001t0001g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44-14042_-44-1404 others(16): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | G | 1 | a0001c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-44-14041G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-44-14041G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362256
|
CG | C | 20 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0116others(17): Show | 20 | HG00280.hp2 HG00735.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-44-14042delC | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362256 | ||||||
| chr8:38362397
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-14182G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362397 | ||||||
| chr8:38362502
|
T | A | 1 | a0001c0001t0001g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44-14287A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362502 | ||||||
| chr8:38362603
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0117a0001c0001t0001g0206others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-14388G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362603 | ||||||
| chr8:38362947
|
A | G | 3 | a0001c0001t0002g0037a0001c0001t0002g0043a0001c0001t0002g0060 | 3 | HG02523.hp2 NA18983.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-44-14732T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38362947 | ||||||
| chr8:38363112
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-44-14897C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363112 | ||||||
| chr8:38363130
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-14915G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363130 | ||||||
| chr8:38363512
|
C | T | 9 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0127others(6): Show | 9 | HG01167.hp1 HG01433.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44-15297G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363512 | ||||||
| chr8:38363639
|
C | CA | 18 | a0001c0001t0001g0098a0001c0001t0001g0141a0001c0001t0001g0146others(15): Show | 18 | HG00735.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44-15425dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363639 | ||||||
| chr8:38363639
|
CA | C | 43 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0118others(40): Show | 43 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-44-15425delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363639 | ||||||
| chr8:38363822
|
G | T | 1 | a0001c0001t0001g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-44-15607C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363822 | ||||||
| chr8:38363950
|
T | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-44-15735A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38363950 | ||||||
| chr8:38364053
|
CT | C | 87 | a0001c0001t0001g0158a0001c0001t0002g0001a0001c0001t0002g0002others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-44-15839delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364053 | ||||||
| chr8:38364088
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-44-15873G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364088 | ||||||
| chr8:38364277
|
A | AAAC | 35 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0097others(32): Show | 35 | HG00438.hp1 HG00735.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.-44-16065_-44-1606 others(7): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364277 | ||||||
| chr8:38364277
|
A | AAACAAC | 97 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-44-16068_-44-1606 others(10): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364277 | ||||||
| chr8:38364277
|
A | AAACAACA others(2): Show |
18 | a0001c0001t0001g0115a0001c0001t0001g0174a0001c0001t0002g0001others(15): Show | 19 | HG00140.hp2 HG00673.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44-16071_-44-1606 others(13): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364277 | ||||||
| chr8:38364277
|
A | AAACAACA others(5): Show |
4 | a0001c0001t0001g0133a0001c0001t0002g0025a0001c0001t0002g0042others(1): Show | 4 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-16074_-44-1606 others(16): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364277 | ||||||
| chr8:38364277
|
A | AAACAACA others(8): Show |
1 | a0001c0001t0002g0014 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-44-16077_-44-1606 others(19): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364277 | ||||||
| chr8:38364316
|
A | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44-16101T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364316 | ||||||
| chr8:38364520
|
T | A | 1 | a0001c0001t0017g0140 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-44-16305A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364520 | ||||||
| chr8:38364555
|
C | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-44-16340G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364555 | ||||||
| chr8:38364710
|
T | G | 1 | a0001c0001t0018g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44-16495A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364710 | ||||||
| chr8:38364976
|
A | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44-16761T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38364976 | ||||||
| chr8:38365079
|
G | A | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+16720C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38365079 | ||||||
| chr8:38365347
|
C | A | 1 | a0001c0001t0002g0009 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-45+16452G>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38365347 | ||||||
| chr8:38365468
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-45+16331C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38365468 | ||||||
| chr8:38365536
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-45+16263C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38365536 | ||||||
| chr8:38365545
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-45+16254A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38365545 | ||||||
| chr8:38365706
|
CAAGTGCT others(4341): Show |
C | 1 | a0001c0001t0002g0067 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-45+11745_-45+1609 others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38365706 | ||||||
| chr8:38366018
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-45+15781A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366018 | ||||||
| chr8:38366110
|
C | CA | 22 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0116others(19): Show | 22 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.-45+15688dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366110 | ||||||
| chr8:38366110
|
CA | C | 8 | a0001c0001t0001g0086a0001c0001t0001g0135a0001c0001t0001g0147others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.-45+15688delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366110 | ||||||
| chr8:38366179
|
C | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(80): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+15620G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366179 | ||||||
| chr8:38366344
|
C | T | 1 | a0001c0001t0018g0221 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-45+15455G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366344 | ||||||
| chr8:38366418
|
C | CT | 7 | a0001c0001t0001g0146a0001c0001t0001g0197a0001c0001t0015g0223others(4): Show | 7 | HG00642.hp1 HG02074.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-45+15380dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366418 | ||||||
| chr8:38366418
|
C | CTTTTTTT others(1): Show |
72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(69): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.-45+15373_-45+1538 others(12): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366418 | ||||||
| chr8:38366418
|
C | CTTTTTTT others(2): Show |
11 | a0001c0001t0002g0013a0001c0001t0002g0030a0001c0001t0002g0031others(8): Show | 11 | HG01243.hp1 HG01978.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-45+15372_-45+1538 others(13): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366418 | ||||||
| chr8:38366418
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0012a0001c0001t0011g0089a0001c0009t0009g0090 | 3 | HG01192.hp2 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-45+15371_-45+1538 others(14): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366418 | ||||||
| chr8:38366418
|
CT | C | 24 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(21): Show | 24 | HG00673.hp1 HG01167.hp1 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-45+15380delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366418 | ||||||
| chr8:38366435
|
G | C | 1 | a0001c0001t0002g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-45+15364C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366435 | ||||||
| chr8:38366477
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-45+15322A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366477 | ||||||
| chr8:38366537
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0117a0001c0001t0001g0206 | 3 | HG02622.hp1 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-45+15262C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366537 | ||||||
| chr8:38366558
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0180others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+15241G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366558 | ||||||
| chr8:38366752
|
T | C | 2 | a0001c0001t0021g0108a0001c0001t0023g0109 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-45+15047A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366752 | ||||||
| chr8:38366768
|
C | T | 1 | a0001c0001t0011g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-45+15031G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38366768 | ||||||
| chr8:38367104
|
A | C | 1 | a0001c0001t0013g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-45+14695T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38367104 | ||||||
| chr8:38367653
|
G | A | 34 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(31): Show | 34 | HG00673.hp1 HG01167.hp1 HG01258.hp2 others(31): Show |
intron_variant | MODIFIER | c.-45+14146C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38367653 | ||||||
| chr8:38367708
|
T | C | 2 | a0001c0001t0001g0106a0006c0012t0001g0172 | 2 | HG00099.hp1 HG00140.hp1 |
intron_variant | MODIFIER | c.-45+14091A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38367708 | ||||||
| chr8:38367831
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-45+13968A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38367831 | ||||||
| chr8:38367911
|
G | C | 2 | a0001c0001t0002g0075a0001c0001t0024g0057 | 2 | HG01081.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-45+13888C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38367911 | ||||||
| chr8:38368577
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-45+13222G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38368577 | ||||||
| chr8:38368595
|
A | G | 8 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0124others(5): Show | 8 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45+13204T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38368595 | ||||||
| chr8:38368759
|
A | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-45+13040T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38368759 | ||||||
| chr8:38369180
|
TGTA | T | 11 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(8): Show | 11 | HG00280.hp2 HG00597.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-45+12616_-45+1261 others(7): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38369180 | ||||||
| chr8:38369727
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-45+12072A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38369727 | ||||||
| chr8:38369846
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-45+11953C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38369846 | ||||||
| chr8:38370013
|
C | T | 2 | a0002c0003t0001g0131a0002c0003t0001g0132 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-45+11786G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370013 | ||||||
| chr8:38370046
|
G | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(78): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-45+11753C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370046 | ||||||
| chr8:38370102
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-45+11697G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370102 | ||||||
| chr8:38370343
|
T | C | 4 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0008t0001g0085others(1): Show | 4 | HG01192.hp1 HG02698.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+11456A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370343 | ||||||
| chr8:38370378
|
G | T | 2 | a0002c0003t0001g0131a0002c0003t0001g0132 | 2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-45+11421C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370378 | ||||||
| chr8:38370380
|
A | AT | 11 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0146others(8): Show | 11 | HG01167.hp2 HG02074.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.-45+11418dupA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370380 | ||||||
| chr8:38370380
|
AT | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0175a0001c0001t0001g0217others(4): Show | 7 | HG00323.hp2 HG02647.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+11418delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370380 | ||||||
| chr8:38370419
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-45+11380G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370419 | ||||||
| chr8:38370482
|
G | A | 1 | a0001c0001t0013g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-45+11317C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370482 | ||||||
| chr8:38370487
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0214 | 3 | HG02723.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-45+11312T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370487 | ||||||
| chr8:38370519
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-45+11280G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370519 | ||||||
| chr8:38370698
|
C | G | 1 | a0001c0001t0002g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-45+11101G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370698 | ||||||
| chr8:38370723
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-45+11076C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38370723 | ||||||
| chr8:38372076
|
T | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-45+9723A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372076 | ||||||
| chr8:38372411
|
G | T | 1 | a0001c0001t0002g0021 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-45+9388C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372411 | ||||||
| chr8:38372495
|
CT | C | 5 | a0001c0001t0001g0176a0001c0001t0002g0023a0001c0001t0002g0058others(2): Show | 5 | HG01167.hp2 HG01256.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+9303delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372495 | ||||||
| chr8:38372542
|
T | C | 2 | a0001c0001t0002g0080a0001c0001t0002g0081 | 2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-45+9257A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372542 | ||||||
| chr8:38372699
|
T | C | 10 | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0127others(7): Show | 10 | HG01167.hp1 HG01433.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45+9100A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372699 | ||||||
| chr8:38372814
|
T | TA | 24 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0134others(21): Show | 24 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-45+8984dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372814 | ||||||
| chr8:38372866
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-45+8933A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372866 | ||||||
| chr8:38372932
|
T | TC | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-45+8866dupG | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372932 | ||||||
| chr8:38372934
|
G | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-45+8865C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372934 | ||||||
| chr8:38372958
|
G | A | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-45+8841C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372958 | ||||||
| chr8:38372967
|
T | G | 2 | a0001c0001t0021g0108a0001c0001t0023g0109 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-45+8832A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372967 | ||||||
| chr8:38372999
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-45+8800C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38372999 | ||||||
| chr8:38373049
|
C | CA | 5 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0192others(2): Show | 5 | HG00741.hp1 HG02723.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+8749dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373049 | ||||||
| chr8:38373049
|
CA | C | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-45+8749delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373049 | ||||||
| chr8:38373451
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-45+8348A>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373451 | ||||||
| chr8:38373524
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-45+8275A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373524 | ||||||
| chr8:38373675
|
C | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+8124G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373675 | ||||||
| chr8:38373796
|
A | T | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-45+8003T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373796 | ||||||
| chr8:38373852
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-45+7947G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373852 | ||||||
| chr8:38373934
|
C | CA | 58 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0001g0099others(55): Show | 58 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-45+7864dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373934 | ||||||
| chr8:38373936
|
A | C | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-45+7863T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373936 | ||||||
| chr8:38373988
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-45+7811C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373988 | ||||||
| chr8:38373996
|
T | C | 17 | a0001c0001t0001g0116a0001c0001t0001g0135a0001c0001t0001g0136others(14): Show | 17 | HG00673.hp1 HG01258.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.-45+7803A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38373996 | ||||||
| chr8:38374356
|
C | T | 133 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(130): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-45+7443G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38374356 | ||||||
| chr8:38374584
|
C | T | 1 | a0001c0001t0025g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-45+7215G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38374584 | ||||||
| chr8:38374685
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-45+7114A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38374685 | ||||||
| chr8:38374768
|
G | A | 13 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(10): Show | 13 | HG00438.hp2 NA18942.hp2 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-45+7031C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38374768 | ||||||
| chr8:38375220
|
G | T | 89 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-45+6579C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38375220 | ||||||
| chr8:38375328
|
T | TA | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(82): Show | 86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.-45+6470dupT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38375328 | ||||||
| chr8:38375536
|
AC | A | 2 | a0001c0001t0002g0030a0001c0001t0002g0031 | 2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-45+6262delG | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38375536 | ||||||
| chr8:38375920
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-45+5879A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38375920 | ||||||
| chr8:38376417
|
A | C | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-45+5382T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38376417 | ||||||
| chr8:38376681
|
C | T | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+5118G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38376681 | ||||||
| chr8:38376771
|
G | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+5028C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38376771 | ||||||
| chr8:38376837
|
T | C | 1 | a0008c0010t0001g0210 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-45+4962A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38376837 | ||||||
| chr8:38376977
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0011 | 2 | NA18966.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-45+4822G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38376977 | ||||||
| chr8:38376991
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-45+4808G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38376991 | ||||||
| chr8:38377002
|
A | T | 1 | a0001c0001t0014g0035 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-45+4797T>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377002 | ||||||
| chr8:38377225
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-45+4574C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377225 | ||||||
| chr8:38377232
|
T | C | 1 | a0001c0013t0001g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-45+4567A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377232 | ||||||
| chr8:38377241
|
CG | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.-45+4557delC | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377241 | ||||||
| chr8:38377409
|
C | G | 7 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(4): Show | 7 | HG00438.hp2 NA18942.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+4390G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377409 | ||||||
| chr8:38377473
|
C | T | 2 | a0001c0001t0010g0113a0001c0001t0011g0089 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-45+4326G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377473 | ||||||
| chr8:38377869
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-45+3930G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377869 | ||||||
| chr8:38377957
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0034 | 2 | NA18941.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-45+3842G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38377957 | ||||||
| chr8:38378008
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-45+3791G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378008 | ||||||
| chr8:38378018
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-45+3781A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378018 | ||||||
| chr8:38378182
|
G | A | 1 | a0001c0001t0022g0213 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-45+3617C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378182 | ||||||
| chr8:38378232
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-45+3567C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378232 | ||||||
| chr8:38378296
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-45+3503C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378296 | ||||||
| chr8:38378459
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-45+3340C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378459 | ||||||
| chr8:38378510
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-45+3289G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378510 | ||||||
| chr8:38378530
|
T | G | 1 | a0001c0001t0002g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-45+3269A>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378530 | ||||||
| chr8:38378531
|
G | T | 1 | a0001c0001t0002g0002 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-45+3268C>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378531 | ||||||
| chr8:38378715
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-45+3084G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378715 | ||||||
| chr8:38378820
|
T | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | NA18978.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-45+2979A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378820 | ||||||
| chr8:38378825
|
CA | C | 9 | a0001c0001t0001g0082a0001c0001t0001g0115a0001c0001t0001g0116others(6): Show | 9 | HG00741.hp2 HG02280.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45+2973delT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378825 | ||||||
| chr8:38378825
|
CAA | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.-45+2972_-45+2973d others(4): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378825 | ||||||
| chr8:38378945
|
G | C | 2 | a0001c0001t0005g0111a0001c0001t0005g0112 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-45+2854C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38378945 | ||||||
| chr8:38379076
|
C | G | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-45+2723G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38379076 | ||||||
| chr8:38379294
|
CT | C | 5 | a0001c0001t0001g0215a0001c0001t0002g0076a0001c0001t0002g0080others(2): Show | 5 | HG01243.hp1 HG01517.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+2504delA | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38379294 | ||||||
| chr8:38379372
|
G | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(83): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-45+2427C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38379372 | ||||||
| chr8:38380045
|
C | G | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+1754G>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38380045 | ||||||
| chr8:38380167
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45+1632C>T | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38380167 | ||||||
| chr8:38380699
|
T | C | 3 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-45+1100A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38380699 | ||||||
| chr8:38380746
|
T | C | 1 | a0001c0009t0009g0090 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+1053A>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38380746 | ||||||
| chr8:38381558
|
G | C | 224 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-45+241C>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381558 | ||||||
| chr8:38381724
|
A | C | 1 | a0001c0001t0001g0216 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-45+75T>G | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381724 | ||||||
| chr8:38381729
|
TAC | T | 32 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.-45+68_-45+69delGT | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381729 | ||||||
| chr8:38381746
|
G | GCA | 8 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(5): Show | 8 | HG00735.hp2 HG02615.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45+51_-45+52dupTG | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381746 | ||||||
| chr8:38381746
|
GCA | G | 23 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 23 | HG00140.hp1 HG01243.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.-45+51_-45+52delTG | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381746 | ||||||
| chr8:38381746
|
GCACA | G | 9 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(6): Show | 9 | HG00323.hp2 HG02622.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45+49_-45+52delTG others(2): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381746 | ||||||
| chr8:38381746
|
GCACACAC others(1): Show |
G | 32 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.-45+45_-45+52delTG others(6): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381746 | ||||||
| chr8:38381746
|
GCACACAC others(3): Show |
G | 49 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0036others(46): Show | 49 | HG00323.hp1 HG00609.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-45+43_-45+52delTG others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381746 | ||||||
| chr8:38381756
|
A | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0003others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.-45+43T>C | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381756 | ||||||
| chr8:38381763
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-45+36G>A | NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381763 | ||||||
| chr8:38381765
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0002g0224a0001c0001t0025g0225 | 2 | HG00408.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-45+24_-45+33delAT others(8): Show |
NSD3 | ENSG00000147548.17 | transcript | ENST00000317025.13 | protein_coding | 1/23 | chr8 | 38381765 |