Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7468 |
|---|---|
| ensemblid | ENSG00000109685.19 |
| hgncid | 12766 |
| symbol | NSD2 |
| name | nuclear receptor binding SET domain protein 2 |
| refseq_nuc | NM_001042424.3 |
| refseq_prot | NP_001035889.1 |
| ensembl_nuc | ENST00000508803.6 |
| ensembl_prot | ENSP00000423972.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 1871393 |
| end | 1982192 |
| strand | + |
| ver | v1.2 |
| region | chr4:1871393-1982192 |
| region5000 | chr4:1866393-1987192 |
| regionname0 | NSD2_chr4_1871393_1982192 |
| regionname5000 | NSD2_chr4_1866393_1987192 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1365 | 127 | 60 | 30 | 20 | 7 | 8 | 16 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0002 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0003 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0004 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4098 | 115 | 49 | 30 | 20 | 7 | 7 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0002 | 0/0 | 4098 | 7 | 7 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0003 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0004 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0005 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0006 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0007 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0008 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0009 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| c0010 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3463 | 92 | 34 | 25 | 18 | 8 | 5 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0002 | 0/0 | 3463 | 8 | 6 | 1 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0003 | 0/0 | 3463 | 4 | 4 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0004 | 0/0 | 3463 | 3 | 2 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0005 | 0/0 | 3459 | 3 | 3 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0006 | 0/0 | 3469 | 3 | 2 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0007 | 0/0 | 3463 | 2 | 2 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0008 | 0/0 | 3463 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0009 | 0/0 | 3463 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0010 | 0/0 | 3463 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0011 | 0/0 | 3463 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0012 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0013 | 0/0 | 3463 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0014 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0015 | 0/0 | 3459 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0016 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0017 | 0/0 | 3463 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0018 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0019 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0020 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0021 | 0/0 | 3463 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| t0022 | 0/0 | 3469 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4098 | 115 | 49 | 30 | 20 | 7 | 7 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002 | 0/0 | 4098 | 7 | 7 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0003 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0004 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0005 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0006 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0009 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0002c0010 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0003c0007 | 0/0 | 4098 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0004c0008 | 0/0 | 4098 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 7560 | 85 | 29 | 25 | 18 | 7 | 4 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0002 | 0/0 | 7560 | 7 | 5 | 1 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0003 | 0/0 | 7560 | 3 | 3 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0004 | 0/0 | 7560 | 3 | 2 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0005 | 0/0 | 7556 | 2 | 2 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0006 | 0/0 | 7566 | 3 | 2 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0007 | 0/0 | 7560 | 2 | 2 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0008 | 0/0 | 7560 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0009 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0010 | 0/0 | 7560 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0011 | 0/0 | 7560 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0012 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0013 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0014 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0017 | 0/0 | 7560 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0018 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0001t0020 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0002 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0003 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0005 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0015 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0019 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0002t0021 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0003t0022 | 0/0 | 7566 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0004t0001 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0005t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0006t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0001c0009t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0002c0010t0016 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0003c0007t0001 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| a0004c0008t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | copy fasta | chr4 | 1866393 | 1987192 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0014g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0017g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0015g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0019g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0021g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0003t0022g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0005t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0009t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0002c0010t0016g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0003c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0004c0008t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00140 | hp2 | a0003 | c0007 | t0001 | g0126 | EUR | GBR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00741 | hp2 | a0001 | c0001 | t0017 | g0103 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0054 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01361 | hp2 | a0001 | c0001 | t0011 | g0051 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02257 | hp1 | a0001 | c0002 | t0021 | g0035 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02630 | hp1 | a0001 | c0006 | t0001 | g0031 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02723 | hp2 | a0004 | c0008 | t0001 | g0023 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0080 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02896 | hp1 | a0001 | c0009 | t0001 | g0097 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03098 | hp2 | a0001 | c0002 | t0015 | g0002 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03139 | hp1 | a0001 | c0003 | t0022 | g0013 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0123 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03195 | hp2 | a0001 | c0002 | t0019 | g0029 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0072 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0119 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0036 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG04184 | hp1 | a0001 | c0001 | t0013 | g0073 | SAS | BEB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0021 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18945 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19030 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0115 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02559 | hp1 | a0002 | c0010 | t0016 | g0105 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02559 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0081 | REF | REF | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0076 | REF | REF | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1904264
|
C | T | 1 | a0004 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.646C>T | p.His216Tyr | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/22 | 825/7560 | 646/4098 | 216/1365 | chr4 | 1904264 | ||
| chr4:1917014
|
C | T | 1 | a0003 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.904C>T | p.Pro302Ser | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/22 | 1083/7560 | 904/4098 | 302/1365 | chr4 | 1917014 | ||
| chr4:1918543
|
A | G | 1 | a0002 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1330A>G | p.Thr444Ala | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/22 | 1509/7560 | 1330/4098 | 444/1365 | chr4 | 1918543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1900870
|
C | G | 1 | a0002c0010 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.216C>G | p.Pro72Pro | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/22 | 395/7560 | 216/4098 | 72/1365 | chr4 | 1900870 | ||
| chr4:1900882
|
C | T | 1 | a0001c0009 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.228C>T | p.Ala76Ala | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/22 | 407/7560 | 228/4098 | 76/1365 | chr4 | 1900882 | ||
| chr4:1955189
|
C | T | 1 | a0001c0006 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2367C>T | p.Pro789Pro | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 13/22 | 2546/7560 | 2367/4098 | 789/1365 | chr4 | 1955189 | ||
| chr4:1955285
|
G | A | 1 | a0001c0003 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.2463G>A | p.Lys821Lys | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 13/22 | 2642/7560 | 2463/4098 | 821/1365 | chr4 | 1955285 | ||
| chr4:1974865
|
C | T | 1 | a0002c0010 | 1 | HG02559.hp1 | splice_region_variant&synonymous_variant | LOW | c.3375C>T | p.Asp1125Asp | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 19/22 | 3554/7560 | 3375/4098 | 1125/1365 | chr4 | 1974865 | ||
| chr4:1974964
|
C | T | 1 | a0002c0010 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.3474C>T | p.Asp1158Asp | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 19/22 | 3653/7560 | 3474/4098 | 1158/1365 | chr4 | 1974964 | ||
| chr4:1974985
|
C | T | 2 | a0001c0002a0001c0003 | 8 | HG02257.hp1 HG02922.hp2 HG03098.hp2 others(5): Show |
synonymous_variant | LOW | c.3495C>T | p.Ala1165Ala | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 19/22 | 3674/7560 | 3495/4098 | 1165/1365 | chr4 | 1974985 | ||
| chr4:1978711
|
C | T | 1 | a0001c0005 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.3900C>T | p.Pro1300Pro | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 4079/7560 | 3900/4098 | 1300/1365 | chr4 | 1978711 | ||
| chr4:1978834
|
C | T | 1 | a0001c0004 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4023C>T | p.Pro1341Pro | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 4202/7560 | 4023/4098 | 1341/1365 | chr4 | 1978834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1871476
|
A | ACGGCCC | 2 | a0001c0001t0006a0001c0003t0022 | 4 | HG01975.hp2 HG03139.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-88_-83dupGGCCCC | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/22 | 29165 | INFO_REALIGN_3_PRIME | chr4 | 1871476 | ||||
| chr4:1871530
|
C | A | 1 | a0001c0001t0008 | 1 | NA18949.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/22 | 29125 | chr4 | 1871530 | |||||
| chr4:1979076
|
A | G | 1 | a0001c0002t0021 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*167A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 167 | chr4 | 1979076 | |||||
| chr4:1979085
|
C | T | 1 | a0001c0001t0020 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 176 | chr4 | 1979085 | |||||
| chr4:1979205
|
A | G | 3 | a0001c0001t0018a0001c0002t0019a0001c0002t0021 | 3 | HG02257.hp1 HG02559.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 296 | chr4 | 1979205 | |||||
| chr4:1979433
|
G | A | 2 | a0001c0001t0003a0001c0002t0003 | 4 | HG02622.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 524 | chr4 | 1979433 | |||||
| chr4:1979502
|
G | T | 3 | a0001c0001t0002a0001c0001t0017a0001c0002t0002 | 9 | HG00741.hp2 HG01433.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*593G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 593 | chr4 | 1979502 | |||||
| chr4:1979529
|
T | A | 1 | a0001c0001t0004 | 3 | HG01106.hp2 HG03486.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*620T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 620 | chr4 | 1979529 | |||||
| chr4:1979529
|
T | G | 2 | a0001c0001t0009a0001c0001t0017 | 2 | HG00741.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*620T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 620 | chr4 | 1979529 | |||||
| chr4:1979994
|
A | T | 3 | a0001c0002t0019a0001c0002t0021a0002c0010t0016 | 3 | HG02257.hp1 HG02559.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1085A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 1085 | chr4 | 1979994 | |||||
| chr4:1980047
|
G | C | 1 | a0001c0001t0010 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 1138 | chr4 | 1980047 | |||||
| chr4:1980255
|
T | C | 1 | a0001c0001t0011 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 1346 | chr4 | 1980255 | |||||
| chr4:1980928
|
C | T | 7 | a0001c0001t0006a0001c0001t0007a0001c0001t0018others(4): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2019C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2019 | chr4 | 1980928 | |||||
| chr4:1981430
|
A | G | 1 | a0001c0002t0015 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2521A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2521 | chr4 | 1981430 | |||||
| chr4:1981543
|
C | T | 2 | a0001c0002t0019a0001c0002t0021 | 2 | HG02257.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2634C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2634 | chr4 | 1981543 | |||||
| chr4:1981642
|
G | C | 4 | a0001c0001t0005a0001c0001t0012a0001c0002t0005others(1): Show | 5 | HG02809.hp2 HG02886.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2733G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2733 | chr4 | 1981642 | |||||
| chr4:1981688
|
C | T | 1 | a0001c0001t0012 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2779C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2779 | chr4 | 1981688 | |||||
| chr4:1981826
|
C | G | 3 | a0001c0001t0014a0001c0002t0019a0001c0002t0021 | 3 | HG02109.hp2 HG02257.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2917C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2917 | chr4 | 1981826 | |||||
| chr4:1981846
|
CTGTT | C | 4 | a0001c0001t0005a0001c0001t0012a0001c0002t0005others(1): Show | 5 | HG02809.hp2 HG02886.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2942_*2945delTGTT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 2942 | INFO_REALIGN_3_PRIME | chr4 | 1981846 | ||||
| chr4:1982150
|
A | C | 1 | a0001c0001t0013 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3241A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 22/22 | 3241 | chr4 | 1982150 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1871724
|
C | T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30+182C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1871724 | ||||||
| chr4:1871801
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30+259C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1871801 | ||||||
| chr4:1871814
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30+272C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1871814 | ||||||
| chr4:1872001
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-30+459C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872001 | ||||||
| chr4:1872161
|
A | G | 3 | a0001c0001t0001g0125a0001c0001t0002g0124a0003c0007t0001g0126 | 3 | HG00140.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-30+619A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872161 | ||||||
| chr4:1872198
|
G | C | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-30+656G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872198 | ||||||
| chr4:1872470
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(4): Show | 7 | HG00609.hp2 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+928T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872470 | ||||||
| chr4:1872564
|
T | G | 1 | a0001c0001t0001g0009 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-30+1022T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872564 | ||||||
| chr4:1872564
|
T | TTG | 3 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0127 | 3 | NA18906.hp2 NA18945.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-30+1049_-30+1050d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872564 | |||||
| chr4:1872564
|
T | TTGTG | 2 | a0001c0001t0001g0118a0001c0001t0009g0119 | 2 | HG02886.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-30+1047_-30+1050d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872564 | |||||
| chr4:1872564
|
TTG | T | 5 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0002g0019others(2): Show | 5 | HG01975.hp2 HG02280.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+1049_-30+1050d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872564 | |||||
| chr4:1872579
|
T | TGAGAGAG others(3): Show |
1 | a0001c0001t0001g0010 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-30+1038_-30+1039i others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872579 | |||||
| chr4:1872581
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-30+1039T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872581 | ||||||
| chr4:1872583
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-30+1041T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872583 | ||||||
| chr4:1872585
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-30+1043T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872585 | ||||||
| chr4:1872585
|
TGTGTGTG others(7): Show |
T | 1 | a0001c0002t0015g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-30+1045_-30+1058d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872585 | |||||
| chr4:1872585
|
TGTGTGTG others(11): Show |
T | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30+1045_-30+1062d others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872585 | |||||
| chr4:1872587
|
T | A | 2 | a0001c0001t0001g0010a0001c0002t0005g0001 | 2 | HG00609.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-30+1045T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872587 | ||||||
| chr4:1872587
|
T | TGAGAGAG others(5): Show |
1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+1046_-30+1047i others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872587 | |||||
| chr4:1872587
|
T | TGAGAGAG others(17): Show |
1 | a0001c0001t0001g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-30+1046_-30+1047i others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872587 | |||||
| chr4:1872587
|
T | TGAGAGAG others(19): Show |
1 | a0001c0001t0001g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-30+1046_-30+1047i others(28): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872587 | |||||
| chr4:1872587
|
TGTGTGAG others(7): Show |
T | 1 | a0001c0001t0018g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-30+1047_-30+1060d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872587 | |||||
| chr4:1872587
|
TGTGTGAG others(9): Show |
T | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30+1047_-30+1062d others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872587 | |||||
| chr4:1872589
|
T | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0016others(4): Show | 7 | HG00609.hp1 HG01934.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+1047T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872589 | ||||||
| chr4:1872589
|
T | TGAGAGAG others(3): Show |
1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30+1048_-30+1049i others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872589
|
T | TGAGAGAG others(5): Show |
1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-30+1048_-30+1049i others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872589
|
T | TGAGAGAG others(17): Show |
1 | a0001c0001t0001g0024 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-30+1048_-30+1049i others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872589
|
T | TGAGAGAG others(21): Show |
1 | a0004c0008t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+1048_-30+1049i others(30): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872589
|
TGTGAGAG others(1): Show |
T | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | NA20752.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-30+1049_-30+1056d others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872589
|
TGTGAGAG others(7): Show |
T | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30+1049_-30+1062d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872589
|
TGTGAGAG others(9): Show |
T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30+1049_-30+1064d others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872589 | |||||
| chr4:1872591
|
T | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0016others(17): Show | 20 | HG00609.hp1 HG01934.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-30+1049T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872591 | ||||||
| chr4:1872591
|
T | TGA | 3 | a0001c0001t0001g0063a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG00140.hp1 HG03453.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-30+1093_-30+1094d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGA | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0064others(2): Show | 5 | HG02735.hp1 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+1091_-30+1094d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGA | 3 | a0001c0001t0001g0057a0001c0001t0001g0062a0003c0007t0001g0126 | 3 | HG00140.hp2 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-30+1089_-30+1094d others(8): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(1): Show |
6 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0056others(3): Show | 6 | HG01106.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1087_-30+1094d others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(3): Show |
4 | a0001c0001t0001g0052a0001c0001t0001g0125a0001c0001t0001g0129others(1): Show | 4 | HG01433.hp2 HG01496.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+1085_-30+1094d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(5): Show |
1 | a0001c0001t0011g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-30+1083_-30+1094d others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(7): Show |
3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG02976.hp2 HG03471.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.-30+1081_-30+1094d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(11): Show |
4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0046others(1): Show | 4 | HG00738.hp1 HG01928.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1077_-30+1094d others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(13): Show |
1 | a0001c0001t0001g0039 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-30+1075_-30+1094d others(22): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(17): Show |
1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-30+1071_-30+1094d others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(25): Show |
1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-30+1063_-30+1094d others(34): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGAGAGAG others(147): Show |
1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30+1094_-30+1095i others(156): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGA | 4 | a0001c0001t0001g0009a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02004.hp2 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(8): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(1): Show |
2 | a0001c0001t0001g0098a0001c0009t0001g0097 | 2 | HG02896.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(3): Show |
4 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG01106.hp1 HG02622.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(5): Show |
2 | a0001c0001t0001g0092a0001c0001t0010g0090 | 2 | HG02615.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(7): Show |
1 | a0001c0001t0001g0088 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(9): Show |
1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(11): Show |
1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(15): Show |
1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(24): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(17): Show |
1 | a0001c0001t0001g0085 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(21): Show |
2 | a0001c0001t0001g0083a0001c0001t0003g0086 | 2 | HG01975.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(30): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(23): Show |
1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(32): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGAGAG others(43): Show |
1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(52): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGAG others(1): Show |
3 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0014g0115 | 3 | HG01433.hp1 HG01952.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGAG others(3): Show |
2 | a0001c0001t0001g0114a0001c0001t0001g0117 | 2 | HG01993.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGAG others(7): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0112 | 2 | HG02300.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGAG others(9): Show |
1 | a0001c0001t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(31): Show |
1 | a0001c0001t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(40): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(7): Show |
1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(15): Show |
1 | a0001c0001t0001g0003 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(24): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(19): Show |
1 | a0001c0001t0001g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(28): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(21): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.-30+1050_-30+1051i others(30): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(32): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(36): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
T | TGTGTGTG others(17): Show |
1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+1050_-30+1051i others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
TGAGAGAG others(9): Show |
T | 2 | a0001c0001t0001g0104a0002c0010t0016g0105 | 2 | HG01167.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30+1079_-30+1094d others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872591
|
TGAGAGAG others(11): Show |
T | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0108others(1): Show | 4 | HG02723.hp1 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+1077_-30+1094d others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872591 | |||||
| chr4:1872593
|
A | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0127a0001c0001t0017g0103others(1): Show | 4 | HG00741.hp2 NA18945.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1051A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872593 | ||||||
| chr4:1872595
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0127a0001c0001t0005g0080 | 3 | HG02886.hp2 NA18945.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-30+1053A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872595 | ||||||
| chr4:1872597
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-30+1055A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872597 | ||||||
| chr4:1872609
|
A | T | 2 | a0001c0001t0001g0104a0002c0010t0016g0105 | 2 | HG01167.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-30+1067A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872609 | ||||||
| chr4:1872611
|
A | T | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0002g0108others(1): Show | 4 | HG02723.hp1 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+1069A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872611 | ||||||
| chr4:1872613
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-30+1071A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872613 | ||||||
| chr4:1872623
|
AGAGAGAG others(7): Show |
A | 1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30+1083_-30+1096d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872623 | |||||
| chr4:1872629
|
A | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+1087A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872629 | ||||||
| chr4:1872631
|
A | AGAGAGAG others(18): Show |
1 | a0001c0001t0007g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-30+1094_-30+1095i others(27): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872631 | |||||
| chr4:1872631
|
A | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG01928.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+1089A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872631 | ||||||
| chr4:1872633
|
A | AGAGAGAG others(23): Show |
1 | a0001c0002t0002g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30+1094_-30+1095i others(32): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872633 | |||||
| chr4:1872633
|
A | AGAGAGAG others(19): Show |
1 | a0001c0001t0002g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-30+1094_-30+1095i others(28): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872633 | |||||
| chr4:1872633
|
A | AGAGAGAG others(17): Show |
1 | a0001c0002t0003g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-30+1094_-30+1095i others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872633 | |||||
| chr4:1872633
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-30+1091A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872633 | ||||||
| chr4:1872635
|
A | AGAGAGAG others(17): Show |
1 | a0001c0001t0001g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-30+1094_-30+1095i others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872635 | |||||
| chr4:1872635
|
A | C | 2 | a0001c0001t0001g0117a0001c0001t0009g0119 | 2 | HG02976.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-30+1093A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872635 | ||||||
| chr4:1872635
|
AGC | A | 3 | a0001c0001t0013g0073a0001c0002t0001g0102a0001c0005t0001g0072 | 3 | HG03225.hp2 HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-30+1098_-30+1099d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1872635 | |||||
| chr4:1872637
|
C | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.-30+1095C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872637 | ||||||
| chr4:1872639
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(4): Show | 7 | HG00609.hp2 HG01928.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+1097C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1872639 | ||||||
| chr4:1873268
|
A | G | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+1726A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873268 | ||||||
| chr4:1873584
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-30+2042C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873584 | ||||||
| chr4:1873618
|
T | G | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+2076T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873618 | ||||||
| chr4:1873799
|
G | GTT | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.-30+2257_-30+2258i others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873799 | ||||||
| chr4:1873827
|
A | T | 12 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(9): Show | 12 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+2285A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873827 | ||||||
| chr4:1873974
|
C | A | 1 | a0001c0001t0006g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-30+2432C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873974 | ||||||
| chr4:1873990
|
A | T | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+2448A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1873990 | ||||||
| chr4:1874080
|
T | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+2538T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1874080 | ||||||
| chr4:1874399
|
C | T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+2857C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1874399 | ||||||
| chr4:1874520
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-30+2978G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1874520 | ||||||
| chr4:1874672
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+3130A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1874672 | ||||||
| chr4:1875280
|
CT | C | 21 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0070others(18): Show | 21 | HG01975.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30+3757delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1875280 | |||||
| chr4:1875388
|
C | T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+3846C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1875388 | ||||||
| chr4:1875440
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30+3898C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1875440 | ||||||
| chr4:1875730
|
G | A | 1 | a0001c0001t0008g0106 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-30+4188G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1875730 | ||||||
| chr4:1875865
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0093 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-30+4323C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1875865 | ||||||
| chr4:1876171
|
G | A | 1 | a0001c0002t0002g0038 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30+4629G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1876171 | ||||||
| chr4:1876307
|
T | A | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-30+4765T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1876307 | ||||||
| chr4:1876754
|
C | CT | 11 | a0001c0001t0001g0109a0001c0001t0006g0014a0001c0001t0006g0015others(8): Show | 11 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30+5221dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1876754 | |||||
| chr4:1876859
|
C | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+5317C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1876859 | ||||||
| chr4:1877140
|
GA | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0117a0001c0001t0003g0030others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+5610delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1877140 | |||||
| chr4:1877725
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-30+6183C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1877725 | ||||||
| chr4:1877852
|
C | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+6310C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1877852 | ||||||
| chr4:1877873
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0004g0054 | 2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-30+6331T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1877873 | ||||||
| chr4:1877885
|
A | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+6343A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1877885 | ||||||
| chr4:1878035
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+6493A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878035 | ||||||
| chr4:1878083
|
C | T | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+6541C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878083 | ||||||
| chr4:1878163
|
C | T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+6621C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878163 | ||||||
| chr4:1878168
|
C | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+6626C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878168 | ||||||
| chr4:1878226
|
G | GAT | 12 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0049others(9): Show | 12 | HG00280.hp2 HG01517.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+6709_-30+6710d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878226
|
G | GATAT | 2 | a0001c0001t0001g0025a0001c0001t0001g0046 | 2 | HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-30+6707_-30+6710d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878226
|
G | GATATATA others(3): Show |
1 | a0001c0001t0001g0008 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-30+6701_-30+6710d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878226
|
G | GATATATA others(5): Show |
1 | a0001c0001t0001g0005 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-30+6699_-30+6710d others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878226
|
G | GATATATA others(7): Show |
1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-30+6697_-30+6710d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878226
|
G | GATATATA others(9): Show |
1 | a0001c0001t0001g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-30+6695_-30+6710d others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878226
|
GAT | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0082others(2): Show | 5 | HG00609.hp1 HG00741.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+6709_-30+6710d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878226 | |||||
| chr4:1878239
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+6697A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878239 | ||||||
| chr4:1878239
|
ATATATAT others(14): Show |
A | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-30+6699_-30+6719d others(23): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878239 | |||||
| chr4:1878239
|
ATATATAT others(15): Show |
A | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30+6699_-30+6720d others(24): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878239 | |||||
| chr4:1878243
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+6701A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878243 | ||||||
| chr4:1878247
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-30+6705A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878247 | ||||||
| chr4:1878249
|
A | T | 2 | a0001c0001t0001g0118a0001c0001t0017g0103 | 2 | HG00741.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-30+6707A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878249 | ||||||
| chr4:1878249
|
ATATTTTT others(7): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30+6709_-30+6722d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878249 | |||||
| chr4:1878249
|
ATATTTTT others(9): Show |
A | 2 | a0001c0001t0001g0085a0001c0001t0002g0078 | 2 | HG01167.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-30+6709_-30+6724d others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878249 | |||||
| chr4:1878251
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30+6710_-30+6711i others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0127a0001c0001t0003g0030 | 2 | HG03516.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-30+6710_-30+6711i others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
A | ATATATAT others(9): Show |
1 | a0001c0006t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-30+6710_-30+6711i others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-30+6710_-30+6711i others(19): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
A | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0032others(3): Show | 6 | HG00609.hp1 HG00741.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+6709A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878251 | ||||||
| chr4:1878251
|
AT | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(14): Show | 17 | HG01952.hp1 HG01993.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+6742delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+6733_-30+6742d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
ATTTTTTT others(5): Show |
A | 1 | a0003c0007t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-30+6731_-30+6742d others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30+6730_-30+6742d others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-30+6729_-30+6742d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878251
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+6726_-30+6742d others(19): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1878251 | |||||
| chr4:1878252
|
T | TA | 10 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0062others(7): Show | 10 | HG01361.hp1 HG01517.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+6710_-30+6711i others(3): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878252
|
T | TATA | 8 | a0001c0001t0001g0050a0001c0001t0001g0064a0001c0001t0001g0068others(5): Show | 8 | HG01106.hp2 HG01433.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+6710_-30+6711i others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878252
|
T | TATATATA others(2): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0094 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-30+6710_-30+6711i others(11): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878252
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0006 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-30+6710_-30+6711i others(13): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878252
|
T | TATATATA others(8): Show |
2 | a0001c0001t0001g0022a0001c0001t0001g0083 | 2 | HG01975.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-30+6710_-30+6711i others(17): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878252
|
T | TATATATA others(10): Show |
1 | a0001c0001t0001g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-30+6710_-30+6711i others(19): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878252
|
T | TGTATATA others(58): Show |
1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+6710_-30+6711i others(67): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878252 | ||||||
| chr4:1878253
|
T | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(25): Show | 28 | HG00280.hp2 HG01496.hp1 HG01517.hp2 others(25): Show |
intron_variant | MODIFIER | c.-30+6711T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878253 | ||||||
| chr4:1878254
|
T | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0052others(9): Show | 12 | HG00738.hp2 HG01517.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30+6712T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878254 | ||||||
| chr4:1878255
|
T | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0053others(10): Show | 13 | HG00280.hp2 HG01496.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30+6713T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878255 | ||||||
| chr4:1878256
|
T | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0052others(5): Show | 8 | HG01975.hp1 HG01993.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+6714T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878256 | ||||||
| chr4:1878257
|
T | A | 7 | a0001c0001t0001g0053a0001c0001t0003g0086a0001c0001t0003g0096others(4): Show | 7 | HG01975.hp2 HG02622.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+6715T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878257 | ||||||
| chr4:1878258
|
T | A | 5 | a0001c0001t0001g0004a0001c0001t0001g0083a0001c0001t0001g0109others(2): Show | 5 | HG01975.hp1 HG01993.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+6716T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878258 | ||||||
| chr4:1878259
|
T | A | 4 | a0001c0001t0001g0107a0001c0001t0003g0096a0001c0001t0005g0130others(1): Show | 4 | HG02622.hp1 NA18522.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6717T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878259 | ||||||
| chr4:1878260
|
T | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0083a0001c0001t0001g0104others(5): Show | 8 | HG01167.hp2 HG01975.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+6718T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878260 | ||||||
| chr4:1878261
|
T | A | 3 | a0001c0001t0001g0107a0001c0001t0005g0130a0001c0001t0008g0106 | 3 | NA18522.hp1 NA18949.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-30+6719T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878261 | ||||||
| chr4:1878262
|
T | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0104a0001c0001t0002g0108others(3): Show | 6 | HG01167.hp2 HG01993.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+6720T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878262 | ||||||
| chr4:1878263
|
T | A | 4 | a0001c0001t0001g0107a0001c0001t0005g0130a0001c0001t0008g0106others(1): Show | 4 | HG03139.hp1 NA18522.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6721T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878263 | ||||||
| chr4:1878264
|
T | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0104a0001c0001t0002g0108others(3): Show | 6 | HG01167.hp2 HG01993.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+6722T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878264 | ||||||
| chr4:1878265
|
T | A | 2 | a0001c0001t0005g0130a0001c0003t0022g0013 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-30+6723T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878265 | ||||||
| chr4:1878266
|
T | A | 5 | a0001c0001t0001g0004a0001c0001t0007g0123a0001c0001t0012g0011others(2): Show | 5 | HG01993.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+6724T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878266 | ||||||
| chr4:1878267
|
T | A | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+6725T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878267 | ||||||
| chr4:1878268
|
T | A | 3 | a0001c0001t0001g0004a0001c0001t0007g0123a0001c0001t0012g0011 | 3 | HG01993.hp2 HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-30+6726T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878268 | ||||||
| chr4:1878270
|
T | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+6728T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878270 | ||||||
| chr4:1878327
|
C | T | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30+6785C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878327 | ||||||
| chr4:1878508
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0046others(14): Show | 17 | HG00280.hp2 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-30+6966G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878508 | ||||||
| chr4:1878592
|
T | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+7050T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878592 | ||||||
| chr4:1878911
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+7369G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878911 | ||||||
| chr4:1878973
|
T | C | 16 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0005g0130others(13): Show | 16 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+7431T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1878973 | ||||||
| chr4:1879042
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-30+7500A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1879042 | ||||||
| chr4:1879375
|
T | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-30+7833T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1879375 | ||||||
| chr4:1879511
|
G | A | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+7969G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1879511 | ||||||
| chr4:1879532
|
T | A | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+7990T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1879532 | ||||||
| chr4:1879646
|
C | G | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30+8104C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1879646 | ||||||
| chr4:1879824
|
T | TTG | 14 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0052others(11): Show | 14 | HG01517.hp1 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+8316_-30+8317d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
T | TTGTG | 4 | a0001c0001t0001g0017a0001c0001t0001g0091a0001c0001t0001g0116others(1): Show | 4 | HG01952.hp1 HG02293.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+8314_-30+8317d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
T | TTGTGTG | 3 | a0001c0001t0018g0020a0001c0002t0019g0029a0001c0002t0021g0035 | 3 | HG02257.hp1 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-30+8312_-30+8317d others(8): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+8308_-30+8317d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
TTG | T | 7 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(4): Show | 7 | HG00741.hp2 HG01167.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+8316_-30+8317d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
TTGTG | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0003g0086others(1): Show | 4 | HG02622.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+8314_-30+8317d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0070a0001c0003t0022g0013 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30+8308_-30+8317d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1879824
|
TTGTGTGT others(5): Show |
T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-30+8306_-30+8317d others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1879824 | |||||
| chr4:1880011
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-30+8469G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1880011 | ||||||
| chr4:1880353
|
CT | C | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+8814delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1880353 | |||||
| chr4:1880612
|
C | CA | 8 | a0001c0001t0001g0024a0001c0001t0001g0071a0001c0001t0001g0109others(5): Show | 8 | HG02922.hp2 HG03139.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+9084dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1880612 | |||||
| chr4:1880612
|
C | CAA | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30+9083_-30+9084d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1880612 | |||||
| chr4:1880705
|
G | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+9163G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1880705 | ||||||
| chr4:1880758
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-30+9216A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1880758 | ||||||
| chr4:1881003
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0071others(1): Show | 4 | NA18945.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+9461C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881003 | ||||||
| chr4:1881204
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-30+9662C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881204 | ||||||
| chr4:1881269
|
C | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+9727C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881269 | ||||||
| chr4:1881324
|
G | A | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-30+9782G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881324 | ||||||
| chr4:1881326
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-30+9784G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881326 | ||||||
| chr4:1881361
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+9819T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881361 | ||||||
| chr4:1881453
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0093 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-30+9911C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881453 | ||||||
| chr4:1881562
|
T | C | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-30+10020T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881562 | ||||||
| chr4:1881646
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-30+10104C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881646 | ||||||
| chr4:1881920
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0041others(5): Show | 8 | HG00140.hp2 HG00609.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+10378A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1881920 | ||||||
| chr4:1882402
|
T | C | 9 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(6): Show | 9 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+10860T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882402 | ||||||
| chr4:1882534
|
G | A | 6 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+10992G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882534 | ||||||
| chr4:1882539
|
C | T | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-30+10997C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882539 | ||||||
| chr4:1882553
|
A | C | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-30+11011A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882553 | ||||||
| chr4:1882553
|
A | G | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+11011A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882553 | ||||||
| chr4:1882556
|
C | G | 3 | a0001c0001t0005g0130a0001c0001t0014g0115a0001c0001t0020g0021 | 3 | HG02109.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+11014C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882556 | ||||||
| chr4:1882872
|
C | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+11330C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1882872 | ||||||
| chr4:1883010
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-30+11468T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883010 | ||||||
| chr4:1883260
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-30+11718T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883260 | ||||||
| chr4:1883324
|
C | T | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30+11782C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883324 | ||||||
| chr4:1883452
|
C | T | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-30+11910C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883452 | ||||||
| chr4:1883631
|
C | CA | 16 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0082others(13): Show | 16 | HG00741.hp1 HG01167.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.-30+12107dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1883631 | |||||
| chr4:1883676
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+12134C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883676 | ||||||
| chr4:1883826
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-30+12284C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883826 | ||||||
| chr4:1883896
|
C | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-30+12354C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1883896 | ||||||
| chr4:1884222
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-30+12680A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1884222 | ||||||
| chr4:1884678
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+13136C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1884678 | ||||||
| chr4:1884833
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+13291G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1884833 | ||||||
| chr4:1884979
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+13437G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1884979 | ||||||
| chr4:1885068
|
C | A | 1 | a0001c0002t0015g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-30+13526C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885068 | ||||||
| chr4:1885116
|
A | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+13574A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885116 | ||||||
| chr4:1885117
|
A | T | 1 | a0001c0001t0001g0050 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-30+13575A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885117 | ||||||
| chr4:1885123
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-30+13581T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885123 | ||||||
| chr4:1885123
|
TA | T | 16 | a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0005g0130others(13): Show | 16 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+13586delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1885123 | |||||
| chr4:1885124
|
A | T | 1 | a0001c0001t0001g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-30+13582A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885124 | ||||||
| chr4:1885193
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-30+13651C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885193 | ||||||
| chr4:1885196
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-30+13654T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885196 | ||||||
| chr4:1885457
|
T | G | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-30+13915T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885457 | ||||||
| chr4:1885507
|
G | A | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+13965G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885507 | ||||||
| chr4:1885628
|
G | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+14086G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885628 | ||||||
| chr4:1885662
|
A | T | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+14120A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885662 | ||||||
| chr4:1885832
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0093 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-30+14290G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885832 | ||||||
| chr4:1885911
|
A | G | 2 | a0001c0001t0001g0104a0001c0001t0002g0108 | 2 | HG01167.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-30+14369A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1885911 | ||||||
| chr4:1886071
|
C | A | 1 | a0001c0009t0001g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-30+14529C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886071 | ||||||
| chr4:1886388
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-29-14238A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886388 | ||||||
| chr4:1886482
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0004g0058a0001c0001t0004g0095 | 3 | HG01106.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-29-14144C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886482 | ||||||
| chr4:1886483
|
G | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-14143G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886483 | ||||||
| chr4:1886550
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-29-14076G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886550 | ||||||
| chr4:1886916
|
G | A | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-29-13710G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886916 | ||||||
| chr4:1886980
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-13646C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1886980 | ||||||
| chr4:1887081
|
G | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-13545G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1887081 | ||||||
| chr4:1887209
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-13417A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1887209 | ||||||
| chr4:1887550
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-13076A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1887550 | ||||||
| chr4:1887903
|
CT | C | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-12716delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1887903 | |||||
| chr4:1887914
|
T | G | 3 | a0001c0001t0001g0094a0001c0001t0004g0058a0001c0001t0004g0095 | 3 | HG01106.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-29-12712T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1887914 | ||||||
| chr4:1887921
|
T | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0001g0075others(6): Show | 9 | HG00741.hp2 HG01952.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-12705T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1887921 | ||||||
| chr4:1887941
|
C | T | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-29-12685C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1887941 | ||||||
| chr4:1888135
|
G | T | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-29-12491G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1888135 | ||||||
| chr4:1888410
|
C | CA | 11 | a0001c0001t0001g0016a0001c0001t0001g0039a0001c0001t0001g0064others(8): Show | 11 | HG00741.hp2 HG01433.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-12189dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1888410 | |||||
| chr4:1888410
|
CA | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-29-12189delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1888410 | |||||
| chr4:1888410
|
CAAAAAA | C | 6 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-12194_-29-1218 others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1888410 | |||||
| chr4:1888442
|
T | C | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29-12184T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1888442 | ||||||
| chr4:1888460
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-29-12166T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1888460 | ||||||
| chr4:1888569
|
T | A | 1 | a0001c0001t0011g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29-12057T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1888569 | ||||||
| chr4:1888845
|
C | T | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-29-11781C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1888845 | ||||||
| chr4:1888901
|
AT | A | 6 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0015g0002others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-11709delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1888901 | |||||
| chr4:1889152
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29-11474C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1889152 | ||||||
| chr4:1889189
|
C | T | 4 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0060others(1): Show | 4 | HG02976.hp2 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-11437C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1889189 | ||||||
| chr4:1889628
|
G | A | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-10998G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1889628 | ||||||
| chr4:1889787
|
G | A | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-29-10839G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1889787 | ||||||
| chr4:1890096
|
T | C | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-29-10530T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1890096 | ||||||
| chr4:1890119
|
A | C | 1 | a0001c0001t0002g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-29-10507A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1890119 | ||||||
| chr4:1890596
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-10030C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1890596 | ||||||
| chr4:1890606
|
A | G | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-10020A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1890606 | ||||||
| chr4:1890778
|
A | G | 3 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0121 | 3 | HG00280.hp2 HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-29-9848A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1890778 | ||||||
| chr4:1890817
|
C | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-9809C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1890817 | ||||||
| chr4:1891116
|
G | C | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-9510G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891116 | ||||||
| chr4:1891200
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-29-9426G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891200 | ||||||
| chr4:1891440
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-29-9186A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891440 | ||||||
| chr4:1891474
|
C | T | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-9152C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891474 | ||||||
| chr4:1891524
|
T | G | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-9102T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891524 | ||||||
| chr4:1891632
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-8994C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891632 | ||||||
| chr4:1891669
|
G | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(8): Show | 11 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-8957G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891669 | ||||||
| chr4:1891688
|
C | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-8938C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891688 | ||||||
| chr4:1891739
|
T | C | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-8887T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891739 | ||||||
| chr4:1891822
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-29-8804A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891822 | ||||||
| chr4:1891862
|
A | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0039a0001c0001t0001g0043others(1): Show | 4 | NA18945.hp2 NA19000.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-8764A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891862 | ||||||
| chr4:1891875
|
A | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(9): Show | 12 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29-8751A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891875 | ||||||
| chr4:1891901
|
G | A | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-29-8725G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891901 | ||||||
| chr4:1891924
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-29-8702A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1891924 | ||||||
| chr4:1892365
|
T | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0001t0001g0084others(4): Show | 7 | HG00280.hp2 HG00738.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-8261T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1892365 | ||||||
| chr4:1892509
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0008g0106 | 3 | NA18949.hp2 NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-29-8117G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1892509 | ||||||
| chr4:1892572
|
CT | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-8043delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1892572 | |||||
| chr4:1892639
|
C | T | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-29-7987C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1892639 | ||||||
| chr4:1892658
|
C | CCT | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-7966_-29-7965d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1892658 | |||||
| chr4:1892672
|
G | A | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-29-7954G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1892672 | ||||||
| chr4:1893094
|
T | C | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29-7532T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893094 | ||||||
| chr4:1893337
|
A | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-7289A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893337 | ||||||
| chr4:1893536
|
GTTTTTTG others(10): Show |
G | 2 | a0001c0001t0001g0033a0001c0001t0004g0054 | 2 | HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-29-7078_-29-7062d others(19): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1893536 | |||||
| chr4:1893543
|
G | GT | 4 | a0001c0001t0001g0068a0001c0001t0001g0107a0001c0001t0002g0124others(1): Show | 4 | HG01433.hp2 HG03516.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-7067dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1893543 | |||||
| chr4:1893543
|
G | T | 2 | a0001c0001t0007g0123a0001c0009t0001g0097 | 2 | HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-29-7083G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893543 | ||||||
| chr4:1893552
|
T | G | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-7074T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893552 | ||||||
| chr4:1893553
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-29-7073T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893553 | ||||||
| chr4:1893555
|
T | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0025others(9): Show | 12 | HG01517.hp2 HG01934.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29-7071T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893555 | ||||||
| chr4:1893555
|
T | TTTG | 4 | a0001c0001t0018g0020a0001c0002t0015g0002a0001c0002t0019g0029others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-7069_-29-7068i others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1893555 | |||||
| chr4:1893556
|
T | G | 6 | a0001c0001t0003g0086a0001c0001t0003g0096a0001c0001t0005g0130others(3): Show | 6 | HG01361.hp2 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-7070T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893556 | ||||||
| chr4:1893560
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29-7066G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893560 | ||||||
| chr4:1893656
|
ATCC | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-6965_-29-6963d others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1893656 | |||||
| chr4:1893735
|
A | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-6891A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893735 | ||||||
| chr4:1893956
|
A | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-6670A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1893956 | ||||||
| chr4:1894250
|
C | G | 1 | a0001c0001t0001g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-29-6376C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1894250 | ||||||
| chr4:1894334
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-29-6292C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1894334 | ||||||
| chr4:1894621
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0025 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-29-6005G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1894621 | ||||||
| chr4:1894674
|
TA | T | 14 | a0001c0001t0001g0057a0001c0001t0005g0130a0001c0001t0006g0014others(11): Show | 14 | HG01517.hp2 HG01975.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-5935delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1894674 | |||||
| chr4:1894675
|
A | T | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29-5951A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1894675 | ||||||
| chr4:1894709
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0052 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-29-5917C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1894709 | ||||||
| chr4:1895196
|
G | A | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-29-5430G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895196 | ||||||
| chr4:1895255
|
G | C | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-29-5371G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895255 | ||||||
| chr4:1895608
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0003g0030a0001c0006t0001g0031 | 3 | HG02630.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-29-5018C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895608 | ||||||
| chr4:1895717
|
C | T | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-29-4909C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895717 | ||||||
| chr4:1895729
|
T | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-4897T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895729 | ||||||
| chr4:1895748
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-4878T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895748 | ||||||
| chr4:1895851
|
C | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-4775C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895851 | ||||||
| chr4:1895865
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-29-4761G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895865 | ||||||
| chr4:1895991
|
C | T | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-29-4635C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1895991 | ||||||
| chr4:1896083
|
C | T | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-29-4543C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1896083 | ||||||
| chr4:1896135
|
A | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0068others(1): Show | 4 | NA18944.hp1 NA18949.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-4491A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1896135 | ||||||
| chr4:1896285
|
C | G | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-4341C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1896285 | ||||||
| chr4:1896589
|
C | A | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-29-4037C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1896589 | ||||||
| chr4:1896681
|
C | CCTCCCTT others(9): Show |
1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-3943_-29-3942i others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1896681 | |||||
| chr4:1896681
|
C | CCTTCCTT others(5): Show |
13 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(10): Show | 13 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-3936_-29-3935i others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1896681 | |||||
| chr4:1896744
|
CTCTT | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0052 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-29-3871_-29-3868d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1896744 | |||||
| chr4:1896809
|
T | A | 1 | a0004c0008t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-29-3817T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1896809 | ||||||
| chr4:1896843
|
T | C | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-3783T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1896843 | ||||||
| chr4:1897174
|
GA | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(89): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-29-3440delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1897174 | |||||
| chr4:1897230
|
C | T | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-3396C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897230 | ||||||
| chr4:1897321
|
A | T | 3 | a0001c0001t0001g0094a0001c0001t0004g0058a0001c0001t0004g0095 | 3 | HG01106.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-29-3305A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897321 | ||||||
| chr4:1897349
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-29-3277G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897349 | ||||||
| chr4:1897493
|
G | GA | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-3123dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1897493 | |||||
| chr4:1897504
|
T | A | 10 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(7): Show | 10 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-3122T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897504 | ||||||
| chr4:1897558
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0003g0030a0001c0006t0001g0031 | 3 | HG02630.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-29-3068T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897558 | ||||||
| chr4:1897645
|
A | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29-2981A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897645 | ||||||
| chr4:1897823
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-29-2803C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1897823 | ||||||
| chr4:1898074
|
G | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(6): Show | 9 | HG01167.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-2552G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898074 | ||||||
| chr4:1898139
|
T | C | 12 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(9): Show | 12 | HG01975.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-2487T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898139 | ||||||
| chr4:1898273
|
G | GA | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-29-2352dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1898273 | |||||
| chr4:1898380
|
C | T | 19 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(16): Show | 19 | HG01167.hp2 HG01975.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-29-2246C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898380 | ||||||
| chr4:1898387
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-29-2239A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898387 | ||||||
| chr4:1898390
|
T | C | 1 | a0001c0001t0004g0058 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-29-2236T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898390 | ||||||
| chr4:1898474
|
G | C | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-29-2152G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898474 | ||||||
| chr4:1898480
|
C | T | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-29-2146C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898480 | ||||||
| chr4:1898492
|
G | A | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-29-2134G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898492 | ||||||
| chr4:1898585
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-29-2041G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898585 | ||||||
| chr4:1898646
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-1980C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898646 | ||||||
| chr4:1898655
|
G | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-1971G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898655 | ||||||
| chr4:1898672
|
C | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-1954C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898672 | ||||||
| chr4:1898690
|
C | CT | 11 | a0001c0001t0001g0075a0001c0001t0001g0112a0001c0001t0001g0114others(8): Show | 11 | HG01952.hp1 HG01975.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-1920dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 1898690 | |||||
| chr4:1898719
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-1907G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898719 | ||||||
| chr4:1898723
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-1903C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898723 | ||||||
| chr4:1898785
|
A | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-1841A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898785 | ||||||
| chr4:1898858
|
T | G | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-29-1768T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898858 | ||||||
| chr4:1898906
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-29-1720G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1898906 | ||||||
| chr4:1899382
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(6): Show | 9 | HG01167.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-1244G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1899382 | ||||||
| chr4:1899477
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-29-1149A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1899477 | ||||||
| chr4:1899488
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29-1138G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1899488 | ||||||
| chr4:1900182
|
T | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.-29-444T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1900182 | ||||||
| chr4:1900188
|
T | G | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-29-438T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1900188 | ||||||
| chr4:1900317
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-309A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1900317 | ||||||
| chr4:1900510
|
T | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-116T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 1/21 | chr4 | 1900510 | ||||||
| chr4:1901285
|
A | G | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.597+34A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1901285 | ||||||
| chr4:1901792
|
G | T | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.597+541G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1901792 | ||||||
| chr4:1901798
|
C | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.597+547C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1901798 | ||||||
| chr4:1902108
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+857T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1902108 | ||||||
| chr4:1902562
|
CT | C | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.597+1312delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1902562 | ||||||
| chr4:1902573
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.597+1322G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1902573 | ||||||
| chr4:1902627
|
C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0050others(12): Show | 15 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+1376C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1902627 | ||||||
| chr4:1903215
|
A | C | 1 | a0001c0001t0003g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.598-1001A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1903215 | ||||||
| chr4:1903661
|
A | C | 6 | a0001c0001t0018g0020a0001c0002t0005g0001a0001c0002t0015g0002others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-555A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1903661 | ||||||
| chr4:1903731
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.598-485A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1903731 | ||||||
| chr4:1903732
|
A | AT | 11 | a0001c0001t0001g0109a0001c0001t0001g0127a0001c0001t0007g0123others(8): Show | 11 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.598-464dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 1903732 | |||||
| chr4:1903859
|
T | C | 6 | a0001c0001t0018g0020a0001c0002t0005g0001a0001c0002t0015g0002others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-357T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1903859 | ||||||
| chr4:1903934
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.598-282T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1903934 | ||||||
| chr4:1904112
|
G | T | 6 | a0001c0001t0018g0020a0001c0002t0005g0001a0001c0002t0015g0002others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.598-104G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 2/21 | chr4 | 1904112 | ||||||
| chr4:1904425
|
A | T | 6 | a0001c0001t0018g0020a0001c0002t0005g0001a0001c0002t0015g0002others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.760+47A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1904425 | ||||||
| chr4:1904435
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.760+57A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1904435 | ||||||
| chr4:1904562
|
T | C | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.760+184T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1904562 | ||||||
| chr4:1904849
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.760+471G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1904849 | ||||||
| chr4:1904990
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0002g0108 | 2 | HG01167.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.760+612C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1904990 | ||||||
| chr4:1905354
|
C | T | 6 | a0001c0001t0018g0020a0001c0002t0005g0001a0001c0002t0015g0002others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.760+976C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1905354 | ||||||
| chr4:1905849
|
C | T | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.760+1471C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1905849 | ||||||
| chr4:1905933
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.760+1555C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1905933 | ||||||
| chr4:1906261
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.760+1883T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1906261 | ||||||
| chr4:1906299
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.760+1921C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1906299 | ||||||
| chr4:1906446
|
G | A | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.760+2068G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1906446 | ||||||
| chr4:1906455
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.760+2077G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1906455 | ||||||
| chr4:1906650
|
C | G | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.760+2272C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1906650 | ||||||
| chr4:1906654
|
C | CT | 8 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0091others(5): Show | 8 | HG02809.hp2 HG03139.hp1 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.760+2300dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1906654 | |||||
| chr4:1906654
|
C | CTT | 5 | a0001c0001t0001g0039a0001c0001t0006g0014a0001c0001t0006g0015others(2): Show | 5 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.760+2299_760+2300d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1906654 | |||||
| chr4:1906987
|
G | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.760+2609G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1906987 | ||||||
| chr4:1907149
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.760+2771A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1907149 | ||||||
| chr4:1907303
|
A | G | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.760+2925A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1907303 | ||||||
| chr4:1907470
|
CT | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.760+3099delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1907470 | |||||
| chr4:1907553
|
AGAC | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0002g0019others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.760+3176_760+3178d others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1907553 | ||||||
| chr4:1907614
|
TC | T | 2 | a0001c0001t0001g0107a0001c0001t0008g0106 | 2 | NA18949.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.760+3237delC | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1907614 | ||||||
| chr4:1907615
|
C | CT | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(33): Show | 36 | HG00280.hp1 HG00738.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.760+3260dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1907615 | |||||
| chr4:1907615
|
CT | C | 16 | a0001c0001t0001g0048a0001c0001t0001g0053a0001c0001t0001g0060others(13): Show | 16 | HG01975.hp1 HG02004.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.760+3260delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1907615 | |||||
| chr4:1907615
|
CTT | C | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG02559.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.760+3259_760+3260d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1907615 | |||||
| chr4:1907993
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.760+3615C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1907993 | ||||||
| chr4:1908176
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.760+3798C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1908176 | ||||||
| chr4:1908449
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.760+4071G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1908449 | ||||||
| chr4:1908775
|
TTTG | T | 2 | a0001c0002t0002g0038a0001c0002t0003g0045 | 2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.760+4409_760+4411d others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1908775 | |||||
| chr4:1908855
|
C | G | 2 | a0001c0001t0007g0123a0001c0001t0012g0011 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.760+4477C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1908855 | ||||||
| chr4:1908916
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.760+4538G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1908916 | ||||||
| chr4:1909084
|
A | G | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.760+4706A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909084 | ||||||
| chr4:1909096
|
T | C | 15 | a0001c0001t0001g0100a0001c0001t0005g0130a0001c0001t0006g0014others(12): Show | 15 | HG01975.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.760+4718T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909096 | ||||||
| chr4:1909162
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.760+4784A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909162 | ||||||
| chr4:1909164
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0025 | 2 | HG01934.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.760+4786T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909164 | ||||||
| chr4:1909270
|
C | G | 1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.760+4892C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909270 | ||||||
| chr4:1909286
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0020g0021 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.760+4908C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909286 | ||||||
| chr4:1909662
|
A | G | 3 | a0001c0001t0001g0041a0001c0002t0002g0038a0001c0002t0003g0045 | 3 | HG02300.hp2 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.760+5284A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909662 | ||||||
| chr4:1909722
|
C | T | 7 | a0001c0001t0018g0020a0001c0002t0005g0001a0001c0002t0015g0002others(4): Show | 7 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.760+5344C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909722 | ||||||
| chr4:1909748
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.760+5370C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1909748 | ||||||
| chr4:1909944
|
TA | T | 8 | a0001c0001t0004g0058a0001c0001t0005g0130a0001c0001t0018g0020others(5): Show | 8 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.760+5580delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1909944 | |||||
| chr4:1910094
|
TTTTGGAA others(12): Show |
T | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.760+5727_760+5745d others(21): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1910094 | |||||
| chr4:1910170
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.760+5792A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1910170 | ||||||
| chr4:1910491
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.760+6113A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1910491 | ||||||
| chr4:1910783
|
T | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.761-6088T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1910783 | ||||||
| chr4:1911385
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.761-5486C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1911385 | ||||||
| chr4:1911518
|
A | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.761-5353A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1911518 | ||||||
| chr4:1911549
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.761-5322C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1911549 | ||||||
| chr4:1911587
|
C | CA | 5 | a0001c0001t0001g0039a0001c0001t0001g0063a0001c0001t0001g0069others(2): Show | 5 | HG00140.hp1 HG00140.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.761-5264dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1911587 | |||||
| chr4:1911587
|
CA | C | 17 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(14): Show | 17 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.761-5264delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1911587 | |||||
| chr4:1911602
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.761-5269A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1911602 | ||||||
| chr4:1911608
|
G | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0066a0001c0001t0001g0075others(5): Show | 8 | HG00741.hp2 HG01993.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.761-5263G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1911608 | ||||||
| chr4:1911853
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.761-5018G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1911853 | ||||||
| chr4:1912046
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.761-4825T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1912046 | ||||||
| chr4:1913263
|
C | A | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.761-3608C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1913263 | ||||||
| chr4:1913306
|
G | A | 1 | a0001c0001t0017g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.761-3565G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1913306 | ||||||
| chr4:1913820
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.761-3051A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1913820 | ||||||
| chr4:1913952
|
C | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.761-2919C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1913952 | ||||||
| chr4:1914061
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0026others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.761-2810C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914061 | ||||||
| chr4:1914243
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.761-2628G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914243 | ||||||
| chr4:1914545
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.761-2326C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914545 | ||||||
| chr4:1914673
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.761-2198G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914673 | ||||||
| chr4:1914813
|
C | CCATTAAC others(7): Show |
1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.761-2056_761-2043d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1914813 | |||||
| chr4:1914818
|
A | G | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.761-2053A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914818 | ||||||
| chr4:1914882
|
G | A | 1 | a0001c0001t0010g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.761-1989G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914882 | ||||||
| chr4:1914924
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.761-1947A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1914924 | ||||||
| chr4:1915111
|
C | CT | 17 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(14): Show | 17 | HG00741.hp1 HG00741.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.761-1738dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1915111 | |||||
| chr4:1915111
|
CTTTT | C | 4 | a0001c0001t0012g0011a0001c0002t0005g0001a0001c0002t0015g0002others(1): Show | 4 | HG02809.hp2 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.761-1741_761-1738d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1915111 | |||||
| chr4:1915111
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0047a0001c0001t0001g0081a0001c0001t0001g0122 | 3 | HG00738.hp1 HG00738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.761-1751_761-1738d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 1915111 | |||||
| chr4:1915379
|
G | T | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.761-1492G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1915379 | ||||||
| chr4:1915715
|
T | C | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.761-1156T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1915715 | ||||||
| chr4:1915984
|
T | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.761-887T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1915984 | ||||||
| chr4:1915985
|
T | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.761-886T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1915985 | ||||||
| chr4:1916135
|
T | C | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.761-736T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1916135 | ||||||
| chr4:1916161
|
C | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.761-710C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 3/21 | chr4 | 1916161 | ||||||
| chr4:1917095
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.927+58G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917095 | ||||||
| chr4:1917152
|
A | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.927+115A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917152 | ||||||
| chr4:1917257
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.927+220G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917257 | ||||||
| chr4:1917296
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0008 | 2 | HG00609.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.927+259C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917296 | ||||||
| chr4:1917297
|
G | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+260G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917297 | ||||||
| chr4:1917330
|
G | T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.927+293G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917330 | ||||||
| chr4:1917411
|
T | C | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+374T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917411 | ||||||
| chr4:1917594
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.928-547G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917594 | ||||||
| chr4:1917761
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.928-380G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917761 | ||||||
| chr4:1917778
|
C | CT | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0008g0106others(1): Show | 4 | HG02559.hp1 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-343dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr4 | 1917778 | |||||
| chr4:1917778
|
CT | C | 7 | a0001c0001t0005g0080a0001c0001t0012g0011a0001c0001t0018g0020others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-343delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr4 | 1917778 | |||||
| chr4:1917842
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.928-299C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917842 | ||||||
| chr4:1917850
|
C | T | 1 | a0001c0002t0019g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.928-291C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1917850 | ||||||
| chr4:1918007
|
C | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.928-134C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 4/21 | chr4 | 1918007 | ||||||
| chr4:1918995
|
C | T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1410+372C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1918995 | ||||||
| chr4:1919167
|
C | CA | 9 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0077others(6): Show | 9 | HG02630.hp1 HG03041.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1410+565dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1919167 | |||||
| chr4:1919167
|
CA | C | 12 | a0001c0001t0001g0010a0001c0001t0005g0080a0001c0001t0006g0014others(9): Show | 12 | HG00609.hp1 HG01975.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1410+565delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1919167 | |||||
| chr4:1919320
|
C | T | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1410+697C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919320 | ||||||
| chr4:1919350
|
C | A | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1410+727C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919350 | ||||||
| chr4:1919494
|
C | T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1410+871C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919494 | ||||||
| chr4:1919587
|
T | C | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1410+964T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919587 | ||||||
| chr4:1919705
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1410+1082G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919705 | ||||||
| chr4:1919925
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1410+1302A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919925 | ||||||
| chr4:1919929
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1410+1306C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1919929 | ||||||
| chr4:1920108
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1410+1485C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1920108 | ||||||
| chr4:1920206
|
T | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1410+1583T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1920206 | ||||||
| chr4:1920402
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1410+1779C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1920402 | ||||||
| chr4:1920847
|
A | G | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1410+2224A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1920847 | ||||||
| chr4:1920857
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1410+2234C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1920857 | ||||||
| chr4:1920879
|
T | A | 5 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(2): Show | 5 | HG01975.hp2 HG02559.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1410+2256T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1920879 | ||||||
| chr4:1921018
|
A | G | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1410+2395A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921018 | ||||||
| chr4:1921107
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0067 | 2 | NA18612.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1410+2484G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921107 | ||||||
| chr4:1921215
|
G | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1410+2592G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921215 | ||||||
| chr4:1921350
|
G | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1410+2727G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921350 | ||||||
| chr4:1921455
|
C | G | 2 | a0001c0001t0001g0099a0001c0001t0009g0119 | 2 | HG02004.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1410+2832C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921455 | ||||||
| chr4:1921463
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1410+2840A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921463 | ||||||
| chr4:1921651
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1410+3028G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1921651 | ||||||
| chr4:1921781
|
C | CA | 11 | a0001c0001t0001g0084a0001c0001t0001g0125a0001c0001t0002g0074others(8): Show | 11 | HG01496.hp1 HG01496.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1410+3177dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1921781 | |||||
| chr4:1922018
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1410+3395C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922018 | ||||||
| chr4:1922023
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1410+3400T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922023 | ||||||
| chr4:1922082
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1410+3459G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922082 | ||||||
| chr4:1922156
|
A | G | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1410+3533A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922156 | ||||||
| chr4:1922220
|
T | G | 1 | a0001c0001t0001g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1410+3597T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922220 | ||||||
| chr4:1922230
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1410+3607G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922230 | ||||||
| chr4:1922581
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1410+3958A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922581 | ||||||
| chr4:1922700
|
C | T | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1410+4077C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1922700 | ||||||
| chr4:1923316
|
C | CA | 10 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0056others(7): Show | 10 | HG01167.hp2 HG01993.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1410+4715dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1923316 | |||||
| chr4:1923316
|
CA | C | 11 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0083others(8): Show | 11 | HG00738.hp1 HG01167.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1410+4715delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1923316 | |||||
| chr4:1923367
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1410+4744C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1923367 | ||||||
| chr4:1923682
|
GC | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1410+5061delC | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1923682 | |||||
| chr4:1923684
|
C | T | 11 | a0001c0001t0005g0130a0001c0001t0007g0123a0001c0001t0012g0011others(8): Show | 11 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1410+5061C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1923684 | ||||||
| chr4:1923692
|
C | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1410+5069C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1923692 | ||||||
| chr4:1923839
|
C | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1410+5216C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1923839 | ||||||
| chr4:1924228
|
C | T | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1410+5605C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1924228 | ||||||
| chr4:1924324
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0071 | 2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1410+5701A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1924324 | ||||||
| chr4:1924451
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(6): Show | 9 | HG01167.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1410+5828G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1924451 | ||||||
| chr4:1924748
|
C | CA | 14 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0017others(11): Show | 14 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.1411-5867dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1924748 | |||||
| chr4:1924811
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1411-5815T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1924811 | ||||||
| chr4:1925106
|
T | C | 1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1411-5520T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925106 | ||||||
| chr4:1925174
|
C | T | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1411-5452C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925174 | ||||||
| chr4:1925202
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(6): Show | 9 | HG01167.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1411-5424G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925202 | ||||||
| chr4:1925342
|
T | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(8): Show | 11 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1411-5284T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925342 | ||||||
| chr4:1925389
|
CT | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1411-5210delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1925389 | |||||
| chr4:1925389
|
CTT | C | 8 | a0001c0001t0001g0085a0001c0001t0001g0104a0001c0001t0002g0108others(5): Show | 8 | HG01167.hp1 HG01167.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411-5211_1411-521 others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1925389 | |||||
| chr4:1925556
|
A | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1411-5070A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925556 | ||||||
| chr4:1925560
|
G | A | 4 | a0001c0001t0012g0011a0001c0002t0005g0001a0001c0002t0015g0002others(1): Show | 4 | HG02809.hp2 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1411-5066G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925560 | ||||||
| chr4:1925762
|
C | A | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-4864C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925762 | ||||||
| chr4:1925773
|
T | TA | 2 | a0001c0001t0005g0130a0001c0001t0007g0123 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1411-4853_1411-485 others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925773 | ||||||
| chr4:1925773
|
T | TATA | 5 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411-4853_1411-485 others(7): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925773 | ||||||
| chr4:1925774
|
T | A | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1411-4852T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925774 | ||||||
| chr4:1925775
|
T | A | 3 | a0001c0001t0005g0130a0001c0002t0005g0001a0001c0002t0019g0029 | 3 | HG03195.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1411-4851T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925775 | ||||||
| chr4:1925776
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1411-4850T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925776 | ||||||
| chr4:1925778
|
T | A | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1411-4848T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925778 | ||||||
| chr4:1925778
|
T | G | 2 | a0001c0001t0001g0120a0001c0002t0021g0035 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1411-4848T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925778 | ||||||
| chr4:1925782
|
G | T | 4 | a0001c0001t0001g0032a0001c0001t0007g0123a0001c0002t0005g0001others(1): Show | 4 | HG03098.hp2 HG03139.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-4844G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925782 | ||||||
| chr4:1925798
|
GTTTGTT | G | 2 | a0001c0001t0001g0055a0001c0009t0001g0097 | 2 | HG02896.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1411-4811_1411-480 others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1925798 | |||||
| chr4:1925881
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1411-4745A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1925881 | ||||||
| chr4:1926150
|
A | AT | 15 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0107others(12): Show | 15 | HG00741.hp2 HG01433.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.1411-4453dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1926150 | |||||
| chr4:1926150
|
AT | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0083others(3): Show | 6 | HG01167.hp1 HG01975.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-4453delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1926150 | |||||
| chr4:1926573
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0113a0001c0001t0001g0121 | 3 | HG00280.hp2 HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1411-4053C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1926573 | ||||||
| chr4:1926608
|
C | G | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1411-4018C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1926608 | ||||||
| chr4:1926734
|
G | A | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1411-3892G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1926734 | ||||||
| chr4:1926790
|
G | C | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1411-3836G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1926790 | ||||||
| chr4:1926829
|
T | G | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1411-3797T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1926829 | ||||||
| chr4:1927025
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1411-3601A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927025 | ||||||
| chr4:1927547
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1411-3079C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927547 | ||||||
| chr4:1927638
|
G | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1411-2988G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927638 | ||||||
| chr4:1927658
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0071 | 2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1411-2968G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927658 | ||||||
| chr4:1927719
|
G | GA | 20 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0037others(17): Show | 20 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1411-2877dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1927719 | |||||
| chr4:1927719
|
GA | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0018others(27): Show | 30 | HG01952.hp2 HG01975.hp2 HG01993.hp1 others(27): Show |
intron_variant | MODIFIER | c.1411-2877delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1927719 | |||||
| chr4:1927719
|
GAA | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0107a0001c0001t0001g0109others(4): Show | 7 | HG02886.hp2 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-2878_1411-287 others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1927719 | |||||
| chr4:1927719
|
GAAAAAAA others(1): Show |
G | 5 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0015g0002others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411-2884_1411-287 others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1927719 | |||||
| chr4:1927720
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0020g0021 | 2 | NA18522.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1411-2906A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927720 | ||||||
| chr4:1927721
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1411-2905A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927721 | ||||||
| chr4:1927722
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1411-2904A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1927722 | ||||||
| chr4:1928071
|
CT | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0002g0042others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1411-2540delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1928071 | |||||
| chr4:1928203
|
GT | G | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1411-2417delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1928203 | |||||
| chr4:1928587
|
TGTGGTGG others(14): Show |
T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1411-2016_1411-199 others(25): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 1928587 | |||||
| chr4:1928684
|
G | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0017g0103 | 3 | HG00741.hp2 HG02004.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1411-1942G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1928684 | ||||||
| chr4:1929955
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1411-671C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1929955 | ||||||
| chr4:1930058
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1411-568C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1930058 | ||||||
| chr4:1930153
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1411-473G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1930153 | ||||||
| chr4:1930511
|
A | G | 1 | a0001c0001t0011g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1411-115A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1930511 | ||||||
| chr4:1930576
|
A | G | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-50A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 5/21 | chr4 | 1930576 | ||||||
| chr4:1930849
|
C | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1555+79C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1930849 | ||||||
| chr4:1930887
|
T | C | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1555+117T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1930887 | ||||||
| chr4:1930938
|
C | T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1555+168C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1930938 | ||||||
| chr4:1931069
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1555+299G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931069 | ||||||
| chr4:1931086
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1555+316G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931086 | ||||||
| chr4:1931135
|
A | G | 11 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0052others(8): Show | 11 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1555+365A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931135 | ||||||
| chr4:1931216
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0094a0001c0001t0004g0054 | 3 | HG01106.hp1 HG01106.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1555+446C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931216 | ||||||
| chr4:1931232
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1555+462G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931232 | ||||||
| chr4:1931524
|
T | A | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1555+754T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931524 | ||||||
| chr4:1931865
|
C | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0002g0042others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1555+1095C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1931865 | ||||||
| chr4:1932032
|
G | A | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1555+1262G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932032 | ||||||
| chr4:1932191
|
C | G | 1 | a0001c0003t0022g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1555+1421C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932191 | ||||||
| chr4:1932203
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1555+1433A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932203 | ||||||
| chr4:1932439
|
C | CA | 11 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(8): Show | 11 | HG00609.hp2 HG01167.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1555+1690dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1932439 | |||||
| chr4:1932439
|
CA | C | 11 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(8): Show | 11 | HG01975.hp2 HG02559.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1555+1690delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1932439 | |||||
| chr4:1932497
|
A | G | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1555+1727A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932497 | ||||||
| chr4:1932508
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0008 | 2 | HG00609.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1555+1738A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932508 | ||||||
| chr4:1932697
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1555+1927G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932697 | ||||||
| chr4:1932736
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1555+1966G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932736 | ||||||
| chr4:1932871
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1555+2101T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932871 | ||||||
| chr4:1932963
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1556-2181C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1932963 | ||||||
| chr4:1933116
|
G | A | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1556-2028G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933116 | ||||||
| chr4:1933359
|
G | A | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1556-1785G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933359 | ||||||
| chr4:1933390
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1556-1754A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933390 | ||||||
| chr4:1933433
|
C | T | 3 | a0001c0001t0001g0049a0001c0005t0001g0072a0004c0008t0001g0023 | 3 | HG02723.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1556-1711C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933433 | ||||||
| chr4:1933544
|
C | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1556-1600C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933544 | ||||||
| chr4:1933556
|
A | AT | 6 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1556-1577dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1933556 | |||||
| chr4:1933629
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0008g0106 | 3 | NA18949.hp2 NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1556-1515C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933629 | ||||||
| chr4:1933686
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1556-1458G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933686 | ||||||
| chr4:1933743
|
C | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1556-1401C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933743 | ||||||
| chr4:1933747
|
A | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0071 | 2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1556-1397A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933747 | ||||||
| chr4:1933953
|
G | A | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1556-1191G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933953 | ||||||
| chr4:1934012
|
AGTT | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1556-1128_1556-112 others(7): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934012 | |||||
| chr4:1934075
|
A | AT | 7 | a0001c0001t0001g0100a0001c0001t0005g0130a0001c0001t0006g0014others(4): Show | 7 | HG01975.hp2 HG02109.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1556-1059dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934075 | |||||
| chr4:1934356
|
A | AT | 2 | a0001c0001t0001g0100a0001c0001t0005g0130 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1556-786dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934356 | |||||
| chr4:1934439
|
G | A | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1556-705G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934439 | ||||||
| chr4:1934474
|
C | T | 1 | a0001c0006t0001g0031 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1556-670C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934474 | ||||||
| chr4:1934567
|
A | G | 3 | a0001c0001t0012g0011a0001c0002t0005g0001a0001c0002t0015g0002 | 3 | HG02809.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1556-577A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934567 | ||||||
| chr4:1934632
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0002g0108 | 2 | HG01167.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1556-512G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934632 | ||||||
| chr4:1934700
|
T | C | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1556-444T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934700 | ||||||
| chr4:1934728
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1556-416A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934728 | ||||||
| chr4:1934847
|
TA | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0046a0001c0001t0001g0053others(11): Show | 14 | HG01361.hp2 HG01496.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.1556-265delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934847 | |||||
| chr4:1934847
|
TAA | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0049a0001c0001t0001g0081others(9): Show | 12 | HG00741.hp1 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.1556-266_1556-265d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934847 | |||||
| chr4:1934847
|
TAAA | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0067others(3): Show | 6 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1556-267_1556-265d others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934847 | |||||
| chr4:1934847
|
TAAAA | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG00609.hp1 HG01517.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1556-268_1556-265d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934847 | |||||
| chr4:1934847
|
TAAAAAA | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0085a0001c0001t0001g0104others(2): Show | 5 | HG01167.hp1 HG01167.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1556-270_1556-265d others(8): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934847 | |||||
| chr4:1934862
|
A | T | 1 | a0001c0001t0006g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1556-282A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934862 | ||||||
| chr4:1934862
|
AAAAAAAA others(13): Show |
A | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1556-280_1556-261d others(22): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934862 | |||||
| chr4:1934864
|
A | T | 1 | a0001c0001t0006g0028 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1556-280A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934864 | ||||||
| chr4:1934866
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1556-278_1556-277i others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934866 | ||||||
| chr4:1934866
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1556-278_1556-277i others(17): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934866 | ||||||
| chr4:1934866
|
A | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1556-278A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934866 | ||||||
| chr4:1934868
|
A | ATAT | 2 | a0001c0001t0001g0066a0001c0001t0001g0128 | 2 | HG02735.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1556-276_1556-275i others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934868 | ||||||
| chr4:1934868
|
A | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0099others(3): Show | 6 | HG01975.hp2 HG01993.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1556-276A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934868 | ||||||
| chr4:1934869
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1556-273_1556-261d others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934869 | |||||
| chr4:1934870
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1556-273_1556-272i others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934870 | |||||
| chr4:1934870
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1556-274_1556-273i others(13): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934870 | ||||||
| chr4:1934870
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0112 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1556-274_1556-273i others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934870 | ||||||
| chr4:1934870
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1556-274_1556-273i others(17): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934870 | ||||||
| chr4:1934870
|
A | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(12): Show | 15 | HG00741.hp2 HG01934.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1556-274A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934870 | ||||||
| chr4:1934872
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1556-271_1556-270i others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934872 | |||||
| chr4:1934872
|
A | ATAT | 2 | a0001c0001t0001g0026a0001c0001t0001g0098 | 2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1556-272_1556-271i others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934872 | ||||||
| chr4:1934872
|
A | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(16): Show | 19 | HG00741.hp2 HG01934.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.1556-272A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934872 | ||||||
| chr4:1934872
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1556-270_1556-259d others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934872 | |||||
| chr4:1934873
|
AAAAAAAT others(12): Show |
A | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1556-269_1556-251d others(21): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934873 | |||||
| chr4:1934874
|
A | AAT | 5 | a0001c0001t0001g0052a0001c0001t0001g0092a0001c0001t0001g0100others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1556-269_1556-268i others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934874 | |||||
| chr4:1934874
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0018a0001c0001t0001g0129a0001c0001t0013g0073 | 3 | HG02280.hp2 HG04184.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1556-270_1556-269i others(11): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934874 | ||||||
| chr4:1934874
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1556-270_1556-269i others(13): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934874 | ||||||
| chr4:1934874
|
A | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(27): Show | 30 | HG00741.hp2 HG01928.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.1556-270A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934874 | ||||||
| chr4:1934874
|
AAAAAAT | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0024others(5): Show | 8 | HG00609.hp2 HG01361.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1556-268_1556-263d others(8): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934874 | |||||
| chr4:1934876
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1556-267_1556-266i others(22): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934876 | |||||
| chr4:1934876
|
A | AT | 2 | a0001c0001t0001g0094a0001c0001t0004g0054 | 2 | HG01106.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1556-268_1556-267i others(3): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934876 | ||||||
| chr4:1934876
|
A | C | 1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1556-268A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934876 | ||||||
| chr4:1934876
|
A | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(49): Show | 52 | HG00140.hp2 HG00741.hp2 HG01361.hp2 others(49): Show |
intron_variant | MODIFIER | c.1556-268A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934876 | ||||||
| chr4:1934878
|
A | AAAAATAT others(6): Show |
1 | a0001c0001t0003g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1556-265_1556-264i others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 1934878 | |||||
| chr4:1934878
|
A | AT | 2 | a0001c0001t0001g0065a0001c0001t0001g0091 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1556-266_1556-265i others(3): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934878 | ||||||
| chr4:1934878
|
A | ATAT | 2 | a0001c0001t0001g0048a0001c0002t0001g0102 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1556-266_1556-265i others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934878 | ||||||
| chr4:1934878
|
A | T | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1556-266A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934878 | ||||||
| chr4:1934910
|
A | T | 17 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0087others(14): Show | 17 | HG00280.hp2 HG01361.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1556-234A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934910 | ||||||
| chr4:1934973
|
T | C | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1556-171T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1934973 | ||||||
| chr4:1935289
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1674+27C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1935289 | ||||||
| chr4:1935509
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1674+247A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1935509 | ||||||
| chr4:1935597
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0111 | 3 | HG02615.hp1 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1674+335C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1935597 | ||||||
| chr4:1935729
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0093 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1674+467C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1935729 | ||||||
| chr4:1935747
|
G | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(6): Show | 9 | HG01167.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1674+485G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1935747 | ||||||
| chr4:1936553
|
C | G | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1674+1291C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1936553 | ||||||
| chr4:1936593
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0002g0019others(1): Show | 4 | HG02922.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674+1331G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1936593 | ||||||
| chr4:1936667
|
C | CA | 6 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0122others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1674+1427dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1936667 | |||||
| chr4:1936667
|
CA | C | 12 | a0001c0001t0003g0086a0001c0001t0003g0096a0001c0001t0006g0014others(9): Show | 12 | HG01975.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1674+1427delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1936667 | |||||
| chr4:1936747
|
A | G | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1674+1485A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1936747 | ||||||
| chr4:1936815
|
G | C | 1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1674+1553G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1936815 | ||||||
| chr4:1936925
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1675-1526G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1936925 | ||||||
| chr4:1937055
|
A | AT | 4 | a0001c0001t0001g0082a0001c0001t0010g0090a0001c0002t0005g0001others(1): Show | 4 | HG00741.hp1 HG03098.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675-1382dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1937055 | |||||
| chr4:1937096
|
G | A | 1 | a0001c0001t0010g0090 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1675-1355G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937096 | ||||||
| chr4:1937228
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1675-1223A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937228 | ||||||
| chr4:1937373
|
C | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1675-1078C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937373 | ||||||
| chr4:1937453
|
C | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(2): Show | 5 | HG01167.hp2 HG02723.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675-998C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937453 | ||||||
| chr4:1937529
|
A | G | 2 | a0001c0001t0001g0056a0001c0009t0001g0097 | 2 | HG02630.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1675-922A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937529 | ||||||
| chr4:1937548
|
GTGTCT | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1675-897_1675-893d others(7): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1937548 | |||||
| chr4:1937555
|
G | A | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1675-896G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937555 | ||||||
| chr4:1937639
|
A | G | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1675-812A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937639 | ||||||
| chr4:1937797
|
A | G | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1675-654A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1937797 | ||||||
| chr4:1938401
|
CT | C | 8 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(5): Show | 8 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1675-40delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1938401 | |||||
| chr4:1938416
|
C | CT | 20 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0034others(17): Show | 20 | HG00609.hp1 HG01433.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.1675-10dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1938416 | |||||
| chr4:1938416
|
CT | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0002g0078others(3): Show | 6 | HG00140.hp2 HG01496.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675-10delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 1938416 | |||||
| chr4:1938441
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1675-10T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 7/21 | chr4 | 1938441 | ||||||
| chr4:1938636
|
G | A | 1 | a0001c0001t0004g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1756+104G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 8/21 | chr4 | 1938636 | ||||||
| chr4:1939013
|
A | G | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1756+481A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 8/21 | chr4 | 1939013 | ||||||
| chr4:1939036
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0093 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1756+504A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 8/21 | chr4 | 1939036 | ||||||
| chr4:1939165
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1757-489G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 8/21 | chr4 | 1939165 | ||||||
| chr4:1939201
|
T | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1757-453T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 8/21 | chr4 | 1939201 | ||||||
| chr4:1939335
|
T | G | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1757-319T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 8/21 | chr4 | 1939335 | ||||||
| chr4:1940258
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1881+480C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1940258 | ||||||
| chr4:1940268
|
A | G | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1881+490A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1940268 | ||||||
| chr4:1940495
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1881+717G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1940495 | ||||||
| chr4:1940798
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1881+1020T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1940798 | ||||||
| chr4:1941444
|
G | A | 3 | a0001c0001t0018g0020a0001c0002t0019g0029a0001c0002t0021g0035 | 3 | HG02257.hp1 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1881+1666G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1941444 | ||||||
| chr4:1941503
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1881+1725C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1941503 | ||||||
| chr4:1941912
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1881+2134A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1941912 | ||||||
| chr4:1941951
|
A | G | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1881+2173A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1941951 | ||||||
| chr4:1942096
|
A | G | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1881+2318A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1942096 | ||||||
| chr4:1942322
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0008 | 2 | HG00609.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.1881+2544G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1942322 | ||||||
| chr4:1943185
|
A | G | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1881+3407A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1943185 | ||||||
| chr4:1943316
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1881+3538A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1943316 | ||||||
| chr4:1943726
|
C | CA | 4 | a0001c0001t0001g0092a0001c0001t0006g0014a0001c0001t0006g0015others(1): Show | 4 | HG01975.hp2 HG02615.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1881+3957dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr4 | 1943726 | |||||
| chr4:1944241
|
G | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1881+4463G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1944241 | ||||||
| chr4:1944397
|
T | C | 10 | a0001c0001t0002g0079a0001c0001t0007g0123a0001c0001t0012g0011others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1881+4619T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1944397 | ||||||
| chr4:1944573
|
A | G | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1881+4795A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1944573 | ||||||
| chr4:1944589
|
C | G | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1881+4811C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1944589 | ||||||
| chr4:1944597
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1881+4819A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1944597 | ||||||
| chr4:1944751
|
G | A | 1 | a0001c0001t0009g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1881+4973G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1944751 | ||||||
| chr4:1945233
|
G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0067 | 2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1881+5455G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1945233 | ||||||
| chr4:1945389
|
GGT | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1881+5620_1881+562 others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr4 | 1945389 | |||||
| chr4:1945421
|
C | G | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1881+5643C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1945421 | ||||||
| chr4:1945597
|
G | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0041others(5): Show | 8 | HG00140.hp1 HG00609.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1882-5475G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1945597 | ||||||
| chr4:1945608
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1882-5464G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1945608 | ||||||
| chr4:1945731
|
C | T | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1882-5341C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1945731 | ||||||
| chr4:1946074
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1882-4998A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1946074 | ||||||
| chr4:1946096
|
A | C | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1882-4976A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1946096 | ||||||
| chr4:1946143
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1882-4929T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1946143 | ||||||
| chr4:1946392
|
C | T | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1882-4680C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1946392 | ||||||
| chr4:1946639
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1882-4433G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1946639 | ||||||
| chr4:1946699
|
A | T | 1 | a0001c0001t0001g0027 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1882-4373A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1946699 | ||||||
| chr4:1947087
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1882-3985T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1947087 | ||||||
| chr4:1947844
|
T | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(6): Show | 9 | HG01167.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1882-3228T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1947844 | ||||||
| chr4:1948064
|
G | A | 11 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(8): Show | 11 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1882-3008G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1948064 | ||||||
| chr4:1948088
|
G | A | 1 | a0001c0001t0013g0073 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1882-2984G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1948088 | ||||||
| chr4:1948315
|
G | A | 3 | a0001c0001t0018g0020a0001c0002t0019g0029a0001c0002t0021g0035 | 3 | HG02257.hp1 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1882-2757G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1948315 | ||||||
| chr4:1949145
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1882-1927C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1949145 | ||||||
| chr4:1949235
|
T | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0117a0001c0001t0003g0030others(15): Show | 18 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1882-1837T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1949235 | ||||||
| chr4:1949402
|
AGAG | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1882-1669_1882-166 others(7): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1949402 | ||||||
| chr4:1949619
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1882-1453C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1949619 | ||||||
| chr4:1950574
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1882-498A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1950574 | ||||||
| chr4:1950586
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1882-486C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 9/21 | chr4 | 1950586 | ||||||
| chr4:1951261
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2013+58C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951261 | ||||||
| chr4:1951319
|
C | T | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2013+116C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951319 | ||||||
| chr4:1951443
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2013+312_2013+321d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TAC | T | 2 | a0001c0001t0001g0003a0001c0004t0001g0036 | 2 | HG00609.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2013+320_2013+321d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACAC | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0056others(1): Show | 4 | HG01928.hp2 HG02293.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+318_2013+321d others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACAC | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0085a0001c0001t0001g0120others(2): Show | 5 | HG01167.hp1 HG03098.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013+316_2013+321d others(8): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(1): Show |
T | 6 | a0001c0001t0001g0052a0001c0001t0001g0065a0001c0001t0001g0129others(3): Show | 6 | HG02257.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2013+314_2013+321d others(10): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(3): Show |
T | 3 | a0001c0001t0001g0101a0001c0001t0005g0130a0004c0008t0001g0023 | 3 | HG02723.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2013+312_2013+321d others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(5): Show |
T | 15 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(12): Show | 15 | HG00280.hp2 HG01934.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.2013+310_2013+321d others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(7): Show |
T | 8 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0069others(5): Show | 8 | HG01993.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2013+308_2013+321d others(16): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(9): Show |
T | 6 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0084others(3): Show | 6 | HG01496.hp1 HG03209.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.2013+306_2013+321d others(18): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(11): Show |
T | 5 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0116others(2): Show | 5 | HG00140.hp2 HG01952.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.2013+304_2013+321d others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(13): Show |
T | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0057others(6): Show | 9 | HG00609.hp1 HG01106.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2013+302_2013+321d others(22): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(15): Show |
T | 3 | a0001c0001t0001g0062a0001c0001t0001g0112a0001c0005t0001g0072 | 3 | HG01517.hp1 HG02300.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2013+300_2013+321d others(24): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(17): Show |
T | 7 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0063others(4): Show | 7 | HG00140.hp1 HG01361.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2013+298_2013+321d others(26): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(19): Show |
T | 3 | a0001c0001t0001g0037a0001c0001t0001g0075a0001c0001t0001g0082 | 3 | HG00280.hp1 HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2013+296_2013+321d others(28): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(21): Show |
T | 5 | a0001c0001t0001g0066a0001c0001t0002g0078a0001c0001t0004g0058others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013+294_2013+321d others(30): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(23): Show |
T | 4 | a0001c0001t0002g0108a0001c0001t0008g0106a0001c0002t0019g0029others(1): Show | 4 | HG02723.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+292_2013+321d others(32): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(25): Show |
T | 8 | a0001c0001t0001g0068a0001c0001t0001g0104a0001c0001t0001g0107others(5): Show | 8 | HG00741.hp2 HG01167.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2013+290_2013+321d others(34): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(27): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0003g0030 | 3 | HG03516.hp1 HG03579.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2013+288_2013+321d others(36): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(29): Show |
T | 3 | a0001c0001t0001g0050a0001c0001t0012g0011a0001c0002t0021g0035 | 3 | HG02257.hp1 HG02809.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2013+286_2013+321d others(38): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(31): Show |
T | 2 | a0001c0001t0001g0046a0001c0001t0011g0051 | 2 | HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.2013+284_2013+321d others(40): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951443
|
TACACACA others(33): Show |
T | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2013+282_2013+321d others(42): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951443 | |||||
| chr4:1951444
|
A | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 16 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2013+241A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951444 | ||||||
| chr4:1951446
|
A | C | 2 | a0001c0001t0001g0003a0001c0004t0001g0036 | 2 | HG00609.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2013+243A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951446 | ||||||
| chr4:1951448
|
A | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0056others(1): Show | 4 | HG01928.hp2 HG02293.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+245A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951448 | ||||||
| chr4:1951450
|
A | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0085a0001c0001t0001g0120others(1): Show | 4 | HG01167.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2013+247A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951450 | ||||||
| chr4:1951452
|
A | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0129a0001c0001t0006g0015 | 3 | HG02809.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2013+249A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951452 | ||||||
| chr4:1951454
|
A | C | 1 | a0004c0008t0001g0023 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2013+251A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951454 | ||||||
| chr4:1951456
|
A | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0012others(12): Show | 15 | HG00280.hp2 HG01934.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.2013+253A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951456 | ||||||
| chr4:1951458
|
A | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0069a0001c0001t0001g0071others(3): Show | 6 | HG01993.hp1 HG02109.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2013+255A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951458 | ||||||
| chr4:1951460
|
A | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0067a0001c0001t0001g0084others(2): Show | 5 | HG01496.hp1 HG04184.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013+257A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951460 | ||||||
| chr4:1951462
|
A | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0081a0001c0001t0001g0116others(2): Show | 5 | HG00140.hp2 HG01952.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.2013+259A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951462 | ||||||
| chr4:1951464
|
A | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0057others(6): Show | 9 | HG00609.hp1 HG01106.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.2013+261A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951464 | ||||||
| chr4:1951466
|
A | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0112a0001c0005t0001g0072 | 3 | HG01517.hp1 HG02300.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2013+263A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951466 | ||||||
| chr4:1951468
|
A | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0063others(4): Show | 7 | HG00140.hp1 HG01361.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2013+265A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951468 | ||||||
| chr4:1951470
|
A | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0075a0001c0001t0001g0082 | 3 | HG00280.hp1 HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2013+267A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951470 | ||||||
| chr4:1951472
|
A | C | 5 | a0001c0001t0001g0066a0001c0001t0002g0078a0001c0001t0004g0058others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013+269A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951472 | ||||||
| chr4:1951474
|
A | C | 4 | a0001c0001t0002g0108a0001c0001t0008g0106a0001c0002t0019g0029others(1): Show | 4 | HG02723.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2013+271A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951474 | ||||||
| chr4:1951476
|
A | C | 8 | a0001c0001t0001g0068a0001c0001t0001g0104a0001c0001t0001g0107others(5): Show | 8 | HG00741.hp2 HG01167.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2013+273A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951476 | ||||||
| chr4:1951478
|
A | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0003g0030 | 3 | HG03516.hp1 HG03579.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.2013+275A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951478 | ||||||
| chr4:1951480
|
A | C | 3 | a0001c0001t0001g0050a0001c0001t0012g0011a0001c0002t0021g0035 | 3 | HG02257.hp1 HG02809.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2013+277A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951480 | ||||||
| chr4:1951482
|
A | C | 2 | a0001c0001t0001g0046a0001c0001t0011g0051 | 2 | HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.2013+279A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951482 | ||||||
| chr4:1951484
|
A | C | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2013+281A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951484 | ||||||
| chr4:1951494
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2013+291A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951494 | ||||||
| chr4:1951497
|
CACACACA others(20): Show |
C | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2013+296_2013+322d others(29): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951497 | |||||
| chr4:1951503
|
CACACACA others(14): Show |
C | 3 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0122 | 3 | HG00738.hp1 HG00738.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2013+302_2013+322d others(23): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951503 | |||||
| chr4:1951505
|
CACACACA others(12): Show |
C | 2 | a0001c0001t0001g0033a0001c0001t0001g0060 | 2 | HG03453.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2013+304_2013+322d others(21): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951505 | |||||
| chr4:1951505
|
CACACACA others(13): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2013+304_2013+323d others(22): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951505 | |||||
| chr4:1951507
|
CACACACA others(11): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2013+306_2013+323d others(20): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951507 | |||||
| chr4:1951511
|
CACACACA others(6): Show |
C | 1 | a0001c0001t0001g0049 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2013+310_2013+322d others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951511 | |||||
| chr4:1951513
|
CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2013+312_2013+322d others(13): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951513 | |||||
| chr4:1951519
|
CACACA | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0083 | 2 | HG01975.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2013+318_2013+322d others(7): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 1951519 | |||||
| chr4:1951524
|
A | AC | 2 | a0001c0001t0001g0089a0001c0001t0001g0092 | 2 | HG02615.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2013+321_2013+322i others(3): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951524 | ||||||
| chr4:1951769
|
G | A | 1 | a0001c0001t0017g0103 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2014-339G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951769 | ||||||
| chr4:1951830
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2014-278A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951830 | ||||||
| chr4:1951882
|
T | C | 1 | a0001c0001t0002g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2014-226T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 10/21 | chr4 | 1951882 | ||||||
| chr4:1953217
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0026others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2138-107C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 11/21 | chr4 | 1953217 | ||||||
| chr4:1953218
|
A | G | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.2138-106A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 11/21 | chr4 | 1953218 | ||||||
| chr4:1953289
|
C | T | 8 | a0001c0001t0001g0088a0001c0001t0012g0011a0001c0001t0018g0020others(5): Show | 8 | HG02257.hp1 HG02293.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2138-35C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 11/21 | chr4 | 1953289 | ||||||
| chr4:1953561
|
G | C | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2338+37G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 12/21 | chr4 | 1953561 | ||||||
| chr4:1954107
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2338+583C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 12/21 | chr4 | 1954107 | ||||||
| chr4:1954115
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2338+591G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 12/21 | chr4 | 1954115 | ||||||
| chr4:1954185
|
A | T | 4 | a0001c0001t0012g0011a0001c0002t0005g0001a0001c0002t0015g0002others(1): Show | 4 | HG02809.hp2 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338+661A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 12/21 | chr4 | 1954185 | ||||||
| chr4:1954863
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2339-298A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 12/21 | chr4 | 1954863 | ||||||
| chr4:1955423
|
C | T | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2518+83C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 13/21 | chr4 | 1955423 | ||||||
| chr4:1955556
|
G | A | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2519-137G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 13/21 | chr4 | 1955556 | ||||||
| chr4:1956205
|
A | G | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2881+17A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1956205 | ||||||
| chr4:1956444
|
A | G | 106 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.2881+256A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1956444 | ||||||
| chr4:1956614
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2881+426C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1956614 | ||||||
| chr4:1956840
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0099 | 2 | HG01934.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2881+652C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1956840 | ||||||
| chr4:1956923
|
G | A | 1 | a0001c0001t0007g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2881+735G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1956923 | ||||||
| chr4:1956956
|
TAA | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0110 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2881+770_2881+771d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr4 | 1956956 | |||||
| chr4:1957051
|
A | G | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2881+863A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957051 | ||||||
| chr4:1957182
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2882-751G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957182 | ||||||
| chr4:1957288
|
G | T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2882-645G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957288 | ||||||
| chr4:1957294
|
T | G | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2882-639T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957294 | ||||||
| chr4:1957375
|
CTG | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0070others(1): Show | 4 | HG02896.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2882-557_2882-556d others(4): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957375 | ||||||
| chr4:1957378
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0070others(1): Show | 4 | HG02896.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2882-555G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957378 | ||||||
| chr4:1957379
|
G | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0070others(1): Show | 4 | HG02896.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2882-554G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957379 | ||||||
| chr4:1957380
|
T | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0070others(1): Show | 4 | HG02896.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2882-553T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957380 | ||||||
| chr4:1957407
|
C | T | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(2): Show | 5 | HG01167.hp2 HG02723.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.2882-526C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957407 | ||||||
| chr4:1957450
|
A | AT | 6 | a0001c0001t0001g0053a0001c0001t0018g0020a0001c0002t0005g0001others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2882-466dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr4 | 1957450 | |||||
| chr4:1957738
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2882-195C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957738 | ||||||
| chr4:1957810
|
T | A | 6 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0091others(3): Show | 6 | HG02922.hp1 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2882-123T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957810 | ||||||
| chr4:1957828
|
T | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(10): Show | 13 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2882-105T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957828 | ||||||
| chr4:1957891
|
G | T | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2882-42G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 15/21 | chr4 | 1957891 | ||||||
| chr4:1958124
|
G | C | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2985+88G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958124 | ||||||
| chr4:1958165
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2985+129A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958165 | ||||||
| chr4:1958232
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2985+196G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958232 | ||||||
| chr4:1958444
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(2): Show | 5 | HG01167.hp2 HG02723.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.2985+408G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958444 | ||||||
| chr4:1958872
|
C | T | 1 | a0001c0002t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2986-599C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958872 | ||||||
| chr4:1958873
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0041others(3): Show | 6 | HG00140.hp1 HG00609.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.2986-598C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958873 | ||||||
| chr4:1958946
|
G | T | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2986-525G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1958946 | ||||||
| chr4:1959008
|
A | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2986-463A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1959008 | ||||||
| chr4:1959248
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0084 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2986-223G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1959248 | ||||||
| chr4:1959410
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2986-61G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 16/21 | chr4 | 1959410 | ||||||
| chr4:1959759
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3255+19T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1959759 | ||||||
| chr4:1959860
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3255+120T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1959860 | ||||||
| chr4:1959930
|
A | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3255+190A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1959930 | ||||||
| chr4:1959994
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3255+254G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1959994 | ||||||
| chr4:1960271
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3255+531G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960271 | ||||||
| chr4:1960296
|
A | T | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3255+556A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960296 | ||||||
| chr4:1960362
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3255+622G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960362 | ||||||
| chr4:1960541
|
C | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3256-494C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960541 | ||||||
| chr4:1960641
|
G | A | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3256-394G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960641 | ||||||
| chr4:1960807
|
A | G | 15 | a0001c0001t0001g0100a0001c0001t0005g0130a0001c0001t0006g0014others(12): Show | 15 | HG01975.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3256-228A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960807 | ||||||
| chr4:1960875
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3256-160C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960875 | ||||||
| chr4:1960908
|
C | T | 10 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0052others(7): Show | 10 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.3256-127C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960908 | ||||||
| chr4:1960915
|
C | T | 1 | a0001c0001t0012g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3256-120C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960915 | ||||||
| chr4:1960994
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3256-41C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 17/21 | chr4 | 1960994 | ||||||
| chr4:1961175
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3372+24C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1961175 | ||||||
| chr4:1961370
|
C | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.3372+219C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1961370 | ||||||
| chr4:1961514
|
T | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3372+363T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1961514 | ||||||
| chr4:1961861
|
C | T | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3372+710C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1961861 | ||||||
| chr4:1962001
|
A | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3372+850A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1962001 | ||||||
| chr4:1962018
|
C | T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3372+867C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1962018 | ||||||
| chr4:1962167
|
A | G | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3372+1016A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1962167 | ||||||
| chr4:1962222
|
CGTGGGGC others(21): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3372+1075_3372+110 others(32): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1962222 | |||||
| chr4:1962274
|
C | G | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3372+1123C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1962274 | ||||||
| chr4:1962807
|
A | C | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3372+1656A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1962807 | ||||||
| chr4:1962928
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3372+1777C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1962928 | ||||||
| chr4:1963203
|
A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3372+2052A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1963203 | ||||||
| chr4:1963250
|
A | C | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3372+2099A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1963250 | ||||||
| chr4:1963945
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3372+2794C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1963945 | ||||||
| chr4:1964068
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3372+2917G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1964068 | ||||||
| chr4:1964460
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3372+3309G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1964460 | ||||||
| chr4:1964463
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3372+3312A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1964463 | ||||||
| chr4:1964502
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3372+3351C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1964502 | ||||||
| chr4:1964507
|
C | T | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3372+3356C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1964507 | ||||||
| chr4:1964627
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0008g0106 | 2 | NA18949.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3372+3476G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1964627 | ||||||
| chr4:1965051
|
C | CA | 60 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(57): Show | 60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.3372+3924dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1965051 | |||||
| chr4:1965051
|
C | CAA | 5 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0050others(2): Show | 5 | HG01928.hp1 HG01928.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.3372+3923_3372+392 others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1965051 | |||||
| chr4:1965051
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3372+3915_3372+392 others(14): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1965051 | |||||
| chr4:1965051
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0012g0011a0001c0002t0005g0001a0001c0002t0015g0002others(2): Show | 5 | HG02257.hp1 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3372+3914_3372+392 others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1965051 | |||||
| chr4:1965989
|
T | G | 11 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(8): Show | 11 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3372+4838T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1965989 | ||||||
| chr4:1966046
|
A | ATGTATTC others(4): Show |
26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3372+4897_3372+489 others(15): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1966046 | |||||
| chr4:1966371
|
A | ACGTACAT others(1): Show |
115 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.3372+5220_3372+522 others(12): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1966371 | ||||||
| chr4:1966404
|
T | C | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3372+5253T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1966404 | ||||||
| chr4:1966589
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3372+5438G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1966589 | ||||||
| chr4:1966638
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3372+5487C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1966638 | ||||||
| chr4:1966656
|
C | CA | 5 | a0001c0001t0001g0037a0001c0001t0001g0107a0001c0001t0006g0014others(2): Show | 5 | HG00280.hp1 HG01975.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.3372+5522dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1966656 | |||||
| chr4:1966725
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3372+5574T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1966725 | ||||||
| chr4:1966872
|
G | A | 1 | a0001c0001t0005g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3372+5721G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1966872 | ||||||
| chr4:1967305
|
C | G | 7 | a0001c0001t0012g0011a0001c0001t0018g0020a0001c0002t0005g0001others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3372+6154C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967305 | ||||||
| chr4:1967307
|
C | T | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3372+6156C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967307 | ||||||
| chr4:1967433
|
C | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3372+6282C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967433 | ||||||
| chr4:1967446
|
C | T | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3372+6295C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967446 | ||||||
| chr4:1967583
|
A | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3372+6432A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967583 | ||||||
| chr4:1967723
|
G | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3372+6572G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967723 | ||||||
| chr4:1967766
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3372+6615C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967766 | ||||||
| chr4:1967920
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3372+6769G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1967920 | ||||||
| chr4:1968154
|
T | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0052others(8): Show | 11 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.3373-6709T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1968154 | ||||||
| chr4:1968220
|
T | G | 3 | a0001c0001t0002g0042a0001c0002t0002g0038a0001c0002t0003g0045 | 3 | HG02922.hp2 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3373-6643T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1968220 | ||||||
| chr4:1968264
|
G | C | 1 | a0001c0002t0019g0029 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3373-6599G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1968264 | ||||||
| chr4:1968614
|
A | C | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3373-6249A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1968614 | ||||||
| chr4:1968733
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3373-6130C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1968733 | ||||||
| chr4:1968787
|
A | C | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3373-6076A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1968787 | ||||||
| chr4:1969090
|
G | A | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3373-5773G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1969090 | ||||||
| chr4:1969541
|
TA | T | 14 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0109others(11): Show | 14 | HG01167.hp2 HG01975.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.3373-5305delA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1969541 | |||||
| chr4:1969541
|
TAA | T | 11 | a0001c0001t0005g0130a0001c0001t0007g0123a0001c0001t0012g0011others(8): Show | 11 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3373-5306_3373-530 others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1969541 | |||||
| chr4:1969642
|
GGC | G | 5 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(2): Show | 5 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.3373-5216_3373-521 others(6): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1969642 | |||||
| chr4:1969958
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3373-4905A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1969958 | ||||||
| chr4:1970120
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3373-4743C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1970120 | ||||||
| chr4:1970304
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3373-4559G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1970304 | ||||||
| chr4:1970842
|
C | T | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3373-4021C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1970842 | ||||||
| chr4:1971073
|
G | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0033others(3): Show | 6 | HG01517.hp2 HG01934.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.3373-3790G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971073 | ||||||
| chr4:1971230
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3373-3633G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971230 | ||||||
| chr4:1971235
|
C | T | 2 | a0001c0001t0001g0046a0002c0010t0016g0105 | 2 | HG01928.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3373-3628C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971235 | ||||||
| chr4:1971357
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0071a0001c0001t0010g0090 | 3 | NA18945.hp2 NA19000.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.3373-3506C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971357 | ||||||
| chr4:1971570
|
G | A | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3373-3293G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971570 | ||||||
| chr4:1971618
|
G | A | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3373-3245G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971618 | ||||||
| chr4:1971626
|
C | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3373-3237C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971626 | ||||||
| chr4:1971706
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3373-3157G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971706 | ||||||
| chr4:1971899
|
G | C | 1 | a0001c0001t0020g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3373-2964G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971899 | ||||||
| chr4:1971979
|
A | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0125 | 2 | HG01496.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.3373-2884A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1971979 | ||||||
| chr4:1972007
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3373-2856C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972007 | ||||||
| chr4:1972355
|
G | A | 1 | a0001c0001t0008g0106 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3373-2508G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972355 | ||||||
| chr4:1972405
|
C | T | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3373-2458C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972405 | ||||||
| chr4:1972818
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0026others(2): Show | 5 | HG02280.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.3373-2045T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972818 | ||||||
| chr4:1972818
|
T | G | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-2045T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972818 | ||||||
| chr4:1972851
|
C | T | 1 | a0001c0002t0021g0035 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3373-2012C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972851 | ||||||
| chr4:1972933
|
C | G | 14 | a0001c0001t0005g0130a0001c0001t0006g0014a0001c0001t0006g0015others(11): Show | 14 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3373-1930C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1972933 | ||||||
| chr4:1973027
|
T | C | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3373-1836T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973027 | ||||||
| chr4:1973357
|
G | A | 1 | a0001c0002t0015g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3373-1506G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973357 | ||||||
| chr4:1973592
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3373-1271A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973592 | ||||||
| chr4:1973599
|
G | A | 1 | a0001c0001t0005g0080 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3373-1264G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973599 | ||||||
| chr4:1973638
|
C | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3373-1225C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973638 | ||||||
| chr4:1973702
|
T | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3373-1161T>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973702 | ||||||
| chr4:1973791
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3373-1072C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973791 | ||||||
| chr4:1973796
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3373-1067T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973796 | ||||||
| chr4:1973803
|
T | C | 2 | a0001c0001t0005g0130a0001c0001t0020g0021 | 2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3373-1060T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973803 | ||||||
| chr4:1973873
|
G | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0117a0001c0001t0003g0030others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3373-990G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973873 | ||||||
| chr4:1973902
|
A | G | 26 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0107others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3373-961A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973902 | ||||||
| chr4:1973926
|
T | A | 2 | a0001c0001t0003g0086a0001c0001t0003g0096 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3373-937T>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1973926 | ||||||
| chr4:1974038
|
C | T | 2 | a0001c0002t0005g0001a0001c0002t0015g0002 | 2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3373-825C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1974038 | ||||||
| chr4:1974156
|
G | A | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3373-707G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1974156 | ||||||
| chr4:1974215
|
C | CT | 5 | a0001c0001t0001g0022a0001c0001t0001g0057a0001c0001t0001g0117others(2): Show | 5 | HG01517.hp2 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3373-636dupT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1974215 | |||||
| chr4:1974215
|
CT | C | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-636delT | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr4 | 1974215 | |||||
| chr4:1974384
|
T | TG | 4 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028others(1): Show | 4 | HG01975.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3373-479_3373-478i others(3): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1974384 | ||||||
| chr4:1974502
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0117a0001c0001t0003g0030others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3373-361C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1974502 | ||||||
| chr4:1974803
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3373-60C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 18/21 | chr4 | 1974803 | ||||||
| chr4:1975469
|
C | G | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3621+69C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1975469 | ||||||
| chr4:1975517
|
T | TA | 4 | a0001c0001t0001g0041a0001c0001t0001g0084a0001c0001t0001g0112others(1): Show | 4 | HG01433.hp2 HG01496.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.3621+117_3621+118i others(3): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1975517 | ||||||
| chr4:1975664
|
C | T | 3 | a0001c0001t0007g0044a0001c0001t0018g0020a0001c0002t0019g0029 | 3 | HG02559.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3621+264C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1975664 | ||||||
| chr4:1975878
|
T | C | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3621+478T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1975878 | ||||||
| chr4:1975895
|
A | C | 2 | a0001c0001t0001g0046a0001c0001t0011g0051 | 2 | HG01361.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.3621+495A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1975895 | ||||||
| chr4:1975899
|
C | G | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3621+499C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1975899 | ||||||
| chr4:1976017
|
G | A | 10 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(7): Show | 10 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3622-458G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1976017 | ||||||
| chr4:1976062
|
C | G | 2 | a0001c0001t0018g0020a0001c0002t0019g0029 | 2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3622-413C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1976062 | ||||||
| chr4:1976249
|
C | T | 1 | a0002c0010t0016g0105 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3622-226C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1976249 | ||||||
| chr4:1976292
|
C | T | 1 | a0001c0004t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3622-183C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 20/21 | chr4 | 1976292 | ||||||
| chr4:1976795
|
G | A | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0001c0001t0006g0028 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3826+116G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1976795 | ||||||
| chr4:1977051
|
T | C | 26 | a0001c0001t0001g0104a0001c0001t0001g0107a0001c0001t0001g0109others(23): Show | 26 | HG01167.hp2 HG01975.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3826+372T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977051 | ||||||
| chr4:1977182
|
C | T | 11 | a0001c0001t0001g0117a0001c0001t0003g0030a0001c0001t0007g0044others(8): Show | 11 | HG02257.hp1 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3826+503C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977182 | ||||||
| chr4:1977183
|
G | A | 1 | a0001c0001t0014g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3826+504G>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977183 | ||||||
| chr4:1977183
|
G | T | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3826+504G>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977183 | ||||||
| chr4:1977189
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3826+510C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977189 | ||||||
| chr4:1977449
|
A | G | 1 | a0001c0009t0001g0097 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3826+770A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977449 | ||||||
| chr4:1977584
|
T | C | 9 | a0001c0001t0007g0044a0001c0001t0012g0011a0001c0001t0018g0020others(6): Show | 9 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3826+905T>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977584 | ||||||
| chr4:1977707
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3827-931C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977707 | ||||||
| chr4:1977785
|
C | G | 1 | a0001c0001t0011g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3827-853C>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977785 | ||||||
| chr4:1977790
|
C | CA | 8 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0002g0108others(5): Show | 8 | HG01167.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3827-834dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 1977790 | |||||
| chr4:1977790
|
C | CAAA | 7 | a0001c0001t0007g0044a0001c0001t0012g0011a0001c0001t0018g0020others(4): Show | 7 | HG02257.hp1 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3827-836_3827-834d others(5): Show |
NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 1977790 | |||||
| chr4:1977797
|
A | G | 1 | a0001c0001t0007g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3827-841A>G | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977797 | ||||||
| chr4:1977805
|
C | A | 3 | a0001c0001t0003g0086a0001c0001t0003g0096a0002c0010t0016g0105 | 3 | HG02559.hp1 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3827-833C>A | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977805 | ||||||
| chr4:1977851
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3827-787C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977851 | ||||||
| chr4:1977853
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3827-785C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1977853 | ||||||
| chr4:1978058
|
C | T | 1 | a0001c0001t0011g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3827-580C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1978058 | ||||||
| chr4:1978126
|
C | CA | 10 | a0001c0001t0007g0044a0001c0001t0012g0011a0001c0001t0018g0020others(7): Show | 10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.3827-502dupA | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 1978126 | |||||
| chr4:1978233
|
G | C | 16 | a0001c0001t0001g0069a0001c0001t0005g0130a0001c0001t0006g0014others(13): Show | 16 | HG01975.hp2 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.3827-405G>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1978233 | ||||||
| chr4:1978349
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3827-289C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1978349 | ||||||
| chr4:1978425
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3827-213C>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1978425 | ||||||
| chr4:1978619
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3827-19A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1978619 |