Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 29072 |
|---|---|
| ensemblid | ENSG00000181555.22 |
| hgncid | 18420 |
| symbol | SETD2 |
| name | SET domain containing 2, histone lysine methyltransferase |
| refseq_nuc | NM_014159.7 |
| refseq_prot | NP_054878.5 |
| ensembl_nuc | ENST00000409792.4 |
| ensembl_prot | ENSP00000386759.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 47016436 |
| end | 47164113 |
| strand | - |
| ver | v1.2 |
| region | chr3:47016436-47164113 |
| region5000 | chr3:47011436-47169113 |
| regionname0 | SETD2_chr3_47016436_47164113 |
| regionname5000 | SETD2_chr3_47011436_47169113 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 2564 | 130 | 39 | 23 | 47 | 5 | 15 | 34 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002 | 0/1 | 2564 | 107 | 13 | 23 | 52 | 5 | 13 | 37 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0003 | 0/0 | 2564 | 26 | 1 | 5 | 18 | 1 | 1 | 16 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0004 | 0/0 | 2564 | 24 | 23 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0005 | 0/0 | 2564 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0006 | 0/0 | 2564 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0007 | 0/0 | 2564 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0008 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0009 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0010 | 0/0 | 2564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0011 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0012 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0013 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0014 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0015 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0016 | 0/0 | 2564 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0017 | 0/0 | 2564 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0018 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0019 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 7695 | 104 | 13 | 23 | 50 | 5 | 12 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0002 | 1/0 | 7695 | 103 | 14 | 21 | 47 | 5 | 15 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0003 | 0/0 | 7695 | 25 | 0 | 5 | 18 | 1 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0004 | 0/0 | 7695 | 23 | 23 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0005 | 0/0 | 7695 | 21 | 20 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0006 | 0/0 | 7695 | 4 | 4 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0007 | 0/0 | 7695 | 4 | 2 | 2 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0008 | 0/0 | 7695 | 3 | 0 | 0 | 3 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0009 | 0/0 | 7695 | 2 | 2 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0010 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0011 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0012 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0013 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0014 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0015 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0016 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0017 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0018 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0019 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0020 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0021 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0022 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0023 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0024 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0025 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0026 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0027 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| c0028 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 838 | 177 | 51 | 32 | 72 | 6 | 15 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| t0002 | 0/0 | 847 | 69 | 2 | 13 | 40 | 1 | 13 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| t0003 | 0/0 | 841 | 40 | 15 | 9 | 7 | 5 | 4 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| t0004 | 0/0 | 838 | 17 | 17 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| t0005 | 0/0 | 844 | 3 | 1 | 2 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| t0006 | 0/0 | 847 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| t0007 | 1/0 | 847 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 7695 | 103 | 14 | 21 | 47 | 5 | 15 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0005 | 0/0 | 7695 | 21 | 20 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0006 | 0/0 | 7695 | 4 | 4 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0020 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0025 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0001 | 0/1 | 7695 | 104 | 13 | 23 | 50 | 5 | 12 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0016 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0017 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0018 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0003c0003 | 0/0 | 7695 | 25 | 0 | 5 | 18 | 1 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0003c0014 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0004c0004 | 0/0 | 7695 | 23 | 23 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0004c0010 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0005c0007 | 0/0 | 7695 | 4 | 2 | 2 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0006c0008 | 0/0 | 7695 | 3 | 0 | 0 | 3 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0007c0009 | 0/0 | 7695 | 2 | 2 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0008c0028 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0009c0027 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0010c0011 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0011c0023 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0012c0012 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0013c0022 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0014c0021 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0015c0015 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0016c0019 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0017c0013 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0018c0024 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0019c0026 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 8541 | 66 | 2 | 13 | 39 | 1 | 11 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0002t0003 | 0/0 | 8535 | 35 | 12 | 8 | 7 | 4 | 4 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0002t0006 | 0/0 | 8541 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0002t0007 | 1/0 | 8541 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0005t0001 | 0/0 | 8532 | 5 | 5 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0005t0004 | 0/0 | 8532 | 14 | 14 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0005t0005 | 0/0 | 8538 | 2 | 1 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0006t0001 | 0/0 | 8532 | 4 | 4 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0020t0003 | 0/0 | 8535 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0001c0025t0003 | 0/0 | 8535 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0001t0001 | 0/1 | 8532 | 101 | 13 | 22 | 49 | 5 | 11 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0001t0002 | 0/0 | 8541 | 2 | 0 | 0 | 1 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0001t0005 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0016t0001 | 0/0 | 8532 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0017t0001 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0002c0018t0001 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0003c0003t0001 | 0/0 | 8532 | 25 | 0 | 5 | 18 | 1 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0003c0014t0001 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0004c0004t0001 | 0/0 | 8532 | 21 | 21 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0004c0004t0004 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0004c0010t0001 | 0/0 | 8532 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0005c0007t0001 | 0/0 | 8532 | 4 | 2 | 2 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0006c0008t0001 | 0/0 | 8532 | 3 | 0 | 0 | 3 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0007c0009t0003 | 0/0 | 8535 | 2 | 2 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0008c0028t0001 | 0/0 | 8532 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0009c0027t0001 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0010c0011t0001 | 0/0 | 8532 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0011c0023t0003 | 0/0 | 8535 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0012c0012t0004 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0013c0022t0001 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0014c0021t0001 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0015c0015t0001 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0016c0019t0001 | 0/0 | 8532 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0017c0013t0001 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0018c0024t0001 | 0/0 | 8532 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| a0019c0026t0002 | 0/0 | 8541 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | copy fasta | chr3 | 47011436 | 47169113 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0002t0007g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0005t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0006t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0020t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0001c0025t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0016t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0017t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0002c0018t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0003c0014t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0004t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0004c0010t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0005c0007t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0005c0007t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0005c0007t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0005c0007t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0006c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0006c0008t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0006c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0007c0009t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0007c0009t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0008c0028t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0009c0027t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0010c0011t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0011c0023t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0012c0012t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0013c0022t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0014c0021t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0015c0015t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0016c0019t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0017c0013t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0018c0024t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| a0019c0026t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0085 | EUR | GBR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00099 | hp2 | a0002 | c0001 | t0001 | g0247 | EUR | GBR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0193 | EUR | GBR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0082 | EUR | GBR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0026 | EUR | FIN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0201 | EUR | FIN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0153 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00597 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0197 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0237 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0159 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00642 | hp1 | a0002 | c0001 | t0005 | g0073 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | CHS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0162 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0198 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0099 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0191 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0160 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01109 | hp2 | a0004 | c0010 | t0001 | g0137 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01167 | hp1 | a0005 | c0007 | t0001 | g0120 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01169 | hp1 | a0005 | c0007 | t0001 | g0121 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01169 | hp2 | a0016 | c0019 | t0001 | g0151 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0222 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0105 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0228 | AMR | PUR | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0274 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01255 | hp2 | a0001 | c0025 | t0003 | g0083 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01256 | hp1 | a0010 | c0011 | t0001 | g0224 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0076 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0182 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0194 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0053 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0285 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0084 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0216 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0241 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0308 | EUR | IBS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0081 | EUR | IBS | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0109 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0273 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01891 | hp1 | a0001 | c0006 | t0001 | g0272 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01891 | hp2 | a0005 | c0007 | t0001 | g0122 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0227 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0288 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01934 | hp1 | a0001 | c0005 | t0005 | g0072 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0196 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01943 | hp2 | a0002 | c0001 | t0001 | g0250 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0187 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0280 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0240 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0166 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0163 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0097 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0161 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0279 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0215 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0186 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0152 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02027 | hp1 | a0002 | c0017 | t0001 | g0156 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02055 | hp1 | a0004 | c0004 | t0004 | g0124 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0107 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0291 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0255 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0282 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0219 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0226 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02135 | hp2 | a0001 | c0002 | t0006 | g0009 | EAS | KHV | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02145 | hp1 | a0001 | c0020 | t0003 | g0108 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02145 | hp2 | a0002 | c0001 | t0001 | g0221 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0246 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0204 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0111 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02258 | hp2 | a0007 | c0009 | t0003 | g0100 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0096 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0142 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0101 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0195 | AMR | PEL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02451 | hp1 | a0002 | c0001 | t0001 | g0203 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0293 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02572 | hp1 | a0004 | c0004 | t0001 | g0133 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02572 | hp2 | a0001 | c0005 | t0004 | g0305 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02622 | hp1 | a0001 | c0005 | t0004 | g0299 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0116 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0125 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0165 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0123 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0147 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02698 | hp1 | a0018 | c0024 | t0001 | g0164 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0103 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02717 | hp1 | a0002 | c0001 | t0001 | g0178 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02717 | hp2 | a0004 | c0004 | t0001 | g0136 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0172 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02735 | hp2 | a0001 | c0002 | t0003 | g0093 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02809 | hp1 | a0004 | c0004 | t0001 | g0259 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02809 | hp2 | a0001 | c0002 | t0003 | g0114 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02886 | hp1 | a0001 | c0005 | t0004 | g0266 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0220 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02896 | hp1 | a0001 | c0005 | t0004 | g0301 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02896 | hp2 | a0004 | c0004 | t0001 | g0134 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02897 | hp1 | a0004 | c0004 | t0001 | g0130 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02897 | hp2 | a0001 | c0005 | t0004 | g0300 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02922 | hp1 | a0004 | c0004 | t0001 | g0132 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02922 | hp2 | a0001 | c0005 | t0005 | g0074 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0127 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0177 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02970 | hp1 | a0015 | c0015 | t0001 | g0138 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02970 | hp2 | a0012 | c0012 | t0004 | g0268 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03017 | hp1 | a0002 | c0016 | t0001 | g0185 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03041 | hp1 | a0004 | c0004 | t0001 | g0126 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03041 | hp2 | a0002 | c0001 | t0001 | g0261 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0113 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03098 | hp2 | a0001 | c0005 | t0004 | g0262 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03130 | hp1 | a0004 | c0004 | t0001 | g0140 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0102 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0112 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0260 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03209 | hp1 | a0001 | c0006 | t0001 | g0271 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03209 | hp2 | a0007 | c0009 | t0003 | g0104 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03225 | hp1 | a0004 | c0004 | t0001 | g0135 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0110 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03453 | hp1 | a0002 | c0001 | t0001 | g0181 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0294 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0106 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03486 | hp2 | a0004 | c0004 | t0001 | g0129 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0174 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0235 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0169 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0092 | AFR | ESN | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03540 | hp1 | a0017 | c0013 | t0001 | g0139 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03540 | hp2 | a0001 | c0005 | t0004 | g0264 | AFR | GWD | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03579 | hp1 | a0001 | c0005 | t0004 | g0304 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0131 | AFR | MSL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03654 | hp1 | a0008 | c0028 | t0001 | g0211 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0176 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03688 | hp1 | a0002 | c0001 | t0002 | g0001 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0077 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0091 | SAS | BEB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0175 | SAS | BEB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0205 | SAS | BEB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0052 | SAS | BEB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0269 | SAS | BEB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0171 | SAS | BEB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0251 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG04199 | hp2 | a0019 | c0026 | t0002 | g0063 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0168 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0024 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0210 | SAS | STU | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18522 | hp1 | a0001 | c0005 | t0004 | g0302 | AFR | YRI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18522 | hp2 | a0004 | c0004 | t0001 | g0258 | AFR | YRI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | CHB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | CHB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0199 | AFR | YRI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18906 | hp2 | a0001 | c0006 | t0001 | g0270 | AFR | YRI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0192 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18943 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18944 | hp2 | a0006 | c0008 | t0001 | g0206 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0180 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18949 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18951 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0243 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18954 | hp2 | a0006 | c0008 | t0001 | g0208 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0213 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18960 | hp2 | a0002 | c0018 | t0001 | g0170 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0200 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0275 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18967 | hp1 | a0002 | c0001 | t0001 | g0249 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18970 | hp1 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0167 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0232 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18978 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0281 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0289 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0212 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0189 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0297 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0115 | AFR | LWK | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | LWK | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19043 | hp1 | a0003 | c0014 | t0001 | g0307 | AFR | LWK | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0257 | AFR | LWK | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0231 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19079 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19080 | hp1 | a0006 | c0008 | t0001 | g0207 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19080 | hp2 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19081 | hp2 | a0002 | c0001 | t0001 | g0230 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0202 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0278 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0179 | EAS | JPT | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19240 | hp1 | a0004 | c0004 | t0001 | g0141 | AFR | YRI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA19240 | hp2 | a0013 | c0022 | t0001 | g0234 | AFR | YRI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0173 | AFR | ASW | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20129 | hp2 | a0004 | c0004 | t0004 | g0128 | AFR | ASW | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0158 | EUR | TSI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20752 | hp2 | a0011 | c0023 | t0003 | g0098 | EUR | TSI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0079 | EUR | TSI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0155 | EUR | TSI | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0058 | SAS | GIH | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0209 | SAS | GIH | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0080 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02109 | hp2 | a0005 | c0007 | t0001 | g0119 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0149 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02486 | hp2 | a0001 | c0005 | t0004 | g0303 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02559 | hp1 | a0014 | c0021 | t0001 | g0256 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0306 | AFR | ACB | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG06807 | hp1 | a0009 | c0027 | t0001 | g0143 | AFR | USA | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| HG06807 | hp2 | a0001 | c0005 | t0004 | g0263 | AFR | USA | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20300 | hp1 | a0004 | c0004 | t0001 | g0117 | AFR | USA | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0267 | AFR | USA | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA21309 | hp1 | a0001 | c0005 | t0004 | g0265 | AFR | LWK | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| NA21309 | hp2 | a0004 | c0004 | t0001 | g0118 | AFR | LWK | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0214 | REF | REF | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0007 | g0042 | REF | REF | SETD2_chr3_47011436_47169113 | SETD2 | chr3 | 47011436 | 47169113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47062283
|
T | C | 1 | a0015 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.6173A>G | p.Asn2058Ser | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/21 | 6362/8541 | 6173/7695 | 2058/2564 | chr3 | 47062283 | ||
| chr3:47083895
|
G | A | 8 | a0002a0006a0008others(5): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
missense_variant | MODERATE | c.5885C>T | p.Pro1962Leu | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/21 | 6074/8541 | 5885/7695 | 1962/2564 | chr3 | 47083895 | ||
| chr3:47116669
|
T | G | 1 | a0016 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.4540A>C | p.Ile1514Leu | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/21 | 4729/8541 | 4540/7695 | 1514/2564 | chr3 | 47116669 | ||
| chr3:47121178
|
A | G | 1 | a0017 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.3458T>C | p.Ile1153Thr | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 3647/8541 | 3458/7695 | 1153/2564 | chr3 | 47121178 | ||
| chr3:47121250
|
T | G | 1 | a0014 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.3386A>C | p.Asp1129Ala | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 3575/8541 | 3386/7695 | 1129/2564 | chr3 | 47121250 | ||
| chr3:47121396
|
C | T | 1 | a0003 | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
missense_variant | MODERATE | c.3240G>A | p.Met1080Ile | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 3429/8541 | 3240/7695 | 1080/2564 | chr3 | 47121396 | ||
| chr3:47121853
|
G | C | 1 | a0013 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2783C>G | p.Thr928Arg | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2972/8541 | 2783/7695 | 928/2564 | chr3 | 47121853 | ||
| chr3:47121932
|
C | G | 4 | a0004a0005a0009others(1): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
missense_variant | MODERATE | c.2704G>C | p.Glu902Gln | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2893/8541 | 2704/7695 | 902/2564 | chr3 | 47121932 | ||
| chr3:47122093
|
G | A | 1 | a0007 | 2 | HG02258.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.2543C>T | p.Ala848Val | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2732/8541 | 2543/7695 | 848/2564 | chr3 | 47122093 | ||
| chr3:47122334
|
C | G | 1 | a0012 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.2302G>C | p.Val768Leu | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2491/8541 | 2302/7695 | 768/2564 | chr3 | 47122334 | ||
| chr3:47122481
|
T | C | 1 | a0011 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2155A>G | p.Asn719Asp | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2344/8541 | 2155/7695 | 719/2564 | chr3 | 47122481 | ||
| chr3:47122540
|
T | C | 1 | a0018 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2096A>G | p.Asp699Gly | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2285/8541 | 2096/7695 | 699/2564 | chr3 | 47122540 | ||
| chr3:47122787
|
G | A | 1 | a0019 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1849C>T | p.Pro617Ser | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2038/8541 | 1849/7695 | 617/2564 | chr3 | 47122787 | ||
| chr3:47122861
|
G | T | 1 | a0010 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.1775C>A | p.Thr592Lys | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 1964/8541 | 1775/7695 | 592/2564 | chr3 | 47122861 | ||
| chr3:47122902
|
T | A | 1 | a0009 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1734A>T | p.Leu578Phe | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 1923/8541 | 1734/7695 | 578/2564 | chr3 | 47122902 | ||
| chr3:47123380
|
T | C | 1 | a0008 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.1256A>G | p.Tyr419Cys | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 1445/8541 | 1256/7695 | 419/2564 | chr3 | 47123380 | ||
| chr3:47124058
|
G | A | 1 | a0006 | 3 | NA18944.hp2 NA18954.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.578C>T | p.Pro193Leu | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 767/8541 | 578/7695 | 193/2564 | chr3 | 47124058 | ||
| chr3:47124079
|
G | A | 1 | a0005 | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
missense_variant | MODERATE | c.557C>T | p.Pro186Leu | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 746/8541 | 557/7695 | 186/2564 | chr3 | 47124079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47037732
|
A | G | 1 | a0002c0018 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.7284T>C | p.Asp2428Asp | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/21 | 7473/8541 | 7284/7695 | 2428/2564 | chr3 | 47037732 | ||
| chr3:47046502
|
A | T | 1 | a0002c0017 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.7083T>A | p.Pro2361Pro | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/21 | 7272/8541 | 7083/7695 | 2361/2564 | chr3 | 47046502 | ||
| chr3:47046517
|
A | G | 1 | a0002c0016 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.7068T>C | p.Val2356Val | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/21 | 7257/8541 | 7068/7695 | 2356/2564 | chr3 | 47046517 | ||
| chr3:47083771
|
C | T | 1 | a0001c0020 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.6009G>A | p.Val2003Val | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/21 | 6198/8541 | 6009/7695 | 2003/2564 | chr3 | 47083771 | ||
| chr3:47103391
|
A | T | 1 | a0001c0006 | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.4872T>A | p.Ser1624Ser | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/21 | 5061/8541 | 4872/7695 | 1624/2564 | chr3 | 47103391 | ||
| chr3:47120316
|
T | A | 1 | a0007c0009 | 2 | HG02258.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.4320A>T | p.Pro1440Pro | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 4509/8541 | 4320/7695 | 1440/2564 | chr3 | 47120316 | ||
| chr3:47120625
|
T | C | 1 | a0003c0014 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.4011A>G | p.Glu1337Glu | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 4200/8541 | 4011/7695 | 1337/2564 | chr3 | 47120625 | ||
| chr3:47121171
|
A | G | 22 | a0001c0005a0001c0006a0002c0001others(19): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
synonymous_variant | LOW | c.3465T>C | p.Asn1155Asn | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 3654/8541 | 3465/7695 | 1155/2564 | chr3 | 47121171 | ||
| chr3:47121387
|
T | G | 1 | a0007c0009 | 2 | HG02258.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.3249A>C | p.Thr1083Thr | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 3438/8541 | 3249/7695 | 1083/2564 | chr3 | 47121387 | ||
| chr3:47122650
|
T | C | 1 | a0001c0025 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.1986A>G | p.Gln662Gln | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 2175/8541 | 1986/7695 | 662/2564 | chr3 | 47122650 | ||
| chr3:47123651
|
G | T | 1 | a0004c0010 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.985C>A | p.Arg329Arg | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/21 | 1174/8541 | 985/7695 | 329/2564 | chr3 | 47123651 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47016515
|
A | G | 1 | a0001c0002t0006 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 21/21 | 578 | chr3 | 47016515 | |||||
| chr3:47016567
|
A | G | 32 | a0001c0002t0002a0001c0002t0003a0001c0002t0006others(29): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*526T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 21/21 | 526 | chr3 | 47016567 | |||||
| chr3:47164012
|
CGCG | C | 2 | a0001c0005t0005a0002c0001t0005 | 3 | HG00642.hp1 HG01934.hp1 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-91_-89delCGC | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/21 | 89 | chr3 | 47164012 | |||||
| chr3:47164012
|
CGCGGCG | C | 5 | a0001c0002t0003a0001c0020t0003a0001c0025t0003others(2): Show | 40 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-94_-89delCGCCGC | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/21 | 89 | chr3 | 47164012 | |||||
| chr3:47164012
|
CGCGGCGG others(2): Show |
C | 24 | a0001c0005t0001a0001c0005t0004a0001c0006t0001others(21): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
5_prime_UTR_variant | MODIFIER | c.-97_-89delCGCCGCCG others(1): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/21 | 89 | chr3 | 47164012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:47017833
|
C | T | 150 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.7432-94G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47017833 | ||||||
| chr3:47018116
|
G | C | 1 | a0003c0003t0001g0284 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.7432-377C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018116 | ||||||
| chr3:47018173
|
T | C | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.7432-434A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018173 | ||||||
| chr3:47018305
|
GCTGT | G | 3 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058 | 3 | HG03704.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.7432-570_7432-567d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018305 | ||||||
| chr3:47018325
|
C | T | 1 | a0002c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.7432-586G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018325 | ||||||
| chr3:47018358
|
G | C | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.7432-619C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018358 | ||||||
| chr3:47018391
|
T | C | 9 | a0002c0001t0001g0190a0002c0001t0001g0192a0002c0001t0001g0197others(6): Show | 9 | HG00609.hp2 HG00673.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.7432-652A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018391 | ||||||
| chr3:47018454
|
G | T | 31 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0165others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.7432-715C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018454 | ||||||
| chr3:47018684
|
C | G | 2 | a0002c0001t0001g0226a0002c0001t0001g0231 | 2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.7432-945G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018684 | ||||||
| chr3:47018731
|
C | T | 1 | a0002c0001t0001g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.7432-992G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018731 | ||||||
| chr3:47018900
|
C | A | 1 | a0001c0020t0003g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7431+860G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018900 | ||||||
| chr3:47018901
|
C | A | 1 | a0001c0020t0003g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7431+859G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018901 | ||||||
| chr3:47018933
|
T | G | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7431+827A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47018933 | ||||||
| chr3:47019128
|
G | A | 1 | a0002c0001t0001g0159 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7431+632C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47019128 | ||||||
| chr3:47019296
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7431+464G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47019296 | ||||||
| chr3:47019693
|
G | A | 35 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0148others(32): Show | 35 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.7431+67C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47019693 | ||||||
| chr3:47019693
|
G | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7431+67C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 19/20 | chr3 | 47019693 | ||||||
| chr3:47019963
|
C | T | 1 | a0002c0001t0001g0215 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7351-123G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47019963 | ||||||
| chr3:47019964
|
G | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0048 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7351-124C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47019964 | ||||||
| chr3:47020210
|
T | C | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-370A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47020210 | ||||||
| chr3:47020292
|
T | A | 2 | a0001c0002t0003g0102a0001c0002t0003g0114 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.7351-452A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47020292 | ||||||
| chr3:47020671
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7351-831G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47020671 | ||||||
| chr3:47021025
|
A | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7351-1185T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021025 | ||||||
| chr3:47021171
|
T | C | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.7351-1331A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021171 | ||||||
| chr3:47021285
|
C | G | 2 | a0002c0001t0001g0169a0002c0001t0001g0181 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.7351-1445G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021285 | ||||||
| chr3:47021351
|
C | T | 3 | a0004c0004t0001g0257a0004c0004t0001g0259a0004c0004t0001g0260 | 3 | HG02809.hp1 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.7351-1511G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021351 | ||||||
| chr3:47021475
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7351-1635G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021475 | ||||||
| chr3:47021700
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7351-1860A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021700 | ||||||
| chr3:47021834
|
C | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7351-1994G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021834 | ||||||
| chr3:47021924
|
G | A | 1 | a0010c0011t0001g0224 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.7351-2084C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021924 | ||||||
| chr3:47021975
|
C | T | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-2135G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47021975 | ||||||
| chr3:47022007
|
C | T | 1 | a0002c0001t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.7351-2167G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022007 | ||||||
| chr3:47022016
|
G | A | 1 | a0001c0005t0004g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7351-2176C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022016 | ||||||
| chr3:47022017
|
CGTGCCTG others(41): Show |
C | 16 | a0002c0001t0001g0146a0002c0001t0001g0236a0002c0001t0001g0237others(13): Show | 16 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.7351-2225_7351-217 others(52): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022017 | ||||||
| chr3:47022193
|
T | TCA | 28 | a0001c0002t0002g0004a0001c0002t0002g0022a0001c0002t0002g0034others(25): Show | 28 | HG00738.hp2 HG00741.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.7351-2355_7351-235 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
T | TCACA | 55 | a0001c0002t0002g0015a0001c0002t0002g0065a0001c0002t0003g0097others(52): Show | 55 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.7351-2357_7351-235 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
T | TCACACA | 45 | a0001c0002t0003g0110a0001c0005t0001g0123a0001c0006t0001g0270others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.7351-2359_7351-235 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
T | TCACACAC others(1): Show |
13 | a0002c0001t0001g0159a0002c0001t0001g0173a0002c0001t0001g0178others(10): Show | 13 | HG00639.hp2 HG01346.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.7351-2361_7351-235 others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
T | TCACACAC others(3): Show |
13 | a0002c0001t0001g0148a0002c0001t0001g0167a0002c0001t0001g0177others(10): Show | 13 | HG00738.hp1 HG01496.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.7351-2363_7351-235 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
T | TCACACAC others(5): Show |
4 | a0002c0001t0001g0147a0002c0001t0001g0174a0002c0001t0001g0199others(1): Show | 4 | HG00642.hp1 HG02647.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.7351-2365_7351-235 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
TCA | T | 29 | a0001c0002t0002g0024a0001c0002t0003g0086a0001c0002t0003g0087others(26): Show | 29 | HG00544.hp2 HG01109.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.7351-2355_7351-235 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
TCACA | T | 12 | a0001c0002t0003g0091a0001c0002t0003g0103a0002c0001t0001g0150others(9): Show | 12 | HG02074.hp1 HG02280.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.7351-2357_7351-235 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
TCACACAC others(5): Show |
T | 1 | a0001c0002t0002g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7351-2365_7351-235 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022193
|
TCACACAC others(7): Show |
T | 3 | a0001c0002t0003g0105a0001c0002t0003g0107a0003c0003t0001g0308 | 3 | HG01192.hp1 HG01515.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.7351-2367_7351-235 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022193 | ||||||
| chr3:47022234
|
A | C | 3 | a0002c0001t0001g0165a0002c0001t0001g0199a0004c0004t0001g0125 | 3 | HG02630.hp1 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7351-2394T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022234 | ||||||
| chr3:47022420
|
G | A | 50 | a0002c0001t0001g0150a0002c0001t0001g0152a0002c0001t0001g0153others(47): Show | 50 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.7351-2580C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022420 | ||||||
| chr3:47022549
|
A | G | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7351-2709T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022549 | ||||||
| chr3:47022797
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7351-2957C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022797 | ||||||
| chr3:47022946
|
C | A | 146 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0144others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.7351-3106G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47022946 | ||||||
| chr3:47023223
|
A | C | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-3383T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47023223 | ||||||
| chr3:47023228
|
G | A | 1 | a0002c0001t0001g0201 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.7351-3388C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47023228 | ||||||
| chr3:47023266
|
G | A | 1 | a0002c0001t0001g0189 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.7351-3426C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47023266 | ||||||
| chr3:47023591
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7351-3751A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47023591 | ||||||
| chr3:47023696
|
C | T | 1 | a0004c0004t0001g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7351-3856G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47023696 | ||||||
| chr3:47023765
|
C | T | 5 | a0002c0001t0001g0193a0002c0001t0001g0195a0002c0001t0001g0196others(2): Show | 5 | HG00140.hp1 HG00280.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.7351-3925G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47023765 | ||||||
| chr3:47024279
|
T | G | 28 | a0001c0005t0001g0273a0001c0005t0001g0306a0003c0003t0001g0269others(25): Show | 28 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.7351-4439A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024279 | ||||||
| chr3:47024287
|
G | A | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7351-4447C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024287 | ||||||
| chr3:47024288
|
A | C | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7351-4448T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024288 | ||||||
| chr3:47024388
|
C | T | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.7351-4548G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024388 | ||||||
| chr3:47024466
|
C | T | 1 | a0001c0002t0003g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7351-4626G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024466 | ||||||
| chr3:47024467
|
G | A | 1 | a0002c0001t0001g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.7351-4627C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024467 | ||||||
| chr3:47024513
|
C | T | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-4673G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024513 | ||||||
| chr3:47024521
|
G | A | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7351-4681C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024521 | ||||||
| chr3:47024713
|
A | C | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-4873T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024713 | ||||||
| chr3:47024732
|
A | G | 1 | a0004c0004t0001g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7351-4892T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47024732 | ||||||
| chr3:47025288
|
A | G | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7351-5448T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47025288 | ||||||
| chr3:47025318
|
C | A | 1 | a0017c0013t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.7351-5478G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47025318 | ||||||
| chr3:47025748
|
T | C | 2 | a0004c0004t0001g0140a0004c0004t0001g0141 | 2 | HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.7351-5908A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47025748 | ||||||
| chr3:47025906
|
A | G | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-6066T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47025906 | ||||||
| chr3:47025946
|
T | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7351-6106A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47025946 | ||||||
| chr3:47026266
|
C | T | 1 | a0002c0001t0001g0187 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.7351-6426G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026266 | ||||||
| chr3:47026313
|
C | T | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7351-6473G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026313 | ||||||
| chr3:47026347
|
T | C | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-6507A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026347 | ||||||
| chr3:47026393
|
C | T | 3 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058 | 3 | HG03704.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.7351-6553G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026393 | ||||||
| chr3:47026625
|
T | TA | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-6786dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026625 | ||||||
| chr3:47026707
|
CA | C | 150 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.7351-6868delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026707 | ||||||
| chr3:47026781
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.7351-6941C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026781 | ||||||
| chr3:47026832
|
G | T | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7351-6992C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026832 | ||||||
| chr3:47026864
|
G | A | 4 | a0004c0004t0001g0257a0004c0004t0001g0258a0004c0004t0001g0259others(1): Show | 4 | HG02809.hp1 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.7351-7024C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026864 | ||||||
| chr3:47026930
|
A | G | 2 | a0005c0007t0001g0120a0005c0007t0001g0121 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.7351-7090T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026930 | ||||||
| chr3:47026949
|
G | GTA | 4 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0148others(1): Show | 4 | HG02027.hp1 HG02132.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.7351-7111_7351-711 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47026949 | ||||||
| chr3:47027115
|
C | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7351-7275G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027115 | ||||||
| chr3:47027126
|
G | A | 1 | a0001c0002t0002g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7351-7286C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027126 | ||||||
| chr3:47027131
|
C | T | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7351-7291G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027131 | ||||||
| chr3:47027180
|
T | C | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7351-7340A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027180 | ||||||
| chr3:47027198
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7351-7358G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027198 | ||||||
| chr3:47027200
|
T | C | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.7351-7360A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027200 | ||||||
| chr3:47027233
|
G | A | 1 | a0002c0001t0001g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.7351-7393C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027233 | ||||||
| chr3:47027312
|
G | C | 1 | a0002c0001t0001g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.7351-7472C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027312 | ||||||
| chr3:47027336
|
C | CA | 14 | a0001c0002t0002g0028a0001c0005t0001g0115a0001c0005t0001g0306others(11): Show | 14 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.7351-7497dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027336 | ||||||
| chr3:47027336
|
C | CAA | 65 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(62): Show | 65 | HG00280.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.7351-7498_7351-749 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027336 | ||||||
| chr3:47027336
|
C | CAAA | 58 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(55): Show | 58 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.7351-7499_7351-749 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027336 | ||||||
| chr3:47027336
|
C | CAAAA | 10 | a0001c0002t0003g0081a0001c0002t0003g0107a0001c0002t0003g0113others(7): Show | 10 | HG01515.hp2 HG02055.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.7351-7500_7351-749 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027336 | ||||||
| chr3:47027336
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0003g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7351-7506_7351-749 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027336 | ||||||
| chr3:47027336
|
CAAAAAAA others(7): Show |
C | 115 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.7351-7510_7351-749 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027336 | ||||||
| chr3:47027408
|
T | C | 150 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.7351-7568A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027408 | ||||||
| chr3:47027499
|
C | T | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-7659G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027499 | ||||||
| chr3:47027564
|
T | C | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-7724A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027564 | ||||||
| chr3:47027574
|
T | A | 1 | a0002c0001t0002g0001 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7351-7734A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027574 | ||||||
| chr3:47027785
|
T | TG | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-7946_7351-794 others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027785 | ||||||
| chr3:47027786
|
T | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7351-7946A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027786 | ||||||
| chr3:47027788
|
T | G | 115 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.7351-7948A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027788 | ||||||
| chr3:47027800
|
G | GT | 6 | a0001c0002t0003g0089a0001c0002t0003g0097a0001c0005t0004g0303others(3): Show | 6 | HG01981.hp1 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.7351-7961dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027800 | ||||||
| chr3:47027806
|
T | G | 5 | a0002c0001t0001g0158a0002c0001t0001g0209a0002c0001t0001g0229others(2): Show | 5 | HG00642.hp1 HG02698.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.7351-7966A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027806 | ||||||
| chr3:47027885
|
G | A | 2 | a0001c0002t0002g0014a0001c0002t0002g0019 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.7351-8045C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027885 | ||||||
| chr3:47027937
|
G | GC | 19 | a0001c0002t0002g0004a0001c0002t0002g0027a0001c0002t0002g0029others(16): Show | 19 | HG00621.hp2 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.7351-8098dupG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027937 | ||||||
| chr3:47027939
|
C | A | 2 | a0002c0001t0001g0202a0002c0001t0001g0219 | 2 | HG02083.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.7351-8099G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027939 | ||||||
| chr3:47027944
|
C | T | 1 | a0001c0002t0003g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.7351-8104G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47027944 | ||||||
| chr3:47028014
|
G | T | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7351-8174C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47028014 | ||||||
| chr3:47028611
|
T | A | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7351-8771A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47028611 | ||||||
| chr3:47028675
|
G | C | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7351-8835C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47028675 | ||||||
| chr3:47028895
|
G | A | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.7350+8771C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47028895 | ||||||
| chr3:47028927
|
C | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.7350+8739G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47028927 | ||||||
| chr3:47029007
|
C | A | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7350+8659G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029007 | ||||||
| chr3:47029065
|
AT | A | 138 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0006others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.7350+8600delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029065 | ||||||
| chr3:47029087
|
G | A | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7350+8579C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029087 | ||||||
| chr3:47029090
|
G | A | 1 | a0002c0001t0001g0193 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7350+8576C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029090 | ||||||
| chr3:47029206
|
A | G | 1 | a0002c0001t0001g0233 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.7350+8460T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029206 | ||||||
| chr3:47029265
|
T | C | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7350+8401A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029265 | ||||||
| chr3:47029483
|
C | CA | 58 | a0001c0002t0002g0027a0001c0005t0001g0149a0001c0005t0005g0072others(55): Show | 58 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.7350+8182dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029483 | ||||||
| chr3:47029698
|
A | T | 2 | a0005c0007t0001g0120a0005c0007t0001g0121 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.7350+7968T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029698 | ||||||
| chr3:47029699
|
TGATTTGG others(14): Show |
T | 2 | a0005c0007t0001g0120a0005c0007t0001g0121 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.7350+7946_7350+796 others(25): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029699 | ||||||
| chr3:47029812
|
A | G | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+7854T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029812 | ||||||
| chr3:47029889
|
C | T | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7350+7777G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029889 | ||||||
| chr3:47029967
|
C | T | 1 | a0002c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7350+7699G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47029967 | ||||||
| chr3:47030111
|
C | T | 2 | a0002c0001t0001g0209a0002c0001t0001g0210 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.7350+7555G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47030111 | ||||||
| chr3:47030162
|
A | G | 1 | a0002c0001t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7350+7504T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47030162 | ||||||
| chr3:47030324
|
T | G | 1 | a0002c0018t0001g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.7350+7342A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47030324 | ||||||
| chr3:47030580
|
C | T | 1 | a0001c0002t0003g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7350+7086G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47030580 | ||||||
| chr3:47031128
|
A | G | 1 | a0002c0001t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.7350+6538T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031128 | ||||||
| chr3:47031131
|
T | A | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7350+6535A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031131 | ||||||
| chr3:47031152
|
T | C | 1 | a0003c0003t0001g0289 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.7350+6514A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031152 | ||||||
| chr3:47031267
|
A | G | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7350+6399T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031267 | ||||||
| chr3:47031320
|
T | C | 1 | a0012c0012t0004g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7350+6346A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031320 | ||||||
| chr3:47031369
|
G | A | 1 | a0002c0001t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.7350+6297C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031369 | ||||||
| chr3:47031735
|
T | C | 1 | a0001c0002t0002g0026 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7350+5931A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031735 | ||||||
| chr3:47031776
|
C | T | 115 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.7350+5890G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031776 | ||||||
| chr3:47031864
|
A | G | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7350+5802T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031864 | ||||||
| chr3:47031899
|
T | C | 25 | a0002c0001t0001g0165a0004c0004t0001g0116a0004c0004t0001g0117others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.7350+5767A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47031899 | ||||||
| chr3:47032094
|
G | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+5572C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032094 | ||||||
| chr3:47032341
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7350+5325G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032341 | ||||||
| chr3:47032375
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+5291A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032375 | ||||||
| chr3:47032454
|
A | G | 2 | a0001c0002t0002g0044a0001c0002t0002g0060 | 2 | NA18957.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.7350+5212T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032454 | ||||||
| chr3:47032497
|
T | G | 2 | a0002c0001t0001g0244a0002c0001t0001g0245 | 2 | NA18943.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.7350+5169A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032497 | ||||||
| chr3:47032540
|
A | G | 2 | a0001c0002t0002g0035a0001c0002t0002g0057 | 2 | HG01109.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.7350+5126T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032540 | ||||||
| chr3:47032553
|
A | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7350+5113T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032553 | ||||||
| chr3:47032688
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+4978C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032688 | ||||||
| chr3:47032924
|
A | G | 1 | a0002c0001t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7350+4742T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032924 | ||||||
| chr3:47032981
|
T | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7350+4685A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47032981 | ||||||
| chr3:47033365
|
A | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+4301T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033365 | ||||||
| chr3:47033416
|
T | C | 105 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.7350+4250A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033416 | ||||||
| chr3:47033437
|
G | A | 108 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.7350+4229C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033437 | ||||||
| chr3:47033549
|
G | A | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7350+4117C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033549 | ||||||
| chr3:47033643
|
C | A | 1 | a0001c0002t0003g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.7350+4023G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033643 | ||||||
| chr3:47033652
|
A | AT | 105 | a0001c0002t0002g0034a0001c0002t0002g0050a0001c0005t0001g0123others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.7350+4013dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033652 | ||||||
| chr3:47033652
|
A | ATT | 96 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0010others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.7350+4012_7350+401 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033652 | ||||||
| chr3:47033652
|
A | ATTT | 39 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(36): Show | 39 | HG00597.hp1 HG00639.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.7350+4011_7350+401 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033652 | ||||||
| chr3:47033652
|
AT | A | 7 | a0004c0004t0001g0117a0004c0004t0001g0140a0004c0004t0001g0141others(4): Show | 7 | HG01167.hp1 HG02280.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.7350+4013delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033652 | ||||||
| chr3:47033652
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.7350+4002_7350+401 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033652 | ||||||
| chr3:47033691
|
C | T | 1 | a0001c0002t0003g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7350+3975G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033691 | ||||||
| chr3:47033939
|
A | G | 290 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.7350+3727T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47033939 | ||||||
| chr3:47034012
|
C | T | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7350+3654G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47034012 | ||||||
| chr3:47034113
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+3553G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47034113 | ||||||
| chr3:47034568
|
C | T | 1 | a0001c0002t0002g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.7350+3098G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47034568 | ||||||
| chr3:47034582
|
G | C | 1 | a0001c0002t0002g0069 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.7350+3084C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47034582 | ||||||
| chr3:47034604
|
G | A | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7350+3062C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47034604 | ||||||
| chr3:47034673
|
C | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7350+2993G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47034673 | ||||||
| chr3:47035175
|
T | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7350+2491A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035175 | ||||||
| chr3:47035425
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7350+2241C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035425 | ||||||
| chr3:47035459
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7350+2207A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035459 | ||||||
| chr3:47035587
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7350+2079A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035587 | ||||||
| chr3:47035676
|
A | G | 1 | a0001c0002t0002g0054 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.7350+1990T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035676 | ||||||
| chr3:47035686
|
G | T | 1 | a0004c0010t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7350+1980C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035686 | ||||||
| chr3:47035735
|
G | A | 1 | a0001c0005t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7350+1931C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035735 | ||||||
| chr3:47035828
|
G | T | 2 | a0004c0004t0001g0142a0009c0027t0001g0143 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.7350+1838C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47035828 | ||||||
| chr3:47036160
|
T | C | 1 | a0004c0004t0001g0130 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.7350+1506A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036160 | ||||||
| chr3:47036358
|
C | T | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.7350+1308G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036358 | ||||||
| chr3:47036539
|
A | G | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7350+1127T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036539 | ||||||
| chr3:47036571
|
C | A | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7350+1095G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036571 | ||||||
| chr3:47036905
|
T | TAAAAAAA others(5): Show |
3 | a0002c0001t0001g0231a0004c0004t0001g0258a0006c0008t0001g0208 | 3 | NA18522.hp2 NA18954.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.7350+760_7350+761i others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036905
|
T | TAAAAAAA others(6): Show |
121 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.7350+760_7350+761i others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036905
|
T | TAAAAAAA others(7): Show |
60 | a0001c0005t0004g0263a0001c0005t0004g0265a0001c0005t0004g0266others(57): Show | 60 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.7350+760_7350+761i others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036905
|
T | TAAAAAAA others(8): Show |
9 | a0001c0005t0001g0306a0001c0005t0004g0262a0001c0005t0004g0303others(6): Show | 9 | HG00673.hp2 HG02071.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.7350+760_7350+761i others(17): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036905
|
T | TAAAAAAA others(10): Show |
1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7350+760_7350+761i others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036905
|
T | TAAAAAAA others(11): Show |
3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7350+760_7350+761i others(20): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036905
|
T | TTAAAAAA others(6): Show |
1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7350+760_7350+761i others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036905 | ||||||
| chr3:47036915
|
A | AAAAAAAA others(6): Show |
1 | a0002c0001t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.7350+750_7350+751i others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47036915 | ||||||
| chr3:47037059
|
CT | C | 50 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0010others(47): Show | 50 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.7350+606delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTT | C | 19 | a0001c0002t0002g0049a0001c0002t0002g0070a0001c0002t0003g0077others(16): Show | 19 | HG01070.hp2 HG01192.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.7350+605_7350+606d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTT | C | 99 | a0001c0006t0001g0293a0002c0001t0001g0144a0002c0001t0001g0145others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.7350+604_7350+606d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTT | C | 9 | a0001c0005t0001g0149a0001c0005t0001g0306a0001c0005t0005g0072others(6): Show | 9 | HG01255.hp1 HG01934.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.7350+603_7350+606d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTTT | C | 62 | a0001c0005t0001g0273a0001c0005t0004g0262a0001c0005t0004g0263others(59): Show | 62 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(59): Show |
intron_variant | MODIFIER | c.7350+602_7350+606d others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTTTT | C | 13 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0005g0074others(10): Show | 13 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.7350+601_7350+606d others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0001t0001g0241 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7350+597_7350+606d others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7350+596_7350+606d others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTTTTT others(5): Show |
C | 1 | a0007c0009t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7350+595_7350+606d others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037059
|
CTTTTTTT others(10): Show |
C | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.7350+590_7350+606d others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037059 | ||||||
| chr3:47037280
|
C | A | 1 | a0016c0019t0001g0151 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.7350+386G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037280 | ||||||
| chr3:47037281
|
T | TC | 44 | a0001c0002t0002g0013a0001c0002t0002g0018a0001c0002t0002g0020others(41): Show | 44 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.7350+384dupG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037281 | ||||||
| chr3:47037282
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+384G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037282 | ||||||
| chr3:47037288
|
C | T | 31 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0165others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.7350+378G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037288 | ||||||
| chr3:47037307
|
G | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7350+359C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037307 | ||||||
| chr3:47037378
|
G | A | 1 | a0002c0001t0001g0188 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.7350+288C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037378 | ||||||
| chr3:47037622
|
G | A | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.7350+44C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 18/20 | chr3 | 47037622 | ||||||
| chr3:47038431
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7239-654G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038431 | ||||||
| chr3:47038515
|
T | G | 1 | a0002c0001t0002g0002 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.7239-738A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038515 | ||||||
| chr3:47038630
|
A | C | 1 | a0002c0001t0001g0195 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.7239-853T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038630 | ||||||
| chr3:47038636
|
A | C | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7239-859T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038636 | ||||||
| chr3:47038637
|
A | C | 197 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.7239-860T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038637 | ||||||
| chr3:47038695
|
G | A | 1 | a0002c0001t0001g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7239-918C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038695 | ||||||
| chr3:47038855
|
C | T | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7239-1078G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47038855 | ||||||
| chr3:47039237
|
T | C | 1 | a0003c0003t0001g0269 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.7239-1460A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039237 | ||||||
| chr3:47039508
|
C | T | 1 | a0002c0001t0001g0253 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7239-1731G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039508 | ||||||
| chr3:47039509
|
G | A | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.7239-1732C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039509 | ||||||
| chr3:47039711
|
C | CA | 7 | a0001c0002t0002g0021a0001c0002t0002g0022a0001c0002t0002g0025others(4): Show | 7 | HG00280.hp1 HG00741.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.7239-1935dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039711 | ||||||
| chr3:47039711
|
CA | C | 72 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.7239-1935delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039711 | ||||||
| chr3:47039711
|
CAA | C | 162 | a0001c0005t0001g0115a0001c0005t0001g0149a0001c0005t0001g0273others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.7239-1936_7239-193 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039711 | ||||||
| chr3:47039725
|
A | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7239-1948T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039725 | ||||||
| chr3:47039919
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7239-2142G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039919 | ||||||
| chr3:47039920
|
G | A | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7239-2143C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039920 | ||||||
| chr3:47039941
|
C | G | 1 | a0002c0001t0001g0213 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.7239-2164G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47039941 | ||||||
| chr3:47040074
|
T | G | 1 | a0007c0009t0003g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7239-2297A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040074 | ||||||
| chr3:47040297
|
C | A | 1 | a0001c0002t0003g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.7238+2264G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040297 | ||||||
| chr3:47040359
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7238+2202C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040359 | ||||||
| chr3:47040451
|
T | C | 1 | a0002c0001t0001g0217 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7238+2110A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040451 | ||||||
| chr3:47040569
|
A | AT | 28 | a0001c0002t0002g0013a0001c0002t0002g0015a0001c0002t0002g0020others(25): Show | 28 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.7238+1991dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTT | 73 | a0001c0005t0001g0273a0001c0006t0001g0272a0001c0006t0001g0293others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.7238+1987_7238+199 others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTT | 50 | a0001c0005t0001g0123a0001c0005t0004g0263a0001c0005t0004g0265others(47): Show | 50 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.7238+1986_7238+199 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT | 36 | a0001c0005t0004g0262a0001c0005t0004g0264a0001c0005t0004g0266others(33): Show | 36 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.7238+1985_7238+199 others(11): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT others(1): Show |
12 | a0001c0005t0001g0115a0002c0001t0001g0152a0002c0001t0001g0153others(9): Show | 12 | HG00558.hp1 HG01928.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.7238+1984_7238+199 others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT others(2): Show |
6 | a0001c0005t0001g0149a0003c0003t0001g0274a0003c0003t0001g0276others(3): Show | 6 | HG01255.hp1 HG02074.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.7238+1983_7238+199 others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT others(3): Show |
2 | a0003c0003t0001g0278a0003c0003t0001g0296 | 2 | NA18970.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.7238+1982_7238+199 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT others(5): Show |
1 | a0003c0003t0001g0280 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.7238+1980_7238+199 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT others(7): Show |
1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7238+1978_7238+199 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
A | ATTTTTTT others(9): Show |
1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7238+1976_7238+199 others(20): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040569
|
ATTTT | A | 12 | a0004c0004t0001g0116a0004c0004t0001g0125a0004c0004t0001g0126others(9): Show | 12 | HG02572.hp1 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.7238+1988_7238+199 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040569 | ||||||
| chr3:47040995
|
T | C | 1 | a0001c0002t0003g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7238+1566A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47040995 | ||||||
| chr3:47041025
|
T | G | 1 | a0001c0002t0003g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7238+1536A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47041025 | ||||||
| chr3:47041284
|
T | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7238+1277A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47041284 | ||||||
| chr3:47041605
|
T | C | 1 | a0019c0026t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7238+956A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47041605 | ||||||
| chr3:47041652
|
C | G | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7238+909G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47041652 | ||||||
| chr3:47041878
|
G | A | 1 | a0001c0002t0002g0050 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.7238+683C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47041878 | ||||||
| chr3:47042123
|
C | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7238+438G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47042123 | ||||||
| chr3:47042131
|
G | A | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.7238+430C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47042131 | ||||||
| chr3:47042292
|
C | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7238+269G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47042292 | ||||||
| chr3:47042508
|
C | T | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7238+53G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 17/20 | chr3 | 47042508 | ||||||
| chr3:47043058
|
C | T | 4 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0064others(1): Show | 4 | NA18953.hp2 NA18961.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.7099-358G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47043058 | ||||||
| chr3:47043369
|
A | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.7099-669T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47043369 | ||||||
| chr3:47043776
|
T | G | 2 | a0001c0002t0003g0079a0001c0002t0003g0081 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.7099-1076A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47043776 | ||||||
| chr3:47044200
|
A | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.7099-1500T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044200 | ||||||
| chr3:47044344
|
C | CA | 7 | a0001c0002t0002g0033a0001c0002t0002g0034a0001c0002t0002g0056others(4): Show | 7 | HG00741.hp1 HG01346.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.7099-1645dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(3): Show |
1 | a0001c0005t0004g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.7099-1654_7099-164 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(4): Show |
1 | a0001c0005t0004g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7099-1655_7099-164 others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(5): Show |
4 | a0001c0002t0002g0036a0001c0002t0002g0055a0001c0002t0002g0062others(1): Show | 4 | HG02080.hp1 NA18940.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.7099-1656_7099-164 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(7): Show |
2 | a0001c0005t0004g0263a0002c0001t0001g0255 | 2 | HG02074.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.7099-1658_7099-164 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(8): Show |
1 | a0004c0004t0004g0128 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7099-1659_7099-164 others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(9): Show |
2 | a0001c0002t0002g0069a0001c0002t0003g0096 | 2 | HG01975.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.7099-1660_7099-164 others(20): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(10): Show |
1 | a0001c0005t0004g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7099-1661_7099-164 others(21): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(11): Show |
1 | a0001c0002t0002g0005 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7099-1662_7099-164 others(22): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(13): Show |
2 | a0001c0002t0002g0031a0001c0005t0004g0300 | 2 | HG02897.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.7099-1664_7099-164 others(24): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(14): Show |
3 | a0001c0002t0002g0004a0001c0005t0004g0301a0001c0005t0004g0304 | 3 | HG02896.hp1 HG03579.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.7099-1665_7099-164 others(25): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(15): Show |
1 | a0001c0002t0002g0016 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.7099-1666_7099-164 others(26): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0002g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.7099-1667_7099-164 others(27): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
C | CAAAAAAA others(28): Show |
1 | a0001c0002t0002g0027 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.7099-1679_7099-164 others(39): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CA | C | 31 | a0001c0002t0002g0022a0001c0002t0002g0052a0001c0002t0002g0053others(28): Show | 31 | HG00140.hp2 HG00642.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.7099-1645delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAA | C | 26 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0024others(23): Show | 26 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.7099-1646_7099-164 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAA | C | 15 | a0001c0002t0002g0029a0001c0002t0003g0095a0001c0002t0003g0102others(12): Show | 15 | HG00544.hp1 HG00621.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.7099-1647_7099-164 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAA | C | 6 | a0001c0002t0002g0006a0001c0002t0002g0014a0001c0002t0002g0015others(3): Show | 6 | HG00639.hp1 HG02071.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.7099-1650_7099-164 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA | C | 7 | a0001c0002t0002g0018a0001c0002t0002g0019a0001c0002t0002g0028others(4): Show | 7 | HG03453.hp2 HG03654.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.7099-1651_7099-164 others(11): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0002g0008a0001c0002t0002g0048 | 2 | HG03492.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.7099-1654_7099-164 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(4): Show |
C | 6 | a0001c0002t0002g0047a0001c0002t0002g0060a0001c0002t0002g0065others(3): Show | 6 | HG01891.hp1 HG03209.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.7099-1655_7099-164 others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0002t0002g0003a0001c0002t0002g0044a0015c0015t0001g0138 | 3 | HG00673.hp1 HG02970.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.7099-1656_7099-164 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.7099-1657_7099-164 others(17): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(7): Show |
C | 6 | a0001c0005t0004g0265a0002c0001t0001g0196a0002c0001t0001g0222others(3): Show | 6 | HG01175.hp1 HG01934.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.7099-1658_7099-164 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(8): Show |
C | 46 | a0001c0002t0002g0017a0001c0002t0002g0057a0001c0002t0003g0075others(43): Show | 46 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.7099-1659_7099-164 others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(9): Show |
C | 63 | a0001c0002t0002g0035a0001c0005t0001g0306a0002c0001t0001g0147others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.7099-1660_7099-164 others(20): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(10): Show |
C | 1 | a0002c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7099-1661_7099-164 others(21): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7099-1662_7099-164 others(22): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7099-1663_7099-164 others(23): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(13): Show |
C | 1 | a0002c0001t0001g0144 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.7099-1664_7099-164 others(24): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(14): Show |
C | 3 | a0001c0002t0003g0111a0002c0001t0001g0172a0007c0009t0003g0100 | 3 | HG02258.hp1 HG02258.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.7099-1665_7099-164 others(25): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(15): Show |
C | 2 | a0001c0002t0003g0112a0001c0002t0003g0113 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7099-1666_7099-164 others(26): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0002t0002g0049 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.7099-1669_7099-164 others(29): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044344
|
CAAAAAAA others(20): Show |
C | 2 | a0001c0002t0002g0041a0019c0026t0002g0063 | 2 | HG04199.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.7099-1671_7099-164 others(31): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044344 | ||||||
| chr3:47044387
|
G | T | 9 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0029others(6): Show | 9 | HG00621.hp2 HG02080.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.7099-1687C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044387 | ||||||
| chr3:47044398
|
G | T | 7 | a0002c0001t0001g0165a0004c0004t0001g0117a0004c0004t0001g0140others(4): Show | 7 | HG02280.hp2 HG02630.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.7099-1698C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044398 | ||||||
| chr3:47044558
|
G | A | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.7099-1858C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044558 | ||||||
| chr3:47044635
|
C | T | 1 | a0002c0001t0001g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.7098+1852G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044635 | ||||||
| chr3:47044757
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.7098+1730G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044757 | ||||||
| chr3:47044921
|
G | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7098+1566C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47044921 | ||||||
| chr3:47045028
|
C | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.7098+1459G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045028 | ||||||
| chr3:47045063
|
C | T | 1 | a0002c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.7098+1424G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045063 | ||||||
| chr3:47045162
|
C | T | 1 | a0001c0002t0003g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.7098+1325G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045162 | ||||||
| chr3:47045519
|
T | TA | 17 | a0001c0002t0002g0024a0001c0002t0002g0043a0001c0002t0002g0050others(14): Show | 17 | HG00544.hp1 HG01978.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.7098+967dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045519 | ||||||
| chr3:47045519
|
TA | T | 41 | a0001c0005t0001g0273a0001c0005t0001g0306a0001c0005t0004g0263others(38): Show | 41 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.7098+967delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045519 | ||||||
| chr3:47045685
|
T | TA | 190 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.7098+801dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045685 | ||||||
| chr3:47045721
|
A | G | 3 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058 | 3 | HG03704.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.7098+766T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045721 | ||||||
| chr3:47045748
|
G | A | 1 | a0012c0012t0004g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7098+739C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045748 | ||||||
| chr3:47045779
|
A | AT | 7 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0019others(4): Show | 7 | HG01256.hp2 HG02027.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.7098+707dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045779 | ||||||
| chr3:47045779
|
AT | A | 37 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(34): Show | 37 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.7098+707delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045779 | ||||||
| chr3:47045862
|
G | A | 1 | a0001c0002t0003g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.7098+625C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045862 | ||||||
| chr3:47045942
|
C | T | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7098+545G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045942 | ||||||
| chr3:47045972
|
A | T | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.7098+515T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47045972 | ||||||
| chr3:47046050
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7098+437G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046050 | ||||||
| chr3:47046167
|
G | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.7098+320C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046167 | ||||||
| chr3:47046252
|
G | A | 8 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(5): Show | 8 | HG00544.hp2 HG02735.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.7098+235C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046252 | ||||||
| chr3:47046346
|
AT | A | 7 | a0002c0001t0001g0190a0002c0001t0001g0192a0002c0001t0001g0197others(4): Show | 7 | HG00609.hp2 HG00673.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.7098+140delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046346 | ||||||
| chr3:47046347
|
T | A | 119 | a0001c0002t0002g0029a0001c0005t0001g0115a0001c0005t0001g0123others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.7098+140A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046347 | ||||||
| chr3:47046352
|
T | A | 11 | a0001c0005t0005g0074a0002c0001t0001g0190a0002c0001t0001g0192others(8): Show | 11 | HG00609.hp2 HG00673.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.7098+135A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046352 | ||||||
| chr3:47046353
|
A | T | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7098+134T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046353 | ||||||
| chr3:47046358
|
A | G | 1 | a0002c0001t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.7098+129T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046358 | ||||||
| chr3:47046359
|
A | G | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.7098+128T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046359 | ||||||
| chr3:47046388
|
A | C | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7098+99T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 16/20 | chr3 | 47046388 | ||||||
| chr3:47046670
|
A | C | 1 | a0001c0002t0002g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6964-49T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47046670 | ||||||
| chr3:47046679
|
C | T | 1 | a0001c0002t0002g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6964-58G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47046679 | ||||||
| chr3:47046904
|
A | C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6964-283T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47046904 | ||||||
| chr3:47047167
|
A | G | 2 | a0002c0001t0001g0179a0002c0001t0001g0218 | 2 | NA19004.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.6964-546T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047167 | ||||||
| chr3:47047178
|
T | A | 37 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.6964-557A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047178 | ||||||
| chr3:47047198
|
A | G | 1 | a0003c0003t0001g0269 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6964-577T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047198 | ||||||
| chr3:47047200
|
A | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6964-579T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047200 | ||||||
| chr3:47047204
|
C | T | 1 | a0001c0002t0002g0011 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6964-583G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047204 | ||||||
| chr3:47047335
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6964-714G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047335 | ||||||
| chr3:47047574
|
A | G | 1 | a0001c0002t0002g0026 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6964-953T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047574 | ||||||
| chr3:47047947
|
A | G | 3 | a0002c0001t0001g0209a0002c0001t0001g0210a0008c0028t0001g0211 | 3 | HG03654.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6964-1326T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47047947 | ||||||
| chr3:47048111
|
G | A | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6964-1490C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048111 | ||||||
| chr3:47048164
|
C | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6964-1543G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048164 | ||||||
| chr3:47048205
|
C | T | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6964-1584G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048205 | ||||||
| chr3:47048375
|
C | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6964-1754G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048375 | ||||||
| chr3:47048427
|
C | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6964-1806G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048427 | ||||||
| chr3:47048471
|
A | T | 1 | a0001c0002t0002g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6964-1850T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048471 | ||||||
| chr3:47048562
|
CA | C | 15 | a0004c0004t0001g0116a0004c0004t0001g0125a0004c0004t0001g0126others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.6964-1942delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048562 | ||||||
| chr3:47048563
|
A | T | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6964-1942T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048563 | ||||||
| chr3:47048651
|
A | T | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.6964-2030T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048651 | ||||||
| chr3:47048652
|
T | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6964-2031A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048652 | ||||||
| chr3:47048731
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6964-2110C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048731 | ||||||
| chr3:47048958
|
G | A | 2 | a0001c0002t0003g0102a0001c0002t0003g0114 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.6964-2337C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048958 | ||||||
| chr3:47048967
|
A | G | 1 | a0002c0001t0001g0189 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.6964-2346T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47048967 | ||||||
| chr3:47049016
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6964-2395C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049016 | ||||||
| chr3:47049085
|
G | A | 32 | a0001c0005t0001g0273a0001c0005t0001g0306a0001c0006t0001g0270others(29): Show | 32 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.6964-2464C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049085 | ||||||
| chr3:47049171
|
T | C | 33 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0165others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.6964-2550A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049171 | ||||||
| chr3:47049247
|
T | A | 1 | a0002c0001t0001g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6964-2626A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049247 | ||||||
| chr3:47049252
|
T | A | 1 | a0001c0005t0005g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6964-2631A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049252 | ||||||
| chr3:47049253
|
T | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6964-2632A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049253 | ||||||
| chr3:47049304
|
A | AAT | 9 | a0001c0002t0002g0006a0001c0002t0002g0011a0001c0002t0002g0022others(6): Show | 9 | HG01167.hp2 HG01934.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.6964-2685_6964-268 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
A | AATAT | 14 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(11): Show | 14 | HG00544.hp2 HG00597.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.6964-2687_6964-268 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
A | AATATAT | 12 | a0001c0002t0002g0003a0001c0002t0002g0023a0001c0002t0002g0027others(9): Show | 12 | HG00639.hp1 HG00673.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.6964-2689_6964-268 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
A | AATATATA others(1): Show |
8 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0019others(5): Show | 8 | HG02071.hp2 HG02559.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.6964-2691_6964-268 others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
A | AATATATA others(3): Show |
6 | a0001c0002t0002g0025a0001c0002t0002g0046a0001c0002t0003g0086others(3): Show | 6 | NA18612.hp2 NA18979.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.6964-2693_6964-268 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
A | AATATATA others(5): Show |
2 | a0001c0002t0002g0043a0003c0003t0001g0286 | 2 | HG02083.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.6964-2695_6964-268 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AAT | A | 10 | a0001c0002t0002g0010a0001c0002t0002g0013a0001c0002t0002g0018others(7): Show | 10 | HG01109.hp1 HG01261.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.6964-2685_6964-268 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATAT | A | 5 | a0001c0002t0002g0034a0001c0002t0003g0105a0001c0002t0003g0106others(2): Show | 5 | HG01192.hp1 HG01346.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.6964-2687_6964-268 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATAT | A | 6 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0078others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.6964-2689_6964-268 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(1): Show |
A | 9 | a0001c0002t0002g0066a0001c0002t0003g0077a0001c0002t0003g0079others(6): Show | 9 | HG01255.hp2 HG01433.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.6964-2691_6964-268 others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(3): Show |
A | 5 | a0001c0002t0002g0032a0001c0002t0002g0051a0001c0002t0003g0080others(2): Show | 5 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.6964-2693_6964-268 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(5): Show |
A | 3 | a0001c0005t0005g0074a0001c0006t0001g0293a0015c0015t0001g0138 | 3 | HG02451.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.6964-2695_6964-268 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(7): Show |
A | 4 | a0001c0002t0002g0024a0001c0002t0003g0097a0003c0003t0001g0275others(1): Show | 4 | HG01515.hp1 HG01981.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.6964-2697_6964-268 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(9): Show |
A | 19 | a0001c0002t0002g0058a0003c0003t0001g0274a0003c0003t0001g0276others(16): Show | 19 | HG01255.hp1 HG01358.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.6964-2699_6964-268 others(20): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(17): Show |
A | 1 | a0002c0001t0001g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6964-2707_6964-268 others(28): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(19): Show |
A | 147 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0144others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.6964-2709_6964-268 others(30): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(23): Show |
A | 2 | a0007c0009t0003g0100a0007c0009t0003g0104 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.6964-2713_6964-268 others(34): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049304
|
AATATATA others(25): Show |
A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6964-2715_6964-268 others(36): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049304 | ||||||
| chr3:47049335
|
A | G | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6964-2714T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049335 | ||||||
| chr3:47049345
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0003g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6964-2725_6964-272 others(22): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049345 | ||||||
| chr3:47049345
|
A | ATATATAT others(9): Show |
2 | a0001c0002t0003g0111a0001c0002t0003g0112 | 2 | HG02258.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.6964-2725_6964-272 others(20): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049345 | ||||||
| chr3:47049374
|
C | CT | 180 | a0001c0002t0002g0049a0001c0002t0003g0075a0001c0002t0003g0076others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.6964-2754dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049374 | ||||||
| chr3:47049412
|
G | A | 1 | a0001c0002t0002g0055 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.6964-2791C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049412 | ||||||
| chr3:47049747
|
A | ATATATAT others(26): Show |
2 | a0002c0001t0001g0152a0002c0001t0001g0153 | 2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.6964-3127_6964-312 others(37): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049747 | ||||||
| chr3:47049797
|
C | CTA | 52 | a0001c0005t0001g0273a0001c0005t0001g0306a0001c0005t0004g0262others(49): Show | 52 | HG00558.hp1 HG01255.hp1 HG01358.hp2 others(49): Show |
intron_variant | MODIFIER | c.6964-3177_6964-317 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049797 | ||||||
| chr3:47049797
|
C | CTATGAGT others(28): Show |
147 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.6964-3177_6964-317 others(39): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049797 | ||||||
| chr3:47049865
|
T | C | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6964-3244A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049865 | ||||||
| chr3:47049867
|
T | C | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6964-3246A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049867 | ||||||
| chr3:47049912
|
A | ATTTATAT others(25): Show |
1 | a0001c0002t0002g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6964-3323_6964-329 others(36): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049912 | ||||||
| chr3:47049913
|
T | TTTATA | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6964-3297_6964-329 others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049913 | ||||||
| chr3:47049993
|
T | G | 1 | a0013c0022t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6964-3372A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47049993 | ||||||
| chr3:47050015
|
CAT | C | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6964-3396_6964-339 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050015 | ||||||
| chr3:47050326
|
T | C | 1 | a0003c0014t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6964-3705A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050326 | ||||||
| chr3:47050398
|
A | C | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6964-3777T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050398 | ||||||
| chr3:47050568
|
C | T | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6964-3947G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050568 | ||||||
| chr3:47050722
|
TC | T | 3 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0064 | 3 | NA18953.hp2 NA18961.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.6964-4102delG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050722 | ||||||
| chr3:47050723
|
C | CCTTTTTT others(4): Show |
1 | a0002c0001t0001g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.6964-4103_6964-410 others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CT | 10 | a0001c0002t0002g0015a0001c0002t0002g0019a0001c0002t0002g0027others(7): Show | 10 | HG00621.hp2 HG01433.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.6964-4103dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTCTTTTT others(3): Show |
1 | a0002c0001t0001g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6964-4103_6964-410 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTT | 11 | a0001c0005t0004g0262a0001c0005t0004g0264a0001c0005t0004g0265others(8): Show | 11 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.6964-4105_6964-410 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTT | 7 | a0001c0005t0001g0115a0001c0005t0004g0263a0001c0005t0004g0266others(4): Show | 7 | HG02886.hp1 HG02970.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.6964-4106_6964-410 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTT | 25 | a0002c0001t0001g0165a0004c0004t0001g0116a0004c0004t0001g0118others(22): Show | 25 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.6964-4107_6964-410 others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTT | 11 | a0001c0005t0001g0123a0002c0001t0001g0144a0002c0001t0001g0240others(8): Show | 11 | HG01169.hp1 HG01256.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.6964-4108_6964-410 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTTT | 29 | a0002c0001t0001g0145a0002c0001t0001g0146a0002c0001t0001g0148others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.6964-4109_6964-410 others(11): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTTT others(1): Show |
34 | a0002c0001t0001g0154a0002c0001t0001g0163a0002c0001t0001g0166others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.6964-4110_6964-410 others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTTT others(2): Show |
19 | a0002c0001t0001g0147a0002c0001t0001g0152a0002c0001t0001g0159others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.6964-4111_6964-410 others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTTT others(3): Show |
9 | a0002c0001t0001g0155a0002c0001t0001g0158a0002c0001t0001g0174others(6): Show | 9 | HG00738.hp1 HG02965.hp2 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.6964-4112_6964-410 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTTT others(4): Show |
4 | a0002c0001t0001g0150a0002c0001t0001g0167a0002c0001t0001g0210others(1): Show | 4 | HG04228.hp2 NA18975.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.6964-4113_6964-410 others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | CTTTTTTT others(6): Show |
2 | a0002c0001t0001g0209a0002c0001t0001g0261 | 2 | HG03041.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6964-4115_6964-410 others(17): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
C | T | 2 | a0001c0002t0002g0067a0002c0018t0001g0170 | 2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.6964-4102G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
CT | C | 37 | a0001c0002t0002g0023a0001c0002t0002g0046a0001c0002t0002g0056others(34): Show | 37 | HG00639.hp1 HG01070.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.6964-4103delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050723
|
CTTTTT | C | 8 | a0001c0005t0001g0149a0001c0005t0005g0072a0002c0001t0001g0190others(5): Show | 8 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.6964-4107_6964-410 others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050723 | ||||||
| chr3:47050889
|
C | T | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6964-4268G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47050889 | ||||||
| chr3:47051538
|
C | A | 1 | a0001c0002t0002g0049 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.6964-4917G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051538 | ||||||
| chr3:47051544
|
A | G | 1 | a0002c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6964-4923T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051544 | ||||||
| chr3:47051654
|
A | T | 1 | a0001c0002t0006g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.6964-5033T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051654 | ||||||
| chr3:47051699
|
T | C | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6964-5078A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051699 | ||||||
| chr3:47051714
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6964-5093A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051714 | ||||||
| chr3:47051716
|
C | A | 4 | a0002c0001t0001g0195a0002c0001t0001g0196a0002c0001t0001g0201others(1): Show | 4 | HG00280.hp2 HG01175.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.6964-5095G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051716 | ||||||
| chr3:47051977
|
G | A | 1 | a0001c0005t0004g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6963+4844C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47051977 | ||||||
| chr3:47052148
|
A | G | 33 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0165others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.6963+4673T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47052148 | ||||||
| chr3:47052580
|
G | C | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6963+4241C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47052580 | ||||||
| chr3:47052629
|
C | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6963+4192G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47052629 | ||||||
| chr3:47052734
|
C | T | 4 | a0002c0001t0001g0171a0002c0001t0001g0209a0002c0001t0001g0210others(1): Show | 4 | HG03654.hp1 HG03942.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.6963+4087G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47052734 | ||||||
| chr3:47052742
|
G | C | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6963+4079C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47052742 | ||||||
| chr3:47052840
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6963+3981G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47052840 | ||||||
| chr3:47053121
|
C | T | 148 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0144others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.6963+3700G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053121 | ||||||
| chr3:47053236
|
A | C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6963+3585T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053236 | ||||||
| chr3:47053327
|
T | G | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6963+3494A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053327 | ||||||
| chr3:47053668
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6963+3153C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053668 | ||||||
| chr3:47053773
|
C | A | 22 | a0003c0003t0001g0274a0003c0003t0001g0275a0003c0003t0001g0276others(19): Show | 22 | HG01255.hp1 HG01358.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.6963+3048G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053773 | ||||||
| chr3:47053815
|
T | C | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.6963+3006A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053815 | ||||||
| chr3:47053913
|
C | T | 2 | a0002c0001t0001g0177a0002c0001t0001g0199 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6963+2908G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47053913 | ||||||
| chr3:47054026
|
C | G | 1 | a0002c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6963+2795G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054026 | ||||||
| chr3:47054028
|
A | G | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.6963+2793T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054028 | ||||||
| chr3:47054243
|
T | C | 23 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.6963+2578A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054243 | ||||||
| chr3:47054250
|
C | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6963+2571G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054250 | ||||||
| chr3:47054259
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6963+2562A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054259 | ||||||
| chr3:47054351
|
A | T | 1 | a0002c0001t0001g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6963+2470T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054351 | ||||||
| chr3:47054382
|
C | T | 4 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(1): Show | 4 | HG02132.hp1 NA18951.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6963+2439G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054382 | ||||||
| chr3:47054444
|
G | A | 1 | a0002c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.6963+2377C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054444 | ||||||
| chr3:47054600
|
G | A | 2 | a0002c0001t0001g0236a0002c0001t0001g0238 | 2 | NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.6963+2221C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054600 | ||||||
| chr3:47054724
|
A | G | 3 | a0002c0001t0001g0172a0002c0001t0001g0215a0010c0011t0001g0224 | 3 | HG01256.hp1 HG02004.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.6963+2097T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054724 | ||||||
| chr3:47054950
|
T | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6963+1871A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47054950 | ||||||
| chr3:47055033
|
C | T | 37 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(34): Show | 37 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.6963+1788G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47055033 | ||||||
| chr3:47055206
|
T | G | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6963+1615A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47055206 | ||||||
| chr3:47055448
|
G | A | 1 | a0002c0017t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6963+1373C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47055448 | ||||||
| chr3:47055930
|
G | A | 10 | a0001c0005t0004g0262a0001c0005t0004g0264a0001c0005t0004g0294others(7): Show | 10 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.6963+891C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47055930 | ||||||
| chr3:47055985
|
C | T | 1 | a0003c0003t0001g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.6963+836G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47055985 | ||||||
| chr3:47056012
|
C | CA | 22 | a0001c0002t0002g0004a0001c0002t0002g0007a0001c0002t0002g0013others(19): Show | 22 | HG00621.hp2 HG01261.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.6963+808dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
C | CAA | 19 | a0001c0002t0002g0008a0001c0002t0002g0011a0001c0002t0002g0020others(16): Show | 19 | HG00280.hp1 HG01070.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.6963+807_6963+808d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
C | CAAA | 14 | a0001c0002t0002g0021a0001c0002t0002g0071a0001c0002t0003g0088others(11): Show | 14 | HG00544.hp2 HG01175.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.6963+806_6963+808d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
C | CAAAA | 7 | a0001c0002t0003g0077a0001c0002t0003g0079a0001c0002t0003g0082others(4): Show | 7 | HG00140.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.6963+805_6963+808d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
C | CAAAAA | 7 | a0001c0002t0003g0075a0001c0002t0003g0080a0001c0002t0003g0081others(4): Show | 7 | HG00099.hp1 HG00735.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.6963+804_6963+808d others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAA | C | 15 | a0001c0005t0001g0115a0001c0005t0004g0262a0001c0005t0004g0263others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6963+805_6963+808d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAA | C | 33 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(30): Show | 33 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.6963+803_6963+808d others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAAA | C | 38 | a0001c0005t0001g0123a0001c0005t0001g0273a0001c0005t0001g0306others(35): Show | 38 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.6963+802_6963+808d others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAAA others(1): Show |
C | 56 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0148others(53): Show | 56 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.6963+801_6963+808d others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAAA others(2): Show |
C | 51 | a0002c0001t0001g0147a0002c0001t0001g0150a0002c0001t0001g0152others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.6963+800_6963+808d others(11): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAAA others(3): Show |
C | 1 | a0002c0001t0001g0231 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.6963+799_6963+808d others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0002g0010 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6963+798_6963+808d others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056012
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6963+797_6963+808d others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056012 | ||||||
| chr3:47056062
|
T | TA | 9 | a0001c0002t0002g0052a0001c0002t0002g0070a0001c0002t0002g0071others(6): Show | 9 | HG01070.hp2 HG01175.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.6963+758dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056062 | ||||||
| chr3:47056062
|
TA | T | 6 | a0001c0002t0002g0033a0001c0002t0003g0081a0002c0001t0001g0230others(3): Show | 6 | HG00741.hp1 HG01515.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.6963+758delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056062 | ||||||
| chr3:47056073
|
A | G | 28 | a0001c0002t0003g0101a0001c0005t0001g0306a0003c0003t0001g0269others(25): Show | 28 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.6963+748T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056073 | ||||||
| chr3:47056091
|
G | A | 1 | a0013c0022t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6963+730C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056091 | ||||||
| chr3:47056092
|
A | AT | 80 | a0002c0001t0001g0147a0002c0001t0001g0150a0002c0001t0001g0152others(77): Show | 80 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.6963+728dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056092 | ||||||
| chr3:47056092
|
A | ATATTTAT others(5): Show |
1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6963+728_6963+729i others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056092 | ||||||
| chr3:47056092
|
ATTTTTAT others(1): Show |
A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6963+721_6963+728d others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056092 | ||||||
| chr3:47056092
|
ATTTTTAT others(4): Show |
A | 1 | a0002c0001t0001g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.6963+718_6963+728d others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056092 | ||||||
| chr3:47056094
|
T | A | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6963+727A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
T | TA | 4 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(1): Show | 4 | HG02132.hp1 NA18951.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6963+726_6963+727i others(3): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
T | TTTTA | 17 | a0001c0002t0002g0032a0001c0002t0002g0041a0001c0002t0002g0049others(14): Show | 17 | HG00609.hp1 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.6963+723_6963+726d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
T | TTTTTA | 10 | a0002c0001t0001g0163a0002c0001t0001g0171a0002c0001t0001g0184others(7): Show | 10 | HG00280.hp2 HG01256.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.6963+726_6963+727i others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
T | TTTTTATT others(6): Show |
1 | a0002c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.6963+726_6963+727i others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
T | TTTTTATT others(10): Show |
1 | a0002c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6963+726_6963+727i others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
T | TTTTTTTA others(5): Show |
1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6963+726_6963+727i others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
TTTTA | T | 75 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0006others(72): Show | 75 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.6963+723_6963+726d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
TTTTATTT others(1): Show |
T | 6 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0006t0001g0270others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.6963+719_6963+726d others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
TTTTATTT others(5): Show |
T | 3 | a0001c0002t0002g0054a0001c0002t0003g0099a0011c0023t0003g0098 | 3 | HG00738.hp2 NA19084.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.6963+715_6963+726d others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056094
|
TTTTATTT others(9): Show |
T | 17 | a0001c0002t0002g0046a0001c0002t0003g0075a0001c0002t0003g0076others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.6963+711_6963+726d others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056094 | ||||||
| chr3:47056095
|
TTTA | T | 18 | a0002c0001t0001g0159a0002c0001t0001g0168a0002c0001t0001g0215others(15): Show | 18 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.6963+723_6963+725d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056095 | ||||||
| chr3:47056098
|
A | T | 4 | a0001c0002t0002g0012a0002c0001t0001g0189a0002c0001t0001g0216others(1): Show | 4 | HG01169.hp2 HG01433.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.6963+723T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056098 | ||||||
| chr3:47056102
|
A | T | 1 | a0001c0002t0003g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6963+719T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056102 | ||||||
| chr3:47056337
|
G | A | 2 | a0002c0001t0001g0177a0002c0001t0001g0199 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6963+484C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056337 | ||||||
| chr3:47056495
|
G | A | 37 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(34): Show | 37 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.6963+326C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056495 | ||||||
| chr3:47056538
|
T | C | 2 | a0006c0008t0001g0207a0006c0008t0001g0208 | 2 | NA18954.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.6963+283A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056538 | ||||||
| chr3:47056718
|
T | C | 1 | a0002c0001t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6963+103A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 15/20 | chr3 | 47056718 | ||||||
| chr3:47057984
|
G | T | 1 | a0002c0001t0001g0163 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6294-494C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47057984 | ||||||
| chr3:47058013
|
G | A | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6294-523C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058013 | ||||||
| chr3:47058440
|
C | CA | 121 | a0001c0002t0002g0003a0001c0002t0002g0007a0001c0002t0002g0012others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.6294-951dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAA | 44 | a0001c0002t0002g0008a0001c0005t0004g0262a0001c0005t0004g0265others(41): Show | 44 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.6294-952_6294-951d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA | 6 | a0001c0005t0001g0115a0004c0004t0001g0117a0004c0004t0001g0141others(3): Show | 6 | HG02280.hp2 HG03139.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.6294-957_6294-951d others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA others(5): Show |
1 | a0004c0004t0001g0126 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6294-962_6294-951d others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA others(6): Show |
7 | a0004c0004t0001g0118a0004c0004t0001g0127a0004c0004t0001g0131others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.6294-963_6294-951d others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA others(7): Show |
4 | a0004c0004t0001g0116a0004c0004t0001g0125a0004c0004t0001g0135others(1): Show | 4 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.6294-964_6294-951d others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA others(8): Show |
5 | a0004c0004t0001g0129a0004c0004t0001g0130a0004c0004t0001g0136others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.6294-965_6294-951d others(17): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA others(9): Show |
2 | a0004c0004t0001g0133a0004c0010t0001g0137 | 2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.6294-966_6294-951d others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058440
|
C | CAAAAAAA others(16): Show |
1 | a0004c0004t0001g0134 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.6294-973_6294-951d others(25): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058440 | ||||||
| chr3:47058456
|
A | C | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6294-966T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058456 | ||||||
| chr3:47058458
|
A | AAAC | 6 | a0003c0003t0001g0278a0003c0003t0001g0280a0003c0003t0001g0282others(3): Show | 6 | HG01952.hp2 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.6294-969_6294-968i others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058458 | ||||||
| chr3:47058458
|
A | AAC | 20 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(17): Show | 20 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.6294-969_6294-968i others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058458 | ||||||
| chr3:47058464
|
AC | A | 3 | a0001c0005t0001g0149a0001c0005t0005g0072a0001c0006t0001g0293 | 3 | HG01934.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.6294-975delG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058464 | ||||||
| chr3:47058465
|
C | A | 196 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0273others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.6294-975G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058465 | ||||||
| chr3:47058471
|
G | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6294-981C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058471 | ||||||
| chr3:47058604
|
G | A | 1 | a0001c0002t0006g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.6294-1114C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058604 | ||||||
| chr3:47058660
|
A | C | 1 | a0002c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.6294-1170T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058660 | ||||||
| chr3:47058885
|
C | G | 37 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(34): Show | 37 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.6294-1395G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058885 | ||||||
| chr3:47058930
|
G | A | 1 | a0003c0003t0001g0291 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6294-1440C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058930 | ||||||
| chr3:47058944
|
G | A | 1 | a0004c0004t0001g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6294-1454C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058944 | ||||||
| chr3:47058962
|
T | TTTGTTG | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6294-1478_6294-147 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47058962 | ||||||
| chr3:47059108
|
C | CT | 23 | a0001c0002t0002g0003a0001c0002t0002g0008a0001c0002t0002g0013others(20): Show | 23 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.6294-1619dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059108 | ||||||
| chr3:47059108
|
CT | C | 152 | a0001c0002t0002g0047a0001c0005t0001g0149a0001c0005t0004g0262others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.6294-1619delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059108 | ||||||
| chr3:47059108
|
CTT | C | 36 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0273others(33): Show | 36 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.6294-1620_6294-161 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059108 | ||||||
| chr3:47059120
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6294-1630A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059120 | ||||||
| chr3:47059121
|
T | C | 151 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.6294-1631A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059121 | ||||||
| chr3:47059209
|
C | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6294-1719G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059209 | ||||||
| chr3:47059363
|
G | A | 1 | a0002c0001t0001g0200 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.6294-1873C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059363 | ||||||
| chr3:47059571
|
C | A | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.6294-2081G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059571 | ||||||
| chr3:47059618
|
C | T | 1 | a0004c0004t0001g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6294-2128G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059618 | ||||||
| chr3:47059816
|
T | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6294-2326A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059816 | ||||||
| chr3:47059934
|
CCACCATG others(7): Show |
C | 1 | a0002c0001t0001g0146 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.6293+2215_6293+222 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47059934 | ||||||
| chr3:47060102
|
C | CA | 7 | a0001c0002t0002g0067a0002c0001t0001g0161a0002c0001t0001g0163others(4): Show | 7 | HG01978.hp2 HG01981.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.6293+2060dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47060102 | ||||||
| chr3:47060261
|
C | T | 1 | a0002c0001t0001g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6293+1902G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47060261 | ||||||
| chr3:47060328
|
T | C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6293+1835A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47060328 | ||||||
| chr3:47060645
|
T | A | 2 | a0002c0001t0001g0190a0002c0001t0001g0223 | 2 | NA18949.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.6293+1518A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47060645 | ||||||
| chr3:47060899
|
T | TAATTCAA others(30): Show |
1 | a0002c0001t0001g0146 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.6293+1263_6293+126 others(41): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47060899 | ||||||
| chr3:47061001
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6293+1162C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061001 | ||||||
| chr3:47061125
|
G | A | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.6293+1038C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061125 | ||||||
| chr3:47061199
|
C | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6293+964G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061199 | ||||||
| chr3:47061317
|
C | A | 4 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(1): Show | 4 | HG02132.hp1 NA18951.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6293+846G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061317 | ||||||
| chr3:47061792
|
A | T | 1 | a0002c0001t0001g0201 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.6293+371T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061792 | ||||||
| chr3:47061886
|
C | T | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6293+277G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061886 | ||||||
| chr3:47061978
|
G | GCTA | 5 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(2): Show | 5 | NA18951.hp2 NA19000.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.6293+182_6293+184d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 14/20 | chr3 | 47061978 | ||||||
| chr3:47062371
|
G | T | 1 | a0001c0002t0003g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6110-25C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062371 | ||||||
| chr3:47062371
|
GTT | G | 196 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.6110-27_6110-26del others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062371 | ||||||
| chr3:47062377
|
T | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6110-31A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062377 | ||||||
| chr3:47062501
|
AAG | A | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.6110-157_6110-156d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062501 | ||||||
| chr3:47062885
|
G | C | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6110-539C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062885 | ||||||
| chr3:47062935
|
C | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6110-589G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062935 | ||||||
| chr3:47062986
|
C | T | 4 | a0001c0005t0004g0263a0001c0005t0004g0265a0001c0005t0004g0266others(1): Show | 4 | HG02886.hp1 HG06807.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.6110-640G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47062986 | ||||||
| chr3:47063131
|
A | G | 1 | a0002c0001t0001g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6110-785T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063131 | ||||||
| chr3:47063679
|
T | C | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.6110-1333A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063679 | ||||||
| chr3:47063713
|
T | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6110-1367A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063713 | ||||||
| chr3:47063857
|
C | A | 4 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0064others(1): Show | 4 | NA18953.hp2 NA18961.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.6110-1511G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063857 | ||||||
| chr3:47063940
|
G | A | 3 | a0002c0001t0001g0158a0002c0001t0001g0159a0002c0001t0001g0160 | 3 | HG00639.hp2 HG01070.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.6110-1594C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063940 | ||||||
| chr3:47063986
|
A | C | 1 | a0002c0017t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.6110-1640T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063986 | ||||||
| chr3:47063988
|
GA | G | 235 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.6110-1643delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063988 | ||||||
| chr3:47063997
|
A | C | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.6110-1651T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47063997 | ||||||
| chr3:47064091
|
A | G | 1 | a0002c0001t0001g0201 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.6110-1745T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47064091 | ||||||
| chr3:47064201
|
C | T | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6110-1855G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47064201 | ||||||
| chr3:47064389
|
A | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6110-2043T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47064389 | ||||||
| chr3:47064817
|
A | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6109+2253T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47064817 | ||||||
| chr3:47064897
|
G | C | 1 | a0001c0005t0005g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6109+2173C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47064897 | ||||||
| chr3:47065056
|
G | A | 1 | a0003c0003t0001g0298 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6109+2014C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065056 | ||||||
| chr3:47065259
|
G | A | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6109+1811C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065259 | ||||||
| chr3:47065334
|
A | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6109+1736T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065334 | ||||||
| chr3:47065339
|
A | G | 2 | a0001c0002t0003g0099a0011c0023t0003g0098 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.6109+1731T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065339 | ||||||
| chr3:47065371
|
CA | C | 38 | a0001c0002t0003g0091a0001c0005t0001g0273a0001c0005t0001g0306others(35): Show | 38 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(35): Show |
intron_variant | MODIFIER | c.6109+1698delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065371 | ||||||
| chr3:47065558
|
G | A | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6109+1512C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065558 | ||||||
| chr3:47065899
|
A | G | 3 | a0002c0001t0001g0150a0002c0001t0001g0167a0002c0001t0001g0225 | 3 | NA18964.hp2 NA18975.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.6109+1171T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47065899 | ||||||
| chr3:47066057
|
C | T | 1 | a0002c0001t0001g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6109+1013G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066057 | ||||||
| chr3:47066202
|
CTTTAT | C | 4 | a0001c0005t0001g0115a0001c0005t0001g0149a0001c0005t0005g0072others(1): Show | 4 | HG01515.hp1 HG01934.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6109+863_6109+867d others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066202 | ||||||
| chr3:47066541
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6109+529C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066541 | ||||||
| chr3:47066704
|
T | TAAGAATG others(2545): Show |
1 | a0001c0002t0003g0081 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.6109+365_6109+366i others(2554): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066704 | ||||||
| chr3:47066704
|
T | TAAGAATG others(2673): Show |
1 | a0001c0002t0003g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6109+365_6109+366i others(2682): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066704 | ||||||
| chr3:47066834
|
T | TAAAGATT others(332): Show |
1 | a0002c0001t0001g0195 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.6109+235_6109+236i others(341): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066834 | ||||||
| chr3:47066840
|
C | T | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6109+230G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066840 | ||||||
| chr3:47066871
|
G | A | 23 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.6109+199C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066871 | ||||||
| chr3:47066970
|
G | C | 1 | a0001c0005t0004g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6109+100C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 13/20 | chr3 | 47066970 | ||||||
| chr3:47067164
|
T | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6061-46A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067164 | ||||||
| chr3:47067301
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.6061-183T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067301 | ||||||
| chr3:47067331
|
A | G | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6061-213T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067331 | ||||||
| chr3:47067392
|
C | G | 1 | a0002c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.6061-274G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067392 | ||||||
| chr3:47067400
|
G | A | 9 | a0002c0001t0001g0152a0002c0001t0001g0153a0002c0001t0001g0166others(6): Show | 9 | HG00558.hp1 HG01978.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.6061-282C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067400 | ||||||
| chr3:47067406
|
C | CT | 48 | a0001c0002t0002g0028a0001c0002t0002g0029a0001c0002t0002g0061others(45): Show | 48 | HG00621.hp2 HG01109.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.6061-289dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067406 | ||||||
| chr3:47067406
|
CT | C | 74 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.6061-289delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067406 | ||||||
| chr3:47067406
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0002g0026 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6061-300_6061-289d others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067406 | ||||||
| chr3:47067576
|
C | T | 1 | a0002c0001t0001g0163 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6061-458G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067576 | ||||||
| chr3:47067690
|
G | A | 2 | a0004c0004t0001g0142a0009c0027t0001g0143 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.6061-572C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47067690 | ||||||
| chr3:47068343
|
T | G | 1 | a0001c0002t0002g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.6061-1225A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068343 | ||||||
| chr3:47068378
|
T | A | 1 | a0002c0001t0001g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6061-1260A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068378 | ||||||
| chr3:47068489
|
CTATCTT | C | 13 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(10): Show | 13 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.6061-1377_6061-137 others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068489 | ||||||
| chr3:47068493
|
CT | C | 37 | a0001c0002t0002g0011a0001c0002t0002g0044a0001c0002t0003g0087others(34): Show | 37 | HG01070.hp1 HG01175.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.6061-1376delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068493 | ||||||
| chr3:47068493
|
CTT | C | 147 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.6061-1377_6061-137 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068493 | ||||||
| chr3:47068695
|
C | T | 1 | a0002c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6061-1577G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068695 | ||||||
| chr3:47068738
|
T | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6061-1620A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47068738 | ||||||
| chr3:47069213
|
C | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6061-2095G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47069213 | ||||||
| chr3:47069232
|
A | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6061-2114T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47069232 | ||||||
| chr3:47069325
|
G | A | 1 | a0002c0001t0001g0166 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6061-2207C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47069325 | ||||||
| chr3:47069620
|
T | C | 2 | a0002c0001t0001g0195a0002c0001t0001g0196 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.6061-2502A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47069620 | ||||||
| chr3:47070508
|
A | G | 1 | a0001c0005t0004g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.6061-3390T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47070508 | ||||||
| chr3:47070585
|
A | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.6061-3467T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47070585 | ||||||
| chr3:47070586
|
T | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6061-3468A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47070586 | ||||||
| chr3:47070762
|
C | A | 1 | a0002c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.6061-3644G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47070762 | ||||||
| chr3:47071280
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6061-4162G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47071280 | ||||||
| chr3:47071539
|
T | C | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6061-4421A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47071539 | ||||||
| chr3:47072034
|
C | T | 1 | a0001c0002t0003g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.6061-4916G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072034 | ||||||
| chr3:47072123
|
A | C | 2 | a0001c0002t0002g0047a0001c0002t0002g0048 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.6061-5005T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072123 | ||||||
| chr3:47072240
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.6061-5122C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072240 | ||||||
| chr3:47072264
|
C | T | 115 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.6061-5146G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072264 | ||||||
| chr3:47072387
|
A | C | 1 | a0002c0001t0001g0248 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6061-5269T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072387 | ||||||
| chr3:47072674
|
G | A | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6061-5556C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072674 | ||||||
| chr3:47072698
|
C | A | 1 | a0002c0001t0001g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6061-5580G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072698 | ||||||
| chr3:47072721
|
A | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6061-5603T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072721 | ||||||
| chr3:47072781
|
T | TA | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.6061-5664dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072781 | ||||||
| chr3:47072930
|
G | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6061-5812C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47072930 | ||||||
| chr3:47073049
|
T | C | 1 | a0002c0001t0002g0001 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6061-5931A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073049 | ||||||
| chr3:47073150
|
CA | C | 197 | a0001c0005t0001g0123a0001c0005t0001g0149a0001c0005t0001g0273others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.6061-6033delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073150 | ||||||
| chr3:47073207
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6061-6089G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073207 | ||||||
| chr3:47073414
|
T | C | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.6061-6296A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073414 | ||||||
| chr3:47073458
|
G | A | 4 | a0004c0004t0001g0257a0004c0004t0001g0258a0004c0004t0001g0259others(1): Show | 4 | HG02809.hp1 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.6061-6340C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073458 | ||||||
| chr3:47073660
|
T | C | 1 | a0002c0001t0001g0213 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.6061-6542A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073660 | ||||||
| chr3:47073711
|
T | A | 1 | a0002c0001t0001g0213 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.6061-6593A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073711 | ||||||
| chr3:47073824
|
C | T | 1 | a0002c0001t0001g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6061-6706G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47073824 | ||||||
| chr3:47074197
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6061-7079C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47074197 | ||||||
| chr3:47074652
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6061-7534C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47074652 | ||||||
| chr3:47074724
|
CCT | C | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.6061-7608_6061-760 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47074724 | ||||||
| chr3:47074834
|
G | C | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6061-7716C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47074834 | ||||||
| chr3:47075051
|
G | A | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6061-7933C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075051 | ||||||
| chr3:47075325
|
C | T | 1 | a0001c0002t0003g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6061-8207G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075325 | ||||||
| chr3:47075482
|
T | C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.6060+8238A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075482 | ||||||
| chr3:47075521
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6060+8199C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075521 | ||||||
| chr3:47075556
|
C | A | 1 | a0001c0002t0003g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6060+8164G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075556 | ||||||
| chr3:47075564
|
C | CA | 6 | a0001c0002t0002g0038a0001c0002t0002g0064a0001c0002t0003g0089others(3): Show | 6 | HG02258.hp1 HG03098.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.6060+8155dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075564 | ||||||
| chr3:47075564
|
CA | C | 7 | a0001c0002t0002g0046a0001c0002t0002g0047a0001c0002t0002g0068others(4): Show | 7 | HG00738.hp2 HG01255.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.6060+8155delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075564 | ||||||
| chr3:47075564
|
CAAA | C | 15 | a0001c0006t0001g0293a0002c0001t0001g0147a0002c0001t0001g0154others(12): Show | 15 | HG00639.hp2 HG00738.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.6060+8153_6060+815 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075564 | ||||||
| chr3:47075564
|
CAAAA | C | 173 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0273others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.6060+8152_6060+815 others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075564 | ||||||
| chr3:47075564
|
CAAAAA | C | 10 | a0001c0005t0001g0149a0001c0005t0005g0072a0001c0005t0005g0074others(7): Show | 10 | HG01256.hp1 HG01934.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.6060+8151_6060+815 others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075564 | ||||||
| chr3:47075564
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0016t0001g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.6060+8142_6060+815 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075564 | ||||||
| chr3:47075586
|
A | G | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6060+8134T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075586 | ||||||
| chr3:47075656
|
A | C | 1 | a0001c0002t0003g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.6060+8064T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075656 | ||||||
| chr3:47075777
|
C | T | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.6060+7943G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47075777 | ||||||
| chr3:47076172
|
A | G | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6060+7548T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076172 | ||||||
| chr3:47076220
|
T | C | 1 | a0001c0002t0003g0107 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6060+7500A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076220 | ||||||
| chr3:47076306
|
T | G | 4 | a0002c0001t0001g0242a0002c0001t0001g0243a0002c0001t0001g0244others(1): Show | 4 | NA18943.hp1 NA18953.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.6060+7414A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076306 | ||||||
| chr3:47076478
|
T | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6060+7242A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076478 | ||||||
| chr3:47076582
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6060+7138G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076582 | ||||||
| chr3:47076621
|
C | T | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6060+7099G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076621 | ||||||
| chr3:47076857
|
C | T | 3 | a0002c0001t0001g0180a0002c0001t0001g0188a0002c0001t0001g0229 | 3 | NA18940.hp1 NA18947.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.6060+6863G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076857 | ||||||
| chr3:47076909
|
G | A | 1 | a0001c0005t0004g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6060+6811C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47076909 | ||||||
| chr3:47077040
|
A | C | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6060+6680T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077040 | ||||||
| chr3:47077335
|
G | A | 1 | a0001c0005t0004g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6060+6385C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077335 | ||||||
| chr3:47077378
|
C | T | 1 | a0002c0001t0001g0205 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6060+6342G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077378 | ||||||
| chr3:47077733
|
G | C | 1 | a0002c0001t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.6060+5987C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077733 | ||||||
| chr3:47077785
|
C | A | 1 | a0001c0005t0004g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6060+5935G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077785 | ||||||
| chr3:47077810
|
A | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6060+5910T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077810 | ||||||
| chr3:47077811
|
G | C | 2 | a0001c0002t0002g0025a0001c0002t0002g0051 | 2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.6060+5909C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077811 | ||||||
| chr3:47077840
|
C | G | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6060+5880G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47077840 | ||||||
| chr3:47078021
|
C | T | 33 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0165others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.6060+5699G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078021 | ||||||
| chr3:47078085
|
A | G | 23 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(20): Show | 23 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.6060+5635T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078085 | ||||||
| chr3:47078116
|
A | G | 2 | a0002c0001t0001g0152a0002c0001t0001g0153 | 2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.6060+5604T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078116 | ||||||
| chr3:47078286
|
A | G | 1 | a0002c0001t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6060+5434T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078286 | ||||||
| chr3:47078519
|
C | CT | 35 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0015others(32): Show | 35 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.6060+5200dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078519 | ||||||
| chr3:47078519
|
CT | C | 130 | a0001c0002t0003g0106a0001c0005t0001g0123a0001c0005t0004g0262others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.6060+5200delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078519 | ||||||
| chr3:47078653
|
G | A | 1 | a0011c0023t0003g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6060+5067C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078653 | ||||||
| chr3:47078882
|
C | A | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6060+4838G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078882 | ||||||
| chr3:47078886
|
A | G | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6060+4834T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47078886 | ||||||
| chr3:47079023
|
TA | T | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.6060+4696delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079023 | ||||||
| chr3:47079107
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6060+4613C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079107 | ||||||
| chr3:47079150
|
G | A | 202 | a0001c0002t0003g0099a0001c0002t0003g0106a0001c0005t0001g0115others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.6060+4570C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079150 | ||||||
| chr3:47079400
|
C | T | 1 | a0001c0002t0002g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6060+4320G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079400 | ||||||
| chr3:47079437
|
T | A | 1 | a0010c0011t0001g0224 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.6060+4283A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079437 | ||||||
| chr3:47079650
|
A | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6060+4070T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079650 | ||||||
| chr3:47079696
|
C | T | 2 | a0003c0003t0001g0283a0003c0003t0001g0284 | 2 | NA19070.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6060+4024G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079696 | ||||||
| chr3:47079783
|
C | A | 2 | a0005c0007t0001g0120a0005c0007t0001g0121 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.6060+3937G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079783 | ||||||
| chr3:47079804
|
T | G | 2 | a0003c0003t0001g0283a0003c0003t0001g0284 | 2 | NA19070.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.6060+3916A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079804 | ||||||
| chr3:47079849
|
C | T | 2 | a0002c0001t0001g0182a0002c0001t0001g0194 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.6060+3871G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079849 | ||||||
| chr3:47079904
|
A | C | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.6060+3816T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079904 | ||||||
| chr3:47079988
|
C | G | 1 | a0002c0001t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6060+3732G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47079988 | ||||||
| chr3:47080292
|
T | C | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6060+3428A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47080292 | ||||||
| chr3:47080411
|
A | G | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.6060+3309T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47080411 | ||||||
| chr3:47080421
|
G | A | 1 | a0001c0005t0005g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.6060+3299C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47080421 | ||||||
| chr3:47080482
|
C | T | 1 | a0002c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.6060+3238G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47080482 | ||||||
| chr3:47080554
|
G | T | 1 | a0002c0001t0001g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.6060+3166C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47080554 | ||||||
| chr3:47080840
|
G | A | 1 | a0002c0001t0001g0163 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.6060+2880C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47080840 | ||||||
| chr3:47081149
|
C | T | 1 | a0002c0001t0002g0002 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6060+2571G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47081149 | ||||||
| chr3:47081565
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6060+2155A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47081565 | ||||||
| chr3:47081917
|
G | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6060+1803C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47081917 | ||||||
| chr3:47082164
|
C | T | 1 | a0002c0001t0001g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.6060+1556G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47082164 | ||||||
| chr3:47082325
|
T | G | 8 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(5): Show | 8 | HG00544.hp2 HG02735.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.6060+1395A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47082325 | ||||||
| chr3:47082709
|
A | G | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6060+1011T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47082709 | ||||||
| chr3:47082723
|
G | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6060+997C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47082723 | ||||||
| chr3:47083099
|
T | C | 1 | a0002c0001t0001g0167 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.6060+621A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083099 | ||||||
| chr3:47083161
|
A | T | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6060+559T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083161 | ||||||
| chr3:47083271
|
T | A | 77 | a0002c0001t0001g0147a0002c0001t0001g0150a0002c0001t0001g0152others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.6060+449A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083271 | ||||||
| chr3:47083292
|
T | C | 4 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0047others(1): Show | 4 | HG03491.hp1 HG03492.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.6060+428A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083292 | ||||||
| chr3:47083420
|
A | C | 2 | a0002c0001t0001g0154a0002c0001t0001g0230 | 2 | HG02071.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.6060+300T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083420 | ||||||
| chr3:47083454
|
G | A | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.6060+266C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083454 | ||||||
| chr3:47083717
|
T | C | 1 | a0001c0002t0003g0076 | 1 | HG01256.hp2 | splice_region_variant&intron_variant | LOW | c.6060+3A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 12/20 | chr3 | 47083717 | ||||||
| chr3:47084426
|
CT | C | 197 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(194): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.5398-45delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47084426 | ||||||
| chr3:47084431
|
T | C | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5398-49A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47084431 | ||||||
| chr3:47084894
|
C | CT | 13 | a0001c0002t0002g0016a0001c0002t0002g0020a0001c0002t0002g0021others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.5398-513dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47084894 | ||||||
| chr3:47084984
|
G | A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.5398-602C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47084984 | ||||||
| chr3:47085053
|
C | T | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.5398-671G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085053 | ||||||
| chr3:47085093
|
T | C | 4 | a0005c0007t0001g0119a0005c0007t0001g0120a0005c0007t0001g0121others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.5398-711A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085093 | ||||||
| chr3:47085221
|
G | C | 1 | a0002c0001t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5398-839C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085221 | ||||||
| chr3:47085285
|
T | C | 2 | a0002c0001t0001g0244a0002c0001t0001g0245 | 2 | NA18943.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.5398-903A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085285 | ||||||
| chr3:47085474
|
T | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5397+721A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085474 | ||||||
| chr3:47085856
|
T | C | 2 | a0002c0001t0001g0154a0002c0001t0001g0230 | 2 | HG02071.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.5397+339A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085856 | ||||||
| chr3:47085858
|
TTA | T | 11 | a0002c0001t0001g0236a0002c0001t0001g0237a0002c0001t0001g0238others(8): Show | 11 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.5397+335_5397+336d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085858 | ||||||
| chr3:47085936
|
A | G | 1 | a0001c0002t0002g0036 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5397+259T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 11/20 | chr3 | 47085936 | ||||||
| chr3:47086383
|
G | A | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5278-69C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47086383 | ||||||
| chr3:47086571
|
T | A | 2 | a0002c0001t0001g0177a0002c0001t0001g0199 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5278-257A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47086571 | ||||||
| chr3:47086720
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.5278-406G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47086720 | ||||||
| chr3:47087035
|
TA | T | 60 | a0002c0001t0001g0147a0002c0001t0001g0150a0002c0001t0001g0152others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.5278-722delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087035 | ||||||
| chr3:47087137
|
C | T | 1 | a0019c0026t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.5278-823G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087137 | ||||||
| chr3:47087208
|
C | CA | 31 | a0001c0002t0002g0004a0002c0001t0001g0150a0002c0001t0001g0167others(28): Show | 31 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.5278-895dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087208 | ||||||
| chr3:47087615
|
C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0005 | 2 | NA18949.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.5277+498G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087615 | ||||||
| chr3:47087684
|
T | C | 1 | a0002c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5277+429A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087684 | ||||||
| chr3:47087737
|
C | T | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5277+376G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087737 | ||||||
| chr3:47087867
|
G | A | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5277+246C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087867 | ||||||
| chr3:47087874
|
C | CAGG | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.5277+238_5277+239i others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087874 | ||||||
| chr3:47087964
|
TAAAC | T | 152 | a0001c0002t0002g0032a0001c0002t0002g0058a0001c0002t0003g0095others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.5277+145_5277+148d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087964 | ||||||
| chr3:47087992
|
C | T | 4 | a0004c0004t0001g0257a0004c0004t0001g0259a0004c0004t0001g0260others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.5277+121G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087992 | ||||||
| chr3:47087992
|
CAAAT | C | 21 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(18): Show | 21 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.5277+117_5277+120d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087992 | ||||||
| chr3:47087996
|
T | C | 5 | a0001c0002t0003g0109a0003c0003t0001g0295a0003c0003t0001g0296others(2): Show | 5 | HG01884.hp1 NA18945.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.5277+117A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47087996 | ||||||
| chr3:47088000
|
T | C | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5277+113A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 10/20 | chr3 | 47088000 | ||||||
| chr3:47088267
|
T | C | 1 | a0001c0002t0002g0069 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5143-20A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088267 | ||||||
| chr3:47088294
|
A | C | 7 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0003g0092others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.5143-47T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088294 | ||||||
| chr3:47088303
|
C | A | 1 | a0002c0001t0001g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5143-56G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088303 | ||||||
| chr3:47088305
|
A | C | 1 | a0002c0001t0001g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.5143-58T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088305 | ||||||
| chr3:47088410
|
TAAC | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.5143-166_5143-164d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088410 | ||||||
| chr3:47088413
|
C | T | 224 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.5143-166G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088413 | ||||||
| chr3:47088487
|
A | C | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5143-240T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088487 | ||||||
| chr3:47088495
|
C | CTTA | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.5143-251_5143-249d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088495 | ||||||
| chr3:47088609
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5143-362A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088609 | ||||||
| chr3:47088727
|
A | G | 2 | a0001c0002t0002g0025a0001c0002t0002g0051 | 2 | HG00558.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.5143-480T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088727 | ||||||
| chr3:47088958
|
C | T | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5143-711G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47088958 | ||||||
| chr3:47089144
|
G | A | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5143-897C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47089144 | ||||||
| chr3:47089243
|
T | C | 1 | a0002c0016t0001g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5143-996A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47089243 | ||||||
| chr3:47089438
|
T | C | 8 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(5): Show | 8 | HG00544.hp2 HG02735.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.5143-1191A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47089438 | ||||||
| chr3:47089554
|
A | G | 4 | a0005c0007t0001g0119a0005c0007t0001g0120a0005c0007t0001g0121others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.5143-1307T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47089554 | ||||||
| chr3:47089993
|
A | T | 2 | a0001c0002t0003g0084a0001c0025t0003g0083 | 2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.5143-1746T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47089993 | ||||||
| chr3:47090023
|
G | A | 3 | a0001c0002t0003g0111a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5143-1776C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090023 | ||||||
| chr3:47090105
|
G | A | 173 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(170): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.5143-1858C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090105 | ||||||
| chr3:47090143
|
A | G | 4 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(1): Show | 4 | HG02132.hp1 NA18951.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5143-1896T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090143 | ||||||
| chr3:47090183
|
G | A | 1 | a0001c0002t0002g0030 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.5143-1936C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090183 | ||||||
| chr3:47090453
|
G | A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.5143-2206C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090453 | ||||||
| chr3:47090643
|
G | A | 5 | a0004c0004t0001g0118a0005c0007t0001g0119a0005c0007t0001g0120others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.5143-2396C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090643 | ||||||
| chr3:47090981
|
T | G | 2 | a0002c0001t0001g0226a0002c0001t0001g0231 | 2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5143-2734A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47090981 | ||||||
| chr3:47091491
|
G | A | 1 | a0002c0001t0001g0187 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5143-3244C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47091491 | ||||||
| chr3:47091682
|
C | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.5143-3435G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47091682 | ||||||
| chr3:47091911
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5143-3664G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47091911 | ||||||
| chr3:47091913
|
C | T | 30 | a0004c0004t0001g0116a0004c0004t0001g0117a0004c0004t0001g0118others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.5143-3666G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47091913 | ||||||
| chr3:47091955
|
A | C | 1 | a0002c0001t0001g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5143-3708T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47091955 | ||||||
| chr3:47092096
|
G | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5143-3849C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47092096 | ||||||
| chr3:47092127
|
T | C | 13 | a0002c0001t0001g0155a0002c0001t0001g0158a0002c0001t0001g0159others(10): Show | 13 | HG00639.hp2 HG00735.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.5143-3880A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47092127 | ||||||
| chr3:47092377
|
T | C | 274 | a0001c0002t0002g0003a0001c0002t0002g0006a0001c0002t0002g0007others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.5143-4130A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47092377 | ||||||
| chr3:47093127
|
G | A | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.5142+4828C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093127 | ||||||
| chr3:47093284
|
C | CT | 21 | a0001c0002t0002g0043a0001c0002t0002g0055a0001c0005t0001g0123others(18): Show | 21 | HG01943.hp2 HG02083.hp2 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.5142+4670dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093284 | ||||||
| chr3:47093284
|
C | CTT | 22 | a0004c0004t0001g0116a0004c0004t0001g0117a0004c0004t0001g0118others(19): Show | 22 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.5142+4669_5142+467 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093284 | ||||||
| chr3:47093394
|
T | C | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.5142+4561A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093394 | ||||||
| chr3:47093443
|
T | C | 1 | a0002c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5142+4512A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093443 | ||||||
| chr3:47093503
|
C | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.5142+4452G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093503 | ||||||
| chr3:47093547
|
G | A | 2 | a0002c0001t0001g0195a0002c0001t0001g0196 | 2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.5142+4408C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093547 | ||||||
| chr3:47093559
|
T | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.5142+4396A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093559 | ||||||
| chr3:47093888
|
A | G | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5142+4067T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47093888 | ||||||
| chr3:47094094
|
GT | G | 15 | a0002c0001t0001g0236a0002c0001t0001g0237a0002c0001t0001g0238others(12): Show | 15 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.5142+3860delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47094094 | ||||||
| chr3:47094554
|
T | G | 2 | a0002c0001t0001g0154a0002c0001t0001g0230 | 2 | HG02071.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.5142+3401A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47094554 | ||||||
| chr3:47094785
|
T | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5142+3170A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47094785 | ||||||
| chr3:47095168
|
C | T | 1 | a0001c0005t0004g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5142+2787G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47095168 | ||||||
| chr3:47095336
|
A | G | 1 | a0001c0002t0003g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5142+2619T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47095336 | ||||||
| chr3:47095675
|
C | T | 20 | a0004c0004t0001g0116a0004c0004t0001g0118a0004c0004t0001g0125others(17): Show | 20 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.5142+2280G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47095675 | ||||||
| chr3:47095952
|
C | T | 2 | a0002c0001t0001g0236a0002c0001t0001g0238 | 2 | NA18981.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.5142+2003G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47095952 | ||||||
| chr3:47096003
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG00558.hp1 HG01891.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5142+1952C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096003 | ||||||
| chr3:47096027
|
A | T | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5142+1928T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096027 | ||||||
| chr3:47096332
|
A | T | 1 | a0003c0003t0001g0275 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5142+1623T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096332 | ||||||
| chr3:47096400
|
T | C | 1 | a0002c0001t0001g0210 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5142+1555A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096400 | ||||||
| chr3:47096449
|
G | A | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5142+1506C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096449 | ||||||
| chr3:47096571
|
C | CA | 24 | a0001c0002t0002g0015a0001c0002t0002g0017a0001c0002t0002g0018others(21): Show | 24 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.5142+1383dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096571 | ||||||
| chr3:47096582
|
AAAAAAAA others(8): Show |
A | 1 | a0002c0001t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5142+1358_5142+137 others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096582 | ||||||
| chr3:47096583
|
AAAAAAAA others(7): Show |
A | 115 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.5142+1358_5142+137 others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096583 | ||||||
| chr3:47096594
|
AAAG | A | 30 | a0001c0005t0001g0306a0001c0005t0004g0263a0001c0005t0004g0265others(27): Show | 30 | HG01255.hp1 HG01515.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.5142+1358_5142+136 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096594 | ||||||
| chr3:47096595
|
AAG | A | 28 | a0001c0005t0001g0123a0001c0005t0001g0273a0001c0005t0004g0264others(25): Show | 28 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.5142+1358_5142+135 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096595 | ||||||
| chr3:47096596
|
A | G | 3 | a0001c0002t0003g0080a0001c0002t0003g0099a0019c0026t0002g0063 | 3 | HG00738.hp2 HG02109.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.5142+1359T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096596 | ||||||
| chr3:47096596
|
AG | A | 15 | a0001c0005t0001g0115a0001c0005t0004g0262a0004c0004t0001g0125others(12): Show | 15 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.5142+1358delC | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096596 | ||||||
| chr3:47096597
|
G | A | 5 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.5142+1358C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096597 | ||||||
| chr3:47096680
|
A | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.5142+1275T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096680 | ||||||
| chr3:47096686
|
G | A | 1 | a0002c0001t0001g0183 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5142+1269C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096686 | ||||||
| chr3:47096734
|
G | A | 33 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(30): Show | 33 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.5142+1221C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096734 | ||||||
| chr3:47096739
|
G | C | 287 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0005others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.5142+1216C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096739 | ||||||
| chr3:47096754
|
A | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.5142+1201T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096754 | ||||||
| chr3:47096756
|
C | A | 8 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(5): Show | 8 | HG00544.hp2 HG02735.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.5142+1199G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096756 | ||||||
| chr3:47096763
|
A | G | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.5142+1192T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096763 | ||||||
| chr3:47096876
|
T | C | 1 | a0001c0002t0003g0095 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.5142+1079A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47096876 | ||||||
| chr3:47097218
|
G | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.5142+737C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47097218 | ||||||
| chr3:47097388
|
T | C | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.5142+567A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47097388 | ||||||
| chr3:47097409
|
C | G | 1 | a0001c0002t0002g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5142+546G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47097409 | ||||||
| chr3:47097706
|
G | C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.5142+249C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47097706 | ||||||
| chr3:47097825
|
T | C | 1 | a0001c0002t0002g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5142+130A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 9/20 | chr3 | 47097825 | ||||||
| chr3:47098110
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.5016-29C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098110 | ||||||
| chr3:47098140
|
T | C | 1 | a0004c0004t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5016-59A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098140 | ||||||
| chr3:47098157
|
G | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5016-76C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098157 | ||||||
| chr3:47098265
|
T | G | 1 | a0001c0002t0002g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.5016-184A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098265 | ||||||
| chr3:47098657
|
A | G | 1 | a0002c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5016-576T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098657 | ||||||
| chr3:47098733
|
T | C | 1 | a0001c0002t0002g0049 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.5016-652A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098733 | ||||||
| chr3:47098800
|
A | T | 4 | a0001c0002t0002g0067a0001c0006t0001g0270a0001c0006t0001g0271others(1): Show | 4 | HG01891.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.5016-719T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098800 | ||||||
| chr3:47098841
|
G | A | 1 | a0004c0004t0001g0117 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5016-760C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098841 | ||||||
| chr3:47098941
|
T | C | 1 | a0001c0002t0002g0058 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5016-860A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47098941 | ||||||
| chr3:47099024
|
C | G | 1 | a0002c0001t0001g0155 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5016-943G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099024 | ||||||
| chr3:47099117
|
G | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5016-1036C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099117 | ||||||
| chr3:47099177
|
T | G | 1 | a0002c0001t0001g0184 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.5016-1096A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099177 | ||||||
| chr3:47099439
|
C | A | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5016-1358G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099439 | ||||||
| chr3:47099562
|
C | T | 1 | a0001c0002t0003g0113 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5016-1481G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099562 | ||||||
| chr3:47099565
|
T | C | 1 | a0002c0001t0001g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5016-1484A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099565 | ||||||
| chr3:47099872
|
A | C | 1 | a0007c0009t0003g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5015+1586T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47099872 | ||||||
| chr3:47100613
|
C | T | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.5015+845G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100613 | ||||||
| chr3:47100619
|
C | T | 1 | a0002c0001t0001g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5015+839G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100619 | ||||||
| chr3:47100662
|
C | T | 1 | a0002c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5015+796G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100662 | ||||||
| chr3:47100792
|
C | T | 2 | a0002c0001t0001g0226a0002c0001t0001g0231 | 2 | HG02135.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.5015+666G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100792 | ||||||
| chr3:47100870
|
C | T | 4 | a0002c0001t0001g0157a0002c0001t0001g0183a0002c0001t0001g0184others(1): Show | 4 | HG00544.hp1 HG02015.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.5015+588G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100870 | ||||||
| chr3:47100871
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5015+587C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100871 | ||||||
| chr3:47100918
|
G | A | 1 | a0001c0005t0004g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5015+540C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47100918 | ||||||
| chr3:47101009
|
C | CA | 52 | a0001c0002t0002g0008a0001c0002t0002g0041a0001c0002t0002g0067others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.5015+448dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47101009 | ||||||
| chr3:47101009
|
CA | C | 32 | a0001c0002t0002g0047a0001c0002t0003g0093a0001c0002t0003g0094others(29): Show | 32 | HG00544.hp2 HG01255.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.5015+448delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47101009 | ||||||
| chr3:47101166
|
G | A | 1 | a0001c0002t0002g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5015+292C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47101166 | ||||||
| chr3:47101417
|
TCC | T | 168 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.5015+39_5015+40del others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 8/20 | chr3 | 47101417 | ||||||
| chr3:47101575
|
C | G | 1 | a0002c0001t0001g0194 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4918-20G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101575 | ||||||
| chr3:47101597
|
A | AGT | 71 | a0001c0002t0002g0006a0001c0002t0002g0014a0001c0002t0002g0019others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.4918-44_4918-43dup others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
A | AGTGT | 17 | a0001c0002t0003g0075a0001c0002t0003g0081a0001c0005t0001g0123others(14): Show | 17 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.4918-46_4918-43dup others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
A | AGTGTGT | 3 | a0001c0002t0003g0084a0001c0002t0003g0097a0002c0001t0001g0245 | 3 | HG01433.hp1 HG01981.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.4918-48_4918-43dup others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
A | AGTGTGTG others(3): Show |
1 | a0002c0001t0001g0244 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.4918-52_4918-43dup others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
AGT | A | 36 | a0001c0002t0002g0039a0001c0002t0002g0045a0001c0002t0002g0046others(33): Show | 36 | HG00738.hp2 HG01884.hp2 HG02004.hp1 others(33): Show |
intron_variant | MODIFIER | c.4918-44_4918-43del others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
AGTGT | A | 29 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0005t0001g0115others(26): Show | 29 | HG01070.hp2 HG01175.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.4918-46_4918-43del others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
AGTGTGT | A | 5 | a0001c0002t0002g0047a0001c0002t0002g0048a0002c0017t0001g0156others(2): Show | 5 | HG02027.hp1 HG02280.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.4918-48_4918-43del others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101597
|
AGTGTGTG others(5): Show |
A | 2 | a0001c0005t0001g0306a0002c0001t0001g0230 | 2 | HG02559.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.4918-54_4918-43del others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101597 | ||||||
| chr3:47101625
|
T | C | 1 | a0002c0001t0001g0200 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4918-70A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101625 | ||||||
| chr3:47101627
|
T | C | 1 | a0002c0001t0001g0200 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.4918-72A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101627 | ||||||
| chr3:47101631
|
T | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4918-76A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101631 | ||||||
| chr3:47101633
|
T | C | 13 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0047others(10): Show | 13 | HG01884.hp2 HG01978.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.4918-78A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101633 | ||||||
| chr3:47101633
|
T | TGC | 15 | a0001c0002t0003g0107a0004c0004t0001g0116a0004c0004t0001g0125others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.4918-80_4918-79dup others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101633 | ||||||
| chr3:47101841
|
A | G | 1 | a0013c0022t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4918-286T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101841 | ||||||
| chr3:47101849
|
TTTTAA | T | 4 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0064others(1): Show | 4 | NA18953.hp2 NA18961.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.4918-299_4918-295d others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101849 | ||||||
| chr3:47101959
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4918-404A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47101959 | ||||||
| chr3:47102001
|
A | C | 1 | a0001c0005t0004g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4918-446T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102001 | ||||||
| chr3:47102250
|
G | C | 1 | a0001c0002t0003g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4918-695C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102250 | ||||||
| chr3:47102421
|
C | G | 1 | a0002c0001t0001g0155 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4918-866G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102421 | ||||||
| chr3:47102499
|
T | C | 3 | a0001c0002t0003g0111a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4917+847A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102499 | ||||||
| chr3:47102507
|
C | A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4917+839G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102507 | ||||||
| chr3:47102772
|
C | CA | 155 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0017others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.4917+573dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102772 | ||||||
| chr3:47102772
|
C | CAA | 12 | a0002c0001t0001g0196a0002c0001t0001g0204a0002c0001t0001g0210others(9): Show | 12 | HG00621.hp1 HG01934.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.4917+572_4917+573d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102772 | ||||||
| chr3:47102772
|
CA | C | 24 | a0003c0003t0001g0269a0003c0003t0001g0275a0003c0003t0001g0276others(21): Show | 24 | HG01358.hp2 HG01515.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.4917+573delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102772 | ||||||
| chr3:47102833
|
A | G | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4917+513T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102833 | ||||||
| chr3:47102929
|
T | C | 1 | a0001c0002t0006g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4917+417A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47102929 | ||||||
| chr3:47103009
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4917+337A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 7/20 | chr3 | 47103009 | ||||||
| chr3:47103744
|
G | GCA | 150 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0005g0074others(147): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.4840-323_4840-322d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47103744 | ||||||
| chr3:47103988
|
T | C | 1 | a0001c0002t0002g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4840-565A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47103988 | ||||||
| chr3:47104100
|
G | C | 1 | a0001c0002t0002g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4840-677C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104100 | ||||||
| chr3:47104237
|
A | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4840-814T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104237 | ||||||
| chr3:47104404
|
G | T | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4840-981C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104404 | ||||||
| chr3:47104515
|
G | A | 1 | a0001c0002t0002g0035 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4840-1092C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104515 | ||||||
| chr3:47104626
|
T | C | 3 | a0002c0001t0001g0180a0002c0001t0001g0188a0002c0001t0001g0229 | 3 | NA18940.hp1 NA18947.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4840-1203A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104626 | ||||||
| chr3:47104657
|
A | G | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4840-1234T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104657 | ||||||
| chr3:47104801
|
G | A | 1 | a0001c0002t0002g0058 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4839+1196C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47104801 | ||||||
| chr3:47105073
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4839+924C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105073 | ||||||
| chr3:47105335
|
G | A | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4839+662C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105335 | ||||||
| chr3:47105371
|
C | T | 15 | a0004c0004t0001g0116a0004c0004t0001g0125a0004c0004t0001g0126others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.4839+626G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105371 | ||||||
| chr3:47105410
|
T | TA | 180 | a0001c0005t0001g0115a0001c0005t0001g0149a0001c0005t0004g0262others(177): Show | 180 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(177): Show |
intron_variant | MODIFIER | c.4839+586dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105410 | ||||||
| chr3:47105410
|
T | TAA | 19 | a0001c0005t0001g0123a0001c0005t0001g0273a0001c0005t0001g0306others(16): Show | 19 | HG00280.hp2 HG01175.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.4839+585_4839+586d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105410 | ||||||
| chr3:47105442
|
C | T | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.4839+555G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105442 | ||||||
| chr3:47105450
|
A | C | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4839+547T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105450 | ||||||
| chr3:47105535
|
T | A | 2 | a0001c0002t0002g0015a0001c0002t0002g0039 | 2 | HG02071.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.4839+462A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105535 | ||||||
| chr3:47105586
|
G | A | 2 | a0002c0001t0001g0187a0002c0001t0001g0214 | 2 | HG01952.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4839+411C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105586 | ||||||
| chr3:47105903
|
C | CA | 12 | a0001c0002t0002g0025a0001c0002t0002g0035a0001c0002t0002g0051others(9): Show | 12 | HG00558.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.4839+93dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105903 | ||||||
| chr3:47105903
|
CA | C | 55 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0273others(52): Show | 55 | HG00609.hp2 HG01109.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.4839+93delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105903 | ||||||
| chr3:47105903
|
CAA | C | 126 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.4839+92_4839+93del others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 6/20 | chr3 | 47105903 | ||||||
| chr3:47106209
|
A | C | 1 | a0001c0002t0002g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4716-89T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106209 | ||||||
| chr3:47106493
|
T | TA | 45 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0015others(42): Show | 45 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.4716-374dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAA | 18 | a0001c0002t0002g0006a0001c0002t0002g0059a0001c0002t0002g0062others(15): Show | 18 | HG00738.hp2 HG01433.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.4716-375_4716-374d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAA | 12 | a0001c0005t0001g0149a0001c0005t0005g0072a0001c0005t0005g0074others(9): Show | 12 | HG01934.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.4716-378_4716-374d others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAA | 11 | a0001c0002t0003g0097a0004c0004t0001g0117a0004c0004t0001g0125others(8): Show | 11 | HG01981.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.4716-379_4716-374d others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAAA others(4): Show |
1 | a0004c0010t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4716-384_4716-374d others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAAA others(9): Show |
1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4716-389_4716-374d others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAAA others(12): Show |
1 | a0005c0007t0001g0121 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.4716-392_4716-374d others(21): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAAA others(13): Show |
2 | a0005c0007t0001g0119a0005c0007t0001g0120 | 2 | HG01167.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4716-393_4716-374d others(22): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAAA others(14): Show |
1 | a0004c0004t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4716-394_4716-374d others(23): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
T | TAAAAAAA others(15): Show |
1 | a0005c0007t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4716-395_4716-374d others(24): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAA | T | 9 | a0001c0005t0004g0263a0001c0005t0004g0264a0001c0005t0004g0265others(6): Show | 9 | HG02486.hp2 HG02886.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.4716-376_4716-374d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAAAAA | T | 19 | a0001c0005t0001g0273a0002c0001t0001g0163a0002c0001t0001g0175others(16): Show | 19 | HG00099.hp2 HG00642.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.4716-379_4716-374d others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAAAAAA | T | 92 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.4716-380_4716-374d others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4716-384_4716-374d others(13): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0002t0002g0069 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4716-386_4716-374d others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAAAAAA others(9): Show |
T | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4716-389_4716-374d others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106493
|
TAAAAAAA others(10): Show |
T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.4716-390_4716-374d others(19): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106493 | ||||||
| chr3:47106496
|
A | T | 2 | a0001c0005t0004g0262a0001c0005t0004g0304 | 2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4716-376T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106496 | ||||||
| chr3:47106497
|
A | T | 9 | a0001c0005t0004g0263a0001c0005t0004g0264a0001c0005t0004g0265others(6): Show | 9 | HG02486.hp2 HG02886.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.4716-377T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106497 | ||||||
| chr3:47106498
|
A | T | 4 | a0001c0005t0004g0299a0001c0005t0004g0301a0001c0005t0004g0305others(1): Show | 4 | HG02572.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4716-378T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106498 | ||||||
| chr3:47106526
|
A | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4716-406T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106526 | ||||||
| chr3:47106811
|
C | CA | 116 | a0001c0002t0002g0015a0001c0002t0002g0039a0002c0001t0001g0144others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.4716-692dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106811 | ||||||
| chr3:47106846
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4716-726C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47106846 | ||||||
| chr3:47107168
|
T | C | 2 | a0001c0002t0003g0079a0001c0002t0003g0081 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4716-1048A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107168 | ||||||
| chr3:47107445
|
G | A | 4 | a0004c0004t0001g0117a0004c0004t0001g0140a0004c0004t0001g0141others(1): Show | 4 | HG03130.hp1 HG03540.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4716-1325C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107445 | ||||||
| chr3:47107461
|
G | GTA | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4716-1343_4716-134 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107461 | ||||||
| chr3:47107604
|
T | A | 1 | a0001c0002t0002g0043 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4716-1484A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107604 | ||||||
| chr3:47107720
|
CG | C | 62 | a0001c0002t0002g0006a0001c0002t0002g0012a0001c0002t0002g0014others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.4716-1601delC | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107720 | ||||||
| chr3:47107720
|
CGGGGGGG others(3): Show |
C | 13 | a0002c0001t0001g0163a0002c0001t0001g0166a0002c0001t0001g0168others(10): Show | 13 | HG00597.hp2 HG00673.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.4716-1610_4716-160 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107720 | ||||||
| chr3:47107720
|
CGGGGGGG others(4): Show |
C | 136 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0005g0074others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4716-1611_4716-160 others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107720 | ||||||
| chr3:47107720
|
CGGGGGGG others(5): Show |
C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4716-1612_4716-160 others(16): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107720 | ||||||
| chr3:47107723
|
G | C | 18 | a0001c0005t0001g0306a0001c0006t0001g0270a0001c0006t0001g0271others(15): Show | 18 | HG01358.hp2 HG01891.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.4716-1603C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107723 | ||||||
| chr3:47107726
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4716-1606C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107726 | ||||||
| chr3:47107729
|
G | T | 41 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(38): Show | 41 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.4716-1609C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107729 | ||||||
| chr3:47107730
|
T | C | 13 | a0003c0003t0001g0274a0003c0003t0001g0276a0003c0003t0001g0277others(10): Show | 13 | HG01255.hp1 HG01515.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.4716-1610A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107730 | ||||||
| chr3:47107730
|
T | G | 43 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0007others(40): Show | 43 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.4716-1610A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107730 | ||||||
| chr3:47107733
|
G | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4716-1613C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107733 | ||||||
| chr3:47107735
|
G | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4716-1615C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107735 | ||||||
| chr3:47107736
|
G | C | 1 | a0002c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4716-1616C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107736 | ||||||
| chr3:47107737
|
G | T | 2 | a0002c0001t0001g0189a0002c0001t0005g0073 | 2 | HG00642.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.4716-1617C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107737 | ||||||
| chr3:47107785
|
A | C | 1 | a0001c0005t0004g0263 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4716-1665T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107785 | ||||||
| chr3:47107803
|
T | C | 3 | a0005c0007t0001g0119a0005c0007t0001g0120a0005c0007t0001g0121 | 3 | HG01167.hp1 HG01169.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4716-1683A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107803 | ||||||
| chr3:47107814
|
T | TA | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.4716-1695dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107814 | ||||||
| chr3:47107949
|
C | T | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.4716-1829G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47107949 | ||||||
| chr3:47108079
|
G | A | 1 | a0003c0003t0001g0291 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4716-1959C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108079 | ||||||
| chr3:47108234
|
A | G | 1 | a0002c0001t0001g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4716-2114T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108234 | ||||||
| chr3:47108332
|
T | C | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4716-2212A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108332 | ||||||
| chr3:47108384
|
C | T | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4716-2264G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108384 | ||||||
| chr3:47108539
|
A | T | 1 | a0001c0002t0006g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4716-2419T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108539 | ||||||
| chr3:47108651
|
C | T | 1 | a0004c0004t0001g0258 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4716-2531G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108651 | ||||||
| chr3:47108748
|
T | A | 1 | a0002c0017t0001g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4716-2628A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108748 | ||||||
| chr3:47108779
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.4716-2659G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108779 | ||||||
| chr3:47108786
|
C | A | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4716-2666G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108786 | ||||||
| chr3:47108804
|
A | G | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4716-2684T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47108804 | ||||||
| chr3:47109128
|
C | T | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4716-3008G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109128 | ||||||
| chr3:47109171
|
G | A | 2 | a0007c0009t0003g0100a0007c0009t0003g0104 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4716-3051C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109171 | ||||||
| chr3:47109225
|
C | T | 1 | a0001c0002t0003g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4716-3105G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109225 | ||||||
| chr3:47109226
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4716-3106C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109226 | ||||||
| chr3:47109237
|
G | A | 1 | a0001c0002t0002g0022 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4716-3117C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109237 | ||||||
| chr3:47109379
|
C | T | 1 | a0002c0001t0001g0167 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4716-3259G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109379 | ||||||
| chr3:47109604
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4716-3484G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109604 | ||||||
| chr3:47109784
|
G | T | 1 | a0001c0002t0006g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4716-3664C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109784 | ||||||
| chr3:47109911
|
G | A | 9 | a0002c0001t0001g0152a0002c0001t0001g0153a0002c0001t0001g0166others(6): Show | 9 | HG00558.hp1 HG01978.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.4716-3791C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109911 | ||||||
| chr3:47109941
|
G | A | 1 | a0002c0001t0001g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4716-3821C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109941 | ||||||
| chr3:47109985
|
C | CA | 9 | a0001c0002t0003g0075a0001c0002t0003g0090a0001c0002t0003g0101others(6): Show | 9 | HG00597.hp2 HG00735.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4716-3866dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47109985 | ||||||
| chr3:47110454
|
G | C | 1 | a0004c0004t0001g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4715+3422C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47110454 | ||||||
| chr3:47110654
|
C | T | 1 | a0002c0001t0001g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4715+3222G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47110654 | ||||||
| chr3:47110946
|
G | A | 1 | a0001c0002t0003g0109 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4715+2930C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47110946 | ||||||
| chr3:47111074
|
T | TC | 58 | a0001c0005t0001g0123a0002c0001t0001g0152a0002c0001t0001g0153others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.4715+2801dupG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111074 | ||||||
| chr3:47111077
|
T | C | 90 | a0001c0005t0001g0115a0002c0001t0001g0144a0002c0001t0001g0145others(87): Show | 90 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.4715+2799A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111077 | ||||||
| chr3:47111079
|
T | A | 58 | a0001c0005t0001g0123a0002c0001t0001g0152a0002c0001t0001g0153others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.4715+2797A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
T | TA | 10 | a0001c0002t0002g0022a0001c0002t0002g0024a0001c0002t0002g0030others(7): Show | 10 | HG00099.hp1 HG00597.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.4715+2796dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
T | TAA | 69 | a0001c0002t0003g0106a0001c0005t0001g0115a0002c0001t0001g0147others(66): Show | 69 | HG00280.hp2 HG00544.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4715+2795_4715+279 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
T | TAAA | 11 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(8): Show | 11 | HG00735.hp1 HG02055.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.4715+2794_4715+279 others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
TA | T | 68 | a0001c0002t0002g0003a0001c0002t0002g0005a0001c0002t0002g0006others(65): Show | 68 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.4715+2796delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
TAA | T | 30 | a0001c0002t0002g0060a0001c0002t0002g0069a0001c0005t0001g0306others(27): Show | 30 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.4715+2795_4715+279 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
TAAAAAAA others(3): Show |
T | 5 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(2): Show | 5 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4715+2787_4715+279 others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111079
|
TAAAAAAA others(4): Show |
T | 4 | a0004c0004t0001g0117a0004c0004t0001g0140a0004c0004t0001g0141others(1): Show | 4 | HG03130.hp1 HG03540.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4715+2786_4715+279 others(15): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111079 | ||||||
| chr3:47111170
|
G | A | 2 | a0004c0004t0004g0124a0015c0015t0001g0138 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.4715+2706C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111170 | ||||||
| chr3:47111390
|
A | AC | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4715+2485dupG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111390 | ||||||
| chr3:47111398
|
T | A | 1 | a0002c0001t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4715+2478A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111398 | ||||||
| chr3:47111502
|
C | T | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4715+2374G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111502 | ||||||
| chr3:47111577
|
T | A | 1 | a0001c0005t0005g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4715+2299A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111577 | ||||||
| chr3:47111654
|
C | T | 3 | a0003c0003t0001g0276a0003c0003t0001g0277a0003c0003t0001g0278 | 3 | NA19066.hp2 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4715+2222G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111654 | ||||||
| chr3:47111787
|
T | C | 2 | a0004c0004t0004g0124a0004c0004t0004g0128 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4715+2089A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111787 | ||||||
| chr3:47111820
|
C | T | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4715+2056G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47111820 | ||||||
| chr3:47112105
|
A | G | 1 | a0001c0006t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4715+1771T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112105 | ||||||
| chr3:47112115
|
C | CT | 7 | a0001c0002t0002g0004a0001c0002t0002g0020a0001c0002t0002g0021others(4): Show | 7 | HG00597.hp1 NA18949.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.4715+1760dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112115 | ||||||
| chr3:47112115
|
CT | C | 182 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.4715+1760delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112115 | ||||||
| chr3:47112115
|
CTT | C | 16 | a0002c0001t0001g0150a0002c0001t0001g0160a0002c0001t0001g0161others(13): Show | 16 | HG00735.hp1 HG01070.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.4715+1759_4715+176 others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112115 | ||||||
| chr3:47112342
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4715+1534G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112342 | ||||||
| chr3:47112343
|
G | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4715+1533C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112343 | ||||||
| chr3:47112344
|
C | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4715+1532G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112344 | ||||||
| chr3:47112351
|
G | A | 4 | a0005c0007t0001g0119a0005c0007t0001g0120a0005c0007t0001g0121others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.4715+1525C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112351 | ||||||
| chr3:47112419
|
T | G | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.4715+1457A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112419 | ||||||
| chr3:47112528
|
C | T | 3 | a0001c0002t0002g0011a0001c0002t0002g0022a0001c0002t0002g0053 | 3 | HG01358.hp1 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.4715+1348G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112528 | ||||||
| chr3:47112692
|
C | T | 1 | a0002c0001t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4715+1184G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112692 | ||||||
| chr3:47112753
|
C | T | 1 | a0001c0002t0003g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4715+1123G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112753 | ||||||
| chr3:47112843
|
G | T | 1 | a0002c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4715+1033C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47112843 | ||||||
| chr3:47113106
|
C | CT | 201 | a0001c0002t0002g0047a0001c0002t0002g0048a0001c0005t0001g0115others(198): Show | 201 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.4715+769dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113106 | ||||||
| chr3:47113161
|
T | G | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4715+715A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113161 | ||||||
| chr3:47113165
|
G | A | 3 | a0002c0001t0001g0180a0002c0001t0001g0188a0002c0001t0001g0229 | 3 | NA18940.hp1 NA18947.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.4715+711C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113165 | ||||||
| chr3:47113323
|
A | G | 5 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(2): Show | 5 | NA18951.hp2 NA19000.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.4715+553T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113323 | ||||||
| chr3:47113526
|
A | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4715+350T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113526 | ||||||
| chr3:47113599
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4715+277G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113599 | ||||||
| chr3:47113610
|
G | A | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4715+266C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113610 | ||||||
| chr3:47113663
|
G | A | 1 | a0001c0002t0002g0025 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4715+213C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113663 | ||||||
| chr3:47113763
|
C | T | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4715+113G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 5/20 | chr3 | 47113763 | ||||||
| chr3:47114037
|
T | C | 1 | a0004c0010t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4587-33A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114037 | ||||||
| chr3:47114290
|
A | G | 1 | a0001c0006t0001g0271 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4587-286T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114290 | ||||||
| chr3:47114374
|
C | T | 15 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(12): Show | 15 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.4587-370G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114374 | ||||||
| chr3:47114489
|
C | T | 22 | a0003c0003t0001g0274a0003c0003t0001g0275a0003c0003t0001g0276others(19): Show | 22 | HG01255.hp1 HG01358.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.4587-485G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114489 | ||||||
| chr3:47114639
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4587-635C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114639 | ||||||
| chr3:47114684
|
C | A | 2 | a0001c0002t0002g0014a0001c0002t0002g0019 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.4587-680G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114684 | ||||||
| chr3:47114876
|
C | CA | 15 | a0001c0002t0002g0016a0001c0002t0002g0044a0001c0002t0002g0045others(12): Show | 15 | HG00621.hp1 HG01175.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.4587-873dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114876 | ||||||
| chr3:47114876
|
CA | C | 15 | a0001c0002t0002g0025a0001c0002t0002g0029a0001c0002t0002g0046others(12): Show | 15 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.4587-873delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114876 | ||||||
| chr3:47114876
|
CAA | C | 26 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0117others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.4587-874_4587-873d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47114876 | ||||||
| chr3:47115282
|
G | A | 1 | a0001c0002t0003g0082 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4587-1278C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47115282 | ||||||
| chr3:47115440
|
T | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.4586+1183A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47115440 | ||||||
| chr3:47115554
|
T | G | 2 | a0003c0003t0001g0283a0003c0003t0001g0284 | 2 | NA19070.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.4586+1069A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47115554 | ||||||
| chr3:47116028
|
G | A | 1 | a0002c0001t0002g0001 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4586+595C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47116028 | ||||||
| chr3:47116136
|
T | TAAGATTT others(318): Show |
1 | a0002c0001t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4586+486_4586+487i others(327): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47116136 | ||||||
| chr3:47116439
|
C | G | 1 | a0003c0014t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4586+184G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 4/20 | chr3 | 47116439 | ||||||
| chr3:47116766
|
A | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4455-12T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47116766 | ||||||
| chr3:47117134
|
C | T | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4455-380G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117134 | ||||||
| chr3:47117274
|
A | C | 28 | a0001c0005t0001g0273a0001c0005t0001g0306a0003c0003t0001g0269others(25): Show | 28 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.4455-520T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117274 | ||||||
| chr3:47117275
|
A | AC | 144 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0144others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.4455-522_4455-521i others(3): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117275 | ||||||
| chr3:47117277
|
A | C | 5 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058others(2): Show | 5 | HG02280.hp1 HG03486.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.4455-523T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117277 | ||||||
| chr3:47117281
|
C | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4455-527G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117281 | ||||||
| chr3:47117282
|
A | C | 1 | a0002c0001t0001g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4455-528T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117282 | ||||||
| chr3:47117283
|
A | C | 2 | a0001c0005t0004g0304a0001c0006t0001g0293 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4455-529T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117283 | ||||||
| chr3:47117283
|
AAC | A | 57 | a0001c0005t0001g0306a0001c0005t0004g0262a0001c0005t0004g0263others(54): Show | 57 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(54): Show |
intron_variant | MODIFIER | c.4455-531_4455-530d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117283 | ||||||
| chr3:47117284
|
AC | A | 132 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(129): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.4455-531delG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117284 | ||||||
| chr3:47117285
|
C | A | 11 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058others(8): Show | 11 | HG02451.hp2 HG02630.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.4455-531G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117285 | ||||||
| chr3:47117287
|
A | C | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.4455-533T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117287 | ||||||
| chr3:47117463
|
C | T | 1 | a0002c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4455-709G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117463 | ||||||
| chr3:47117762
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.4455-1008G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117762 | ||||||
| chr3:47117786
|
G | A | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4455-1032C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47117786 | ||||||
| chr3:47118198
|
G | A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG01358.hp2 HG02486.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4455-1444C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118198 | ||||||
| chr3:47118228
|
A | G | 1 | a0011c0023t0003g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4455-1474T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118228 | ||||||
| chr3:47118436
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4455-1682A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118436 | ||||||
| chr3:47118594
|
G | A | 1 | a0004c0004t0001g0259 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4454+1588C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118594 | ||||||
| chr3:47118633
|
C | A | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4454+1549G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118633 | ||||||
| chr3:47118637
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4454+1545G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118637 | ||||||
| chr3:47118779
|
T | C | 1 | a0001c0002t0003g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4454+1403A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118779 | ||||||
| chr3:47118832
|
T | C | 1 | a0001c0002t0002g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4454+1350A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118832 | ||||||
| chr3:47118924
|
C | G | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4454+1258G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47118924 | ||||||
| chr3:47119033
|
C | A | 1 | a0005c0007t0001g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4454+1149G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119033 | ||||||
| chr3:47119087
|
G | A | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4454+1095C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119087 | ||||||
| chr3:47119396
|
A | T | 2 | a0003c0003t0001g0308a0003c0014t0001g0307 | 2 | HG01515.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4454+786T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119396 | ||||||
| chr3:47119449
|
T | G | 1 | a0001c0002t0003g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4454+733A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119449 | ||||||
| chr3:47119502
|
T | C | 1 | a0002c0001t0001g0226 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4454+680A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119502 | ||||||
| chr3:47119654
|
A | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4454+528T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119654 | ||||||
| chr3:47119724
|
T | C | 200 | a0001c0002t0002g0015a0001c0005t0001g0115a0001c0005t0001g0123others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.4454+458A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119724 | ||||||
| chr3:47119941
|
C | T | 1 | a0001c0002t0003g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4454+241G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 3/20 | chr3 | 47119941 | ||||||
| chr3:47124876
|
C | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.88-328G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47124876 | ||||||
| chr3:47124915
|
T | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.88-367A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47124915 | ||||||
| chr3:47124966
|
A | G | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.88-418T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47124966 | ||||||
| chr3:47125245
|
G | A | 2 | a0002c0001t0001g0203a0002c0001t0001g0204 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.88-697C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125245 | ||||||
| chr3:47125256
|
T | C | 2 | a0001c0002t0002g0047a0001c0002t0002g0048 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.88-708A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125256 | ||||||
| chr3:47125342
|
TA | T | 200 | a0001c0002t0002g0028a0001c0005t0001g0115a0001c0005t0001g0123others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.88-795delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125342 | ||||||
| chr3:47125463
|
T | A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.88-915A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125463 | ||||||
| chr3:47125468
|
A | C | 2 | a0001c0002t0002g0016a0002c0001t0001g0175 | 2 | HG03834.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.88-920T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125468 | ||||||
| chr3:47125495
|
T | C | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.88-947A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125495 | ||||||
| chr3:47125716
|
G | C | 1 | a0001c0002t0002g0018 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.87+932C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125716 | ||||||
| chr3:47125719
|
T | C | 28 | a0001c0005t0001g0273a0001c0005t0001g0306a0003c0003t0001g0269others(25): Show | 28 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(25): Show |
intron_variant | MODIFIER | c.87+929A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125719 | ||||||
| chr3:47125846
|
T | A | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.87+802A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47125846 | ||||||
| chr3:47126319
|
A | C | 1 | a0002c0001t0001g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.87+329T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47126319 | ||||||
| chr3:47126426
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.87+222A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47126426 | ||||||
| chr3:47126632
|
G | A | 1 | a0002c0001t0001g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.87+16C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 2/20 | chr3 | 47126632 | ||||||
| chr3:47126729
|
T | C | 4 | a0001c0002t0003g0091a0001c0002t0003g0103a0001c0002t0003g0105others(1): Show | 4 | HG01192.hp1 HG02055.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-66A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47126729 | ||||||
| chr3:47126814
|
C | CA | 4 | a0005c0007t0001g0119a0005c0007t0001g0120a0005c0007t0001g0121others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-152dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47126814 | ||||||
| chr3:47127236
|
T | C | 1 | a0002c0001t0001g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.72-573A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127236 | ||||||
| chr3:47127349
|
T | TA | 142 | a0001c0002t0002g0071a0001c0002t0003g0097a0001c0005t0001g0306others(139): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.72-687dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127349 | ||||||
| chr3:47127601
|
C | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.72-938G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127601 | ||||||
| chr3:47127885
|
G | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.72-1222C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127885 | ||||||
| chr3:47127993
|
T | TCA | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0003g0097 | 3 | HG01981.hp1 NA18965.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.72-1332_72-1331dup others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127993 | ||||||
| chr3:47127993
|
TCA | T | 172 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(169): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.72-1332_72-1331del others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127993 | ||||||
| chr3:47127997
|
A | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72-1334T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47127997 | ||||||
| chr3:47128649
|
A | T | 1 | a0002c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.72-1986T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47128649 | ||||||
| chr3:47128946
|
C | T | 1 | a0004c0004t0001g0117 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.72-2283G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47128946 | ||||||
| chr3:47129117
|
A | C | 20 | a0004c0004t0001g0116a0004c0004t0001g0118a0004c0004t0001g0125others(17): Show | 20 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.72-2454T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47129117 | ||||||
| chr3:47129448
|
A | G | 1 | a0001c0002t0002g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.72-2785T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47129448 | ||||||
| chr3:47129464
|
T | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-2801A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47129464 | ||||||
| chr3:47129665
|
C | T | 1 | a0017c0013t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72-3002G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47129665 | ||||||
| chr3:47129889
|
AAAAGAAA others(4): Show |
A | 1 | a0002c0001t0001g0216 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.72-3237_72-3227del others(11): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47129889 | ||||||
| chr3:47130387
|
A | G | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.72-3724T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47130387 | ||||||
| chr3:47130818
|
T | C | 1 | a0002c0001t0001g0245 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.72-4155A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47130818 | ||||||
| chr3:47130897
|
A | G | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72-4234T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47130897 | ||||||
| chr3:47130917
|
T | C | 37 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(34): Show | 37 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.72-4254A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47130917 | ||||||
| chr3:47131064
|
T | C | 2 | a0007c0009t0003g0100a0007c0009t0003g0104 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.72-4401A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131064 | ||||||
| chr3:47131204
|
A | G | 1 | a0004c0004t0001g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72-4541T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131204 | ||||||
| chr3:47131228
|
C | A | 1 | a0001c0002t0003g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-4565G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131228 | ||||||
| chr3:47131374
|
C | T | 15 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(12): Show | 15 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.72-4711G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131374 | ||||||
| chr3:47131445
|
G | A | 6 | a0002c0001t0001g0171a0002c0001t0001g0174a0002c0001t0001g0205others(3): Show | 6 | HG03491.hp2 HG03654.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-4782C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131445 | ||||||
| chr3:47131556
|
G | T | 2 | a0001c0002t0002g0012a0001c0002t0002g0027 | 2 | NA18975.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.72-4893C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131556 | ||||||
| chr3:47131764
|
CT | C | 6 | a0002c0001t0001g0172a0002c0001t0001g0233a0006c0008t0001g0206others(3): Show | 6 | HG01256.hp1 HG02735.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-5102delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47131764 | ||||||
| chr3:47132055
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72-5392G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132055 | ||||||
| chr3:47132096
|
G | A | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.72-5433C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132096 | ||||||
| chr3:47132131
|
C | CT | 31 | a0001c0002t0003g0097a0001c0005t0001g0123a0002c0001t0001g0236others(28): Show | 31 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.72-5469dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132131 | ||||||
| chr3:47132131
|
CT | C | 8 | a0001c0002t0003g0112a0001c0002t0003g0113a0001c0005t0001g0273others(5): Show | 8 | HG01884.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-5469delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132131 | ||||||
| chr3:47132159
|
A | C | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.72-5496T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132159 | ||||||
| chr3:47132193
|
C | T | 2 | a0001c0002t0002g0010a0001c0002t0002g0052 | 2 | HG03704.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.72-5530G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132193 | ||||||
| chr3:47132322
|
T | C | 3 | a0006c0008t0001g0206a0006c0008t0001g0207a0006c0008t0001g0208 | 3 | NA18944.hp2 NA18954.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.72-5659A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132322 | ||||||
| chr3:47132408
|
G | A | 1 | a0003c0003t0001g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.72-5745C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132408 | ||||||
| chr3:47132505
|
A | G | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-5842T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132505 | ||||||
| chr3:47132521
|
G | C | 1 | a0002c0001t0001g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.72-5858C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132521 | ||||||
| chr3:47132664
|
CG | C | 199 | a0001c0002t0002g0014a0001c0005t0001g0115a0001c0005t0001g0123others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.72-6002delC | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132664 | ||||||
| chr3:47132759
|
A | T | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6096T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132759 | ||||||
| chr3:47132760
|
C | A | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6097G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132760 | ||||||
| chr3:47132761
|
T | C | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6098A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132761 | ||||||
| chr3:47132763
|
A | T | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6100T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132763 | ||||||
| chr3:47132765
|
A | G | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6102T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132765 | ||||||
| chr3:47132767
|
A | G | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6104T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132767 | ||||||
| chr3:47132768
|
C | A | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6105G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132768 | ||||||
| chr3:47132769
|
A | T | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.72-6106T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132769 | ||||||
| chr3:47132853
|
T | A | 199 | a0001c0002t0002g0014a0001c0005t0001g0115a0001c0005t0001g0123others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.72-6190A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132853 | ||||||
| chr3:47132960
|
T | C | 1 | a0015c0015t0001g0138 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.72-6297A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47132960 | ||||||
| chr3:47133070
|
T | C | 1 | a0003c0003t0001g0291 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.72-6407A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133070 | ||||||
| chr3:47133149
|
G | C | 3 | a0002c0001t0001g0209a0002c0001t0001g0210a0008c0028t0001g0211 | 3 | HG03654.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.72-6486C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133149 | ||||||
| chr3:47133191
|
A | G | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72-6528T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133191 | ||||||
| chr3:47133214
|
A | T | 3 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058 | 3 | HG03704.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.72-6551T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133214 | ||||||
| chr3:47133250
|
G | A | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72-6587C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133250 | ||||||
| chr3:47133352
|
T | C | 1 | a0002c0001t0001g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.72-6689A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133352 | ||||||
| chr3:47133704
|
G | A | 31 | a0002c0001t0001g0155a0002c0001t0001g0157a0002c0001t0001g0158others(28): Show | 31 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.72-7041C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133704 | ||||||
| chr3:47133778
|
G | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72-7115C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133778 | ||||||
| chr3:47133854
|
A | G | 1 | a0013c0022t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72-7191T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133854 | ||||||
| chr3:47133888
|
T | C | 1 | a0002c0001t0001g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.72-7225A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47133888 | ||||||
| chr3:47134102
|
C | G | 3 | a0002c0001t0001g0190a0002c0001t0001g0192a0002c0001t0001g0223 | 3 | NA18942.hp1 NA18949.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.72-7439G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134102 | ||||||
| chr3:47134142
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72-7479A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134142 | ||||||
| chr3:47134196
|
A | C | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-7533T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134196 | ||||||
| chr3:47134374
|
T | C | 1 | a0001c0005t0004g0262 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.72-7711A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134374 | ||||||
| chr3:47134397
|
A | T | 1 | a0001c0002t0003g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.72-7734T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134397 | ||||||
| chr3:47134715
|
C | T | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72-8052G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134715 | ||||||
| chr3:47134803
|
T | C | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.72-8140A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47134803 | ||||||
| chr3:47135367
|
C | T | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72-8704G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47135367 | ||||||
| chr3:47135456
|
T | G | 200 | a0001c0002t0002g0014a0001c0005t0001g0115a0001c0005t0001g0123others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.72-8793A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47135456 | ||||||
| chr3:47135712
|
A | T | 1 | a0002c0001t0001g0191 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.72-9049T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47135712 | ||||||
| chr3:47135791
|
C | T | 1 | a0001c0002t0002g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72-9128G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47135791 | ||||||
| chr3:47135898
|
G | A | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.72-9235C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47135898 | ||||||
| chr3:47135929
|
T | C | 1 | a0002c0001t0001g0189 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.72-9266A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47135929 | ||||||
| chr3:47136079
|
G | A | 1 | a0002c0001t0001g0165 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72-9416C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136079 | ||||||
| chr3:47136282
|
C | T | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.72-9619G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136282 | ||||||
| chr3:47136287
|
T | C | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.72-9624A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136287 | ||||||
| chr3:47136430
|
A | G | 1 | a0002c0001t0001g0161 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.72-9767T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136430 | ||||||
| chr3:47136499
|
A | C | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72-9836T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136499 | ||||||
| chr3:47136639
|
A | T | 4 | a0002c0001t0001g0178a0002c0001t0001g0216a0002c0001t0005g0073others(1): Show | 4 | HG00642.hp1 HG01169.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-9976T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136639 | ||||||
| chr3:47136782
|
C | T | 1 | a0004c0004t0001g0258 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.72-10119G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47136782 | ||||||
| chr3:47137087
|
T | C | 1 | a0002c0001t0001g0241 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.72-10424A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47137087 | ||||||
| chr3:47137335
|
G | A | 1 | a0001c0002t0002g0016 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.72-10672C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47137335 | ||||||
| chr3:47137427
|
G | A | 4 | a0003c0003t0001g0275a0003c0003t0001g0289a0003c0003t0001g0290others(1): Show | 4 | NA18965.hp1 NA18981.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-10764C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47137427 | ||||||
| chr3:47137571
|
T | C | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72-10908A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47137571 | ||||||
| chr3:47137764
|
G | A | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72-11101C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47137764 | ||||||
| chr3:47138096
|
C | T | 1 | a0001c0005t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.72-11433G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138096 | ||||||
| chr3:47138097
|
G | A | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.72-11434C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138097 | ||||||
| chr3:47138372
|
C | T | 1 | a0001c0002t0002g0026 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.72-11709G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138372 | ||||||
| chr3:47138412
|
C | T | 1 | a0002c0001t0001g0190 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72-11749G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138412 | ||||||
| chr3:47138482
|
C | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72-11819G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138482 | ||||||
| chr3:47138755
|
G | A | 2 | a0003c0003t0001g0286a0003c0003t0001g0287 | 2 | NA18952.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.72-12092C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138755 | ||||||
| chr3:47138903
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-12240C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47138903 | ||||||
| chr3:47139093
|
A | G | 1 | a0002c0001t0001g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.72-12430T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47139093 | ||||||
| chr3:47139726
|
C | T | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.72-13063G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47139726 | ||||||
| chr3:47139846
|
A | C | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.72-13183T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47139846 | ||||||
| chr3:47140171
|
C | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.72-13508G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140171 | ||||||
| chr3:47140325
|
A | C | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.72-13662T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140325 | ||||||
| chr3:47140325
|
A | G | 1 | a0001c0002t0002g0025 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.72-13662T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140325 | ||||||
| chr3:47140528
|
C | T | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.72-13865G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140528 | ||||||
| chr3:47140699
|
A | G | 1 | a0001c0002t0002g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.72-14036T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140699 | ||||||
| chr3:47140820
|
G | A | 5 | a0002c0001t0001g0251a0002c0001t0001g0252a0002c0001t0001g0253others(2): Show | 5 | HG02074.hp2 HG04199.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-14157C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140820 | ||||||
| chr3:47140866
|
T | C | 5 | a0002c0001t0001g0161a0002c0001t0001g0162a0002c0001t0001g0163others(2): Show | 5 | HG00735.hp1 HG01192.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-14203A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140866 | ||||||
| chr3:47140996
|
G | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-14333C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47140996 | ||||||
| chr3:47141037
|
A | G | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.72-14374T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141037 | ||||||
| chr3:47141045
|
T | G | 1 | a0018c0024t0001g0164 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72-14382A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141045 | ||||||
| chr3:47141133
|
A | T | 1 | a0001c0002t0003g0092 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.72-14470T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141133 | ||||||
| chr3:47141297
|
T | C | 202 | a0001c0002t0003g0099a0001c0002t0003g0106a0001c0005t0001g0115others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.72-14634A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141297 | ||||||
| chr3:47141547
|
A | G | 2 | a0002c0001t0001g0252a0002c0001t0001g0253 | 2 | NA18612.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.72-14884T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141547 | ||||||
| chr3:47141749
|
C | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.72-15086G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141749 | ||||||
| chr3:47141859
|
T | A | 1 | a0001c0002t0002g0051 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.72-15196A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141859 | ||||||
| chr3:47141992
|
C | G | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.72-15329G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47141992 | ||||||
| chr3:47142107
|
G | C | 1 | a0004c0004t0001g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.72-15444C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142107 | ||||||
| chr3:47142276
|
G | A | 27 | a0001c0005t0004g0294a0003c0003t0001g0269a0003c0003t0001g0274others(24): Show | 27 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.72-15613C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142276 | ||||||
| chr3:47142501
|
T | A | 1 | a0001c0005t0004g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72-15838A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142501 | ||||||
| chr3:47142565
|
C | T | 2 | a0001c0002t0002g0023a0001c0002t0002g0024 | 2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.72-15902G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142565 | ||||||
| chr3:47142666
|
T | C | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72-16003A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142666 | ||||||
| chr3:47142670
|
CT | C | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.72-16008delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142670 | ||||||
| chr3:47142692
|
G | A | 148 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0144others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.72-16029C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142692 | ||||||
| chr3:47142921
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-16258G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142921 | ||||||
| chr3:47142947
|
G | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.72-16284C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47142947 | ||||||
| chr3:47143043
|
G | A | 3 | a0001c0002t0002g0010a0001c0002t0002g0052a0001c0002t0002g0058 | 3 | HG03704.hp2 HG03927.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.72-16380C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47143043 | ||||||
| chr3:47143245
|
G | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-16582C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47143245 | ||||||
| chr3:47143417
|
T | C | 1 | a0005c0007t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.72-16754A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47143417 | ||||||
| chr3:47143691
|
T | C | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72-17028A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47143691 | ||||||
| chr3:47143835
|
C | T | 1 | a0001c0002t0003g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.72-17172G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47143835 | ||||||
| chr3:47143956
|
C | T | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72-17293G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47143956 | ||||||
| chr3:47144160
|
C | G | 36 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(33): Show | 36 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-17497G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144160 | ||||||
| chr3:47144162
|
G | A | 6 | a0002c0001t0001g0152a0002c0001t0001g0153a0002c0001t0001g0212others(3): Show | 6 | HG00558.hp1 HG02015.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-17499C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144162 | ||||||
| chr3:47144349
|
A | G | 1 | a0013c0022t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72-17686T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144349 | ||||||
| chr3:47144360
|
C | T | 1 | a0001c0005t0004g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72-17697G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144360 | ||||||
| chr3:47144414
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.72-17751C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144414 | ||||||
| chr3:47144585
|
C | T | 3 | a0001c0002t0002g0011a0001c0002t0002g0022a0001c0002t0002g0053 | 3 | HG01358.hp1 HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.72-17922G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144585 | ||||||
| chr3:47144595
|
T | A | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.72-17932A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144595 | ||||||
| chr3:47144629
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72-17966C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144629 | ||||||
| chr3:47144844
|
G | A | 6 | a0002c0001t0001g0168a0004c0004t0001g0125a0004c0004t0001g0133others(3): Show | 6 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.72-18181C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144844 | ||||||
| chr3:47144909
|
C | T | 1 | a0002c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72-18246G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47144909 | ||||||
| chr3:47145013
|
G | T | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.72-18350C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145013 | ||||||
| chr3:47145079
|
A | T | 4 | a0001c0002t0002g0020a0001c0002t0002g0021a0001c0002t0002g0064others(1): Show | 4 | NA18953.hp2 NA18961.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-18416T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145079 | ||||||
| chr3:47145288
|
G | A | 1 | a0002c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.71+18566C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145288 | ||||||
| chr3:47145374
|
T | A | 1 | a0003c0014t0001g0307 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.71+18480A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145374 | ||||||
| chr3:47145447
|
T | C | 1 | a0002c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.71+18407A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145447 | ||||||
| chr3:47145516
|
T | A | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.71+18338A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145516 | ||||||
| chr3:47145585
|
C | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.71+18269G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145585 | ||||||
| chr3:47145837
|
C | T | 3 | a0001c0002t0003g0111a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.71+18017G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145837 | ||||||
| chr3:47145838
|
G | A | 1 | a0002c0001t0001g0214 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.71+18016C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47145838 | ||||||
| chr3:47146003
|
G | A | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.71+17851C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146003 | ||||||
| chr3:47146004
|
AGACCCTG others(3): Show |
A | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.71+17840_71+17849d others(12): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146004 | ||||||
| chr3:47146015
|
C | A | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.71+17839G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146015 | ||||||
| chr3:47146015
|
C | CA | 31 | a0001c0002t0002g0053a0001c0002t0002g0054a0001c0002t0002g0055others(28): Show | 31 | HG00738.hp2 HG01358.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.71+17838dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146015 | ||||||
| chr3:47146015
|
C | CAA | 9 | a0001c0005t0001g0123a0001c0005t0001g0273a0001c0005t0005g0074others(6): Show | 9 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+17837_71+17838d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146015 | ||||||
| chr3:47146015
|
C | CAAA | 76 | a0001c0006t0001g0271a0002c0001t0001g0144a0002c0001t0001g0145others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.71+17836_71+17838d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146015 | ||||||
| chr3:47146015
|
C | CAAAA | 32 | a0002c0001t0001g0148a0002c0001t0001g0154a0002c0001t0001g0166others(29): Show | 32 | HG00597.hp2 HG00673.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.71+17835_71+17838d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146015 | ||||||
| chr3:47146521
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+17333C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146521 | ||||||
| chr3:47146625
|
T | TA | 194 | a0001c0002t0002g0013a0001c0002t0002g0057a0001c0005t0001g0115others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.71+17228dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146625 | ||||||
| chr3:47146831
|
G | C | 1 | a0001c0002t0002g0058 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.71+17023C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146831 | ||||||
| chr3:47146854
|
C | G | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71+17000G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146854 | ||||||
| chr3:47146923
|
G | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0059 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.71+16931C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146923 | ||||||
| chr3:47146931
|
C | T | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.71+16923G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47146931 | ||||||
| chr3:47147202
|
A | G | 2 | a0001c0002t0002g0014a0001c0002t0002g0019 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.71+16652T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147202 | ||||||
| chr3:47147323
|
A | AT | 160 | a0001c0002t0002g0013a0001c0002t0003g0090a0001c0005t0001g0115others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.71+16530dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147323 | ||||||
| chr3:47147323
|
A | ATT | 9 | a0001c0005t0001g0149a0001c0005t0005g0072a0002c0001t0001g0175others(6): Show | 9 | HG01175.hp1 HG01934.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.71+16529_71+16530d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147323 | ||||||
| chr3:47147443
|
C | G | 1 | a0002c0001t0001g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.71+16411G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147443 | ||||||
| chr3:47147480
|
G | A | 1 | a0002c0001t0001g0222 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.71+16374C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147480 | ||||||
| chr3:47147621
|
C | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.71+16233G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147621 | ||||||
| chr3:47147640
|
T | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+16214A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147640 | ||||||
| chr3:47147796
|
G | A | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+16058C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147796 | ||||||
| chr3:47147860
|
T | G | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.71+15994A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147860 | ||||||
| chr3:47147885
|
G | A | 148 | a0001c0005t0001g0115a0001c0005t0001g0123a0002c0001t0001g0144others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.71+15969C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147885 | ||||||
| chr3:47147892
|
T | C | 1 | a0004c0010t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.71+15962A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147892 | ||||||
| chr3:47147917
|
C | CA | 44 | a0001c0002t0002g0060a0001c0002t0003g0086a0001c0002t0003g0087others(41): Show | 44 | HG00544.hp2 HG00642.hp1 HG01358.hp2 others(41): Show |
intron_variant | MODIFIER | c.71+15936dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147917 | ||||||
| chr3:47147917
|
CA | C | 12 | a0001c0002t0002g0018a0002c0001t0001g0144a0002c0001t0001g0155others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.71+15936delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47147917 | ||||||
| chr3:47148110
|
TTTG | T | 53 | a0001c0002t0002g0017a0001c0002t0003g0075a0001c0002t0003g0076others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.71+15741_71+15743d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148110 | ||||||
| chr3:47148110
|
TTTGTTG | T | 179 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(176): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.71+15738_71+15743d others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148110 | ||||||
| chr3:47148110
|
TTTGTTGT others(5): Show |
T | 7 | a0001c0002t0003g0099a0001c0005t0001g0273a0001c0006t0001g0270others(4): Show | 7 | HG00738.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+15732_71+15743d others(14): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148110 | ||||||
| chr3:47148192
|
G | A | 3 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272 | 3 | HG01891.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.71+15662C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148192 | ||||||
| chr3:47148258
|
G | A | 1 | a0001c0020t0003g0108 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.71+15596C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148258 | ||||||
| chr3:47148271
|
C | G | 1 | a0002c0001t0001g0250 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.71+15583G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148271 | ||||||
| chr3:47148291
|
G | A | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.71+15563C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148291 | ||||||
| chr3:47148604
|
T | G | 3 | a0002c0001t0001g0150a0002c0001t0001g0167a0002c0001t0001g0225 | 3 | NA18964.hp2 NA18975.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.71+15250A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148604 | ||||||
| chr3:47148720
|
A | C | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.71+15134T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148720 | ||||||
| chr3:47148730
|
T | C | 32 | a0001c0005t0001g0115a0001c0005t0001g0123a0004c0004t0001g0116others(29): Show | 32 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.71+15124A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148730 | ||||||
| chr3:47148804
|
G | C | 1 | a0002c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.71+15050C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148804 | ||||||
| chr3:47148826
|
C | A | 27 | a0001c0005t0004g0294a0003c0003t0001g0269a0003c0003t0001g0274others(24): Show | 27 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.71+15028G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148826 | ||||||
| chr3:47148838
|
G | T | 1 | a0002c0018t0001g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.71+15016C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47148838 | ||||||
| chr3:47149015
|
A | G | 1 | a0002c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71+14839T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149015 | ||||||
| chr3:47149029
|
A | C | 1 | a0004c0004t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71+14825T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149029 | ||||||
| chr3:47149342
|
C | T | 1 | a0002c0001t0001g0247 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.71+14512G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149342 | ||||||
| chr3:47149392
|
A | G | 1 | a0002c0001t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.71+14462T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149392 | ||||||
| chr3:47149402
|
A | C | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+14452T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149402 | ||||||
| chr3:47149423
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+14431C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149423 | ||||||
| chr3:47149669
|
C | T | 1 | a0002c0001t0001g0168 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.71+14185G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149669 | ||||||
| chr3:47149859
|
G | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.71+13995C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149859 | ||||||
| chr3:47149898
|
T | A | 1 | a0002c0001t0001g0226 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.71+13956A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47149898 | ||||||
| chr3:47150028
|
C | CT | 10 | a0001c0002t0002g0014a0001c0002t0002g0015a0001c0002t0002g0016others(7): Show | 10 | HG01981.hp1 HG02071.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.71+13825dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
C | CTTT | 8 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(5): Show | 8 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.71+13823_71+13825d others(5): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
C | CTTTT | 14 | a0001c0005t0001g0273a0001c0005t0004g0262a0001c0005t0004g0263others(11): Show | 14 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.71+13822_71+13825d others(6): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
C | CTTTTT | 29 | a0001c0005t0001g0149a0001c0005t0004g0299a0001c0005t0005g0072others(26): Show | 29 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+13821_71+13825d others(7): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
C | CTTTTTT | 6 | a0001c0005t0001g0123a0001c0005t0001g0306a0001c0005t0004g0294others(3): Show | 6 | HG02074.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+13820_71+13825d others(8): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
C | CTTTTTTT | 121 | a0001c0005t0001g0115a0002c0001t0001g0144a0002c0001t0001g0145others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.71+13819_71+13825d others(9): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
C | CTTTTTTT others(1): Show |
18 | a0002c0001t0001g0155a0002c0001t0001g0157a0002c0001t0001g0158others(15): Show | 18 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.71+13818_71+13825d others(10): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150028
|
CT | C | 7 | a0001c0002t0002g0061a0001c0002t0002g0069a0001c0002t0003g0085others(4): Show | 7 | HG00099.hp1 HG01975.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+13825delA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150028 | ||||||
| chr3:47150153
|
C | T | 1 | a0012c0012t0004g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+13701G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150153 | ||||||
| chr3:47150241
|
C | T | 1 | a0002c0001t0001g0246 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.71+13613G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150241 | ||||||
| chr3:47150242
|
G | A | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71+13612C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150242 | ||||||
| chr3:47150285
|
G | A | 1 | a0001c0005t0004g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+13569C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150285 | ||||||
| chr3:47150415
|
T | C | 1 | a0001c0002t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.71+13439A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150415 | ||||||
| chr3:47150481
|
A | G | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.71+13373T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150481 | ||||||
| chr3:47150507
|
G | C | 30 | a0004c0004t0001g0116a0004c0004t0001g0117a0004c0004t0001g0118others(27): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.71+13347C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150507 | ||||||
| chr3:47150600
|
G | C | 1 | a0004c0004t0001g0260 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71+13254C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150600 | ||||||
| chr3:47150748
|
G | A | 1 | a0002c0001t0001g0229 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.71+13106C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150748 | ||||||
| chr3:47150869
|
G | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+12985C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150869 | ||||||
| chr3:47150920
|
TA | T | 112 | a0001c0002t0002g0013a0001c0002t0002g0070a0002c0001t0001g0144others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.71+12933delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150920 | ||||||
| chr3:47150932
|
A | G | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02071.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+12922T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47150932 | ||||||
| chr3:47151017
|
T | C | 1 | a0001c0005t0001g0123 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.71+12837A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151017 | ||||||
| chr3:47151165
|
C | T | 2 | a0002c0001t0001g0152a0002c0001t0001g0153 | 2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.71+12689G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151165 | ||||||
| chr3:47151274
|
A | T | 239 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.71+12580T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151274 | ||||||
| chr3:47151328
|
T | A | 29 | a0001c0005t0001g0273a0001c0005t0001g0306a0001c0005t0004g0294others(26): Show | 29 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+12526A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151328 | ||||||
| chr3:47151372
|
A | T | 1 | a0001c0002t0002g0012 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.71+12482T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151372 | ||||||
| chr3:47151405
|
G | A | 1 | a0002c0001t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.71+12449C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151405 | ||||||
| chr3:47151457
|
C | T | 1 | a0005c0007t0001g0119 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.71+12397G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151457 | ||||||
| chr3:47151544
|
C | T | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.71+12310G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151544 | ||||||
| chr3:47151712
|
AC | A | 4 | a0001c0006t0001g0270a0001c0006t0001g0271a0001c0006t0001g0272others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+12141delG | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151712 | ||||||
| chr3:47151758
|
C | T | 1 | a0019c0026t0002g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.71+12096G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151758 | ||||||
| chr3:47151759
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+12095C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151759 | ||||||
| chr3:47151827
|
C | CA | 7 | a0001c0002t0002g0064a0001c0002t0002g0065a0001c0002t0002g0066others(4): Show | 7 | HG01884.hp1 HG04199.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+12026dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151827 | ||||||
| chr3:47151827
|
CA | C | 185 | a0001c0002t0002g0011a0001c0005t0001g0115a0001c0005t0001g0273others(182): Show | 185 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.71+12026delT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151827 | ||||||
| chr3:47151942
|
T | C | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.71+11912A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151942 | ||||||
| chr3:47151951
|
C | G | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.71+11903G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47151951 | ||||||
| chr3:47152199
|
T | C | 1 | a0001c0005t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.71+11655A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152199 | ||||||
| chr3:47152514
|
C | T | 1 | a0001c0002t0002g0010 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.71+11340G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152514 | ||||||
| chr3:47152522
|
A | C | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+11332T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152522 | ||||||
| chr3:47152736
|
G | T | 1 | a0001c0002t0003g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.71+11118C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152736 | ||||||
| chr3:47152764
|
C | G | 1 | a0012c0012t0004g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+11090G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152764 | ||||||
| chr3:47152860
|
C | T | 1 | a0004c0004t0001g0118 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71+10994G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152860 | ||||||
| chr3:47152938
|
T | A | 1 | a0001c0002t0003g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71+10916A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152938 | ||||||
| chr3:47152946
|
C | G | 1 | a0016c0019t0001g0151 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.71+10908G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152946 | ||||||
| chr3:47152970
|
A | G | 1 | a0001c0002t0006g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.71+10884T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47152970 | ||||||
| chr3:47153153
|
A | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10701T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153153 | ||||||
| chr3:47153154
|
G | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10700C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153154 | ||||||
| chr3:47153156
|
G | A | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10698C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153156 | ||||||
| chr3:47153159
|
T | TTTAATTT others(9): Show |
26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10694_71+10695i others(18): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153159 | ||||||
| chr3:47153162
|
C | T | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10692G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153162 | ||||||
| chr3:47153163
|
T | TTA | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10690_71+10691i others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153163 | ||||||
| chr3:47153275
|
TATTAACC others(17): Show |
T | 1 | a0001c0002t0003g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.71+10555_71+10578d others(26): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153275 | ||||||
| chr3:47153758
|
G | GA | 7 | a0001c0005t0001g0306a0004c0004t0001g0117a0004c0004t0001g0140others(4): Show | 7 | HG02280.hp2 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+10095dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153758 | ||||||
| chr3:47153758
|
G | GAA | 26 | a0003c0003t0001g0269a0003c0003t0001g0274a0003c0003t0001g0275others(23): Show | 26 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.71+10094_71+10095d others(4): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47153758 | ||||||
| chr3:47154124
|
G | A | 1 | a0013c0022t0001g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71+9730C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154124 | ||||||
| chr3:47154140
|
A | G | 212 | a0001c0002t0002g0069a0001c0002t0003g0086a0001c0002t0003g0087others(209): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.71+9714T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154140 | ||||||
| chr3:47154170
|
G | A | 15 | a0004c0004t0001g0116a0004c0004t0001g0125a0004c0004t0001g0126others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.71+9684C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154170 | ||||||
| chr3:47154176
|
C | A | 15 | a0004c0004t0001g0116a0004c0004t0001g0125a0004c0004t0001g0126others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.71+9678G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154176 | ||||||
| chr3:47154237
|
C | T | 2 | a0001c0002t0002g0007a0001c0002t0002g0008 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.71+9617G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154237 | ||||||
| chr3:47154471
|
G | T | 3 | a0001c0002t0003g0111a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.71+9383C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154471 | ||||||
| chr3:47154618
|
G | A | 1 | a0002c0001t0001g0235 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.71+9236C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154618 | ||||||
| chr3:47154719
|
C | A | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.71+9135G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154719 | ||||||
| chr3:47154722
|
G | A | 15 | a0002c0001t0001g0236a0002c0001t0001g0237a0002c0001t0001g0238others(12): Show | 15 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.71+9132C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154722 | ||||||
| chr3:47154769
|
G | A | 1 | a0001c0005t0005g0072 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.71+9085C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154769 | ||||||
| chr3:47154866
|
C | T | 1 | a0012c0012t0004g0268 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71+8988G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154866 | ||||||
| chr3:47154941
|
C | A | 1 | a0002c0001t0001g0250 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.71+8913G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154941 | ||||||
| chr3:47154993
|
C | CA | 34 | a0001c0002t0002g0067a0001c0005t0001g0273a0001c0005t0001g0306others(31): Show | 34 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.71+8860dupT | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154993 | ||||||
| chr3:47154993
|
C | CAA | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+8859_71+8860dup others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47154993 | ||||||
| chr3:47155090
|
C | T | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.71+8764G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155090 | ||||||
| chr3:47155221
|
T | G | 2 | a0001c0005t0005g0074a0015c0015t0001g0138 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.71+8633A>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155221 | ||||||
| chr3:47155261
|
T | C | 5 | a0002c0001t0001g0251a0002c0001t0001g0252a0002c0001t0001g0253others(2): Show | 5 | HG02074.hp2 HG04199.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.71+8593A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155261 | ||||||
| chr3:47155329
|
G | C | 1 | a0001c0006t0001g0293 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71+8525C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155329 | ||||||
| chr3:47155390
|
A | T | 2 | a0001c0005t0001g0149a0001c0005t0005g0072 | 2 | HG01934.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.71+8464T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155390 | ||||||
| chr3:47155663
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.71+8191C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155663 | ||||||
| chr3:47155841
|
G | T | 13 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(10): Show | 13 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.71+8013C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47155841 | ||||||
| chr3:47156942
|
A | G | 1 | a0001c0002t0003g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.71+6912T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47156942 | ||||||
| chr3:47156947
|
C | G | 199 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.71+6907G>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47156947 | ||||||
| chr3:47157035
|
G | A | 3 | a0001c0002t0003g0111a0001c0002t0003g0112a0001c0002t0003g0113 | 3 | HG02258.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.71+6819C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157035 | ||||||
| chr3:47157045
|
G | C | 6 | a0004c0004t0001g0117a0004c0004t0001g0140a0004c0004t0001g0141others(3): Show | 6 | HG02280.hp2 HG03130.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+6809C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157045 | ||||||
| chr3:47157149
|
G | A | 1 | a0001c0005t0004g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+6705C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157149 | ||||||
| chr3:47157219
|
C | T | 1 | a0004c0004t0001g0117 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.71+6635G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157219 | ||||||
| chr3:47157313
|
A | C | 1 | a0001c0002t0002g0006 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.71+6541T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157313 | ||||||
| chr3:47157336
|
G | A | 116 | a0002c0001t0001g0144a0002c0001t0001g0145a0002c0001t0001g0146others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.71+6518C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157336 | ||||||
| chr3:47157527
|
C | T | 5 | a0001c0002t0003g0086a0001c0002t0003g0087a0001c0002t0003g0088others(2): Show | 5 | NA18951.hp2 NA19000.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+6327G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157527 | ||||||
| chr3:47157598
|
G | A | 1 | a0001c0002t0002g0069 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.71+6256C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157598 | ||||||
| chr3:47157741
|
C | T | 1 | a0004c0004t0001g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.71+6113G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157741 | ||||||
| chr3:47157857
|
G | A | 1 | a0014c0021t0001g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.71+5997C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47157857 | ||||||
| chr3:47158029
|
A | G | 4 | a0003c0003t0001g0295a0003c0003t0001g0296a0003c0003t0001g0297others(1): Show | 4 | NA18945.hp1 NA18970.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+5825T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47158029 | ||||||
| chr3:47158373
|
A | G | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.71+5481T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47158373 | ||||||
| chr3:47158683
|
T | A | 1 | a0001c0005t0001g0149 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.71+5171A>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47158683 | ||||||
| chr3:47158965
|
C | T | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+4889G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47158965 | ||||||
| chr3:47159102
|
C | T | 1 | a0002c0001t0001g0150 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.71+4752G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47159102 | ||||||
| chr3:47159966
|
C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0005 | 2 | NA18949.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.71+3888G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47159966 | ||||||
| chr3:47160258
|
T | C | 4 | a0003c0003t0001g0295a0003c0003t0001g0296a0003c0003t0001g0297others(1): Show | 4 | NA18945.hp1 NA18970.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+3596A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47160258 | ||||||
| chr3:47160282
|
A | G | 1 | a0004c0004t0001g0257 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71+3572T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47160282 | ||||||
| chr3:47160467
|
A | AT | 74 | a0001c0005t0001g0123a0001c0005t0001g0149a0001c0005t0001g0273others(71): Show | 74 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(71): Show |
intron_variant | MODIFIER | c.71+3386dupA | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47160467 | ||||||
| chr3:47160467
|
A | ATT | 14 | a0001c0005t0001g0115a0001c0005t0004g0262a0001c0005t0004g0263others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+3385_71+3386dup others(2): Show |
SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47160467 | ||||||
| chr3:47160498
|
C | T | 11 | a0001c0002t0003g0075a0001c0002t0003g0076a0001c0002t0003g0077others(8): Show | 11 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.71+3356G>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47160498 | ||||||
| chr3:47160629
|
A | G | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+3225T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47160629 | ||||||
| chr3:47161828
|
T | C | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.71+2026A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47161828 | ||||||
| chr3:47161934
|
T | C | 1 | a0001c0005t0005g0074 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.71+1920A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47161934 | ||||||
| chr3:47162095
|
A | C | 1 | a0001c0002t0002g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.71+1759T>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162095 | ||||||
| chr3:47162284
|
A | T | 14 | a0001c0005t0004g0262a0001c0005t0004g0263a0001c0005t0004g0264others(11): Show | 14 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.71+1570T>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162284 | ||||||
| chr3:47162292
|
TG | T | 4 | a0004c0004t0001g0257a0004c0004t0001g0258a0004c0004t0001g0259others(1): Show | 4 | HG02809.hp1 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.71+1561delC | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162292 | ||||||
| chr3:47162293
|
G | T | 195 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.71+1561C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162293 | ||||||
| chr3:47162390
|
C | A | 1 | a0002c0001t0001g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.71+1464G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162390 | ||||||
| chr3:47162641
|
G | C | 1 | a0001c0002t0003g0114 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.71+1213C>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162641 | ||||||
| chr3:47162868
|
A | G | 1 | a0003c0003t0001g0269 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71+986T>C | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47162868 | ||||||
| chr3:47163028
|
T | C | 33 | a0001c0005t0001g0273a0001c0005t0001g0306a0001c0005t0004g0294others(30): Show | 33 | HG01255.hp1 HG01358.hp2 HG01515.hp1 others(30): Show |
intron_variant | MODIFIER | c.71+826A>G | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47163028 | ||||||
| chr3:47163367
|
G | A | 7 | a0001c0005t0004g0299a0001c0005t0004g0300a0001c0005t0004g0301others(4): Show | 7 | HG02486.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+487C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47163367 | ||||||
| chr3:47163449
|
G | T | 152 | a0001c0005t0001g0115a0001c0005t0001g0123a0001c0005t0001g0149others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.71+405C>A | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47163449 | ||||||
| chr3:47163496
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+358C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47163496 | ||||||
| chr3:47163537
|
G | A | 1 | a0001c0005t0001g0306 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.71+317C>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47163537 | ||||||
| chr3:47163619
|
C | A | 2 | a0003c0003t0001g0308a0003c0014t0001g0307 | 2 | HG01515.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.71+235G>T | SETD2 | ENSG00000181555.22 | transcript | ENST00000409792.4 | protein_coding | 1/20 | chr3 | 47163619 |