Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MEFSI others(1360): Show |
chr4 | 1866393 | 1987192 |
| a0002 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | MEFSI others(1360): Show |
chr4 | 1866393 | 1987192 |
| a0003 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | MEFSI others(1360): Show |
chr4 | 1866393 | 1987192 |
| a0004 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | MEFSI others(1360): Show |
chr4 | 1866393 | 1987192 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4095 | 115 | 49 | 30 | 20 | 7 | 7 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0001c0002 | 0/0 | 4095 | 7 | 7 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0001c0003 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0001c0004 | 0/0 | 4095 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0001c0005 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0001c0006 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0001c0009 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0002c0007 | 0/0 | 4095 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0003c0010 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
chr4 | 1866393 | 1987192 | ||
| a0004c0008 | 0/0 | 4095 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | ATGGA others(4090): Show |
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 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0002 | 0/0 | 7560 | 7 | 5 | 1 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0003 | 0/0 | 7560 | 3 | 3 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0004 | 0/0 | 7560 | 3 | 2 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0005 | 0/0 | 7556 | 2 | 2 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7551): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0006 | 0/0 | 7566 | 3 | 2 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7561): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0007 | 0/0 | 7560 | 2 | 2 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0008 | 0/0 | 7560 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0009 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0010 | 0/0 | 7560 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0011 | 0/0 | 7560 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0012 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7551): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0013 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0014 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0017 | 0/0 | 7560 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0018 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0001t0020 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0002 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0003 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0005 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7551): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0015 | 0/0 | 7556 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7551): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0019 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0002t0021 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0003t0022 | 0/0 | 7566 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7561): Show |
chr4 | 1866393 | 1987192 |
| a0001c0004t0001 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0005t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0006t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0001c0009t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0002c0007t0001 | 0/0 | 7560 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0003c0010t0016 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| a0004c0008t0001 | 0/0 | 7560 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | GGCGC others(7555): Show |
chr4 | 1866393 | 1987192 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0051 | 1/0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0054 | 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 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0001g0126 | 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 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0002g0116 | 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 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0005g0035 | 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 |
| a0001c0001t0006g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0009g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0011g0076 | 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 |
| a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0014g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0017g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0018g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0001t0020g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0015g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0019g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0002t0021g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0003t0022g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0001c0009t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0002c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0003c0010t0016g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| a0004c0008t0001g0091 | 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 | g0109 | EUR | GBR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00140 | hp2 | a0002 | c0007 | t0001 | g0125 | EUR | GBR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0067 | 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 | g0006 | EAS | CHS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG00741 | hp2 | a0001 | c0001 | t0017 | g0053 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01361 | hp2 | a0001 | c0001 | t0011 | g0076 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0075 | 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 | g0064 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | IBS | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02257 | hp1 | a0001 | c0002 | t0021 | g0017 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02630 | hp1 | a0001 | c0006 | t0001 | g0058 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02723 | hp2 | a0004 | c0008 | t0001 | g0091 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0039 | 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 | g0040 | 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 | g0122 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02896 | hp1 | a0001 | c0009 | t0001 | g0041 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0023 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03098 | hp2 | a0001 | c0002 | t0015 | g0001 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03139 | hp1 | a0001 | c0003 | t0022 | g0020 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03195 | hp2 | a0001 | c0002 | t0019 | g0019 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0087 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03239 | hp2 | a0001 | c0001 | t0009 | g0123 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0102 | SAS | PJL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG04184 | hp1 | a0001 | c0001 | t0013 | g0101 | SAS | BEB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0012 | 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 | g0111 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0086 | 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 | g0106 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0114 | 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 | g0117 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0105 | 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 | g0104 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19030 | hp2 | a0001 | c0002 | t0005 | g0002 | 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 | g0112 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | YRI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0029 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02559 | hp1 | a0003 | c0010 | t0016 | g0119 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG02559 | hp2 | a0001 | c0001 | t0018 | g0018 | AFR | ACB | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0120 | REF | REF | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0051 | REF | REF | NSD2_chr4_1866393_1987192 | NSD2 | chr4 | 1866393 | 1987192 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002 | 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 | a0003 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1900870 | C | G | 1 | a0003c0010 | 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 | a0003c0010 | 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 | a0003c0010 | 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 | a0001c0002 a0001c0003 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1871476 | A | ACGGCCC | 2 | a0001c0001t0006 a0001c0003t0022 |
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 | a0001c0001t0018 a0001c0002t0019 a0001c0002t0021 |
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 | a0001c0001t0003 a0001c0002t0003 |
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 | a0001c0001t0002 a0001c0001t0017 a0001c0002t0002 |
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 | a0001c0001t0009 a0001c0001t0017 |
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 | a0001c0002t0019 a0001c0002t0021 a0003c0010t0016 |
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 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0018 others(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 | a0001c0002t0019 a0001c0002t0021 |
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 | a0001c0001t0005 a0001c0001t0012 a0001c0002t0005 others(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 | a0001c0001t0014 a0001c0002t0019 a0001c0002t0021 |
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 | a0001c0001t0005 a0001c0001t0012 a0001c0002t0005 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0001g0126 a0001c0001t0002g0124 a0002c0007t0001g0125 |
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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0127 |
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 | a0001c0001t0001g0122 a0001c0001t0009g0123 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0002g0013 others(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 | a0001c0002t0015g0001 | 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 | a0001c0001t0001g0010 a0001c0002t0005g0002 |
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 | a0001c0003t0022g0020 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0018g0018 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0084 | 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 | a0004c0008t0001g0091 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0092 |
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 | a0001c0002t0021g0017 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0109 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0002c0007t0001g0125 |
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 | a0001c0001t0001g0031 a0001c0001t0001g0073 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0126 a0001c0001t0001g0129 others(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 | a0001c0001t0011g0076 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0071 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0104 | 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 | a0001c0001t0001g0089 | 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 | a0001c0004t0001g0102 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0054 a0001c0009t0001g0041 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0085 others(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 | a0001c0001t0001g0049 a0001c0001t0010g0106 |
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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0080 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0107 | 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 | TGTGTGAG others(1): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0075 a0001c0001t0014g0029 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0043 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0105 |
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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0007 |
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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0118 a0003c0010t0016g0119 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0002g0116 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0017g0053 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0127 a0001c0001t0005g0035 |
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 | a0001c0001t0001g0118 a0003c0010t0016g0119 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0002g0116 others(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 | a0001c0001t0001g0113 | 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0007g0034 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0002t0002g0022 | 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 | a0001c0001t0002g0026 | 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 | a0001c0002t0003g0023 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0028 a0001c0001t0009g0123 |
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 | a0001c0001t0013g0101 a0001c0002t0001g0094 a0001c0005t0001g0087 |
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 | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(56): Show |
59 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(56): 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0006g0015 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0007g0021 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0109 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0008g0114 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0002t0002g0022 | 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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0117 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0003g0056 others(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 | a0001c0001t0001g0028 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0062 a0001c0001t0004g0063 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0003c0010t0016g0119 | 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 | a0001c0003t0022g0020 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0062 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0105 a0001c0001t0001g0107 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0002t0021g0017 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0122 a0001c0001t0017g0053 |
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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0098 a0001c0001t0002g0095 |
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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0127 a0001c0001t0003g0056 |
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 | a0001c0006t0001g0058 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0043 others(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 | a0001c0003t0022g0020 | 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 | a0002c0007t0001g0125 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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(4): Show |
1 | a0001c0001t0001g0007 | 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 | a0001c0001t0001g0057 a0001c0001t0001g0080 |
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 | a0001c0001t0001g0077 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(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 | 11 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(8): Show |
11 | HG00738.hp2 HG01517.hp1 HG01928.hp2 others(8): 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 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0031 a0001c0001t0003g0036 a0001c0001t0003g0037 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0115 a0001c0001t0003g0036 a0001c0001t0005g0130 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0080 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0115 a0001c0001t0005g0130 a0001c0001t0008g0114 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0116 others(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 | a0001c0001t0001g0115 a0001c0001t0005g0130 a0001c0001t0008g0114 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0116 others(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 | a0001c0001t0005g0130 a0001c0003t0022g0020 |
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 | a0001c0001t0001g0005 a0001c0001t0007g0021 a0001c0001t0012g0011 others(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 | a0001c0003t0022g0020 | 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 | a0001c0001t0001g0005 a0001c0001t0007g0021 a0001c0001t0012g0011 |
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 | a0001c0001t0007g0021 | 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 | 16 | a0001c0001t0001g0009 a0001c0001t0001g0062 a0001c0001t0001g0064 others(13): Show |
16 | HG00280.hp2 HG00738.hp2 HG01106.hp2 others(13): 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0005g0130 others(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 | a0001c0001t0001g0055 | 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 | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0003t0022g0020 | 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 | a0001c0002t0021g0017 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0031 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0055 a0001c0001t0001g0081 others(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 | a0001c0001t0018g0018 a0001c0002t0019g0019 a0001c0002t0021g0017 |
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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0003g0036 others(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 | a0001c0001t0001g0027 a0001c0003t0022g0020 |
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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0105 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0108 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0073 a0001c0001t0001g0081 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0004t0001g0102 | 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 | a0001c0001t0007g0034 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0005g0130 a0001c0001t0014g0029 a0001c0001t0020g0111 |
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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0066 | 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 | a0001c0003t0022g0020 | 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 | a0001c0001t0013g0101 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0107 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0007g0021 | 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 | a0001c0002t0015g0001 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0005g0130 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0013g0101 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
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 | a0001c0009t0001g0041 | 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 | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): 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 | a0001c0001t0001g0085 a0001c0001t0004g0030 a0001c0001t0004g0072 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0007g0034 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0085 a0001c0001t0004g0030 a0001c0001t0004g0072 |
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 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(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 | a0001c0001t0014g0029 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0075 others(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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0011g0076 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0015g0001 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0002g0026 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0075 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0100 a0001c0001t0001g0104 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0097 | 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 | 6 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0070 others(3): Show |
6 | HG00280.hp2 HG00738.hp2 HG01433.hp1 others(3): 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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0008g0114 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0002t0021g0017 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0062 a0001c0001t0004g0063 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0115 a0001c0001t0002g0124 others(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 | a0001c0001t0007g0021 a0001c0009t0001g0041 |
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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0071 others(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 | a0001c0001t0018g0018 a0001c0002t0015g0001 a0001c0002t0019g0019 others(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 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0005g0130 others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0068 a0001c0001t0005g0130 a0001c0001t0006g0015 others(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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0028 a0001c0001t0003g0056 a0001c0006t0001g0058 |
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 | a0001c0002t0021g0017 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0013g0101 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0079 others(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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0003c0010t0016g0119 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0004c0008t0001g0091 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0001g0085 a0001c0001t0004g0030 a0001c0001t0004g0072 |
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 | a0001c0001t0001g0068 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0001g0028 a0001c0001t0003g0056 a0001c0006t0001g0058 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0004g0030 | 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 | a0001c0001t0004g0030 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0013g0101 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0009g0123 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0007g0021 | 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 | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): 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 | a0001c0001t0014g0029 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0092 | 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 | 14 | a0001c0001t0001g0009 a0001c0001t0001g0064 a0001c0001t0001g0065 others(11): Show |
14 | HG00280.hp2 HG00738.hp2 HG01361.hp2 others(11): 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 | a0001c0001t0003g0037 | 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 | a0001c0001t0018g0018 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0007g0021 others(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 | a0001c0001t0018g0018 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0018g0018 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0018g0018 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
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 | a0001c0001t0018g0018 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0003t0022g0020 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0048 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0001g0113 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0104 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0002g0013 others(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 | a0001c0001t0001g0115 a0001c0001t0008g0114 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0032 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0059 | 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 | a0001c0002t0002g0022 a0001c0002t0003g0023 |
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 | a0001c0001t0007g0021 a0001c0001t0012g0011 |
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 | a0001c0001t0001g0071 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0061 a0001c0001t0005g0130 a0001c0001t0006g0015 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0090 |
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 | a0001c0001t0001g0092 | 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 | a0001c0001t0002g0112 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0108 a0001c0002t0002g0022 a0001c0002t0003g0023 |
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 | a0001c0001t0018g0018 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0001g0099 | 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 | a0001c0001t0004g0030 a0001c0001t0005g0130 a0001c0001t0018g0018 others(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 | a0001c0004t0001g0102 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0109 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0042 others(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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0061 | 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 | a0001c0003t0022g0020 | 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 | a0001c0001t0017g0053 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0010g0106 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0012g0011 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | 2 | a0001c0001t0001g0077 a0001c0001t0001g0097 |
2 | HG00738.hp1 HG00738.hp2 |
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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0008g0114 others(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 | a0001c0001t0005g0035 a0001c0001t0012g0011 a0001c0001t0018g0018 others(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 | a0001c0001t0001g0078 | 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 | a0001c0002t0019g0019 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0054 a0001c0001t0001g0088 a0001c0001t0001g0099 others(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 | a0001c0001t0001g0010 a0001c0001t0005g0035 a0001c0001t0006g0015 others(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 | a0001c0001t0020g0111 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0003g0056 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0059 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0007g0034 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0096 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0042 a0001c0001t0009g0123 |
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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0126 a0001c0001t0002g0046 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0013g0101 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0100 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0097 others(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 | a0001c0001t0001g0070 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0005g0130 a0001c0001t0007g0021 a0001c0001t0012g0011 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0007g0021 | 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 | a0001c0002t0021g0017 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0081 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0002g0112 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): 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 | a0001c0001t0001g0098 a0001c0001t0001g0118 a0001c0001t0002g0116 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0012g0011 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0005g0130 a0001c0001t0007g0021 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): 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 | a0001c0001t0005g0130 a0001c0002t0005g0002 a0001c0002t0019g0019 |
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 | a0001c0001t0001g0060 | 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 | a0001c0001t0013g0101 | 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 | a0001c0001t0001g0113 a0001c0002t0021g0017 |
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 | a0001c0001t0001g0012 a0001c0001t0007g0021 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0073 a0001c0009t0001g0041 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0075 |
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 | a0001c0003t0022g0020 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0003t0022g0020 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0024 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0015g0001 others(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 | a0001c0001t0001g0078 a0001c0001t0020g0111 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0059 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0026 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0017g0053 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0011g0076 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0062 a0001c0001t0001g0085 a0001c0001t0004g0063 |
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 | a0001c0001t0001g0089 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0026 others(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 | a0001c0002t0021g0017 | 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 | a0001c0003t0022g0020 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0028 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 |
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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0108 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0020g0111 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0071 a0001c0005t0001g0087 a0004c0008t0001g0091 |
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 | a0001c0001t0007g0021 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0008g0114 |
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 | a0001c0001t0009g0123 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0009 a0001c0001t0001g0083 |
2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1556-1397A>C | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 6/21 | chr4 | 1933747 | |||||||
| chr4:1934012 | AGTT | A | 7 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0061 a0001c0001t0005g0130 a0001c0001t0006g0015 others(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 | a0001c0001t0001g0061 a0001c0001t0005g0130 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0006t0001g0058 | 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 | a0001c0001t0012g0011 a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0118 a0001c0001t0002g0116 |
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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0062 others(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 | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0075 others(8): Show |
11 | HG00741.hp1 HG01433.hp1 HG01433.hp2 others(8): 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 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(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 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0098 others(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 | a0001c0001t0006g0110 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0006g0110 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0039 a0001c0001t0001g0128 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0003 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0039 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0014g0029 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0129 a0001c0001t0013g0101 |
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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0085 a0001c0001t0004g0063 |
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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(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 | a0001c0001t0003g0036 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0055 |
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 | a0001c0001t0001g0033 a0001c0002t0001g0094 |
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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0055 others(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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0014g0029 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0002g0013 others(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 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0097 others(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 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0006g0015 others(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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0107 a0001c0001t0010g0106 a0001c0002t0005g0002 others(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 | a0001c0001t0010g0106 | 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 | a0001c0001t0001g0038 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0103 a0001c0009t0001g0041 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0007g0034 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0040 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0002g0095 others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0004g0072 | 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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0009g0123 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0080 | 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 | a0001c0001t0014g0029 | 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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 a0001c0002t0021g0017 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0003c0010t0016g0119 | 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0008 |
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 | a0001c0001t0005g0035 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0001g0049 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0001t0002g0112 a0001c0001t0007g0021 a0001c0001t0012g0011 others(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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0004t0001g0102 | 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 | a0001c0001t0009g0123 | 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 | a0001c0001t0001g0069 a0001c0001t0001g0100 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0014g0029 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0081 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0014g0029 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0052 | 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 | a0001c0004t0001g0102 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0013g0101 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 a0001c0002t0021g0017 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0003g0056 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0057 | 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 | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0060 | 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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0006 a0001c0004t0001g0102 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0081 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0098 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0121 a0001c0001t0005g0130 a0004c0008t0001g0091 |
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 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0069 others(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 | 4 | a0001c0001t0001g0038 a0001c0001t0001g0092 a0001c0001t0010g0106 others(1): Show |
4 | HG00140.hp2 HG01952.hp1 NA18945.hp2 others(1): 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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0005t0001g0087 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0089 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0039 a0001c0001t0002g0095 a0001c0001t0004g0030 others(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 | a0001c0001t0002g0116 a0001c0001t0008g0114 a0001c0002t0019g0019 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0074 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0117 a0001c0001t0003g0056 |
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 | a0001c0001t0001g0079 a0001c0001t0012g0011 a0001c0002t0021g0017 |
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 | a0001c0001t0001g0065 a0001c0001t0011g0076 |
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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0052 others(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 | a0001c0001t0001g0006 a0001c0004t0001g0102 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0081 a0001c0001t0001g0103 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0098 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0006g0016 |
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 | a0004c0008t0001g0091 | 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 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0069 others(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 | 4 | a0001c0001t0001g0038 a0001c0001t0001g0092 a0001c0001t0010g0106 others(1): Show |
4 | HG00140.hp2 HG01952.hp1 NA18945.hp2 others(1): 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 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0061 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0005t0001g0087 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0089 a0001c0001t0001g0107 |
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 | a0001c0001t0001g0039 a0001c0001t0002g0095 a0001c0001t0004g0030 others(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 | a0001c0001t0002g0116 a0001c0001t0008g0114 a0001c0002t0019g0019 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0074 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0117 a0001c0001t0003g0056 |
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 | a0001c0001t0001g0079 a0001c0001t0012g0011 a0001c0002t0021g0017 |
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 | a0001c0001t0001g0065 a0001c0001t0011g0076 |
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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0001c0001t0001g0048 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0077 a0001c0001t0001g0097 |
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 | a0001c0001t0001g0032 a0001c0001t0001g0062 |
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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0096 |
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 | a0001c0001t0001g0049 a0001c0001t0001g0059 |
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 | a0001c0001t0017g0053 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0052 others(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 | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): 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 | a0001c0001t0001g0070 a0001c0001t0012g0011 a0001c0001t0018g0018 others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0012g0011 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0004t0001g0102 | 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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | 105 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0090 |
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 | a0001c0001t0007g0034 | 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 | a0001c0001t0001g0009 a0001c0001t0001g0105 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0001g0117 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0073 others(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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0031 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0001g0074 | 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 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(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 | a0001c0002t0001g0094 | 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 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0081 others(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 | a0001c0001t0014g0029 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0109 |
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 | 61 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
61 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(58): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0080 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0048 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0061 a0001c0001t0005g0130 a0001c0001t0006g0015 others(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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0006 | 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 | 60 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): 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 | a0001c0001t0007g0021 | 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 | a0001c0004t0001g0102 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0003c0010t0016g0119 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0070 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0115 a0001c0001t0008g0114 |
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 | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(56): Show |
59 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(56): 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 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0079 others(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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0012g0011 a0001c0002t0005g0002 a0001c0002t0015g0001 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 |
114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0115 a0001c0001t0006g0015 others(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 | a0001c0001t0001g0004 | 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 | a0001c0001t0012g0011 a0001c0001t0018g0018 a0001c0002t0005g0002 others(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 | a0001c0001t0005g0035 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0020g0111 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0032 others(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 | a0001c0001t0002g0026 a0001c0002t0002g0022 a0001c0002t0003g0023 |
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 | a0001c0002t0019g0019 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0117 others(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 | a0001c0001t0005g0130 a0001c0001t0007g0021 a0001c0001t0012g0011 others(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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0068 others(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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0065 a0003c0010t0016g0119 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0010g0106 |
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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0020g0111 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0020g0111 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0126 |
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 | a0001c0001t0001g0078 | 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 | a0001c0001t0008g0114 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0052 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0002t0021g0017 | 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 | a0001c0001t0005g0130 a0001c0001t0006g0015 a0001c0001t0006g0016 others(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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0002t0015g0001 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0077 | 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 | a0001c0001t0005g0130 a0001c0001t0020g0111 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0003g0056 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0115 others(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 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
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 | a0001c0002t0005g0002 a0001c0002t0015g0001 |
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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0068 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0003g0056 others(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 | a0001c0001t0001g0068 | 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 | a0003c0010t0016g0119 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0108 others(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 | a0001c0001t0007g0034 a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | |||||||
| chr4:1975895 | A | C | 2 | a0001c0001t0001g0065 a0001c0001t0011g0076 |
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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | a0001c0001t0018g0018 a0001c0002t0019g0019 |
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 | a0003c0010t0016g0119 | 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 | a0001c0004t0001g0102 | 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 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0110 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | a0001c0001t0001g0028 a0001c0001t0003g0056 a0001c0001t0007g0034 others(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 | a0001c0001t0014g0029 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0082 | 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 | a0001c0009t0001g0041 | 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 | a0001c0001t0007g0034 a0001c0001t0012g0011 a0001c0001t0018g0018 others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0011g0076 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0118 a0001c0001t0002g0116 others(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 | a0001c0001t0007g0034 a0001c0001t0012g0011 a0001c0001t0018g0018 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0003c0010t0016g0119 |
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 | a0001c0001t0001g0107 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0011g0076 | 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 | a0001c0001t0007g0034 a0001c0001t0012g0011 a0001c0001t0018g0018 others(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 | a0001c0001t0001g0088 a0001c0001t0005g0130 a0001c0001t0006g0015 others(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 | a0001c0001t0001g0096 | 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 | a0001c0001t0001g0082 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3827-19A>T | NSD2 | ENSG00000109685.19 | transcript | ENST00000508803.6 | protein_coding | 21/21 | chr4 | 1978619 |