Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84193 |
| ensemblid | ENSG00000183576.13 |
| hgncid | 20493 |
| symbol | SETD3 |
| name | SET domain containing 3, actin N3(tau)-histidine methyltransferase |
| refseq_nuc | NM_032233.3 |
| refseq_prot | NP_115609.2 |
| ensembl_nuc | ENST00000331768.10 |
| ensembl_prot | ENSP00000327436.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 99397748 |
| end | 99480859 |
| strand | - |
| ver | v1.2 |
| region | chr14:99397748-99480859 |
| region5000 | chr14:99392748-99485859 |
| regionname0 | SETD3_chr14_99397748_99480859 |
| regionname5000 | SETD3_chr14_99392748_99485859 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 594 | 287 | 74 | 46 | 123 | 12 | 30 | 99 | SETD3_chr14_99392748_99485859 | SETD3 | MGKKS others(589): Show |
chr14 | 99392748 | 99485859 |
| a0002 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | MGKKS others(589): Show |
chr14 | 99392748 | 99485859 |
| a0003 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | MGKKS others(589): Show |
chr14 | 99392748 | 99485859 |
| a0004 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | MGKKS others(589): Show |
chr14 | 99392748 | 99485859 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1782 | 268 | 56 | 46 | 122 | 12 | 30 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0001c0002 | 0/0 | 1782 | 10 | 10 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0001c0003 | 0/0 | 1782 | 4 | 4 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0001c0004 | 0/0 | 1782 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0001c0007 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0001c0008 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0001c0010 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0002c0006 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0003c0005 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 | ||
| a0004c0009 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | ATGGG others(1777): Show |
chr14 | 99392748 | 99485859 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2856 | 261 | 54 | 45 | 119 | 12 | 29 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0001t0003 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0001t0004 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0001t0006 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0001t0007 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0001t0008 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0001t0009 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0002t0002 | 0/0 | 2856 | 9 | 9 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0002t0005 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0003t0001 | 0/0 | 2856 | 4 | 4 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0004t0001 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0007t0002 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0008t0001 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0001c0010t0001 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0002c0006t0002 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0003c0005t0010 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| a0004c0009t0001 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | AGGCT others(2851): Show |
chr14 | 99392748 | 99485859 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0001t0009g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0002t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0007t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0008t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0001c0010t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0002c0006t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0003c0005t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| a0004c0009t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00408 | hp1 | a0001 | c0008 | t0001 | g0105 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0139 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0113 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02055 | hp1 | a0001 | c0007 | t0002 | g0145 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CDX | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CDX | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0281 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02630 | hp2 | a0002 | c0006 | t0002 | g0144 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0134 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02970 | hp2 | a0001 | c0010 | t0001 | g0155 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03209 | hp1 | a0003 | c0005 | t0010 | g0283 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0204 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19006 | hp2 | a0004 | c0009 | t0001 | g0047 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0143 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ASW | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0156 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0280 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | USA | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0032 | REF | REF | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0154 | REF | REF | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99398807 | C | A | 1 | a0003 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1657G>T | p.Val553Leu | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 1797/2856 | 1657/1785 | 553/594 | chr14 | 99398807 | |||
| chr14:99399009 | G | T | 1 | a0002 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1455C>A | p.Asn485Lys | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 1595/2856 | 1455/1785 | 485/594 | chr14 | 99399009 | |||
| chr14:99463548 | T | C | 1 | a0004 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.134A>G | p.Lys45Arg | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/13 | 274/2856 | 134/1785 | 45/594 | chr14 | 99463548 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99404235 | A | G | 3 | a0001c0002 a0001c0007 a0002c0006 |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
synonymous_variant | LOW | c.1167T>C | p.Cys389Cys | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/13 | 1307/2856 | 1167/1785 | 389/594 | chr14 | 99404235 | |||
| chr14:99405261 | T | C | 2 | a0001c0007 a0002c0006 |
2 | HG02055.hp1 HG02630.hp2 |
synonymous_variant | LOW | c.1035A>G | p.Lys345Lys | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/13 | 1175/2856 | 1035/1785 | 345/594 | chr14 | 99405261 | |||
| chr14:99458303 | G | A | 1 | a0001c0008 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.651C>T | p.Tyr217Tyr | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/13 | 791/2856 | 651/1785 | 217/594 | chr14 | 99458303 | |||
| chr14:99458311 | G | T | 1 | a0001c0004 | 2 | HG02486.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.643C>A | p.Arg215Arg | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/13 | 783/2856 | 643/1785 | 215/594 | chr14 | 99458311 | |||
| chr14:99458390 | G | A | 1 | a0001c0010 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.564C>T | p.Tyr188Tyr | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/13 | 704/2856 | 564/1785 | 188/594 | chr14 | 99458390 | |||
| chr14:99461306 | A | G | 1 | a0001c0003 | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
synonymous_variant | LOW | c.231T>C | p.Asp77Asp | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/13 | 371/2856 | 231/1785 | 77/594 | chr14 | 99461306 | |||
| chr14:99465734 | T | C | 1 | a0001c0010 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.72A>G | p.Glu24Glu | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/13 | 212/2856 | 72/1785 | 24/594 | chr14 | 99465734 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99397840 | C | G | 1 | a0001c0001t0006 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 839 | chr14 | 99397840 | ||||||
| chr14:99397860 | C | A | 1 | a0001c0001t0003 | 2 | HG02451.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*819G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 819 | chr14 | 99397860 | ||||||
| chr14:99398078 | T | C | 1 | a0003c0005t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*601A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 601 | chr14 | 99398078 | ||||||
| chr14:99398087 | A | G | 1 | a0001c0002t0005 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 592 | chr14 | 99398087 | ||||||
| chr14:99398166 | A | AT | 4 | a0001c0002t0002 a0001c0002t0005 a0001c0007t0002 others(1): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*512dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 512 | chr14 | 99398166 | ||||||
| chr14:99398186 | C | A | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 493 | chr14 | 99398186 | ||||||
| chr14:99398363 | G | A | 1 | a0001c0001t0008 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 316 | chr14 | 99398363 | ||||||
| chr14:99398616 | G | A | 1 | a0001c0001t0009 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*63C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 63 | chr14 | 99398616 | ||||||
| chr14:99398633 | C | T | 4 | a0001c0002t0002 a0001c0002t0005 a0001c0007t0002 others(1): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*46G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 46 | chr14 | 99398633 | ||||||
| chr14:99480782 | G | A | 1 | a0003c0005t0010 | 1 | HG03209.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/13 | chr14 | 99480782 | |||||||
| chr14:99480793 | C | G | 1 | a0001c0001t0004 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/13 | 14988 | chr14 | 99480793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:99399181 | G | C | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1339-56C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399181 | |||||||
| chr14:99399195 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-70G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399195 | |||||||
| chr14:99399271 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1339-146A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399271 | |||||||
| chr14:99399335 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1339-210G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399335 | |||||||
| chr14:99399391 | C | T | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1339-266G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399391 | |||||||
| chr14:99399447 | ATG | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1339-324_1339-323d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399447 | |||||||
| chr14:99399476 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1339-351A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399476 | |||||||
| chr14:99399489 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1339-364C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399489 | |||||||
| chr14:99399586 | T | G | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-461A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399586 | |||||||
| chr14:99399741 | A | AT | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0158 others(6): Show |
9 | HG00735.hp2 HG02055.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338+357dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | |||||||
| chr14:99399741 | ATT | A | 24 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0070 others(21): Show |
24 | HG00738.hp1 HG02027.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1338+356_1338+357d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | |||||||
| chr14:99399741 | ATTT | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1338+355_1338+357d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | |||||||
| chr14:99399741 | ATTTT | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0101 others(8): Show |
11 | HG00099.hp2 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1338+354_1338+357d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | |||||||
| chr14:99399743 | T | A | 1 | a0001c0001t0001g0254 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1338+356A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399743 | |||||||
| chr14:99399744 | T | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0044 a0001c0001t0001g0070 others(19): Show |
22 | HG00738.hp1 HG02027.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1338+355A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399744 | |||||||
| chr14:99399745 | T | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1338+354A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399745 | |||||||
| chr14:99399746 | T | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0101 others(8): Show |
11 | HG00099.hp2 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1338+353A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399746 | |||||||
| chr14:99399747 | T | A | 1 | a0001c0001t0001g0278 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1338+352A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399747 | |||||||
| chr14:99399835 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+264G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399835 | |||||||
| chr14:99399846 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1338+253C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399846 | |||||||
| chr14:99399982 | C | T | 17 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0065 others(14): Show |
17 | HG00099.hp2 HG00673.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1338+117G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399982 | |||||||
| chr14:99400031 | G | A | 10 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+68C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99400031 | |||||||
| chr14:99400315 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1178-56C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400315 | |||||||
| chr14:99400385 | C | T | 6 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1178-126G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400385 | |||||||
| chr14:99400392 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1178-133C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400392 | |||||||
| chr14:99400439 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1178-180C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400439 | |||||||
| chr14:99400502 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1178-243C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400502 | |||||||
| chr14:99400931 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1178-672C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400931 | |||||||
| chr14:99400975 | A | T | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1178-716T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400975 | |||||||
| chr14:99401138 | CA | C | 17 | a0001c0001t0001g0029 a0001c0001t0001g0150 a0001c0001t0001g0151 others(14): Show |
17 | HG01515.hp2 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1178-880delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401138 | |||||||
| chr14:99401161 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178-902G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401161 | |||||||
| chr14:99401190 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1178-931G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401190 | |||||||
| chr14:99401402 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1178-1143G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401402 | |||||||
| chr14:99401553 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1178-1294T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401553 | |||||||
| chr14:99401575 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1178-1316T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401575 | |||||||
| chr14:99401688 | A | G | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1178-1429T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401688 | |||||||
| chr14:99401971 | A | AGCACAGG others(4): Show |
12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178-1713_1178-171 others(15): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401971 | |||||||
| chr14:99401973 | G | A | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178-1714C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401973 | |||||||
| chr14:99402079 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1178-1820C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402079 | |||||||
| chr14:99402150 | G | C | 2 | a0001c0001t0003g0021 a0001c0001t0003g0108 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1178-1891C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402150 | |||||||
| chr14:99402198 | G | A | 24 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(21): Show |
24 | HG00558.hp2 HG00673.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1178-1939C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402198 | |||||||
| chr14:99402324 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1177+1901A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402324 | |||||||
| chr14:99402334 | A | G | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1177+1891T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402334 | |||||||
| chr14:99402492 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1177+1733C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402492 | |||||||
| chr14:99402637 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1177+1588C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402637 | |||||||
| chr14:99402833 | A | C | 10 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(7): Show |
10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177+1392T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402833 | |||||||
| chr14:99402835 | T | C | 1 | a0001c0002t0002g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1177+1390A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402835 | |||||||
| chr14:99402918 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1177+1307A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402918 | |||||||
| chr14:99402939 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1177+1286A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402939 | |||||||
| chr14:99402949 | T | C | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1177+1276A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402949 | |||||||
| chr14:99402959 | T | G | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+1266A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402959 | |||||||
| chr14:99403076 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1177+1149G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403076 | |||||||
| chr14:99403127 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0087 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+1098C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403127 | |||||||
| chr14:99403193 | A | G | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+1032T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403193 | |||||||
| chr14:99403252 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02615.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+973G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403252 | |||||||
| chr14:99403298 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+927G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403298 | |||||||
| chr14:99403330 | A | C | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+895T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403330 | |||||||
| chr14:99403447 | A | ACTCTCTC others(7): Show |
1 | a0001c0001t0001g0240 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1177+777_1177+778i others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403447 | |||||||
| chr14:99403449 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1177+776T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403449 | |||||||
| chr14:99403451 | A | ACTCTCTC others(3): Show |
1 | a0003c0005t0010g0283 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1177+773_1177+774i others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | |||||||
| chr14:99403451 | A | ACTCTCTC others(5): Show |
1 | a0001c0001t0001g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1177+773_1177+774i others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | |||||||
| chr14:99403451 | A | T | 1 | a0001c0001t0001g0240 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1177+774T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | |||||||
| chr14:99403451 | ACACACTC others(1): Show |
A | 3 | a0001c0002t0002g0147 a0001c0007t0002g0145 a0002c0006t0002g0144 |
3 | HG02055.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1177+766_1177+773d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | |||||||
| chr14:99403451 | ACACACTC others(3): Show |
A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1177+764_1177+773d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | |||||||
| chr14:99403451 | ACACACTC others(11): Show |
A | 4 | a0001c0002t0002g0134 a0001c0002t0002g0279 a0001c0002t0002g0280 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+756_1177+773d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | |||||||
| chr14:99403453 | A | ACTCT | 5 | a0001c0001t0001g0174 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
5 | HG00099.hp1 HG00280.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177+771_1177+772i others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | A | ACTCTCTC others(11): Show |
1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1177+771_1177+772i others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | A | ACTCTCTC others(13): Show |
4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0178 others(1): Show |
4 | HG00558.hp2 NA18956.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+771_1177+772i others(22): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | A | ACTCTCTC others(15): Show |
2 | a0001c0001t0001g0175 a0001c0001t0001g0186 |
2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1177+771_1177+772i others(24): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | A | ACTCTCTC others(17): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0180 |
2 | HG03041.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1177+771_1177+772i others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | A | ACTCTCTC others(25): Show |
1 | a0001c0001t0001g0167 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1177+771_1177+772i others(34): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | A | T | 6 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG00673.hp2 HG01123.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177+772T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | ACACTCTC others(3): Show |
A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+762_1177+771d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403453 | ACACTCTC others(9): Show |
A | 4 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(1): Show |
4 | HG02451.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+756_1177+771d others(18): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | |||||||
| chr14:99403455 | A | ACACT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0063 a0001c0001t0001g0271 others(6): Show |
9 | HG00423.hp2 NA18522.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1177+769_1177+770i others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCT | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0058 others(35): Show |
39 | HG00408.hp2 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1177+766_1177+769d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCTCTC others(1): Show |
6 | a0001c0001t0001g0197 a0001c0001t0001g0208 a0001c0001t0001g0210 others(3): Show |
6 | HG03098.hp2 NA18941.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177+762_1177+769d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCTCTC others(3): Show |
2 | a0001c0001t0001g0200 a0001c0001t0001g0242 |
2 | NA18948.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1177+760_1177+769d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCTCTC others(11): Show |
3 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0001g0182 |
3 | HG03540.hp1 NA18951.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1177+752_1177+769d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCTCTC others(13): Show |
2 | a0001c0001t0001g0177 a0001c0001t0001g0184 |
2 | HG03579.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1177+750_1177+769d others(22): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCTCTC others(15): Show |
1 | a0001c0001t0001g0172 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1177+748_1177+769d others(24): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | ACTCTCTC others(17): Show |
1 | a0001c0001t0001g0166 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1177+746_1177+769d others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | A | T | 23 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0163 others(20): Show |
23 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.1177+770T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACT | A | 8 | a0001c0001t0001g0062 a0001c0001t0001g0110 a0001c0001t0001g0111 others(5): Show |
8 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177+768_1177+769d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACTCT | A | 3 | a0001c0001t0001g0005 a0001c0004t0001g0156 a0001c0004t0001g0157 |
4 | HG01257.hp2 HG01258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+766_1177+769d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACTCTCT | A | 9 | a0001c0001t0001g0039 a0001c0001t0001g0068 a0001c0001t0001g0076 others(6): Show |
9 | HG02965.hp2 NA18961.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.1177+764_1177+769d others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACTCTCTC others(1): Show |
A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1177+762_1177+769d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACTCTCTC others(3): Show |
A | 2 | a0001c0001t0001g0125 a0001c0001t0008g0121 |
2 | NA18951.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1177+760_1177+769d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACTCTCTC others(5): Show |
A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0149 |
2 | HG00738.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1177+758_1177+769d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403455 | ACTCTCTC others(7): Show |
A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1177+756_1177+769d others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | |||||||
| chr14:99403457 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1177+768A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403457 | |||||||
| chr14:99403459 | T | A | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0148 others(4): Show |
7 | HG01496.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177+766A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403459 | |||||||
| chr14:99403461 | T | A | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+764A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403461 | |||||||
| chr14:99403463 | T | A | 11 | a0001c0001t0001g0039 a0001c0001t0001g0076 a0001c0001t0001g0118 others(8): Show |
11 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1177+762A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403463 | |||||||
| chr14:99403465 | T | A | 1 | a0001c0001t0001g0046 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1177+760A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403465 | |||||||
| chr14:99403467 | T | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0125 a0001c0001t0008g0121 |
3 | NA18951.hp1 NA18956.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1177+758A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403467 | |||||||
| chr14:99403472 | CTCTCTCT others(11): Show |
C | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1177+735_1177+752d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403472 | |||||||
| chr14:99403488 | CTTTCTCT others(5): Show |
C | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1177+725_1177+736d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403488 | |||||||
| chr14:99403489 | T | TCTCTCTC others(8): Show |
1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1177+735_1177+736i others(17): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403489 | |||||||
| chr14:99403489 | T | TCTCTCTC others(12): Show |
1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1177+735_1177+736i others(21): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403489 | |||||||
| chr14:99403489 | T | TCTCTCTC others(14): Show |
1 | a0001c0001t0001g0171 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1177+735_1177+736i others(23): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403489 | |||||||
| chr14:99403490 | T | C | 9 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(6): Show |
9 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1177+735A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403490 | |||||||
| chr14:99403597 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+628G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403597 | |||||||
| chr14:99403674 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1177+551C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403674 | |||||||
| chr14:99404003 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1177+222A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99404003 | |||||||
| chr14:99404097 | T | C | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+128A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99404097 | |||||||
| chr14:99404199 | A | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+26T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99404199 | |||||||
| chr14:99404451 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1092-141T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404451 | |||||||
| chr14:99404570 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1092-260G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404570 | |||||||
| chr14:99404574 | T | A | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1092-264A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404574 | |||||||
| chr14:99404626 | TAAC | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1092-319_1092-317d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404626 | |||||||
| chr14:99404673 | T | G | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092-363A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404673 | |||||||
| chr14:99404707 | C | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1092-397G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404707 | |||||||
| chr14:99404844 | A | G | 8 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1091+361T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404844 | |||||||
| chr14:99405475 | T | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.925-104A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99405475 | |||||||
| chr14:99405724 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.925-353T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99405724 | |||||||
| chr14:99405966 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.924+550A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99405966 | |||||||
| chr14:99406092 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.924+424C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406092 | |||||||
| chr14:99406092 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.924+424C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406092 | |||||||
| chr14:99406107 | C | T | 3 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 |
3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.924+409G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406107 | |||||||
| chr14:99406198 | G | GT | 21 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(18): Show |
21 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.924+317dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406198 | |||||||
| chr14:99406318 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.924+198G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406318 | |||||||
| chr14:99406360 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.924+156C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406360 | |||||||
| chr14:99406497 | G | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+19C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406497 | |||||||
| chr14:99406507 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0003t0001g0140 |
3 | HG02723.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.924+9C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406507 | |||||||
| chr14:99406613 | A | T | 1 | a0001c0001t0001g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.850-23T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406613 | |||||||
| chr14:99406654 | C | T | 8 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-64G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406654 | |||||||
| chr14:99406828 | T | A | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-238A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406828 | |||||||
| chr14:99406889 | C | T | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-299G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406889 | |||||||
| chr14:99406896 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.850-306C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406896 | |||||||
| chr14:99407134 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.850-544A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407134 | |||||||
| chr14:99407261 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
4 | HG01123.hp1 HG01884.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-671C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407261 | |||||||
| chr14:99407280 | C | T | 20 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(17): Show |
20 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.850-690G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407280 | |||||||
| chr14:99407330 | G | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-740C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407330 | |||||||
| chr14:99407341 | C | T | 14 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
14 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.850-751G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407341 | |||||||
| chr14:99407366 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.850-776A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407366 | |||||||
| chr14:99407496 | T | C | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-906A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407496 | |||||||
| chr14:99407538 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0239 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.850-948T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407538 | |||||||
| chr14:99407554 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.850-964C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407554 | |||||||
| chr14:99407606 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.850-1016G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407606 | |||||||
| chr14:99407782 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.850-1192C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407782 | |||||||
| chr14:99407804 | C | A | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-1214G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407804 | |||||||
| chr14:99407806 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.850-1216A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407806 | |||||||
| chr14:99407813 | C | G | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-1223G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407813 | |||||||
| chr14:99407819 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.850-1229C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407819 | |||||||
| chr14:99407895 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1305C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407895 | |||||||
| chr14:99407897 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1307T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407897 | |||||||
| chr14:99407900 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1310A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407900 | |||||||
| chr14:99407903 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1313T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407903 | |||||||
| chr14:99407908 | A | T | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1318T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407908 | |||||||
| chr14:99407920 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.850-1330C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407920 | |||||||
| chr14:99408102 | T | C | 10 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1512A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99408102 | |||||||
| chr14:99408451 | T | A | 10 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1861A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99408451 | |||||||
| chr14:99408748 | T | G | 1 | a0001c0004t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-2158A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99408748 | |||||||
| chr14:99409071 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.850-2481T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409071 | |||||||
| chr14:99409074 | G | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-2484C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409074 | |||||||
| chr14:99409150 | C | T | 7 | a0001c0002t0002g0133 a0001c0002t0002g0134 a0001c0002t0002g0147 others(4): Show |
7 | HG02258.hp2 HG02809.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-2560G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409150 | |||||||
| chr14:99409326 | T | C | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2736A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409326 | |||||||
| chr14:99409330 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-2740T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409330 | |||||||
| chr14:99409367 | A | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0049 others(1): Show |
4 | HG02683.hp1 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2777T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409367 | |||||||
| chr14:99409376 | A | G | 23 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0150 others(20): Show |
23 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.850-2786T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409376 | |||||||
| chr14:99409399 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-2809G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409399 | |||||||
| chr14:99409492 | G | A | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2902C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409492 | |||||||
| chr14:99409813 | C | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG02257.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+3138G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409813 | |||||||
| chr14:99409879 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(133): Show |
141 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.849+3072C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409879 | |||||||
| chr14:99410038 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0078 |
2 | NA18965.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.849+2913A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410038 | |||||||
| chr14:99410149 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+2802C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410149 | |||||||
| chr14:99410168 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(154): Show |
162 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.849+2783T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410168 | |||||||
| chr14:99410287 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.849+2664C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410287 | |||||||
| chr14:99410333 | G | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.849+2618C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410333 | |||||||
| chr14:99410386 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.849+2565C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410386 | |||||||
| chr14:99410512 | T | C | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+2439A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410512 | |||||||
| chr14:99410516 | A | G | 23 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0150 others(20): Show |
23 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.849+2435T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410516 | |||||||
| chr14:99410887 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.849+2064G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410887 | |||||||
| chr14:99411128 | A | AAGAGTGC | 5 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+1816_849+1822d others(9): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411128 | |||||||
| chr14:99411275 | C | T | 11 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+1676G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411275 | |||||||
| chr14:99411306 | A | AAACT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.849+1644_849+1645i others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411306 | |||||||
| chr14:99411387 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.849+1564C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411387 | |||||||
| chr14:99411631 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1320T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411631 | |||||||
| chr14:99411718 | ACT | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1231_849+1232d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411718 | |||||||
| chr14:99411721 | C | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+1230G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411721 | |||||||
| chr14:99411799 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
9 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+1152C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411799 | |||||||
| chr14:99411800 | T | C | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.849+1151A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411800 | |||||||
| chr14:99411891 | C | T | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+1060G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411891 | |||||||
| chr14:99411978 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.849+973A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411978 | |||||||
| chr14:99412112 | C | G | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.849+839G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412112 | |||||||
| chr14:99412167 | C | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | NA18952.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.849+784G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412167 | |||||||
| chr14:99412244 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(74): Show |
79 | HG00099.hp2 HG00408.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.849+707C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412244 | |||||||
| chr14:99412389 | C | T | 11 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+562G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412389 | |||||||
| chr14:99412720 | A | G | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.849+231T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412720 | |||||||
| chr14:99412733 | C | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+218G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412733 | |||||||
| chr14:99412810 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+141A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412810 | |||||||
| chr14:99412825 | T | C | 3 | a0001c0002t0005g0143 a0001c0007t0002g0145 a0002c0006t0002g0144 |
3 | HG02055.hp1 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.849+126A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412825 | |||||||
| chr14:99412837 | T | C | 6 | a0001c0001t0001g0243 a0001c0002t0002g0130 a0001c0002t0002g0131 others(3): Show |
6 | HG02451.hp2 HG02809.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+114A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412837 | |||||||
| chr14:99412855 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.849+96C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412855 | |||||||
| chr14:99412870 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.849+81T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412870 | |||||||
| chr14:99413230 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.735-165G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413230 | |||||||
| chr14:99413276 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.735-211G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413276 | |||||||
| chr14:99413376 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.735-311G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413376 | |||||||
| chr14:99413475 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.734+401C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413475 | |||||||
| chr14:99413675 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.734+201A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413675 | |||||||
| chr14:99413856 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.734+20G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413856 | |||||||
| chr14:99413995 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.676-61C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99413995 | |||||||
| chr14:99414150 | T | G | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-216A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414150 | |||||||
| chr14:99414252 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.676-318T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414252 | |||||||
| chr14:99414332 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-398C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414332 | |||||||
| chr14:99414398 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.676-464C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414398 | |||||||
| chr14:99414541 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.676-607G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414541 | |||||||
| chr14:99414670 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-736A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414670 | |||||||
| chr14:99414786 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-852A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414786 | |||||||
| chr14:99414786 | T | TAGAC | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.676-853_676-852ins others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414786 | |||||||
| chr14:99414786 | T | TAGGC | 4 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0050 others(1): Show |
4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-853_676-852ins others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414786 | |||||||
| chr14:99414860 | T | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG02257.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.676-926A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414860 | |||||||
| chr14:99414862 | C | T | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-928G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414862 | |||||||
| chr14:99414903 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0278 |
2 | HG02293.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.676-969A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414903 | |||||||
| chr14:99415144 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-1210A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415144 | |||||||
| chr14:99415214 | G | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-1280C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415214 | |||||||
| chr14:99415263 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.676-1329T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415263 | |||||||
| chr14:99415337 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-1403C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415337 | |||||||
| chr14:99415351 | C | T | 1 | a0001c0002t0002g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.676-1417G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415351 | |||||||
| chr14:99415824 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676-1890C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415824 | |||||||
| chr14:99415912 | G | A | 1 | a0001c0001t0006g0084 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.676-1978C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415912 | |||||||
| chr14:99416192 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676-2258A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99416192 | |||||||
| chr14:99416519 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.676-2585A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99416519 | |||||||
| chr14:99417133 | T | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-3199A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417133 | |||||||
| chr14:99417251 | C | T | 8 | a0001c0001t0001g0252 a0001c0001t0001g0258 a0001c0001t0001g0261 others(5): Show |
8 | HG00544.hp1 HG01346.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-3317G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417251 | |||||||
| chr14:99417463 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.676-3529T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417463 | |||||||
| chr14:99417734 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.676-3800G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417734 | |||||||
| chr14:99417988 | T | TCTCTACC others(22): Show |
1 | a0001c0001t0001g0116 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.676-4083_676-4055d others(31): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417988 | |||||||
| chr14:99418013 | A | G | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-4079T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418013 | |||||||
| chr14:99418244 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-4310A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418244 | |||||||
| chr14:99418417 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.676-4483G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418417 | |||||||
| chr14:99418727 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.676-4793A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418727 | |||||||
| chr14:99418764 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.676-4830A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418764 | |||||||
| chr14:99418953 | G | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-5019C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418953 | |||||||
| chr14:99419085 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.676-5151G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419085 | |||||||
| chr14:99419087 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.676-5153G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419087 | |||||||
| chr14:99419098 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.676-5164G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419098 | |||||||
| chr14:99419130 | T | C | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-5196A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419130 | |||||||
| chr14:99419227 | T | C | 2 | a0001c0002t0002g0280 a0001c0002t0002g0281 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.676-5293A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419227 | |||||||
| chr14:99419260 | C | T | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-5326G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419260 | |||||||
| chr14:99419262 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0199 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.676-5328G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419262 | |||||||
| chr14:99419295 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.676-5361G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419295 | |||||||
| chr14:99419359 | T | C | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-5425A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419359 | |||||||
| chr14:99419475 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-5541A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419475 | |||||||
| chr14:99419723 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676-5789G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419723 | |||||||
| chr14:99419762 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.676-5828C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419762 | |||||||
| chr14:99419773 | TCAAAAAA others(5): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
10 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.676-5851_676-5840d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419773 | |||||||
| chr14:99419774 | CA | C | 14 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.676-5841delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419774 | |||||||
| chr14:99419775 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.676-5852_676-5842d others(13): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419775 | |||||||
| chr14:99419784 | AAC | A | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-5852_676-5851d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419784 | |||||||
| chr14:99419785 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.676-5851T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419785 | |||||||
| chr14:99419787 | A | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-5853T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419787 | |||||||
| chr14:99420078 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.676-6144A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420078 | |||||||
| chr14:99420102 | C | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-6168G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420102 | |||||||
| chr14:99420111 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-6177G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420111 | |||||||
| chr14:99420446 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.676-6512C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420446 | |||||||
| chr14:99420532 | A | T | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(3): Show |
6 | HG00408.hp2 HG01928.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-6598T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420532 | |||||||
| chr14:99420765 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
129 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.676-6831G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420765 | |||||||
| chr14:99420815 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.676-6881G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420815 | |||||||
| chr14:99420831 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-6897G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420831 | |||||||
| chr14:99420947 | CG | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0060 others(23): Show |
27 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-7014delC | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGG | C | 23 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0085 others(20): Show |
23 | HG00735.hp1 HG01109.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.676-7015_676-7014d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGG | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0044 others(20): Show |
23 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.676-7016_676-7014d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGG | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
100 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.676-7017_676-7014d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGG | C | 28 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0016 others(25): Show |
28 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.676-7018_676-7014d others(7): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(3): Show |
C | 4 | a0001c0001t0001g0225 a0001c0002t0002g0134 a0001c0002t0002g0279 others(1): Show |
4 | HG01891.hp2 HG02809.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-7023_676-7014d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(4): Show |
C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
10 | HG01123.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.676-7024_676-7014d others(13): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(5): Show |
C | 4 | a0001c0002t0002g0133 a0001c0002t0002g0281 a0002c0006t0002g0144 others(1): Show |
4 | HG02258.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-7025_676-7014d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(6): Show |
C | 2 | a0001c0001t0001g0228 a0001c0007t0002g0145 |
2 | HG02055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.676-7026_676-7014d others(15): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(7): Show |
C | 3 | a0001c0002t0002g0147 a0001c0002t0005g0143 a0001c0010t0001g0155 |
3 | HG02970.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.676-7027_676-7014d others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(10): Show |
C | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.676-7030_676-7014d others(19): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420947 | CGGGGGGG others(17): Show |
C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0186 |
2 | NA18986.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.676-7037_676-7014d others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | |||||||
| chr14:99420956 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.676-7022C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420956 | |||||||
| chr14:99420959 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.676-7025C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420959 | |||||||
| chr14:99420961 | G | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0197 a0001c0001t0001g0232 |
3 | HG01169.hp2 HG02293.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.676-7027C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420961 | |||||||
| chr14:99420962 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.676-7028C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420962 | |||||||
| chr14:99420963 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.676-7029C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420963 | |||||||
| chr14:99420964 | G | C | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-7030C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420964 | |||||||
| chr14:99420964 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.676-7030C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420964 | |||||||
| chr14:99420967 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
126 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.676-7033C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420967 | |||||||
| chr14:99420967 | GGGGGGGG others(3): Show |
G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.676-7043_676-7034d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420967 | |||||||
| chr14:99420968 | G | T | 6 | a0001c0001t0001g0207 a0001c0003t0001g0139 a0001c0003t0001g0140 others(3): Show |
6 | HG01891.hp2 HG02083.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-7034C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420968 | |||||||
| chr14:99420969 | G | GT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0190 a0001c0001t0001g0198 others(3): Show |
6 | HG01099.hp2 HG03491.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-7036_676-7035i others(3): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420969 | |||||||
| chr14:99420969 | G | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0059 others(75): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.676-7035C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420969 | |||||||
| chr14:99420972 | G | T | 4 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-7038C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420972 | |||||||
| chr14:99420973 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
142 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.676-7039C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420973 | |||||||
| chr14:99420976 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-7042C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420976 | |||||||
| chr14:99420983 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.676-7049C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420983 | |||||||
| chr14:99421028 | C | CGTTTCTT others(1): Show |
4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-7102_676-7095d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421028 | |||||||
| chr14:99421044 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.676-7110C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421044 | |||||||
| chr14:99421112 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
7 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-7178C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421112 | |||||||
| chr14:99421235 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.676-7301G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421235 | |||||||
| chr14:99421512 | C | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-7578G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421512 | |||||||
| chr14:99421606 | A | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-7672T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421606 | |||||||
| chr14:99421777 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-7843C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421777 | |||||||
| chr14:99421789 | A | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-7855T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421789 | |||||||
| chr14:99422017 | G | A | 2 | a0001c0002t0002g0130 a0001c0002t0002g0131 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.676-8083C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422017 | |||||||
| chr14:99422078 | T | C | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-8144A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422078 | |||||||
| chr14:99422260 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | NA18964.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.676-8326C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422260 | |||||||
| chr14:99422368 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.676-8434T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422368 | |||||||
| chr14:99422550 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.676-8616G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422550 | |||||||
| chr14:99422561 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.676-8627C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422561 | |||||||
| chr14:99422623 | TAGG | T | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.676-8692_676-8690d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422623 | |||||||
| chr14:99422678 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.676-8744G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422678 | |||||||
| chr14:99422691 | A | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-8757T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422691 | |||||||
| chr14:99422824 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.676-8890G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422824 | |||||||
| chr14:99422836 | C | G | 11 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-8902G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422836 | |||||||
| chr14:99422914 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-8980C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422914 | |||||||
| chr14:99422943 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-9009C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422943 | |||||||
| chr14:99423043 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.676-9109G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423043 | |||||||
| chr14:99423051 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.676-9117C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423051 | |||||||
| chr14:99423167 | G | T | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-9233C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423167 | |||||||
| chr14:99423250 | A | G | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.676-9316T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423250 | |||||||
| chr14:99423285 | T | C | 12 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(9): Show |
12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.676-9351A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423285 | |||||||
| chr14:99423350 | G | A | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-9416C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423350 | |||||||
| chr14:99423406 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.676-9472T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423406 | |||||||
| chr14:99423588 | C | CA | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(80): Show |
85 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.676-9655dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAA | 17 | a0001c0001t0001g0034 a0001c0001t0001g0194 a0001c0001t0001g0199 others(14): Show |
17 | HG00423.hp2 HG02293.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.676-9656_676-9655d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0088 others(6): Show |
10 | HG01346.hp1 HG01928.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.676-9658_676-9655d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0099 |
3 | HG01167.hp2 HG02602.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.676-9666_676-9655d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0050 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.676-9667_676-9655d others(15): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.676-9668_676-9655d others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0146 |
2 | HG00735.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.676-9669_676-9655d others(17): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0059 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.676-9671_676-9655d others(19): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0069 |
2 | HG00738.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.676-9672_676-9655d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0019 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-9673_676-9655d others(21): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(13): Show |
6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0057 others(3): Show |
6 | HG02074.hp1 HG02074.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-9674_676-9655d others(22): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0053 others(2): Show |
5 | HG00673.hp1 HG01952.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.676-9675_676-9655d others(23): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0282 a0001c0008t0001g0105 |
2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.676-9676_676-9655d others(24): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(16): Show |
4 | a0001c0001t0001g0017 a0001c0001t0001g0065 a0001c0001t0001g0092 others(1): Show |
4 | HG02083.hp2 NA18957.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-9677_676-9655d others(25): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(17): Show |
6 | a0001c0001t0001g0041 a0001c0001t0001g0054 a0001c0001t0001g0056 others(3): Show |
6 | HG01952.hp2 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-9678_676-9655d others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(18): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0028 others(4): Show |
8 | HG01243.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-9679_676-9655d others(27): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(19): Show |
9 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0051 others(6): Show |
9 | HG01081.hp1 HG01192.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-9680_676-9655d others(28): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(20): Show |
4 | a0001c0001t0001g0128 a0001c0001t0001g0136 a0001c0001t0006g0084 others(1): Show |
4 | HG01496.hp2 HG02056.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(29): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0003g0021 |
3 | HG02886.hp2 HG03098.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(30): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(22): Show |
1 | a0001c0001t0003g0108 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.676-9655_676-9654i others(31): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(23): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0107 a0001c0001t0001g0114 others(2): Show |
5 | HG01169.hp2 HG03139.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(32): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(24): Show |
9 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(6): Show |
9 | HG01069.hp2 HG01496.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(33): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0109 a0001c0001t0001g0125 |
2 | NA18964.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(35): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(27): Show |
7 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(36): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(28): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0100 |
3 | HG02615.hp2 HG02886.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(37): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0091 |
2 | HG02809.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(38): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-9655_676-9654i others(39): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(31): Show |
3 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0124 |
3 | NA18977.hp2 NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(40): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.676-9655_676-9654i others(41): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(33): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG02895.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(42): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(37): Show |
1 | a0001c0001t0001g0020 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(46): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(39): Show |
1 | a0001c0001t0001g0082 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(48): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CAAAAAAA others(45): Show |
1 | a0001c0001t0001g0095 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(54): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | C | CACAAAAA others(28): Show |
1 | a0001c0001t0001g0022 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(37): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0093 a0001c0002t0002g0130 a0001c0002t0002g0131 others(5): Show |
8 | HG02451.hp2 HG02809.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-9662_676-9655d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0229 others(3): Show |
6 | HG00408.hp2 HG01928.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-9663_676-9655d others(11): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423588 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.676-9664_676-9655d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | |||||||
| chr14:99423676 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0050 others(1): Show |
4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-9742T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423676 | |||||||
| chr14:99423821 | C | T | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-9887G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423821 | |||||||
| chr14:99424042 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.676-10108T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424042 | |||||||
| chr14:99424175 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.676-10241A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424175 | |||||||
| chr14:99424240 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-10306C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424240 | |||||||
| chr14:99424290 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.676-10356C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424290 | |||||||
| chr14:99424344 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.676-10410C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424344 | |||||||
| chr14:99424383 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.676-10449T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424383 | |||||||
| chr14:99424747 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.676-10813T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424747 | |||||||
| chr14:99424870 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
9 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-10936A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424870 | |||||||
| chr14:99425226 | C | T | 7 | a0001c0001t0001g0200 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG02056.hp1 NA18941.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-11292G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425226 | |||||||
| chr14:99425481 | G | C | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-11547C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425481 | |||||||
| chr14:99425545 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-11611C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425545 | |||||||
| chr14:99425546 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.676-11612G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425546 | |||||||
| chr14:99425616 | T | A | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-11682A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425616 | |||||||
| chr14:99425707 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0185 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676-11773G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425707 | |||||||
| chr14:99426028 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(148): Show |
156 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.676-12094C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426028 | |||||||
| chr14:99426051 | C | T | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-12117G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426051 | |||||||
| chr14:99426068 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.676-12134G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426068 | |||||||
| chr14:99426069 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.676-12135T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426069 | |||||||
| chr14:99426099 | A | T | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-12165T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426099 | |||||||
| chr14:99426281 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
131 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.676-12347G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426281 | |||||||
| chr14:99426492 | G | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-12558C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426492 | |||||||
| chr14:99426493 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-12559G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426493 | |||||||
| chr14:99426505 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.676-12571C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426505 | |||||||
| chr14:99426707 | C | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-12773G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426707 | |||||||
| chr14:99426758 | CA | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
5 | HG01261.hp2 HG01346.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-12825delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426758 | |||||||
| chr14:99426761 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.676-12827C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426761 | |||||||
| chr14:99426889 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.676-12955C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426889 | |||||||
| chr14:99427064 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.676-13130G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427064 | |||||||
| chr14:99427108 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-13174G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427108 | |||||||
| chr14:99427220 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-13286G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427220 | |||||||
| chr14:99427231 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-13297G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427231 | |||||||
| chr14:99427309 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.676-13375T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427309 | |||||||
| chr14:99427346 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.676-13422_676-1341 others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427346 | |||||||
| chr14:99427409 | A | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.676-13475T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427409 | |||||||
| chr14:99427444 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.676-13510G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427444 | |||||||
| chr14:99427613 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.676-13679G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427613 | |||||||
| chr14:99427732 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-13798C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427732 | |||||||
| chr14:99427802 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.676-13868G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427802 | |||||||
| chr14:99428126 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.676-14192G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428126 | |||||||
| chr14:99428296 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.676-14362T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428296 | |||||||
| chr14:99428297 | C | T | 13 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(10): Show |
13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.676-14363G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428297 | |||||||
| chr14:99428621 | G | A | 5 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.676-14687C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428621 | |||||||
| chr14:99428853 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-14919A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428853 | |||||||
| chr14:99428890 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.676-14956A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428890 | |||||||
| chr14:99428996 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.676-15062G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428996 | |||||||
| chr14:99429073 | A | C | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-15139T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429073 | |||||||
| chr14:99429415 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-15481G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429415 | |||||||
| chr14:99429477 | C | T | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-15543G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429477 | |||||||
| chr14:99429696 | C | G | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-15762G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429696 | |||||||
| chr14:99430006 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.676-16072C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430006 | |||||||
| chr14:99430016 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.676-16082C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430016 | |||||||
| chr14:99430087 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-16153C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430087 | |||||||
| chr14:99430107 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.676-16173C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430107 | |||||||
| chr14:99430227 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-16293T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430227 | |||||||
| chr14:99430276 | T | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-16342A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430276 | |||||||
| chr14:99430658 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.676-16724C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430658 | |||||||
| chr14:99430835 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.676-16901T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430835 | |||||||
| chr14:99430911 | T | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-16977A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430911 | |||||||
| chr14:99430926 | C | A | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-16992G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430926 | |||||||
| chr14:99430971 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-17037G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430971 | |||||||
| chr14:99431494 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-17560A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99431494 | |||||||
| chr14:99431860 | A | G | 11 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-17926T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99431860 | |||||||
| chr14:99432069 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.676-18135G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432069 | |||||||
| chr14:99432195 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.676-18261G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432195 | |||||||
| chr14:99432244 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-18310C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432244 | |||||||
| chr14:99432442 | G | A | 3 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 |
3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.676-18508C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432442 | |||||||
| chr14:99432533 | C | T | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-18599G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432533 | |||||||
| chr14:99432883 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.676-18949A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432883 | |||||||
| chr14:99433419 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.676-19485C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433419 | |||||||
| chr14:99433506 | T | C | 9 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
9 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-19572A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433506 | |||||||
| chr14:99433732 | C | T | 8 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-19798G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433732 | |||||||
| chr14:99433988 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.676-20054G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433988 | |||||||
| chr14:99434020 | C | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.676-20086G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434020 | |||||||
| chr14:99434025 | A | G | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-20091T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434025 | |||||||
| chr14:99434072 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-20138A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434072 | |||||||
| chr14:99434135 | C | T | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.676-20201G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434135 | |||||||
| chr14:99434184 | C | CTG | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.676-20252_676-2025 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434184 | |||||||
| chr14:99434274 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-20340G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434274 | |||||||
| chr14:99434447 | G | A | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-20513C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434447 | |||||||
| chr14:99434465 | C | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-20531G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434465 | |||||||
| chr14:99434480 | G | A | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-20546C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434480 | |||||||
| chr14:99434493 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-20559C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434493 | |||||||
| chr14:99434715 | C | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-20781G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434715 | |||||||
| chr14:99434778 | G | T | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-20844C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434778 | |||||||
| chr14:99434787 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.676-20853A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434787 | |||||||
| chr14:99434796 | G | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-20862C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434796 | |||||||
| chr14:99434847 | C | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-20913G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | C | CA | 43 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0018 others(40): Show |
44 | HG00408.hp2 HG00423.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.676-20914dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | C | CAA | 12 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0165 others(9): Show |
12 | HG01891.hp2 HG02280.hp2 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.676-20915_676-2091 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | C | CAAA | 11 | a0001c0001t0001g0148 a0001c0001t0001g0169 a0001c0001t0001g0170 others(8): Show |
11 | HG00673.hp2 HG01891.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.676-20916_676-2091 others(7): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | C | CAAAA | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0174 others(5): Show |
8 | HG00558.hp2 HG02027.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-20917_676-2091 others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | CA | C | 89 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.676-20914delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | CAA | C | 7 | a0001c0001t0001g0267 a0001c0002t0002g0133 a0001c0002t0002g0134 others(4): Show |
7 | HG01257.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-20915_676-2091 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434847 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0243 |
2 | HG02080.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.676-20926_676-2091 others(17): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | |||||||
| chr14:99434877 | C | A | 13 | a0001c0001t0001g0076 a0001c0001t0001g0150 a0001c0001t0001g0151 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.676-20943G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434877 | |||||||
| chr14:99434878 | A | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-20944T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434878 | |||||||
| chr14:99434943 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.676-21009T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434943 | |||||||
| chr14:99435151 | C | T | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-21217G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435151 | |||||||
| chr14:99435170 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.676-21236T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435170 | |||||||
| chr14:99435228 | C | CATTA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.676-21295_676-2129 others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435228 | |||||||
| chr14:99435349 | C | T | 3 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 |
3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.676-21415G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435349 | |||||||
| chr14:99435515 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.676-21581A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435515 | |||||||
| chr14:99435536 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.676-21602A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435536 | |||||||
| chr14:99435632 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.676-21698C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435632 | |||||||
| chr14:99435735 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.676-21801G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435735 | |||||||
| chr14:99435742 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-21808T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435742 | |||||||
| chr14:99435743 | C | A | 1 | a0001c0001t0001g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-21809G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435743 | |||||||
| chr14:99435744 | CT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
187 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.676-21811delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435744 | |||||||
| chr14:99435745 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-21811A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435745 | |||||||
| chr14:99435777 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-21843C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435777 | |||||||
| chr14:99435800 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-21866C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435800 | |||||||
| chr14:99435926 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.676-21992C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435926 | |||||||
| chr14:99436060 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-22126G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436060 | |||||||
| chr14:99436121 | A | G | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+22158T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436121 | |||||||
| chr14:99436136 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.675+22143C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436136 | |||||||
| chr14:99436393 | T | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+21886A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436393 | |||||||
| chr14:99436477 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.675+21802G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436477 | |||||||
| chr14:99436533 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.675+21746C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436533 | |||||||
| chr14:99436583 | A | G | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+21696T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436583 | |||||||
| chr14:99436746 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.675+21533G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436746 | |||||||
| chr14:99436878 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.675+21401G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436878 | |||||||
| chr14:99437017 | T | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG00544.hp1 HG01346.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.675+21262A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437017 | |||||||
| chr14:99437143 | A | C | 1 | a0001c0002t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.675+21136T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437143 | |||||||
| chr14:99437451 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.675+20828T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437451 | |||||||
| chr14:99437526 | C | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG01123.hp1 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+20753G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437526 | |||||||
| chr14:99437636 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.675+20643G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437636 | |||||||
| chr14:99437662 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675+20617A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437662 | |||||||
| chr14:99437665 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.675+20614C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437665 | |||||||
| chr14:99437685 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.675+20594C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437685 | |||||||
| chr14:99437849 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+20430C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437849 | |||||||
| chr14:99437890 | C | T | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+20389G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437890 | |||||||
| chr14:99437998 | C | G | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+20281G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437998 | |||||||
| chr14:99438162 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.675+20117C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438162 | |||||||
| chr14:99438234 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+20045G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438234 | |||||||
| chr14:99438283 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.675+19996G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438283 | |||||||
| chr14:99438515 | T | G | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+19764A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438515 | |||||||
| chr14:99438697 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.675+19582C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438697 | |||||||
| chr14:99438706 | G | A | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+19573C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438706 | |||||||
| chr14:99438825 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.675+19454G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438825 | |||||||
| chr14:99438826 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0213 |
2 | HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.675+19453C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438826 | |||||||
| chr14:99438838 | T | C | 1 | a0001c0002t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.675+19441A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438838 | |||||||
| chr14:99439416 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.675+18863A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439416 | |||||||
| chr14:99439592 | G | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.675+18687C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439592 | |||||||
| chr14:99439616 | T | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+18663A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439616 | |||||||
| chr14:99439688 | A | ATATGTAT others(53): Show |
1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.675+18531_675+1859 others(64): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439688 | |||||||
| chr14:99439692 | GTATT | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.675+18583_675+1858 others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439692 | |||||||
| chr14:99439710 | A | T | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+18569T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439710 | |||||||
| chr14:99439769 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+18510G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439769 | |||||||
| chr14:99440056 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.675+18223T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440056 | |||||||
| chr14:99440217 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0120 a0001c0001t0001g0122 others(1): Show |
4 | NA18961.hp2 NA18968.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+18062A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440217 | |||||||
| chr14:99440302 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.675+17977T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440302 | |||||||
| chr14:99440513 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.675+17766G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440513 | |||||||
| chr14:99440525 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.675+17754G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440525 | |||||||
| chr14:99440526 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+17753C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440526 | |||||||
| chr14:99440676 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.675+17603G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440676 | |||||||
| chr14:99440942 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.675+17337A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440942 | |||||||
| chr14:99440982 | G | T | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+17297C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440982 | |||||||
| chr14:99441032 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.675+17247G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441032 | |||||||
| chr14:99441046 | C | T | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.675+17233G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441046 | |||||||
| chr14:99441156 | T | C | 1 | a0001c0004t0001g0156 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.675+17123A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441156 | |||||||
| chr14:99441195 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.675+17084A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441195 | |||||||
| chr14:99441537 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+16742G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441537 | |||||||
| chr14:99441559 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.675+16720A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441559 | |||||||
| chr14:99441599 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.675+16680C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441599 | |||||||
| chr14:99441636 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.675+16643T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441636 | |||||||
| chr14:99441720 | G | A | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+16559C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441720 | |||||||
| chr14:99441856 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+16423A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441856 | |||||||
| chr14:99441915 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.675+16364C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441915 | |||||||
| chr14:99441992 | G | A | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+16287C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441992 | |||||||
| chr14:99442045 | G | A | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+16234C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442045 | |||||||
| chr14:99442115 | C | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(23): Show |
27 | HG00423.hp1 HG00558.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.675+16164G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442115 | |||||||
| chr14:99442122 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+16157C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442122 | |||||||
| chr14:99442140 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+16139G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442140 | |||||||
| chr14:99442292 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.675+15987C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442292 | |||||||
| chr14:99442373 | T | A | 1 | a0001c0001t0001g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.675+15906A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442373 | |||||||
| chr14:99442391 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.675+15888G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442391 | |||||||
| chr14:99442411 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.675+15868C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442411 | |||||||
| chr14:99442471 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+15808G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442471 | |||||||
| chr14:99442723 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.675+15556T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442723 | |||||||
| chr14:99442959 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
160 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.675+15320A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442959 | |||||||
| chr14:99443065 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675+15214G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443065 | |||||||
| chr14:99443255 | A | AT | 28 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0053 others(25): Show |
28 | HG01081.hp2 HG01123.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.675+15023dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443255 | |||||||
| chr14:99443255 | A | ATT | 6 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0003t0001g0140 others(3): Show |
6 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+15022_675+1502 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443255 | |||||||
| chr14:99443255 | AT | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0001t0001g0036 others(7): Show |
10 | HG01167.hp1 HG01517.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.675+15023delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443255 | |||||||
| chr14:99443256 | T | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0110 others(5): Show |
9 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.675+15023A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443256 | |||||||
| chr14:99443341 | T | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0050 others(1): Show |
4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.675+14938A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443341 | |||||||
| chr14:99443494 | C | T | 1 | a0001c0004t0001g0156 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.675+14785G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443494 | |||||||
| chr14:99443531 | C | T | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+14748G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443531 | |||||||
| chr14:99443644 | G | A | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+14635C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443644 | |||||||
| chr14:99443722 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+14557A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443722 | |||||||
| chr14:99443724 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.675+14555A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443724 | |||||||
| chr14:99443826 | T | C | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+14453A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443826 | |||||||
| chr14:99443829 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.675+14450G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443829 | |||||||
| chr14:99443851 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+14428G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443851 | |||||||
| chr14:99443885 | T | A | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+14394A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443885 | |||||||
| chr14:99444101 | T | C | 1 | a0001c0007t0002g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.675+14178A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444101 | |||||||
| chr14:99444130 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.675+14149G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444130 | |||||||
| chr14:99444222 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.675+14057T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444222 | |||||||
| chr14:99444261 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.675+14018A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444261 | |||||||
| chr14:99444419 | T | C | 8 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+13860A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444419 | |||||||
| chr14:99444438 | T | C | 14 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0130 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+13841A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444438 | |||||||
| chr14:99444567 | ATCAAAAC others(17): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.675+13688_675+1371 others(28): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444567 | |||||||
| chr14:99444608 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.675+13671G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444608 | |||||||
| chr14:99444631 | G | GTAGGATC others(19): Show |
1 | a0001c0001t0001g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.675+13647_675+1364 others(30): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444631 | |||||||
| chr14:99444804 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0090 others(2): Show |
6 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+13475G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444804 | |||||||
| chr14:99444834 | C | CA | 23 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(20): Show |
23 | HG01361.hp1 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.675+13444dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444834 | |||||||
| chr14:99444885 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.675+13394T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444885 | |||||||
| chr14:99444964 | T | C | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG01123.hp1 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+13315A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444964 | |||||||
| chr14:99444972 | A | G | 5 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+13307T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444972 | |||||||
| chr14:99445007 | G | C | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | NA18953.hp2 NA18974.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.675+13272C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445007 | |||||||
| chr14:99445083 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+13196C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445083 | |||||||
| chr14:99445117 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+13162C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445117 | |||||||
| chr14:99445182 | A | T | 1 | a0001c0008t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.675+13097T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445182 | |||||||
| chr14:99445235 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.675+13044C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445235 | |||||||
| chr14:99445262 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.675+13017G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445262 | |||||||
| chr14:99445422 | T | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+12857A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445422 | |||||||
| chr14:99446013 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.675+12266C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446013 | |||||||
| chr14:99446033 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.675+12246C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446033 | |||||||
| chr14:99446115 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.675+12164C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446115 | |||||||
| chr14:99446117 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+12162G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446117 | |||||||
| chr14:99446165 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.675+12114C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446165 | |||||||
| chr14:99446189 | G | A | 4 | a0001c0001t0001g0177 a0001c0003t0001g0139 a0001c0003t0001g0140 others(1): Show |
4 | HG01891.hp2 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+12090C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446189 | |||||||
| chr14:99446417 | T | C | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+11862A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446417 | |||||||
| chr14:99446479 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+11800G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446479 | |||||||
| chr14:99446543 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.675+11736T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446543 | |||||||
| chr14:99446926 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+11353C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446926 | |||||||
| chr14:99446944 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.675+11335C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446944 | |||||||
| chr14:99446975 | CT | C | 140 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(137): Show |
142 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.675+11303delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446975 | |||||||
| chr14:99446975 | CTT | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.675+11302_675+1130 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446975 | |||||||
| chr14:99447117 | G | A | 2 | a0001c0001t0001g0093 a0001c0010t0001g0155 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.675+11162C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447117 | |||||||
| chr14:99447164 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.675+11115C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447164 | |||||||
| chr14:99447189 | T | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
5 | HG01261.hp2 HG01346.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+11090A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447189 | |||||||
| chr14:99447289 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.675+10990A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447289 | |||||||
| chr14:99447319 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0213 |
2 | HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.675+10960T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447319 | |||||||
| chr14:99447334 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+10945A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447334 | |||||||
| chr14:99447469 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.675+10810T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447469 | |||||||
| chr14:99447542 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0138 |
2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.675+10737G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447542 | |||||||
| chr14:99447586 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+10693C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447586 | |||||||
| chr14:99447589 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.675+10690G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447589 | |||||||
| chr14:99447734 | C | T | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+10545G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447734 | |||||||
| chr14:99447735 | G | A | 1 | a0001c0007t0002g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.675+10544C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447735 | |||||||
| chr14:99447911 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0158 others(47): Show |
52 | HG00408.hp2 HG00544.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.675+10368G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447911 | |||||||
| chr14:99448169 | A | C | 1 | a0001c0001t0001g0064 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.675+10110T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448169 | |||||||
| chr14:99448240 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.675+10039C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448240 | |||||||
| chr14:99448336 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.675+9943C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448336 | |||||||
| chr14:99448488 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG01081.hp1 HG01243.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+9791C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448488 | |||||||
| chr14:99448547 | C | T | 1 | a0001c0008t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.675+9732G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448547 | |||||||
| chr14:99448552 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.675+9727A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448552 | |||||||
| chr14:99448554 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+9725T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448554 | |||||||
| chr14:99448585 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.675+9694G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448585 | |||||||
| chr14:99448835 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.675+9444C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448835 | |||||||
| chr14:99448838 | G | T | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+9441C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448838 | |||||||
| chr14:99448972 | T | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG00735.hp1 HG01069.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.675+9307A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448972 | |||||||
| chr14:99449022 | T | G | 14 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0130 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+9257A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449022 | |||||||
| chr14:99449270 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.675+9009A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449270 | |||||||
| chr14:99449475 | C | A | 8 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+8804G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449475 | |||||||
| chr14:99449534 | A | G | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+8745T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449534 | |||||||
| chr14:99449614 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.675+8665C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449614 | |||||||
| chr14:99449672 | A | G | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+8607T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449672 | |||||||
| chr14:99449792 | A | G | 3 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 |
3 | HG02451.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.675+8487T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449792 | |||||||
| chr14:99449829 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+8450A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449829 | |||||||
| chr14:99449830 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.675+8449T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449830 | |||||||
| chr14:99449960 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675+8319T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449960 | |||||||
| chr14:99450373 | C | T | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+7906G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450373 | |||||||
| chr14:99450814 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.675+7465T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450814 | |||||||
| chr14:99450964 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.675+7315A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450964 | |||||||
| chr14:99450984 | G | C | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.675+7295C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450984 | |||||||
| chr14:99451237 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+7042A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451237 | |||||||
| chr14:99451295 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | NA18952.hp2 NA18968.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.675+6984C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451295 | |||||||
| chr14:99451472 | T | C | 1 | a0001c0004t0001g0157 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.675+6807A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451472 | |||||||
| chr14:99451527 | G | A | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+6752C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451527 | |||||||
| chr14:99451600 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.675+6679C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451600 | |||||||
| chr14:99451606 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.675+6673T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451606 | |||||||
| chr14:99452029 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.675+6250G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452029 | |||||||
| chr14:99452080 | G | C | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+6199C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452080 | |||||||
| chr14:99452170 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+6109C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452170 | |||||||
| chr14:99452200 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.675+6079C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452200 | |||||||
| chr14:99452357 | G | A | 1 | a0001c0001t0004g0008 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.675+5922C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452357 | |||||||
| chr14:99452418 | T | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 |
3 | HG01081.hp1 HG01515.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.675+5861A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452418 | |||||||
| chr14:99452470 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG02055.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+5809G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452470 | |||||||
| chr14:99452666 | A | G | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+5613T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452666 | |||||||
| chr14:99452790 | C | T | 1 | a0002c0006t0002g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.675+5489G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452790 | |||||||
| chr14:99452847 | C | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.675+5432G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452847 | |||||||
| chr14:99452848 | G | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+5431C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452848 | |||||||
| chr14:99452852 | G | T | 14 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0130 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+5427C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452852 | |||||||
| chr14:99452898 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.675+5381C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452898 | |||||||
| chr14:99452905 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.675+5374T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452905 | |||||||
| chr14:99453239 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.675+5040G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453239 | |||||||
| chr14:99453318 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.675+4961C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453318 | |||||||
| chr14:99453591 | G | A | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+4688C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453591 | |||||||
| chr14:99453601 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.675+4678C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453601 | |||||||
| chr14:99453661 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.675+4618G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453661 | |||||||
| chr14:99453673 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.675+4606T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453673 | |||||||
| chr14:99453739 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+4540A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453739 | |||||||
| chr14:99453748 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.675+4531G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453748 | |||||||
| chr14:99453820 | C | T | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+4459G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453820 | |||||||
| chr14:99453841 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.675+4438G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453841 | |||||||
| chr14:99454014 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+4265C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454014 | |||||||
| chr14:99454267 | G | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.675+4012C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454267 | |||||||
| chr14:99454328 | G | C | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+3951C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454328 | |||||||
| chr14:99454408 | C | T | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(123): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.675+3871G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454408 | |||||||
| chr14:99454504 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0220 a0001c0001t0001g0222 others(3): Show |
7 | NA18977.hp1 NA18978.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+3775T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454504 | |||||||
| chr14:99454518 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.675+3761C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454518 | |||||||
| chr14:99454576 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.675+3703A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454576 | |||||||
| chr14:99454666 | C | T | 1 | a0001c0008t0001g0105 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.675+3613G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454666 | |||||||
| chr14:99454678 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+3601T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454678 | |||||||
| chr14:99454703 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.675+3576T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454703 | |||||||
| chr14:99454704 | T | A | 1 | a0001c0001t0001g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.675+3575A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454704 | |||||||
| chr14:99454768 | GT | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.675+3510delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454768 | |||||||
| chr14:99454905 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+3374C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454905 | |||||||
| chr14:99454933 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0115 |
2 | HG00099.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.675+3346C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454933 | |||||||
| chr14:99454949 | T | C | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+3330A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454949 | |||||||
| chr14:99455095 | G | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0278 |
2 | HG02293.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.675+3184C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455095 | |||||||
| chr14:99455096 | G | C | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+3183C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455096 | |||||||
| chr14:99455568 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+2711T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455568 | |||||||
| chr14:99455584 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.675+2695G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455584 | |||||||
| chr14:99455886 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+2393C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455886 | |||||||
| chr14:99455930 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+2349C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455930 | |||||||
| chr14:99456069 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+2210A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456069 | |||||||
| chr14:99456125 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+2154T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456125 | |||||||
| chr14:99456195 | A | G | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+2084T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456195 | |||||||
| chr14:99456201 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+2078C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456201 | |||||||
| chr14:99456256 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.675+2023T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456256 | |||||||
| chr14:99456265 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.675+2014A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456265 | |||||||
| chr14:99456439 | T | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.675+1840A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456439 | |||||||
| chr14:99456445 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.675+1834A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456445 | |||||||
| chr14:99456723 | T | G | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+1556A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456723 | |||||||
| chr14:99456760 | A | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.675+1519T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456760 | |||||||
| chr14:99457070 | C | A | 2 | a0001c0001t0001g0103 a0004c0009t0001g0047 |
2 | NA18979.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.675+1209G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457070 | |||||||
| chr14:99457130 | G | A | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+1149C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457130 | |||||||
| chr14:99457193 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+1086T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457193 | |||||||
| chr14:99457225 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+1054A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457225 | |||||||
| chr14:99457229 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.675+1050C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457229 | |||||||
| chr14:99457250 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.675+1029A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457250 | |||||||
| chr14:99457297 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.675+982G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457297 | |||||||
| chr14:99457520 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.675+759G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457520 | |||||||
| chr14:99457699 | G | A | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(123): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.675+580C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457699 | |||||||
| chr14:99457793 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.675+486A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457793 | |||||||
| chr14:99457883 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+396C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457883 | |||||||
| chr14:99457941 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0104 |
2 | HG01109.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.675+338A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457941 | |||||||
| chr14:99458273 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA18985.hp2 | splice_region_variant&intron_variant | LOW | c.675+6C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99458273 | |||||||
| chr14:99458642 | TAA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.419-109_419-108del others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458642 | |||||||
| chr14:99458663 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | NA18961.hp2 NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.419-128G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458663 | |||||||
| chr14:99458771 | C | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.419-236G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458771 | |||||||
| chr14:99458774 | C | CA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.419-240dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458774 | |||||||
| chr14:99458774 | C | CAA | 12 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0046 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.419-241_419-240dup others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458774 | |||||||
| chr14:99458774 | CA | C | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(120): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.419-240delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458774 | |||||||
| chr14:99458856 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.418+257G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458856 | |||||||
| chr14:99459205 | T | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.346-20A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459205 | |||||||
| chr14:99459235 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.346-50A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459235 | |||||||
| chr14:99459254 | G | A | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.346-69C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459254 | |||||||
| chr14:99459265 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.346-80G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459265 | |||||||
| chr14:99459297 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346-112A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459297 | |||||||
| chr14:99459305 | CTTCAAAT others(5): Show |
C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0050 others(1): Show |
4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-132_346-121del others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459305 | |||||||
| chr14:99459509 | A | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.346-324T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459509 | |||||||
| chr14:99459590 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.346-405A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459590 | |||||||
| chr14:99459704 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346-519C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459704 | |||||||
| chr14:99459706 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.346-521A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459706 | |||||||
| chr14:99459823 | G | C | 3 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 |
3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.346-638C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459823 | |||||||
| chr14:99459899 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.346-714A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459899 | |||||||
| chr14:99460000 | C | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.346-815G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460000 | |||||||
| chr14:99460145 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346-960G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460145 | |||||||
| chr14:99460162 | G | GT | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(126): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.346-978dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460162 | |||||||
| chr14:99460308 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+884T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460308 | |||||||
| chr14:99460419 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.345+773G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460419 | |||||||
| chr14:99460592 | G | A | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+600C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460592 | |||||||
| chr14:99460832 | A | G | 3 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 |
3 | HG02451.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.345+360T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460832 | |||||||
| chr14:99461158 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.345+34A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99461158 | |||||||
| chr14:99461609 | G | A | 5 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-269C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99461609 | |||||||
| chr14:99461647 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.197-307T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99461647 | |||||||
| chr14:99462314 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.197-974A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462314 | |||||||
| chr14:99462460 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.196+1026G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462460 | |||||||
| chr14:99462481 | G | A | 1 | a0001c0002t0002g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+1005C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462481 | |||||||
| chr14:99462587 | G | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(92): Show |
97 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+899C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462587 | |||||||
| chr14:99462593 | G | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.196+893C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462593 | |||||||
| chr14:99462738 | C | T | 1 | a0001c0002t0002g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.196+748G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462738 | |||||||
| chr14:99462903 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0108 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.196+583C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462903 | |||||||
| chr14:99463464 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.196+22C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99463464 | |||||||
| chr14:99463705 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.104-127G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463705 | |||||||
| chr14:99463716 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.104-138G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463716 | |||||||
| chr14:99463804 | G | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.104-226C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463804 | |||||||
| chr14:99463809 | CAA | C | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.104-233_104-232del others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463809 | |||||||
| chr14:99463849 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.104-271A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463849 | |||||||
| chr14:99464203 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-625C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464203 | |||||||
| chr14:99464240 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.104-662G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464240 | |||||||
| chr14:99464386 | G | A | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.104-808C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464386 | |||||||
| chr14:99464629 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.104-1051C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464629 | |||||||
| chr14:99464693 | G | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.103+1010C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464693 | |||||||
| chr14:99464786 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.103+917A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464786 | |||||||
| chr14:99464821 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.103+882A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464821 | |||||||
| chr14:99464903 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.103+800A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464903 | |||||||
| chr14:99464916 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.103+787C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464916 | |||||||
| chr14:99464973 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.103+730G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464973 | |||||||
| chr14:99465494 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.103+209C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465494 | |||||||
| chr14:99465516 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103+187G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465516 | |||||||
| chr14:99465625 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.103+78C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465625 | |||||||
| chr14:99465627 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.103+76C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465627 | |||||||
| chr14:99466004 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-191T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466004 | |||||||
| chr14:99466301 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-8-488T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466301 | |||||||
| chr14:99466388 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-575C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466388 | |||||||
| chr14:99466422 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-8-609C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466422 | |||||||
| chr14:99466485 | C | T | 1 | a0003c0005t0010g0283 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-672G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466485 | |||||||
| chr14:99466600 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-787A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466600 | |||||||
| chr14:99466618 | CGG | C | 21 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0040 others(18): Show |
21 | HG00423.hp1 HG00673.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-807_-8-806delCC | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466618 | |||||||
| chr14:99466618 | CGGG | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-8-808_-8-806delCC others(1): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466618 | |||||||
| chr14:99466621 | G | A | 1 | a0001c0002t0002g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-808C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466621 | |||||||
| chr14:99466622 | G | A | 10 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0133 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-809C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466622 | |||||||
| chr14:99466626 | G | C | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-813C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466626 | |||||||
| chr14:99466631 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-8-818C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466631 | |||||||
| chr14:99466632 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-819C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466632 | |||||||
| chr14:99466646 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0148 |
2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-833C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466646 | |||||||
| chr14:99466885 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1072C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466885 | |||||||
| chr14:99467094 | T | TA | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(123): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-8-1282dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467094 | |||||||
| chr14:99467210 | T | C | 3 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 |
3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-8-1397A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467210 | |||||||
| chr14:99467367 | T | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0158 a0001c0001t0001g0188 others(22): Show |
26 | HG00408.hp2 HG00544.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-1554A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467367 | |||||||
| chr14:99467488 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-1675G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467488 | |||||||
| chr14:99467489 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02615.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1676T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467489 | |||||||
| chr14:99467614 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
7 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1801C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467614 | |||||||
| chr14:99467707 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-1894G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467707 | |||||||
| chr14:99467793 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-8-1980G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467793 | |||||||
| chr14:99467796 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-1983G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467796 | |||||||
| chr14:99467824 | T | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(123): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-8-2011A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467824 | |||||||
| chr14:99467887 | T | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-8-2074A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467887 | |||||||
| chr14:99468000 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-2187C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468000 | |||||||
| chr14:99468106 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-8-2293C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468106 | |||||||
| chr14:99468156 | T | TA | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(115): Show |
120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-8-2344dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468156 | |||||||
| chr14:99468582 | A | G | 26 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(23): Show |
26 | HG00558.hp2 HG00673.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-2769T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468582 | |||||||
| chr14:99468642 | T | TC | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-2830dupG | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468642 | |||||||
| chr14:99468653 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-8-2840G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468653 | |||||||
| chr14:99468681 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-8-2868A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468681 | |||||||
| chr14:99468873 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8-3060C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468873 | |||||||
| chr14:99468924 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-3111T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468924 | |||||||
| chr14:99468972 | A | G | 14 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0130 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-3159T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468972 | |||||||
| chr14:99469020 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-3207G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469020 | |||||||
| chr14:99469541 | T | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-8-3728A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469541 | |||||||
| chr14:99469565 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-8-3752T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469565 | |||||||
| chr14:99469668 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-8-3855G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469668 | |||||||
| chr14:99469682 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-3869C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469682 | |||||||
| chr14:99469889 | C | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-4076G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469889 | |||||||
| chr14:99469898 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-8-4085G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469898 | |||||||
| chr14:99469921 | G | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(117): Show |
122 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-8-4108C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469921 | |||||||
| chr14:99469984 | G | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(117): Show |
122 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-8-4171C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469984 | |||||||
| chr14:99469987 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0245 a0001c0001t0001g0271 others(6): Show |
9 | HG00423.hp2 NA18964.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-4174G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469987 | |||||||
| chr14:99470021 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-8-4208T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470021 | |||||||
| chr14:99470123 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-4310C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470123 | |||||||
| chr14:99470220 | G | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.-8-4407C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470220 | |||||||
| chr14:99470357 | C | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-8-4544G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470357 | |||||||
| chr14:99470381 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-8-4568G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470381 | |||||||
| chr14:99470610 | C | G | 28 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0001g0247 others(25): Show |
28 | HG00544.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-4797G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470610 | |||||||
| chr14:99470610 | C | T | 1 | a0001c0001t0001g0245 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-8-4797G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470610 | |||||||
| chr14:99470653 | C | T | 18 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(15): Show |
18 | HG00558.hp2 HG00673.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-4840G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470653 | |||||||
| chr14:99470657 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-4844G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470657 | |||||||
| chr14:99471012 | C | T | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-5199G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471012 | |||||||
| chr14:99471209 | T | C | 5 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5396A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471209 | |||||||
| chr14:99471292 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8-5479G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471292 | |||||||
| chr14:99471687 | T | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(116): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-8-5874A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471687 | |||||||
| chr14:99471872 | C | T | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-6059G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471872 | |||||||
| chr14:99471875 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-8-6062C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471875 | |||||||
| chr14:99471888 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-6075A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471888 | |||||||
| chr14:99472003 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-6190C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472003 | |||||||
| chr14:99472009 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-6196A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472009 | |||||||
| chr14:99472034 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-8-6221A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472034 | |||||||
| chr14:99472263 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-8-6450C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472263 | |||||||
| chr14:99472280 | T | C | 1 | a0001c0002t0002g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-6467A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472280 | |||||||
| chr14:99472466 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-8-6653A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472466 | |||||||
| chr14:99472531 | T | C | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-8-6718A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472531 | |||||||
| chr14:99472674 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-8-6861T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472674 | |||||||
| chr14:99472872 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-8-7059G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472872 | |||||||
| chr14:99472904 | T | A | 1 | a0001c0002t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8-7091A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472904 | |||||||
| chr14:99473050 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-8-7237G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473050 | |||||||
| chr14:99473265 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG01243.hp1 HG04115.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-8-7452T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473265 | |||||||
| chr14:99473308 | G | A | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9+7420C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473308 | |||||||
| chr14:99473308 | G | T | 1 | a0001c0001t0001g0245 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-9+7420C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473308 | |||||||
| chr14:99473444 | A | C | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9+7284T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473444 | |||||||
| chr14:99473564 | T | C | 1 | a0001c0002t0005g0143 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+7164A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473564 | |||||||
| chr14:99473579 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-9+7149T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473579 | |||||||
| chr14:99473684 | C | G | 4 | a0001c0003t0001g0139 a0001c0003t0001g0140 a0001c0003t0001g0141 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+7044G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473684 | |||||||
| chr14:99473991 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-9+6737C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473991 | |||||||
| chr14:99474064 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG01081.hp1 HG01243.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+6664G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474064 | |||||||
| chr14:99474339 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.-9+6389T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474339 | |||||||
| chr14:99474418 | G | A | 2 | a0001c0004t0001g0156 a0001c0004t0001g0157 |
2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-9+6310C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474418 | |||||||
| chr14:99474549 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9+6179A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474549 | |||||||
| chr14:99474636 | G | A | 8 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0123 others(5): Show |
8 | NA18951.hp1 NA18961.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+6092C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474636 | |||||||
| chr14:99474825 | G | C | 1 | a0001c0003t0001g0141 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-9+5903C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474825 | |||||||
| chr14:99474851 | T | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-9+5877A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474851 | |||||||
| chr14:99474875 | A | AT | 134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(131): Show |
136 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-9+5852dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474875 | |||||||
| chr14:99474875 | A | ATT | 7 | a0001c0001t0001g0146 a0001c0001t0001g0197 a0001c0003t0001g0139 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+5851_-9+5852dup others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474875 | |||||||
| chr14:99474989 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9+5739C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474989 | |||||||
| chr14:99475417 | A | C | 9 | a0001c0001t0001g0164 a0001c0001t0001g0189 a0001c0001t0001g0190 others(6): Show |
9 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+5311T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475417 | |||||||
| chr14:99475659 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-9+5069T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475659 | |||||||
| chr14:99475676 | T | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-9+5052A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475676 | |||||||
| chr14:99475708 | G | A | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-9+5020C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475708 | |||||||
| chr14:99475818 | C | G | 1 | a0002c0006t0002g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+4910G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475818 | |||||||
| chr14:99475840 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-9+4888T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475840 | |||||||
| chr14:99476109 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9+4619T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476109 | |||||||
| chr14:99476355 | G | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(92): Show |
97 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-9+4373C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476355 | |||||||
| chr14:99476393 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-9+4335T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476393 | |||||||
| chr14:99476745 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-9+3983A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476745 | |||||||
| chr14:99476827 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-9+3901G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476827 | |||||||
| chr14:99476911 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9+3817G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476911 | |||||||
| chr14:99477051 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+3677G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477051 | |||||||
| chr14:99477123 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-9+3605A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477123 | |||||||
| chr14:99477126 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-9+3602A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477126 | |||||||
| chr14:99477358 | C | CT | 3 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 |
3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+3369_-9+3370ins others(1): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477358 | |||||||
| chr14:99477425 | T | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-9+3303A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477425 | |||||||
| chr14:99477443 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-9+3285T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477443 | |||||||
| chr14:99477557 | C | A | 5 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+3171G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477557 | |||||||
| chr14:99477723 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0282 |
2 | HG02080.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-9+3005G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477723 | |||||||
| chr14:99477748 | C | CA | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-9+2979dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477748 | |||||||
| chr14:99477748 | C | CAA | 8 | a0001c0001t0001g0128 a0001c0001t0001g0241 a0001c0001t0001g0242 others(5): Show |
8 | HG02145.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+2978_-9+2979dup others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477748 | |||||||
| chr14:99477837 | TGA | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
9 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+2889_-9+2890del others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477837 | |||||||
| chr14:99477945 | A | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-9+2783T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477945 | |||||||
| chr14:99478050 | G | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-9+2678C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478050 | |||||||
| chr14:99478200 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-9+2528G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478200 | |||||||
| chr14:99478422 | C | A | 2 | a0001c0007t0002g0145 a0002c0006t0002g0144 |
2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-9+2306G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478422 | |||||||
| chr14:99478610 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-9+2118C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478610 | |||||||
| chr14:99478904 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+1824A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478904 | |||||||
| chr14:99478996 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-9+1732A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478996 | |||||||
| chr14:99479017 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.-9+1711C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479017 | |||||||
| chr14:99479055 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-9+1673A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479055 | |||||||
| chr14:99479075 | A | C | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG01123.hp1 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1653T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479075 | |||||||
| chr14:99479126 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9+1602C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479126 | |||||||
| chr14:99479355 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0002t0002g0147 |
3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-9+1373C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479355 | |||||||
| chr14:99479386 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9+1342C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479386 | |||||||
| chr14:99479422 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9+1306T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479422 | |||||||
| chr14:99479507 | T | A | 8 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1221A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479507 | |||||||
| chr14:99479569 | C | A | 1 | a0001c0001t0001g0278 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-9+1159G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479569 | |||||||
| chr14:99479570 | T | C | 37 | a0001c0001t0001g0012 a0001c0001t0001g0244 a0001c0001t0001g0245 others(34): Show |
37 | HG00423.hp2 HG00544.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-9+1158A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479570 | |||||||
| chr14:99479889 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+839C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479889 | |||||||
| chr14:99479891 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+837G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479891 | |||||||
| chr14:99479892 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+836C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479892 | |||||||
| chr14:99480046 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-9+682G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480046 | |||||||
| chr14:99480175 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(127): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-9+553G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480175 | |||||||
| chr14:99480210 | A | G | 5 | a0001c0002t0002g0130 a0001c0002t0002g0131 a0001c0002t0002g0132 others(2): Show |
5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+518T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480210 | |||||||
| chr14:99480240 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
131 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+488C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480240 | |||||||
| chr14:99480300 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-9+428A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480300 | |||||||
| chr14:99480351 | A | C | 1 | a0001c0001t0001g0013 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+377T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480351 | |||||||
| chr14:99480353 | C | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-9+375G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480353 | |||||||
| chr14:99480486 | G | A | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(123): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-9+242C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480486 | |||||||
| chr14:99480504 | G | C | 3 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0001c0002t0002g0281 |
3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+224C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480504 | |||||||
| chr14:99480543 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-9+185C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480543 | |||||||
| chr14:99480566 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+162G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480566 | |||||||
| chr14:99480632 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-9+96G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480632 | |||||||
| chr14:99480664 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-9+64G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480664 |