Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55209 |
| ensemblid | ENSG00000168137.20 |
| hgncid | 25566 |
| symbol | SETD5 |
| name | SET domain containing 5 |
| refseq_nuc | NM_001080517.3 |
| refseq_prot | NP_001073986.1 |
| ensembl_nuc | ENST00000402198.7 |
| ensembl_prot | ENSP00000385852.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 9397615 |
| end | 9478154 |
| strand | + |
| ver | v1.2 |
| region | chr3:9397615-9478154 |
| region5000 | chr3:9392615-9483154 |
| regionname0 | SETD5_chr3_9397615_9478154 |
| regionname5000 | SETD5_chr3_9392615_9483154 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1442 | 217 | 76 | 41 | 73 | 12 | 13 | 51 | SETD5_chr3_9392615_9483154 | SETD5 | MSIAI others(1437): Show |
chr3 | 9392615 | 9483154 |
| a0002 | 0/0 | 1442 | 11 | 2 | 4 | 0 | 0 | 5 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | MSIAI others(1437): Show |
chr3 | 9392615 | 9483154 |
| a0003 | 0/0 | 1442 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | MSIAI others(1437): Show |
chr3 | 9392615 | 9483154 |
| a0004 | 0/0 | 1442 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SETD5_chr3_9392615_9483154 | SETD5 | MSIAI others(1437): Show |
chr3 | 9392615 | 9483154 |
| a0005 | 0/0 | 1442 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | MSIAI others(1437): Show |
chr3 | 9392615 | 9483154 |
| a0006 | 0/0 | 1442 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | MSIAI others(1437): Show |
chr3 | 9392615 | 9483154 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4326 | 203 | 67 | 39 | 71 | 11 | 13 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0001c0003 | 0/0 | 4326 | 9 | 8 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0001c0007 | 0/0 | 4326 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0001c0009 | 0/0 | 4326 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0001c0010 | 0/0 | 4326 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0001c0012 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0002c0002 | 0/0 | 4326 | 11 | 2 | 4 | 0 | 0 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0003c0005 | 0/0 | 4326 | 3 | 0 | 3 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0003c0008 | 0/0 | 4326 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0004c0004 | 0/0 | 4326 | 4 | 0 | 0 | 4 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0005c0006 | 0/0 | 4326 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 | ||
| a0006c0011 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | ATGAG others(4321): Show |
chr3 | 9392615 | 9483154 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6928 | 67 | 10 | 13 | 30 | 8 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0002 | 0/0 | 6929 | 34 | 6 | 8 | 14 | 1 | 5 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0003 | 0/0 | 6925 | 18 | 0 | 6 | 8 | 2 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6920): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0004 | 0/0 | 6930 | 15 | 13 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6925): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0005 | 1/0 | 6931 | 10 | 2 | 2 | 4 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6926): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0006 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0007 | 0/0 | 6931 | 6 | 6 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6926): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0008 | 0/0 | 6932 | 6 | 2 | 2 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6927): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0010 | 0/0 | 6927 | 5 | 2 | 2 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6922): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0012 | 0/0 | 6931 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6926): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0014 | 0/0 | 6928 | 4 | 0 | 0 | 4 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0015 | 0/0 | 6933 | 3 | 3 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6928): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0016 | 0/0 | 6940 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6935): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0017 | 0/0 | 6934 | 2 | 1 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6929): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0018 | 0/0 | 6932 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6927): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0020 | 0/0 | 6928 | 2 | 2 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0022 | 0/0 | 6924 | 2 | 1 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6919): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0023 | 0/0 | 6926 | 2 | 0 | 1 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6921): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0024 | 0/0 | 6940 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6935): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0025 | 0/0 | 6935 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6930): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0026 | 0/0 | 6934 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6929): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0027 | 0/0 | 6934 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6929): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0028 | 0/0 | 6932 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6927): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0030 | 0/0 | 6927 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6922): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0031 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0033 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0035 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0036 | 0/0 | 6928 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0038 | 0/0 | 6928 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0039 | 0/0 | 6926 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6921): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0040 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6920): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0041 | 0/0 | 6924 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6919): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0043 | 0/0 | 6925 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6920): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0044 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0045 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6917): Show |
chr3 | 9392615 | 9483154 |
| a0001c0001t0046 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6917): Show |
chr3 | 9392615 | 9483154 |
| a0001c0003t0009 | 0/0 | 6926 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6921): Show |
chr3 | 9392615 | 9483154 |
| a0001c0003t0011 | 0/0 | 6925 | 4 | 4 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6920): Show |
chr3 | 9392615 | 9483154 |
| a0001c0003t0042 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6920): Show |
chr3 | 9392615 | 9483154 |
| a0001c0007t0029 | 0/0 | 6931 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6926): Show |
chr3 | 9392615 | 9483154 |
| a0001c0007t0047 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6914): Show |
chr3 | 9392615 | 9483154 |
| a0001c0009t0002 | 0/0 | 6929 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0001c0010t0001 | 0/0 | 6928 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0001c0012t0037 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0002c0002t0006 | 0/0 | 6928 | 6 | 2 | 1 | 0 | 0 | 3 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0002c0002t0013 | 0/0 | 6929 | 4 | 0 | 2 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0002c0002t0034 | 0/0 | 6927 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6922): Show |
chr3 | 9392615 | 9483154 |
| a0003c0005t0009 | 0/0 | 6926 | 2 | 0 | 2 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6921): Show |
chr3 | 9392615 | 9483154 |
| a0003c0005t0011 | 0/0 | 6925 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6920): Show |
chr3 | 9392615 | 9483154 |
| a0003c0008t0001 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0003c0008t0002 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0004c0004t0019 | 0/0 | 6931 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6926): Show |
chr3 | 9392615 | 9483154 |
| a0004c0004t0021 | 0/0 | 6929 | 2 | 0 | 0 | 2 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0005c0006t0002 | 0/0 | 6929 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6924): Show |
chr3 | 9392615 | 9483154 |
| a0005c0006t0032 | 0/0 | 6928 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| a0006c0011t0001 | 0/0 | 6928 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | AGTGG others(6923): Show |
chr3 | 9392615 | 9483154 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0010g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0014g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0014g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0015g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0015g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0015g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0016g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0016g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0017g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0018g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0020g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0020g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0022g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0022g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0023g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0023g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0024g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0025g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0026g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0027g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0028g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0030g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0031g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0033g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0035g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0036g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0038g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0039g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0040g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0041g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0043g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0044g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0045g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0001t0046g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0003t0042g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0007t0029g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0007t0047g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0009t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0010t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0001c0012t0037g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0006g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0013g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0013g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0013g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0002c0002t0034g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0003c0005t0009g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0003c0005t0009g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0003c0005t0011g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0003c0008t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0003c0008t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0004c0004t0019g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0004c0004t0019g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0004c0004t0021g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0004c0004t0021g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0005c0006t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0005c0006t0032g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| a0006c0011t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | FIN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00544 | hp1 | a0001 | c0001 | t0024 | g0019 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00621 | hp1 | a0001 | c0001 | t0039 | g0223 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00735 | hp1 | a0002 | c0002 | t0006 | g0182 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00735 | hp2 | a0001 | c0001 | t0017 | g0018 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG00741 | hp2 | a0002 | c0002 | t0013 | g0180 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01069 | hp1 | a0003 | c0005 | t0011 | g0200 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01069 | hp2 | a0001 | c0001 | t0028 | g0025 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01070 | hp1 | a0001 | c0001 | t0022 | g0229 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01071 | hp1 | a0003 | c0005 | t0009 | g0201 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01074 | hp2 | a0001 | c0010 | t0001 | g0042 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01099 | hp1 | a0001 | c0003 | t0042 | g0198 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0149 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01175 | hp2 | a0003 | c0005 | t0009 | g0202 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01346 | hp1 | a0002 | c0002 | t0034 | g0187 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01346 | hp2 | a0001 | c0001 | t0010 | g0040 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01433 | hp2 | a0001 | c0001 | t0023 | g0212 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0228 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0227 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0167 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01884 | hp2 | a0005 | c0006 | t0002 | g0101 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02004 | hp1 | a0001 | c0001 | t0040 | g0231 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0133 | AMR | PEL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02040 | hp2 | a0001 | c0001 | t0014 | g0088 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02055 | hp2 | a0001 | c0001 | t0031 | g0235 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02080 | hp2 | a0001 | c0001 | t0014 | g0075 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0111 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02129 | hp2 | a0001 | c0007 | t0047 | g0006 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | KHV | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02145 | hp1 | a0005 | c0006 | t0032 | g0102 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0153 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02572 | hp1 | a0001 | c0003 | t0009 | g0203 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02615 | hp1 | a0001 | c0003 | t0011 | g0196 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0234 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02622 | hp1 | a0001 | c0001 | t0044 | g0178 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02630 | hp2 | a0001 | c0001 | t0045 | g0161 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02647 | hp2 | a0001 | c0003 | t0011 | g0199 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02717 | hp2 | a0001 | c0003 | t0011 | g0204 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02723 | hp1 | a0001 | c0001 | t0035 | g0206 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02723 | hp2 | a0001 | c0001 | t0043 | g0208 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02809 | hp1 | a0001 | c0001 | t0018 | g0169 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0115 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0171 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02895 | hp1 | a0001 | c0003 | t0009 | g0194 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02897 | hp2 | a0001 | c0003 | t0011 | g0195 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0163 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02970 | hp1 | a0001 | c0003 | t0009 | g0193 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02976 | hp1 | a0001 | c0001 | t0046 | g0177 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03017 | hp1 | a0002 | c0002 | t0006 | g0181 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03041 | hp2 | a0001 | c0003 | t0009 | g0197 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03098 | hp1 | a0001 | c0001 | t0022 | g0225 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03098 | hp2 | a0003 | c0008 | t0002 | g0095 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03130 | hp2 | a0001 | c0012 | t0037 | g0207 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03139 | hp2 | a0001 | c0001 | t0016 | g0154 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03195 | hp1 | a0003 | c0008 | t0001 | g0081 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0174 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03453 | hp2 | a0001 | c0001 | t0041 | g0175 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0151 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03491 | hp2 | a0002 | c0002 | t0006 | g0004 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03492 | hp2 | a0002 | c0002 | t0006 | g0004 | SAS | PJL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03540 | hp1 | a0002 | c0002 | t0006 | g0191 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0172 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0233 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03688 | hp1 | a0002 | c0002 | t0013 | g0183 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03831 | hp2 | a0002 | c0002 | t0013 | g0179 | SAS | BEB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | STU | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18906 | hp2 | a0001 | c0001 | t0033 | g0089 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18940 | hp2 | a0004 | c0004 | t0021 | g0022 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18942 | hp1 | a0001 | c0001 | t0030 | g0026 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18942 | hp2 | a0001 | c0001 | t0027 | g0028 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18950 | hp1 | a0001 | c0001 | t0010 | g0013 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18950 | hp2 | a0004 | c0004 | t0019 | g0059 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18952 | hp1 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18957 | hp1 | a0004 | c0004 | t0019 | g0037 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18957 | hp2 | a0001 | c0001 | t0023 | g0217 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18973 | hp2 | a0001 | c0001 | t0036 | g0017 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18983 | hp2 | a0001 | c0001 | t0038 | g0044 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18991 | hp2 | a0001 | c0007 | t0029 | g0005 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19000 | hp2 | a0004 | c0004 | t0021 | g0078 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19030 | hp2 | a0001 | c0001 | t0012 | g0173 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0120 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19043 | hp2 | a0001 | c0001 | t0020 | g0073 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19074 | hp2 | a0001 | c0001 | t0014 | g0031 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19084 | hp1 | a0006 | c0011 | t0001 | g0034 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19089 | hp2 | a0001 | c0001 | t0008 | g0080 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA19240 | hp2 | a0002 | c0002 | t0006 | g0184 | AFR | YRI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA20805 | hp1 | a0001 | c0009 | t0002 | g0135 | EUR | TSI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | TSI | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01123 | hp1 | a0002 | c0002 | t0013 | g0192 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0170 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02486 | hp2 | a0001 | c0001 | t0026 | g0189 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG02559 | hp2 | a0001 | c0001 | t0020 | g0074 | AFR | ACB | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0077 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0165 | AFR | MSL | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA20300 | hp2 | a0001 | c0001 | t0015 | g0118 | AFR | USA | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0127 | REF | REF | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0014 | REF | REF | SETD5_chr3_9392615_9483154 | SETD5 | chr3 | 9392615 | 9483154 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9434386 | G | A | 1 | a0005 | 2 | HG01884.hp2 HG02145.hp1 |
missense_variant | MODERATE | c.230G>A | p.Arg77His | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 5/23 | 769/6931 | 230/4329 | 77/1442 | chr3 | 9434386 | |||
| chr3:9464601 | T | C | 1 | a0004 | 4 | NA18940.hp2 NA18950.hp2 NA18957.hp1 others(1): Show |
missense_variant | MODERATE | c.2653T>C | p.Tyr885His | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/23 | 3192/6931 | 2653/4329 | 885/1442 | chr3 | 9464601 | |||
| chr3:9470658 | A | G | 1 | a0006 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.2924A>G | p.Gln975Arg | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/23 | 3463/6931 | 2924/4329 | 975/1442 | chr3 | 9470658 | |||
| chr3:9473449 | A | G | 1 | a0003 | 5 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(2): Show |
missense_variant | MODERATE | c.3409A>G | p.Met1137Val | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/23 | 3948/6931 | 3409/4329 | 1137/1442 | chr3 | 9473449 | |||
| chr3:9475685 | C | T | 1 | a0002 | 11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
missense_variant | MODERATE | c.3923C>T | p.Thr1308Ile | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 4462/6931 | 3923/4329 | 1308/1442 | chr3 | 9475685 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9434483 | C | T | 1 | a0001c0012 | 1 | HG03130.hp2 | splice_region_variant&synonymous_variant | LOW | c.327C>T | p.Cys109Cys | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 5/23 | 866/6931 | 327/4329 | 109/1442 | chr3 | 9434483 | |||
| chr3:9464492 | T | G | 1 | a0001c0007 | 2 | HG02129.hp2 NA18991.hp2 |
synonymous_variant | LOW | c.2544T>G | p.Leu848Leu | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/23 | 3083/6931 | 2544/4329 | 848/1442 | chr3 | 9464492 | |||
| chr3:9473370 | T | C | 1 | a0001c0009 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.3330T>C | p.Thr1110Thr | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/23 | 3869/6931 | 3330/4329 | 1110/1442 | chr3 | 9473370 | |||
| chr3:9474515 | C | T | 2 | a0001c0003 a0003c0005 |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
synonymous_variant | LOW | c.3564C>T | p.Ser1188Ser | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/23 | 4103/6931 | 3564/4329 | 1188/1442 | chr3 | 9474515 | |||
| chr3:9475893 | C | T | 1 | a0001c0010 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.4131C>T | p.Asn1377Asn | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 4670/6931 | 4131/4329 | 1377/1442 | chr3 | 9475893 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9397651 | T | TGCC | 5 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0025 others(2): Show |
8 | HG00735.hp2 HG02486.hp2 HG02818.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-470_-468dupCGC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31252 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | |||||
| chr3:9397651 | T | TGCCGCCG others(2): Show |
2 | a0001c0001t0016 a0001c0001t0024 |
3 | HG00544.hp1 HG02145.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-476_-468dupCGCCGC others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31252 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | |||||
| chr3:9397651 | TGCC | T | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(22): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
5_prime_UTR_variant | MODIFIER | c.-470_-468delCGC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | |||||
| chr3:9397651 | TGCCGCC | T | 12 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0023 others(9): Show |
38 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-473_-468delCGCCGC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | |||||
| chr3:9397651 | TGCCGCCG others(2): Show |
T | 2 | a0001c0001t0045 a0001c0001t0046 |
2 | HG02630.hp2 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-476_-468delCGCCGC others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | |||||
| chr3:9397651 | TGCCGCCG others(5): Show |
T | 1 | a0001c0007t0047 | 1 | HG02129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-479_-468delCGCCGC others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31253 | INFO_REALIGN_3_PRIME | chr3 | 9397651 | |||||
| chr3:9397684 | C | T | 1 | a0001c0001t0044 | 1 | HG02622.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-470C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | chr3 | 9397684 | |||||||
| chr3:9397781 | C | G | 4 | a0001c0001t0014 a0001c0001t0027 a0004c0004t0019 others(1): Show |
9 | HG02040.hp2 HG02080.hp2 NA18940.hp2 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-373C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | chr3 | 9397781 | |||||||
| chr3:9397857 | C | G | 1 | a0001c0001t0038 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-297C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/23 | 31082 | chr3 | 9397857 | ||||||
| chr3:9424519 | A | G | 1 | a0001c0012t0037 | 1 | HG03130.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-124A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/23 | chr3 | 9424519 | |||||||
| chr3:9428907 | C | T | 1 | a0001c0001t0036 | 1 | NA18973.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/23 | chr3 | 9428907 | |||||||
| chr3:9476210 | T | C | 1 | a0001c0001t0039 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 119 | chr3 | 9476210 | ||||||
| chr3:9476399 | G | A | 1 | a0001c0001t0040 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 308 | chr3 | 9476399 | ||||||
| chr3:9476422 | C | T | 3 | a0001c0001t0035 a0001c0007t0029 a0001c0007t0047 |
3 | HG02129.hp2 HG02723.hp1 NA18991.hp2 |
3_prime_UTR_variant | MODIFIER | c.*331C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 331 | chr3 | 9476422 | ||||||
| chr3:9476459 | TA | T | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
43 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*387delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 387 | INFO_REALIGN_3_PRIME | chr3 | 9476459 | |||||
| chr3:9476459 | TAA | T | 6 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0015 others(3): Show |
12 | HG02129.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*386_*387delAA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 386 | INFO_REALIGN_3_PRIME | chr3 | 9476459 | |||||
| chr3:9476563 | A | G | 1 | a0001c0001t0027 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 472 | chr3 | 9476563 | ||||||
| chr3:9476646 | G | A | 1 | a0001c0001t0030 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 555 | chr3 | 9476646 | ||||||
| chr3:9476764 | C | T | 2 | a0001c0001t0012 a0001c0001t0018 |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*673C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 673 | chr3 | 9476764 | ||||||
| chr3:9476827 | C | T | 17 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(14): Show |
50 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 736 | chr3 | 9476827 | ||||||
| chr3:9476955 | G | A | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*864G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 864 | chr3 | 9476955 | ||||||
| chr3:9477123 | G | C | 13 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0017 others(10): Show |
38 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1032G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1032 | chr3 | 9477123 | ||||||
| chr3:9477178 | G | C | 1 | a0001c0001t0028 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1087G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1087 | chr3 | 9477178 | ||||||
| chr3:9477521 | C | G | 1 | a0005c0006t0032 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1430 | chr3 | 9477521 | ||||||
| chr3:9477679 | AT | A | 13 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(10): Show |
40 | HG01070.hp1 HG01081.hp2 HG01099.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1610delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1610 | INFO_REALIGN_3_PRIME | chr3 | 9477679 | |||||
| chr3:9477864 | T | A | 1 | a0001c0001t0041 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1773T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1773 | chr3 | 9477864 | ||||||
| chr3:9477906 | G | A | 1 | a0001c0001t0028 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1815G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1815 | chr3 | 9477906 | ||||||
| chr3:9478004 | C | CG | 21 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(18): Show |
75 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1920dupG | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 23/23 | 1921 | INFO_REALIGN_3_PRIME | chr3 | 9478004 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:9398070 | T | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+93T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398070 | |||||||
| chr3:9398129 | C | T | 4 | a0001c0001t0004g0236 a0001c0001t0007g0233 a0001c0001t0010g0234 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+152C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398129 | |||||||
| chr3:9398204 | A | G | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-177+227A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398204 | |||||||
| chr3:9398211 | C | T | 1 | a0001c0012t0037g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-177+234C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398211 | |||||||
| chr3:9398373 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+396C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398373 | |||||||
| chr3:9398444 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+467C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398444 | |||||||
| chr3:9398719 | C | T | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-177+742C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398719 | |||||||
| chr3:9398729 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0002g0001 |
2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-177+752G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9398729 | |||||||
| chr3:9399389 | C | T | 86 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(83): Show |
87 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.-177+1412C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399389 | |||||||
| chr3:9399399 | A | G | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+1422A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399399 | |||||||
| chr3:9399496 | A | T | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(13): Show |
17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-177+1519A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399496 | |||||||
| chr3:9399827 | CA | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-177+1867delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9399827 | ||||||
| chr3:9399858 | G | T | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+1881G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399858 | |||||||
| chr3:9399902 | CAG | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0128 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-177+1926_-177+192 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9399902 | |||||||
| chr3:9400035 | A | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0002g0123 others(1): Show |
4 | HG00099.hp1 HG01169.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+2058A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400035 | |||||||
| chr3:9400053 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-177+2076G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400053 | |||||||
| chr3:9400081 | C | T | 1 | a0002c0002t0006g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-177+2104C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400081 | |||||||
| chr3:9400294 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+2317C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400294 | |||||||
| chr3:9400840 | C | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+2863C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400840 | |||||||
| chr3:9400977 | A | G | 1 | a0001c0001t0008g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-177+3000A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400977 | |||||||
| chr3:9400985 | C | A | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+3008C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9400985 | |||||||
| chr3:9401051 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-177+3074A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401051 | |||||||
| chr3:9401206 | A | G | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-177+3229A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401206 | |||||||
| chr3:9401319 | C | G | 1 | a0001c0001t0004g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177+3342C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401319 | |||||||
| chr3:9401370 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-177+3393G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401370 | |||||||
| chr3:9401413 | A | G | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+3436A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401413 | |||||||
| chr3:9401565 | T | C | 1 | a0001c0001t0036g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-177+3588T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401565 | |||||||
| chr3:9401734 | T | C | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-177+3757T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401734 | |||||||
| chr3:9401870 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-177+3893T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9401870 | |||||||
| chr3:9402572 | C | G | 1 | a0001c0001t0010g0013 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-177+4595C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402572 | |||||||
| chr3:9402616 | C | G | 1 | a0001c0001t0010g0013 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-177+4639C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402616 | |||||||
| chr3:9402743 | G | A | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-177+4766G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402743 | |||||||
| chr3:9402974 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0024g0019 |
2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-177+4997T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9402974 | |||||||
| chr3:9403001 | C | T | 1 | a0001c0003t0011g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-177+5024C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403001 | |||||||
| chr3:9403143 | G | T | 1 | a0001c0001t0003g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-177+5166G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403143 | |||||||
| chr3:9403225 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0002g0012 |
2 | HG01258.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-177+5248A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403225 | |||||||
| chr3:9403489 | G | T | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+5512G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403489 | |||||||
| chr3:9403564 | G | A | 1 | a0001c0001t0007g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-177+5587G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9403564 | |||||||
| chr3:9404018 | T | C | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-177+6041T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404018 | |||||||
| chr3:9404067 | A | G | 1 | a0001c0001t0004g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-177+6090A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404067 | |||||||
| chr3:9404312 | T | C | 3 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0044g0178 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-177+6335T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404312 | |||||||
| chr3:9404321 | TAAAG | T | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+6348_-177+635 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9404321 | ||||||
| chr3:9404643 | C | A | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-177+6666C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404643 | |||||||
| chr3:9404714 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-177+6737A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404714 | |||||||
| chr3:9404860 | C | T | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+6883C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9404860 | |||||||
| chr3:9405139 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-177+7162A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405139 | |||||||
| chr3:9405218 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-177+7241C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405218 | |||||||
| chr3:9405369 | C | T | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-177+7392C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405369 | |||||||
| chr3:9405403 | G | A | 25 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(22): Show |
25 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+7426G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405403 | |||||||
| chr3:9405958 | T | A | 6 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(3): Show |
6 | HG01074.hp1 HG01192.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+7981T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9405958 | |||||||
| chr3:9406062 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-177+8085G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406062 | |||||||
| chr3:9406065 | T | G | 1 | a0001c0001t0003g0215 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-177+8088T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406065 | |||||||
| chr3:9406285 | G | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+8308G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406285 | |||||||
| chr3:9406431 | C | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+8454C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406431 | |||||||
| chr3:9406540 | G | A | 18 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(15): Show |
18 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177+8563G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406540 | |||||||
| chr3:9406578 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-177+8601A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406578 | |||||||
| chr3:9406607 | C | CAA | 6 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(3): Show |
6 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+8643_-177+864 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAA | 8 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(5): Show |
8 | HG01099.hp1 HG02615.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-177+8641_-177+864 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAA | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+8639_-177+864 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(3): Show |
23 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(20): Show |
23 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-177+8635_-177+864 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0006g0205 a0001c0001t0007g0155 a0001c0001t0007g0156 |
3 | HG02970.hp2 HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-177+8634_-177+864 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(6): Show |
1 | a0001c0007t0047g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-177+8632_-177+864 others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(7): Show |
1 | a0001c0007t0029g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-177+8631_-177+864 others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(9): Show |
16 | a0001c0001t0003g0211 a0001c0001t0003g0213 a0001c0001t0003g0214 others(13): Show |
16 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177+8644_-177+864 others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(10): Show |
5 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0216 others(2): Show |
5 | HG01192.hp2 HG01978.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+8644_-177+864 others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0016g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(23): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0016g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(24): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406607 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+8644_-177+864 others(25): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9406607 | ||||||
| chr3:9406681 | C | T | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+8704C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406681 | |||||||
| chr3:9406957 | A | G | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-177+8980A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406957 | |||||||
| chr3:9406983 | G | A | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-177+9006G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9406983 | |||||||
| chr3:9407054 | G | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+9077G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407054 | |||||||
| chr3:9407090 | G | A | 1 | a0001c0001t0004g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-177+9113G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407090 | |||||||
| chr3:9407144 | A | G | 1 | a0001c0001t0005g0151 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-177+9167A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407144 | |||||||
| chr3:9407195 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-177+9218G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407195 | |||||||
| chr3:9407283 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-177+9306G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407283 | |||||||
| chr3:9407371 | C | T | 34 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(31): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-177+9394C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407371 | |||||||
| chr3:9407381 | A | G | 7 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0148 others(4): Show |
7 | HG00597.hp2 HG01109.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+9404A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407381 | |||||||
| chr3:9407386 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0002g0105 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-177+9409A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407386 | |||||||
| chr3:9407726 | T | C | 95 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(92): Show |
96 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-177+9749T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407726 | |||||||
| chr3:9407758 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+9781T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407758 | |||||||
| chr3:9407912 | A | C | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(13): Show |
17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-177+9935A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407912 | |||||||
| chr3:9407914 | C | G | 1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-177+9937C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407914 | |||||||
| chr3:9407949 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-177+9972G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407949 | |||||||
| chr3:9407956 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-177+9979C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407956 | |||||||
| chr3:9407980 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-177+10003A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9407980 | |||||||
| chr3:9408000 | C | CAA | 12 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+10034_-177+10 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9408000 | ||||||
| chr3:9408062 | T | C | 4 | a0001c0001t0005g0168 a0001c0001t0012g0170 a0001c0001t0018g0167 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+10085T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408062 | |||||||
| chr3:9408131 | G | T | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+10154G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408131 | |||||||
| chr3:9408228 | C | G | 2 | a0005c0006t0002g0101 a0005c0006t0032g0102 |
2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-177+10251C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408228 | |||||||
| chr3:9408511 | T | C | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-177+10534T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408511 | |||||||
| chr3:9408617 | TC | T | 25 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(22): Show |
25 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+10646delC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9408617 | ||||||
| chr3:9408621 | C | T | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+10644C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408621 | |||||||
| chr3:9408928 | A | G | 1 | a0001c0001t0004g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177+10951A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9408928 | |||||||
| chr3:9409084 | C | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+11107C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409084 | |||||||
| chr3:9409092 | A | T | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+11115A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409092 | |||||||
| chr3:9409155 | G | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+11178G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409155 | |||||||
| chr3:9409528 | C | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+11551C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409528 | |||||||
| chr3:9409554 | T | C | 1 | a0001c0003t0011g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-177+11577T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409554 | |||||||
| chr3:9409599 | C | G | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-177+11622C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409599 | |||||||
| chr3:9409603 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0002g0001 |
2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-177+11626C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409603 | |||||||
| chr3:9409693 | T | A | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-177+11716T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409693 | |||||||
| chr3:9409801 | C | T | 1 | a0001c0001t0002g0010 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-177+11824C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409801 | |||||||
| chr3:9409841 | C | T | 7 | a0001c0001t0005g0168 a0001c0001t0012g0170 a0001c0001t0012g0172 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+11864C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9409841 | |||||||
| chr3:9410023 | T | G | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177+12046T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410023 | |||||||
| chr3:9410157 | C | G | 2 | a0001c0001t0005g0099 a0001c0001t0005g0100 |
2 | NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-177+12180C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410157 | |||||||
| chr3:9410219 | G | A | 1 | a0004c0004t0021g0022 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-177+12242G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410219 | |||||||
| chr3:9410225 | A | G | 1 | a0004c0004t0021g0022 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-177+12248A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410225 | |||||||
| chr3:9410262 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-177+12285T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410262 | |||||||
| chr3:9410336 | T | C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177+12359T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410336 | |||||||
| chr3:9410453 | C | T | 1 | a0001c0001t0004g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-177+12476C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410453 | |||||||
| chr3:9410474 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0098 |
2 | HG00673.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-177+12497C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410474 | |||||||
| chr3:9410504 | G | A | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177+12527G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410504 | |||||||
| chr3:9410560 | G | C | 1 | a0001c0001t0003g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-177+12583G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410560 | |||||||
| chr3:9410804 | C | CTTTT | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-177+12830_-177+12 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9410804 | ||||||
| chr3:9410877 | C | CT | 68 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(65): Show |
69 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.-177+12911dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9410877 | ||||||
| chr3:9410877 | C | CTT | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-177+12910_-177+12 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9410877 | ||||||
| chr3:9410919 | C | T | 10 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(7): Show |
10 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177+12942C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9410919 | |||||||
| chr3:9411453 | G | A | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-13014G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411453 | |||||||
| chr3:9411761 | C | G | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-12706C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411761 | |||||||
| chr3:9411772 | T | C | 2 | a0001c0001t0003g0218 a0001c0001t0023g0217 |
2 | NA18940.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-176-12695T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411772 | |||||||
| chr3:9411776 | T | G | 1 | a0001c0001t0004g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-176-12691T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411776 | |||||||
| chr3:9411976 | T | C | 45 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(42): Show |
46 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-176-12491T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9411976 | |||||||
| chr3:9412387 | G | GT | 51 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0072 others(48): Show |
51 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-176-12050dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | ||||||
| chr3:9412387 | G | GTT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0185 others(8): Show |
11 | HG01099.hp1 HG01175.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.-176-12051_-176-12 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | ||||||
| chr3:9412387 | G | GTTT | 10 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0002g0190 others(7): Show |
10 | HG00323.hp2 HG00735.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.-176-12052_-176-12 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | ||||||
| chr3:9412387 | GT | G | 33 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0128 others(30): Show |
33 | HG01069.hp2 HG01517.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-176-12050delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9412387 | ||||||
| chr3:9412390 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-176-12077T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412390 | |||||||
| chr3:9412399 | T | G | 2 | a0001c0001t0007g0156 a0001c0001t0031g0235 |
2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-176-12068T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412399 | |||||||
| chr3:9412400 | T | G | 26 | a0001c0001t0004g0157 a0001c0001t0004g0158 a0001c0001t0004g0159 others(23): Show |
26 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-176-12067T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412400 | |||||||
| chr3:9412408 | T | G | 1 | a0001c0001t0002g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-176-12059T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412408 | |||||||
| chr3:9412414 | TTTTA | T | 21 | a0001c0001t0003g0209 a0001c0001t0003g0213 a0001c0001t0003g0214 others(18): Show |
21 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-176-12052_-176-12 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412414 | |||||||
| chr3:9412471 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-11996T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412471 | |||||||
| chr3:9412661 | T | G | 1 | a0001c0003t0011g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-176-11806T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412661 | |||||||
| chr3:9412819 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-11648T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412819 | |||||||
| chr3:9412973 | A | G | 1 | a0001c0001t0004g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-176-11494A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412973 | |||||||
| chr3:9412976 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0002g0093 |
2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-176-11491C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9412976 | |||||||
| chr3:9413078 | A | G | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-11389A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413078 | |||||||
| chr3:9413225 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-176-11242T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413225 | |||||||
| chr3:9413238 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-176-11229T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413238 | |||||||
| chr3:9413327 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-11140A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413327 | |||||||
| chr3:9413367 | T | A | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-11100T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413367 | |||||||
| chr3:9413646 | CG | C | 5 | a0001c0001t0001g0068 a0001c0001t0002g0067 a0001c0001t0005g0147 others(2): Show |
5 | HG02074.hp2 NA18906.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-10817delG | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413646 | ||||||
| chr3:9413649 | G | GGGTGTGT | 11 | a0001c0001t0001g0188 a0001c0001t0002g0190 a0001c0001t0026g0189 others(8): Show |
11 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-176-10817_-176-10 others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GGGTGTGT others(4): Show |
1 | a0002c0002t0006g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-176-10817_-176-10 others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GGT | 31 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
32 | HG00597.hp1 HG00673.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-176-10783_-176-10 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GGTGT | 26 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(23): Show |
26 | HG01099.hp1 HG01255.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-10785_-176-10 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GGTGTGT | 11 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0213 others(8): Show |
11 | HG01070.hp1 HG01074.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-176-10787_-176-10 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GGTGTGTG others(1): Show |
13 | a0001c0001t0003g0215 a0001c0001t0003g0216 a0001c0001t0003g0218 others(10): Show |
13 | HG00621.hp1 HG00639.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-176-10789_-176-10 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GGTGTGTG others(3): Show |
4 | a0001c0001t0003g0211 a0001c0001t0003g0230 a0001c0001t0006g0205 others(1): Show |
4 | HG02004.hp1 HG03688.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-10791_-176-10 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413649 | G | GT | 2 | a0001c0001t0002g0069 a0001c0001t0002g0090 |
2 | NA18998.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-176-10818_-176-10 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413649 | |||||||
| chr3:9413649 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-176-10818G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413649 | |||||||
| chr3:9413649 | GGT | G | 70 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0021 others(67): Show |
70 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.-176-10783_-176-10 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413649 | ||||||
| chr3:9413770 | TTTTTG | T | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-10677_-176-10 others(11): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9413770 | ||||||
| chr3:9413840 | T | A | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-176-10627T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413840 | |||||||
| chr3:9413882 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-176-10585A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413882 | |||||||
| chr3:9413912 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-176-10555G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9413912 | |||||||
| chr3:9414027 | G | A | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-10440G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414027 | |||||||
| chr3:9414194 | G | A | 1 | a0001c0001t0017g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-176-10273G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414194 | |||||||
| chr3:9414236 | G | T | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-10231G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414236 | |||||||
| chr3:9414395 | GTGTTGT | G | 3 | a0001c0001t0002g0029 a0003c0008t0001g0081 a0003c0008t0002g0095 |
3 | HG03098.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-176-10064_-176-10 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9414395 | ||||||
| chr3:9414417 | G | C | 18 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(15): Show |
18 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176-10050G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414417 | |||||||
| chr3:9414540 | A | G | 1 | a0001c0001t0005g0062 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-176-9927A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414540 | |||||||
| chr3:9414603 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-9864T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414603 | |||||||
| chr3:9414658 | C | A | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-176-9809C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414658 | |||||||
| chr3:9414680 | T | A | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-176-9787T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414680 | |||||||
| chr3:9414767 | GT | G | 2 | a0001c0003t0009g0194 a0001c0003t0011g0195 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-176-9698delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9414767 | ||||||
| chr3:9414796 | T | C | 1 | a0001c0001t0004g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-176-9671T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414796 | |||||||
| chr3:9414936 | A | G | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-9531A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9414936 | |||||||
| chr3:9415021 | A | C | 34 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(31): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-176-9446A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415021 | |||||||
| chr3:9415068 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-176-9399A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415068 | |||||||
| chr3:9415270 | T | C | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-176-9197T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415270 | |||||||
| chr3:9415577 | A | T | 82 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(79): Show |
83 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-176-8890A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415577 | |||||||
| chr3:9415586 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-176-8881A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415586 | |||||||
| chr3:9415588 | T | A | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-8879T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415588 | |||||||
| chr3:9415589 | T | A | 1 | a0001c0001t0003g0221 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-176-8878T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415589 | |||||||
| chr3:9415621 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-176-8846C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415621 | |||||||
| chr3:9415674 | A | G | 82 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(79): Show |
83 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-176-8793A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415674 | |||||||
| chr3:9415682 | C | T | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-8785C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415682 | |||||||
| chr3:9415802 | G | C | 1 | a0001c0001t0003g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-176-8665G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9415802 | |||||||
| chr3:9416129 | C | G | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-8338C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416129 | |||||||
| chr3:9416183 | GTCT | G | 95 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(92): Show |
96 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-176-8280_-176-827 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9416183 | ||||||
| chr3:9416199 | C | CT | 2 | a0001c0001t0002g0024 a0001c0001t0005g0084 |
2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-176-8267dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9416199 | ||||||
| chr3:9416312 | C | A | 1 | a0001c0001t0002g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-176-8155C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416312 | |||||||
| chr3:9416388 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0010g0071 a0001c0001t0033g0089 |
3 | HG02896.hp1 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-176-8079G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416388 | |||||||
| chr3:9416545 | A | G | 1 | a0001c0003t0011g0204 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-176-7922A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416545 | |||||||
| chr3:9416565 | G | A | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-176-7902G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416565 | |||||||
| chr3:9416623 | A | G | 34 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(31): Show |
34 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.-176-7844A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416623 | |||||||
| chr3:9416940 | T | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0143 |
3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-176-7527T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9416940 | |||||||
| chr3:9417026 | A | T | 37 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(34): Show |
37 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.-176-7441A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417026 | |||||||
| chr3:9417178 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176-7289G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417178 | |||||||
| chr3:9417224 | T | C | 1 | a0001c0001t0002g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-176-7243T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417224 | |||||||
| chr3:9417483 | C | CT | 7 | a0001c0001t0003g0221 a0001c0001t0006g0205 a0001c0001t0008g0080 others(4): Show |
7 | HG02129.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-6970dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417483 | ||||||
| chr3:9417483 | CT | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0098 a0001c0001t0004g0114 others(35): Show |
38 | HG00673.hp1 HG01081.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-176-6970delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417483 | ||||||
| chr3:9417497 | T | C | 1 | a0001c0001t0004g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-176-6970T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417497 | |||||||
| chr3:9417498 | C | T | 27 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(24): Show |
27 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.-176-6969C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417498 | |||||||
| chr3:9417522 | A | G | 95 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(92): Show |
96 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-176-6945A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417522 | |||||||
| chr3:9417578 | C | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-6889C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417578 | |||||||
| chr3:9417611 | A | G | 83 | a0001c0001t0001g0113 a0001c0001t0001g0185 a0001c0001t0001g0186 others(80): Show |
84 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.-176-6856A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417611 | |||||||
| chr3:9417638 | A | G | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-176-6829A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417638 | |||||||
| chr3:9417741 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0010g0071 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-176-6726T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417741 | |||||||
| chr3:9417942 | G | GT | 27 | a0001c0001t0001g0125 a0001c0001t0001g0185 a0001c0001t0001g0186 others(24): Show |
28 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-176-6509dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417942 | ||||||
| chr3:9417942 | G | GTT | 5 | a0001c0001t0022g0225 a0001c0001t0040g0231 a0001c0007t0047g0006 others(2): Show |
5 | HG01123.hp1 HG02004.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-6510_-176-650 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9417942 | ||||||
| chr3:9417947 | T | TG | 18 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(15): Show |
18 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-176-6520_-176-651 others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9417947 | |||||||
| chr3:9418003 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-176-6464C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418003 | |||||||
| chr3:9418107 | AT | A | 9 | a0001c0001t0001g0072 a0001c0001t0001g0106 a0001c0001t0002g0105 others(6): Show |
9 | HG00735.hp2 HG02055.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-176-6346delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9418107 | ||||||
| chr3:9418194 | C | T | 3 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0044g0178 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-176-6273C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418194 | |||||||
| chr3:9418194 | CGCCTCG | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0061 others(6): Show |
9 | HG01109.hp1 HG02809.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.-176-6270_-176-626 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9418194 | ||||||
| chr3:9418322 | G | A | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-176-6145G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418322 | |||||||
| chr3:9418557 | A | G | 1 | a0001c0001t0027g0028 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-176-5910A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418557 | |||||||
| chr3:9418732 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176-5735G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418732 | |||||||
| chr3:9418743 | C | T | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-5724C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418743 | |||||||
| chr3:9418803 | CA | C | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(13): Show |
17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-176-5651delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9418803 | ||||||
| chr3:9418839 | T | C | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-176-5628T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418839 | |||||||
| chr3:9418890 | A | C | 1 | a0001c0001t0001g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-176-5577A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9418890 | |||||||
| chr3:9419073 | C | T | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-5394C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419073 | |||||||
| chr3:9419098 | A | G | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-176-5369A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419098 | |||||||
| chr3:9419206 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-176-5261G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419206 | |||||||
| chr3:9419269 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-5198A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9419269 | |||||||
| chr3:9420238 | GATAATA | G | 9 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176-4217_-176-421 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9420238 | ||||||
| chr3:9420241 | A | G | 11 | a0001c0003t0009g0194 a0001c0003t0009g0197 a0001c0003t0009g0203 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.-176-4226A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420241 | |||||||
| chr3:9420315 | C | G | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-4152C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420315 | |||||||
| chr3:9420362 | T | C | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-4105T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420362 | |||||||
| chr3:9420392 | C | G | 28 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(25): Show |
28 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-4075C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420392 | |||||||
| chr3:9420433 | T | C | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-176-4034T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9420433 | |||||||
| chr3:9420832 | A | AT | 45 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(42): Show |
46 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-176-3624dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9420832 | ||||||
| chr3:9420832 | A | ATT | 46 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(43): Show |
46 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.-176-3625_-176-362 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr3 | 9420832 | ||||||
| chr3:9421137 | A | C | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-3330A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421137 | |||||||
| chr3:9421352 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-176-3115G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421352 | |||||||
| chr3:9421387 | C | G | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-3080C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421387 | |||||||
| chr3:9421446 | T | C | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-176-3021T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421446 | |||||||
| chr3:9421508 | C | T | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-176-2959C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421508 | |||||||
| chr3:9421778 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-176-2689A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9421778 | |||||||
| chr3:9422004 | A | G | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-2463A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422004 | |||||||
| chr3:9422296 | G | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-176-2171G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422296 | |||||||
| chr3:9422299 | T | G | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-176-2168T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422299 | |||||||
| chr3:9422408 | A | G | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.-176-2059A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422408 | |||||||
| chr3:9422474 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-176-1993G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422474 | |||||||
| chr3:9422753 | G | T | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-176-1714G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422753 | |||||||
| chr3:9422827 | A | G | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-176-1640A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422827 | |||||||
| chr3:9422828 | A | G | 1 | a0001c0010t0001g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-176-1639A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9422828 | |||||||
| chr3:9423041 | T | C | 82 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(79): Show |
83 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-176-1426T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423041 | |||||||
| chr3:9423287 | A | G | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-176-1180A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423287 | |||||||
| chr3:9423317 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-176-1150G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423317 | |||||||
| chr3:9423708 | G | A | 2 | a0001c0001t0003g0219 a0001c0001t0003g0220 |
2 | NA19070.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-176-759G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423708 | |||||||
| chr3:9423845 | G | A | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-176-622G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423845 | |||||||
| chr3:9423980 | A | G | 7 | a0001c0001t0001g0072 a0001c0001t0010g0071 a0001c0001t0017g0018 others(4): Show |
7 | HG00735.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-487A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9423980 | |||||||
| chr3:9424095 | A | T | 97 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0185 others(94): Show |
98 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.-176-372A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9424095 | |||||||
| chr3:9424357 | GA | G | 3 | a0003c0005t0009g0201 a0003c0005t0009g0202 a0003c0005t0011g0200 |
3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-176-109delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 1/22 | chr3 | 9424357 | |||||||
| chr3:9424562 | T | C | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-117+36T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9424562 | |||||||
| chr3:9424651 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-117+125C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9424651 | |||||||
| chr3:9424766 | A | G | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.-117+240A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9424766 | |||||||
| chr3:9425036 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-117+510A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425036 | |||||||
| chr3:9425038 | A | G | 2 | a0001c0001t0002g0190 a0002c0002t0006g0191 |
2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-117+512A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425038 | |||||||
| chr3:9425051 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-117+528_-117+529i others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425051 | ||||||
| chr3:9425054 | T | G | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-117+528T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425054 | |||||||
| chr3:9425055 | C | CT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(15): Show |
18 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.-117+552dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTT | 6 | a0001c0001t0001g0007 a0001c0001t0006g0205 a0001c0003t0011g0204 others(3): Show |
6 | HG01071.hp1 HG01099.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-117+550_-117+552d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTTT | 7 | a0001c0001t0022g0225 a0001c0003t0009g0193 a0001c0003t0009g0194 others(4): Show |
7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-117+549_-117+552d others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTTTT | 32 | a0001c0001t0001g0185 a0001c0001t0003g0209 a0001c0001t0003g0210 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-117+548_-117+552d others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTTTTT | 18 | a0001c0001t0001g0188 a0001c0001t0002g0190 a0001c0001t0003g0232 others(15): Show |
19 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-117+547_-117+552d others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0004g0236 a0001c0001t0031g0235 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-117+530_-117+552d others(25): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0007g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-117+552_-117+553i others(29): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0010g0234 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-117+552_-117+553i others(30): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-117+529C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425055 | |||||||
| chr3:9425055 | C | T | 3 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0044g0178 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-117+529C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425055 | |||||||
| chr3:9425055 | CT | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0109 a0001c0001t0001g0143 others(10): Show |
13 | HG00323.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-117+552delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425055 | CTTT | C | 11 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(8): Show |
11 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-117+550_-117+552d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425055 | ||||||
| chr3:9425062 | T | TTTTTTTT others(6): Show |
2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-117+548_-117+549i others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425062 | ||||||
| chr3:9425102 | T | C | 36 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(33): Show |
36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-117+576T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425102 | |||||||
| chr3:9425118 | A | G | 1 | a0001c0001t0003g0209 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-117+592A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425118 | |||||||
| chr3:9425207 | G | A | 26 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(23): Show |
26 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-117+681G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425207 | |||||||
| chr3:9425253 | A | G | 36 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(33): Show |
36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-117+727A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425253 | |||||||
| chr3:9425264 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-117+738G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425264 | |||||||
| chr3:9425377 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-117+851T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425377 | |||||||
| chr3:9425388 | T | C | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(13): Show |
17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-117+862T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425388 | |||||||
| chr3:9425575 | C | CT | 17 | a0001c0001t0001g0138 a0001c0001t0002g0150 a0001c0001t0008g0039 others(14): Show |
17 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-117+1068dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425575 | ||||||
| chr3:9425575 | CT | C | 26 | a0001c0001t0001g0008 a0001c0001t0001g0185 a0001c0001t0001g0186 others(23): Show |
27 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-117+1068delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9425575 | ||||||
| chr3:9425635 | G | T | 1 | a0002c0002t0006g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-117+1109G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425635 | |||||||
| chr3:9425776 | G | A | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-117+1250G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425776 | |||||||
| chr3:9425922 | G | A | 1 | a0001c0007t0047g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-117+1396G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425922 | |||||||
| chr3:9425942 | A | G | 1 | a0001c0003t0042g0198 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-117+1416A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9425942 | |||||||
| chr3:9426005 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-117+1479T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426005 | |||||||
| chr3:9426015 | A | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.-117+1489A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426015 | |||||||
| chr3:9426172 | A | G | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-117+1646A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426172 | |||||||
| chr3:9426210 | TC | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0002g0012 others(1): Show |
4 | HG01258.hp2 HG01934.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-117+1687delC | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr3 | 9426210 | ||||||
| chr3:9426212 | C | CT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(24): Show |
27 | HG00099.hp2 HG00673.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0103 others(16): Show |
19 | HG00597.hp2 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTT | 18 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0048 others(15): Show |
18 | HG00639.hp2 HG01071.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTT | 12 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0051 others(9): Show |
12 | HG00099.hp1 HG01884.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTT | 14 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0053 others(11): Show |
14 | HG00323.hp1 HG00438.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTT | 3 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0005c0006t0032g0102 |
3 | HG00621.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT | 3 | a0001c0001t0001g0065 a0001c0001t0001g0085 a0001c0001t0001g0108 |
3 | HG03516.hp2 NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(11): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0036 a0001c0001t0001g0098 a0001c0001t0001g0126 others(2): Show |
5 | HG01928.hp2 NA18942.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(3): Show |
9 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0061 others(6): Show |
9 | HG00544.hp1 HG00673.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0113 |
2 | HG00544.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0146 a0001c0001t0002g0055 a0004c0004t0021g0022 |
3 | HG02132.hp1 NA18940.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0069 a0004c0004t0019g0059 |
2 | NA18950.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-117+1686_-117+168 others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0005g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-117+1686_-117+168 others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | C | CTTTTTTT others(14): Show |
1 | a0004c0004t0021g0078 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-117+1686_-117+168 others(25): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCT | C | 4 | a0001c0001t0002g0047 a0001c0001t0010g0013 a0001c0001t0030g0026 others(1): Show |
4 | HG02683.hp1 HG02970.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-117+1687_-117+168 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(1): Show |
C | 3 | a0001c0003t0009g0203 a0003c0005t0009g0201 a0003c0005t0011g0200 |
3 | HG01069.hp1 HG01071.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-117+1687_-117+169 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(2): Show |
C | 4 | a0001c0003t0009g0197 a0001c0003t0011g0196 a0001c0003t0011g0199 others(1): Show |
4 | HG01099.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-117+1687_-117+169 others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(3): Show |
C | 3 | a0001c0003t0009g0194 a0001c0003t0011g0195 a0001c0003t0011g0204 |
3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-117+1687_-117+169 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(4): Show |
C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-117+1687_-117+169 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-117+1687_-117+169 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0046 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-117+1687_-117+169 others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(7): Show |
C | 8 | a0001c0001t0001g0091 a0001c0001t0003g0209 a0001c0001t0003g0210 others(5): Show |
8 | HG01192.hp2 HG01433.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(8): Show |
C | 23 | a0001c0001t0001g0185 a0001c0001t0003g0211 a0001c0001t0003g0213 others(20): Show |
23 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(9): Show |
C | 18 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0002g0190 others(15): Show |
19 | HG00323.hp2 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(11): Show |
C | 2 | a0001c0001t0002g0104 a0001c0001t0006g0205 |
2 | HG02071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(22): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(15): Show |
C | 3 | a0001c0001t0005g0100 a0001c0001t0016g0153 a0001c0001t0016g0154 |
3 | HG02145.hp2 HG03139.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(26): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426212 | CCTTTTTT others(16): Show |
C | 27 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(24): Show |
27 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.-117+1687_-117+170 others(27): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426212 | |||||||
| chr3:9426213 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-117+1687C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426213 | |||||||
| chr3:9426275 | G | T | 1 | a0001c0003t0011g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-117+1749G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426275 | |||||||
| chr3:9426343 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-117+1817T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426343 | |||||||
| chr3:9426593 | A | C | 1 | a0001c0007t0029g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-117+2067A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9426593 | |||||||
| chr3:9427519 | C | G | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-116-1304C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427519 | |||||||
| chr3:9427543 | T | A | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-116-1280T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427543 | |||||||
| chr3:9427544 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-116-1279G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427544 | |||||||
| chr3:9427595 | C | T | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0130 others(4): Show |
7 | HG00099.hp2 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-116-1228C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427595 | |||||||
| chr3:9427603 | T | C | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-116-1220T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427603 | |||||||
| chr3:9427620 | T | C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-116-1203T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427620 | |||||||
| chr3:9427711 | C | G | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.-116-1112C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427711 | |||||||
| chr3:9427822 | A | G | 2 | a0001c0003t0009g0194 a0001c0003t0011g0195 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-116-1001A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427822 | |||||||
| chr3:9427937 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-116-886T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427937 | |||||||
| chr3:9427971 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0128 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-116-852G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9427971 | |||||||
| chr3:9428020 | G | A | 1 | a0001c0001t0030g0026 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-116-803G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428020 | |||||||
| chr3:9428032 | G | T | 13 | a0001c0001t0046g0177 a0001c0003t0009g0193 a0001c0003t0009g0194 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-116-791G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428032 | |||||||
| chr3:9428139 | C | T | 1 | a0001c0001t0015g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-116-684C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428139 | |||||||
| chr3:9428140 | G | A | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-116-683G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428140 | |||||||
| chr3:9428271 | A | G | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-116-552A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428271 | |||||||
| chr3:9428307 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-116-516G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428307 | |||||||
| chr3:9428507 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-116-316A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 2/22 | chr3 | 9428507 | |||||||
| chr3:9429493 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.71+484G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9429493 | |||||||
| chr3:9429502 | T | G | 2 | a0001c0001t0001g0106 a0001c0001t0002g0105 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.71+493T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9429502 | |||||||
| chr3:9429548 | G | T | 6 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(3): Show |
6 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.71+539G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9429548 | |||||||
| chr3:9429616 | TA | T | 32 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.71+611delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr3 | 9429616 | ||||||
| chr3:9430095 | A | C | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71+1086A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430095 | |||||||
| chr3:9430216 | T | C | 2 | a0001c0001t0002g0067 a0001c0001t0008g0080 |
2 | HG02074.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.71+1207T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430216 | |||||||
| chr3:9430317 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.71+1308T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430317 | |||||||
| chr3:9430564 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.71+1555C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430564 | |||||||
| chr3:9430773 | C | T | 1 | a0001c0001t0015g0165 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.71+1764C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9430773 | |||||||
| chr3:9431044 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.71+2035C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431044 | |||||||
| chr3:9431237 | A | G | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71+2228A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431237 | |||||||
| chr3:9431518 | A | C | 36 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(33): Show |
36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-2327A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431518 | |||||||
| chr3:9431618 | A | G | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.72-2227A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431618 | |||||||
| chr3:9431950 | G | A | 1 | a0001c0001t0004g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.72-1895G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431950 | |||||||
| chr3:9431985 | T | C | 26 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.72-1860T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9431985 | |||||||
| chr3:9432167 | C | T | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.72-1678C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432167 | |||||||
| chr3:9432176 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.72-1669C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432176 | |||||||
| chr3:9432253 | G | GTTC | 36 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(33): Show |
36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.72-1588_72-1586dup others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr3 | 9432253 | ||||||
| chr3:9432278 | C | G | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72-1567C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432278 | |||||||
| chr3:9432377 | A | G | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.72-1468A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432377 | |||||||
| chr3:9432466 | C | T | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.72-1379C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432466 | |||||||
| chr3:9432987 | G | A | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.72-858G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9432987 | |||||||
| chr3:9433076 | T | C | 1 | a0001c0001t0002g0057 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.72-769T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433076 | |||||||
| chr3:9433158 | C | G | 1 | a0001c0001t0026g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.72-687C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433158 | |||||||
| chr3:9433298 | T | C | 2 | a0002c0002t0013g0179 a0002c0002t0013g0183 |
2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.72-547T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433298 | |||||||
| chr3:9433434 | G | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.72-411G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433434 | |||||||
| chr3:9433630 | C | G | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.72-215C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433630 | |||||||
| chr3:9433732 | T | A | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.72-113T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 3/22 | chr3 | 9433732 | |||||||
| chr3:9434011 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0002g0001 |
2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.177+61T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 4/22 | chr3 | 9434011 | |||||||
| chr3:9434601 | G | T | 1 | a0001c0012t0037g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.329+116G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 5/22 | chr3 | 9434601 | |||||||
| chr3:9435243 | C | CA | 7 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG02080.hp2 HG02895.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.388+383dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | ||||||
| chr3:9435243 | CA | C | 20 | a0001c0001t0001g0072 a0001c0001t0001g0143 a0001c0001t0001g0185 others(17): Show |
21 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+383delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | ||||||
| chr3:9435243 | CAA | C | 72 | a0001c0001t0002g0190 a0001c0001t0003g0209 a0001c0001t0003g0210 others(69): Show |
72 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.388+382_388+383del others(2): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | ||||||
| chr3:9435243 | CAAA | C | 5 | a0001c0001t0004g0119 a0001c0001t0004g0163 a0001c0001t0007g0112 others(2): Show |
5 | HG01070.hp1 HG01081.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+381_388+383del others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435243 | ||||||
| chr3:9435245 | A | C | 1 | a0002c0002t0006g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.388+363A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435245 | |||||||
| chr3:9435278 | C | G | 26 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(23): Show |
26 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.388+396C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435278 | |||||||
| chr3:9435350 | TTC | T | 3 | a0001c0001t0004g0117 a0001c0001t0007g0116 a0001c0001t0015g0120 |
3 | HG02886.hp2 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.389-373_389-372del others(2): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr3 | 9435350 | ||||||
| chr3:9435366 | G | A | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.389-362G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435366 | |||||||
| chr3:9435466 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.389-262T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435466 | |||||||
| chr3:9435540 | C | G | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.389-188C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435540 | |||||||
| chr3:9435546 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.389-182G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435546 | |||||||
| chr3:9435547 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.389-181C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435547 | |||||||
| chr3:9435549 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.389-179A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435549 | |||||||
| chr3:9435621 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0002g0001 |
2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.389-107G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 6/22 | chr3 | 9435621 | |||||||
| chr3:9436153 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.567+247A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9436153 | |||||||
| chr3:9436661 | A | G | 1 | a0001c0001t0002g0055 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.567+755A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9436661 | |||||||
| chr3:9436837 | C | T | 1 | a0001c0001t0003g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.567+931C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9436837 | |||||||
| chr3:9437205 | G | A | 1 | a0001c0001t0012g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.567+1299G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437205 | |||||||
| chr3:9437284 | GTAT | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.567+1383_567+1385d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437284 | ||||||
| chr3:9437458 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(48): Show |
52 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.567+1552G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437458 | |||||||
| chr3:9437516 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.567+1610C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437516 | |||||||
| chr3:9437520 | T | G | 14 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(11): Show |
14 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.567+1614T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437520 | |||||||
| chr3:9437522 | C | CGT | 25 | a0001c0001t0001g0097 a0001c0001t0001g0107 a0001c0001t0001g0109 others(22): Show |
26 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.567+1643_567+1644d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGT | 10 | a0001c0001t0001g0106 a0001c0001t0002g0105 a0001c0001t0026g0189 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.567+1641_567+1644d others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0003g0209 a0001c0001t0006g0205 |
2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.567+1635_567+1644d others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(5): Show |
20 | a0001c0001t0003g0210 a0001c0001t0003g0211 a0001c0001t0003g0213 others(17): Show |
20 | HG00621.hp1 HG01074.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.567+1633_567+1644d others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(7): Show |
13 | a0001c0001t0003g0222 a0001c0001t0003g0226 a0001c0001t0003g0227 others(10): Show |
13 | HG00639.hp1 HG01070.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.567+1631_567+1644d others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(9): Show |
3 | a0001c0001t0004g0157 a0001c0001t0004g0236 a0001c0001t0022g0225 |
3 | HG02572.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.567+1629_567+1644d others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(11): Show |
9 | a0001c0001t0004g0114 a0001c0001t0004g0119 a0001c0001t0004g0164 others(6): Show |
9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+1627_567+1644d others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(13): Show |
3 | a0001c0001t0004g0115 a0001c0001t0007g0112 a0001c0001t0015g0120 |
3 | HG02818.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.567+1625_567+1644d others(22): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(15): Show |
8 | a0001c0001t0004g0117 a0001c0001t0004g0159 a0001c0001t0004g0160 others(5): Show |
8 | HG02258.hp2 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.567+1623_567+1644d others(24): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(17): Show |
5 | a0001c0001t0004g0158 a0001c0001t0004g0162 a0001c0001t0007g0155 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+1621_567+1644d others(26): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437522 | C | CGTGTGTG others(19): Show |
1 | a0001c0001t0004g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.567+1619_567+1644d others(28): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9437522 | ||||||
| chr3:9437671 | G | A | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.567+1765G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437671 | |||||||
| chr3:9437729 | G | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 |
3 | HG00323.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.567+1823G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437729 | |||||||
| chr3:9437819 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.567+1913A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9437819 | |||||||
| chr3:9438002 | CA | C | 91 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(88): Show |
92 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.567+2111delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9438002 | ||||||
| chr3:9438018 | T | A | 4 | a0001c0001t0001g0002 a0001c0001t0002g0010 a0001c0001t0008g0002 others(1): Show |
4 | HG00673.hp2 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+2112T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438018 | |||||||
| chr3:9438061 | C | T | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567+2155C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438061 | |||||||
| chr3:9438128 | A | T | 2 | a0001c0001t0001g0053 a0001c0001t0002g0069 |
2 | NA18990.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.567+2222A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438128 | |||||||
| chr3:9438287 | T | G | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.568-2169T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438287 | |||||||
| chr3:9438393 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.568-2063A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438393 | |||||||
| chr3:9438417 | G | A | 6 | a0001c0001t0012g0170 a0001c0001t0012g0172 a0001c0001t0012g0173 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.568-2039G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438417 | |||||||
| chr3:9438651 | T | A | 1 | a0001c0001t0007g0112 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.568-1805T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9438651 | |||||||
| chr3:9439199 | A | G | 2 | a0002c0002t0006g0182 a0002c0002t0013g0180 |
2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.568-1257A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439199 | |||||||
| chr3:9439200 | C | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.568-1256C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439200 | |||||||
| chr3:9439222 | T | C | 83 | a0001c0001t0001g0068 a0001c0001t0001g0185 a0001c0001t0001g0186 others(80): Show |
84 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.568-1234T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439222 | |||||||
| chr3:9439320 | C | T | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.568-1136C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439320 | |||||||
| chr3:9439352 | ATCAG | A | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.568-1099_568-1096d others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr3 | 9439352 | ||||||
| chr3:9439363 | A | G | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.568-1093A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439363 | |||||||
| chr3:9439373 | A | G | 26 | a0001c0001t0002g0033 a0001c0001t0003g0209 a0001c0001t0003g0210 others(23): Show |
26 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.568-1083A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439373 | |||||||
| chr3:9439429 | G | T | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.568-1027G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439429 | |||||||
| chr3:9439711 | A | G | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.568-745A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439711 | |||||||
| chr3:9439909 | A | G | 32 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.568-547A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9439909 | |||||||
| chr3:9440087 | G | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.568-369G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9440087 | |||||||
| chr3:9440109 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.568-347T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9440109 | |||||||
| chr3:9440225 | A | T | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.568-231A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 7/22 | chr3 | 9440225 | |||||||
| chr3:9440725 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.810+27C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9440725 | |||||||
| chr3:9441226 | G | A | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.811-367G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9441226 | |||||||
| chr3:9441352 | AT | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0002g0067 others(5): Show |
8 | HG02055.hp1 HG02074.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-225delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr3 | 9441352 | ||||||
| chr3:9441415 | A | G | 1 | a0001c0001t0014g0032 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.811-178A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9441415 | |||||||
| chr3:9441435 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.811-158G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 8/22 | chr3 | 9441435 | |||||||
| chr3:9442081 | C | T | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.960-47C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 9/22 | chr3 | 9442081 | |||||||
| chr3:9442280 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077+35A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442280 | |||||||
| chr3:9442472 | T | A | 3 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0044g0178 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1077+227T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442472 | |||||||
| chr3:9442545 | A | G | 1 | a0001c0001t0004g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1077+300A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442545 | |||||||
| chr3:9442748 | G | A | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1077+503G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442748 | |||||||
| chr3:9442796 | G | A | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(13): Show |
17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-512G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442796 | |||||||
| chr3:9442979 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0002g0105 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1078-329G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442979 | |||||||
| chr3:9442998 | C | G | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1078-310C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9442998 | |||||||
| chr3:9443220 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1078-88C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9443220 | |||||||
| chr3:9443235 | G | C | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1078-73G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9443235 | |||||||
| chr3:9443266 | A | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1078-42A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 10/22 | chr3 | 9443266 | |||||||
| chr3:9443638 | CAG | C | 16 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(13): Show |
17 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1187+223_1187+224d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | 9443638 | ||||||
| chr3:9443805 | C | A | 1 | a0003c0008t0002g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1187+388C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443805 | |||||||
| chr3:9443836 | C | G | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1187+419C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443836 | |||||||
| chr3:9443893 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1187+476C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443893 | |||||||
| chr3:9443929 | G | A | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1187+512G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9443929 | |||||||
| chr3:9444047 | G | A | 1 | a0001c0001t0022g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1187+630G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444047 | |||||||
| chr3:9444091 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1187+674C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444091 | |||||||
| chr3:9444282 | T | C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1188-766T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444282 | |||||||
| chr3:9444319 | T | G | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1188-729T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444319 | |||||||
| chr3:9444537 | C | CT | 34 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(31): Show |
34 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1188-501dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr3 | 9444537 | ||||||
| chr3:9444545 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1188-503T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444545 | |||||||
| chr3:9444617 | G | A | 2 | a0001c0001t0022g0229 a0001c0001t0025g0077 |
2 | HG01070.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1188-431G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444617 | |||||||
| chr3:9444699 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1188-349T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444699 | |||||||
| chr3:9444763 | G | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1188-285G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444763 | |||||||
| chr3:9444819 | G | A | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1188-229G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444819 | |||||||
| chr3:9444841 | A | C | 1 | a0001c0001t0001g0011 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1188-207A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444841 | |||||||
| chr3:9444857 | C | T | 3 | a0001c0001t0002g0087 a0001c0001t0010g0013 a0001c0001t0030g0026 |
3 | HG00597.hp1 NA18942.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1188-191C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9444857 | |||||||
| chr3:9445009 | G | T | 14 | a0001c0001t0025g0077 a0001c0001t0046g0177 a0001c0003t0009g0193 others(11): Show |
14 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1188-39G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 11/22 | chr3 | 9445009 | |||||||
| chr3:9445464 | T | C | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1440+164T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 12/22 | chr3 | 9445464 | |||||||
| chr3:9445937 | T | G | 1 | a0001c0001t0038g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1524+197T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445937 | |||||||
| chr3:9445962 | G | GTT | 4 | a0001c0001t0003g0230 a0001c0001t0006g0205 a0001c0007t0029g0005 others(1): Show |
4 | HG02129.hp2 HG04115.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+223_1524+224d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445962 | G | GTTTTTTT others(9): Show |
3 | a0001c0001t0023g0217 a0001c0001t0040g0231 a0001c0001t0043g0208 |
3 | HG02004.hp1 HG02723.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1524+224_1524+225i others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445962 | G | GTTTTTTT others(10): Show |
8 | a0001c0001t0003g0213 a0001c0001t0003g0224 a0001c0001t0003g0226 others(5): Show |
8 | HG01070.hp1 HG01255.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1524+224_1524+225i others(19): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445962 | G | GTTTTTTT others(11): Show |
10 | a0001c0001t0003g0209 a0001c0001t0003g0211 a0001c0001t0003g0214 others(7): Show |
10 | HG01074.hp1 HG01192.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+224_1524+225i others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445962 | G | GTTTTTTT others(12): Show |
7 | a0001c0001t0003g0210 a0001c0001t0003g0216 a0001c0001t0003g0220 others(4): Show |
7 | HG00639.hp1 HG01978.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+224_1524+225i others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445962 | G | GTTTTTTT others(25): Show |
1 | a0001c0001t0017g0171 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1524+224_1524+225i others(34): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445962 | GTTGTTTT others(3): Show |
G | 1 | a0001c0001t0022g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1524+225_1524+234d others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445962 | ||||||
| chr3:9445963 | T | C | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1524+223T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445963 | |||||||
| chr3:9445964 | T | TG | 3 | a0001c0001t0002g0029 a0001c0001t0005g0084 a0003c0008t0002g0095 |
3 | HG03098.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1524+225dupG | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445964 | ||||||
| chr3:9445965 | G | GT | 30 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0068 others(27): Show |
31 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1524+248dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(7): Show |
2 | a0001c0001t0025g0077 a0001c0003t0042g0198 |
2 | HG01099.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1524+235_1524+248d others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(8): Show |
1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+234_1524+248d others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(9): Show |
2 | a0001c0003t0009g0203 a0001c0003t0011g0196 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1524+233_1524+248d others(18): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(12): Show |
3 | a0001c0003t0009g0194 a0001c0003t0011g0195 a0001c0003t0011g0204 |
3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1524+230_1524+248d others(21): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(18): Show |
1 | a0003c0005t0011g0200 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1524+248_1524+249i others(27): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(19): Show |
1 | a0003c0005t0009g0201 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1524+248_1524+249i others(28): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | GTTTTTTT others(20): Show |
1 | a0003c0005t0009g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1524+248_1524+249i others(29): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445965 | G | T | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1524+225G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445965 | |||||||
| chr3:9445965 | GT | G | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1524+248delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445965 | ||||||
| chr3:9445966 | T | G | 6 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0002g0024 others(3): Show |
6 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+226T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445966 | |||||||
| chr3:9445968 | T | TTTTTTTT others(8): Show |
1 | a0001c0003t0011g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1524+242_1524+243i others(17): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445968 | ||||||
| chr3:9445971 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1524+231T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445971 | |||||||
| chr3:9445974 | T | TTTTTTTT others(11): Show |
1 | a0001c0001t0039g0223 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1524+248_1524+249i others(20): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9445974 | ||||||
| chr3:9445988 | T | TTTTTTTT others(7): Show |
1 | a0001c0003t0009g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1524+248_1524+249i others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9445988 | |||||||
| chr3:9446011 | G | A | 3 | a0003c0005t0009g0201 a0003c0005t0009g0202 a0003c0005t0011g0200 |
3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1524+271G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446011 | |||||||
| chr3:9446026 | G | A | 1 | a0001c0001t0004g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1524+286G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446026 | |||||||
| chr3:9446069 | C | T | 1 | a0001c0001t0018g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1524+329C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446069 | |||||||
| chr3:9446095 | C | G | 12 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0197 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1524+355C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446095 | |||||||
| chr3:9446150 | G | A | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1524+410G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446150 | |||||||
| chr3:9446180 | G | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1524+440G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446180 | |||||||
| chr3:9446286 | C | CA | 7 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0085 others(4): Show |
7 | HG00597.hp1 HG00621.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+568dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9446286 | ||||||
| chr3:9446286 | CAAA | C | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0213 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1524+566_1524+568d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9446286 | ||||||
| chr3:9446306 | A | AAC | 32 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0106 others(29): Show |
32 | HG00741.hp1 HG01109.hp2 HG01515.hp2 others(29): Show |
intron_variant | MODIFIER | c.1524+567_1524+568i others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr3 | 9446306 | ||||||
| chr3:9446306 | A | AC | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1524+566_1524+567i others(3): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446306 | |||||||
| chr3:9446306 | A | C | 37 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(34): Show |
37 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1524+566A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446306 | |||||||
| chr3:9446318 | C | T | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+578C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446318 | |||||||
| chr3:9446499 | T | G | 9 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(6): Show |
9 | HG02258.hp2 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525-551T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446499 | |||||||
| chr3:9446507 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1525-543T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446507 | |||||||
| chr3:9446661 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0110 |
2 | HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1525-389T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446661 | |||||||
| chr3:9446704 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG00438.hp2 NA18948.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-346G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446704 | |||||||
| chr3:9446720 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0108 |
2 | HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1525-330C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446720 | |||||||
| chr3:9446771 | G | C | 1 | a0001c0001t0005g0062 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1525-279G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9446771 | |||||||
| chr3:9447031 | C | A | 34 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(31): Show |
34 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1525-19C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 13/22 | chr3 | 9447031 | |||||||
| chr3:9447481 | A | G | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1782+174A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447481 | |||||||
| chr3:9447504 | CTAGCCTC others(13): Show |
C | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783-181_1783-162d others(22): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447504 | |||||||
| chr3:9447525 | A | G | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783-161A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447525 | |||||||
| chr3:9447526 | G | T | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1783-160G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447526 | |||||||
| chr3:9447650 | A | ATTTC | 36 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(33): Show |
36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1783-34_1783-31dup others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr3 | 9447650 | ||||||
| chr3:9447656 | G | A | 36 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(33): Show |
36 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1783-30G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 14/22 | chr3 | 9447656 | |||||||
| chr3:9448053 | T | A | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2103+47T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 15/22 | chr3 | 9448053 | |||||||
| chr3:9448083 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2103+77T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 15/22 | chr3 | 9448083 | |||||||
| chr3:9448164 | G | A | 4 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(1): Show |
4 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2103+158G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 15/22 | chr3 | 9448164 | |||||||
| chr3:9448747 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2346+117C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9448747 | |||||||
| chr3:9448761 | A | G | 1 | a0001c0001t0026g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2346+131A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9448761 | |||||||
| chr3:9448834 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0002g0001 |
2 | NA18948.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2346+204A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9448834 | |||||||
| chr3:9449405 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2346+775A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449405 | |||||||
| chr3:9449425 | G | A | 17 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(14): Show |
17 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2346+795G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449425 | |||||||
| chr3:9449444 | T | C | 32 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(29): Show |
32 | HG01081.hp2 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.2346+814T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449444 | |||||||
| chr3:9449947 | G | A | 7 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(4): Show |
7 | HG00639.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.2346+1317G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449947 | |||||||
| chr3:9449973 | A | T | 3 | a0004c0004t0019g0037 a0004c0004t0019g0059 a0004c0004t0021g0022 |
3 | NA18940.hp2 NA18950.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.2346+1343A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9449973 | |||||||
| chr3:9450256 | C | T | 1 | a0001c0009t0002g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2346+1626C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450256 | |||||||
| chr3:9450276 | A | G | 1 | a0001c0001t0020g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2346+1646A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450276 | |||||||
| chr3:9450311 | A | T | 1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2346+1681A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450311 | |||||||
| chr3:9450348 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0002g0070 a0001c0001t0024g0019 others(1): Show |
4 | HG00544.hp1 NA18970.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.2346+1718T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450348 | |||||||
| chr3:9450422 | A | T | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2346+1792A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450422 | |||||||
| chr3:9450423 | G | A | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2346+1793G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450423 | |||||||
| chr3:9450583 | A | G | 1 | a0001c0001t0005g0151 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2346+1953A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450583 | |||||||
| chr3:9450592 | T | C | 49 | a0001c0001t0001g0068 a0001c0001t0001g0185 a0001c0001t0001g0186 others(46): Show |
50 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.2346+1962T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450592 | |||||||
| chr3:9450656 | T | C | 17 | a0001c0001t0001g0068 a0001c0001t0001g0185 a0001c0001t0001g0186 others(14): Show |
18 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.2346+2026T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450656 | |||||||
| chr3:9450704 | A | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2346+2074A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450704 | |||||||
| chr3:9450749 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2346+2119A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450749 | |||||||
| chr3:9450872 | T | G | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2346+2242T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450872 | |||||||
| chr3:9450923 | T | C | 1 | a0001c0001t0040g0231 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2346+2293T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9450923 | |||||||
| chr3:9451559 | T | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2347-2180T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451559 | |||||||
| chr3:9451560 | A | G | 31 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(28): Show |
31 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.2347-2179A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451560 | |||||||
| chr3:9451566 | A | G | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2347-2173A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451566 | |||||||
| chr3:9451578 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2347-2161G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451578 | |||||||
| chr3:9451631 | C | T | 18 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(15): Show |
19 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2347-2108C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451631 | |||||||
| chr3:9451684 | A | C | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2347-2055A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451684 | |||||||
| chr3:9451727 | C | T | 45 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(42): Show |
45 | HG00621.hp1 HG00639.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.2347-2012C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451727 | |||||||
| chr3:9451728 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2347-2011G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451728 | |||||||
| chr3:9451789 | G | A | 28 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(25): Show |
28 | HG01081.hp2 HG02055.hp2 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.2347-1950G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451789 | |||||||
| chr3:9451956 | C | G | 1 | a0002c0002t0006g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2347-1783C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9451956 | |||||||
| chr3:9452201 | A | T | 1 | a0001c0001t0004g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2347-1538A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452201 | |||||||
| chr3:9452331 | C | G | 1 | a0001c0001t0004g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2347-1408C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452331 | |||||||
| chr3:9452590 | TGTTTACA others(1): Show |
T | 81 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(78): Show |
82 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2347-1140_2347-113 others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452590 | ||||||
| chr3:9452631 | A | G | 30 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(27): Show |
30 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.2347-1108A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452631 | |||||||
| chr3:9452659 | A | AT | 17 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0085 others(14): Show |
17 | HG01069.hp1 HG01099.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2347-1055dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | A | ATT | 10 | a0001c0001t0004g0119 a0001c0001t0041g0175 a0001c0001t0046g0177 others(7): Show |
10 | HG01071.hp1 HG01081.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.2347-1056_2347-105 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | A | ATTT | 21 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(18): Show |
21 | HG01099.hp1 HG02451.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.2347-1057_2347-105 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | A | ATTTT | 8 | a0001c0001t0004g0158 a0001c0001t0004g0160 a0001c0001t0004g0162 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347-1058_2347-105 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | A | ATTTTT | 16 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0002g0190 others(13): Show |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.2347-1059_2347-105 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | A | ATTTTTTT others(4): Show |
1 | a0001c0007t0047g0006 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2347-1065_2347-105 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | A | ATTTTTTT others(5): Show |
1 | a0001c0007t0029g0005 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2347-1066_2347-105 others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | AT | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(47): Show |
51 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2347-1055delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452659 | ATTTTT | A | 32 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0213 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2347-1059_2347-105 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr3 | 9452659 | ||||||
| chr3:9452726 | A | G | 32 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2347-1013A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452726 | |||||||
| chr3:9452813 | C | T | 1 | a0001c0010t0001g0042 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2347-926C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452813 | |||||||
| chr3:9452827 | A | T | 15 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(12): Show |
16 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.2347-912A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452827 | |||||||
| chr3:9452944 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2347-795A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9452944 | |||||||
| chr3:9453093 | T | C | 1 | a0001c0001t0004g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2347-646T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453093 | |||||||
| chr3:9453364 | G | A | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2347-375G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453364 | |||||||
| chr3:9453394 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2347-345C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453394 | |||||||
| chr3:9453435 | C | A | 81 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(78): Show |
82 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2347-304C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453435 | |||||||
| chr3:9453659 | C | G | 1 | a0001c0001t0005g0100 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2347-80C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453659 | |||||||
| chr3:9453699 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2347-40A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453699 | |||||||
| chr3:9453701 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
106 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2347-38A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 16/22 | chr3 | 9453701 | |||||||
| chr3:9454243 | G | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2476+375G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454243 | |||||||
| chr3:9454260 | G | T | 3 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0044g0178 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2476+392G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454260 | |||||||
| chr3:9454293 | T | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0045 others(2): Show |
5 | HG01346.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476+425T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454293 | |||||||
| chr3:9454478 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2476+610G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454478 | |||||||
| chr3:9454524 | G | T | 3 | a0001c0001t0001g0082 a0001c0001t0002g0090 a0001c0001t0036g0017 |
3 | NA18973.hp2 NA18999.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2476+656G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454524 | |||||||
| chr3:9454546 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2476+678C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454546 | |||||||
| chr3:9454564 | G | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2476+696G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454564 | |||||||
| chr3:9454576 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2476+708C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454576 | |||||||
| chr3:9454622 | C | CA | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0051 others(20): Show |
23 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.2476+782dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | C | CAA | 5 | a0001c0001t0001g0054 a0001c0001t0001g0082 a0001c0001t0002g0046 others(2): Show |
5 | HG00621.hp2 HG02074.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476+781_2476+782d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0006g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2476+773_2476+782d others(12): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | C | CAAAAAAA others(4): Show |
1 | a0002c0002t0013g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2476+772_2476+782d others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | CA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2476+782delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | CAA | C | 6 | a0001c0001t0002g0024 a0001c0001t0003g0226 a0001c0001t0003g0230 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2476+781_2476+782d others(4): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | CAAA | C | 34 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0004g0114 others(31): Show |
34 | HG01070.hp1 HG01081.hp2 HG01516.hp1 others(31): Show |
intron_variant | MODIFIER | c.2476+780_2476+782d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0186 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2476+772_2476+782d others(13): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454622 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0026g0189 others(1): Show |
4 | HG00323.hp2 HG01515.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2476+771_2476+782d others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9454622 | ||||||
| chr3:9454637 | A | C | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2476+769A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454637 | |||||||
| chr3:9454638 | A | C | 29 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(26): Show |
29 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.2476+770A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454638 | |||||||
| chr3:9454639 | A | C | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2476+771A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454639 | |||||||
| chr3:9454644 | A | C | 2 | a0001c0001t0008g0039 a0001c0001t0008g0079 |
2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2476+776A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9454644 | |||||||
| chr3:9455168 | C | CT | 27 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0108 others(24): Show |
27 | HG01099.hp2 HG01109.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.2476+1322dupT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | ||||||
| chr3:9455168 | C | CTT | 5 | a0001c0001t0001g0138 a0001c0001t0004g0119 a0001c0001t0004g0236 others(2): Show |
5 | HG01081.hp2 HG01175.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2476+1321_2476+132 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | ||||||
| chr3:9455168 | C | CTTT | 20 | a0001c0001t0003g0215 a0001c0001t0003g0216 a0001c0001t0003g0218 others(17): Show |
20 | HG01884.hp1 HG02129.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.2476+1320_2476+132 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | ||||||
| chr3:9455168 | C | CTTTT | 13 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(10): Show |
13 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.2476+1319_2476+132 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | ||||||
| chr3:9455168 | CT | C | 12 | a0001c0001t0002g0190 a0001c0001t0033g0089 a0002c0002t0006g0004 others(9): Show |
13 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2476+1322delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455168 | ||||||
| chr3:9455173 | T | C | 11 | a0001c0001t0002g0190 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+1305T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455173 | |||||||
| chr3:9455175 | T | C | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2476+1307T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455175 | |||||||
| chr3:9455193 | A | G | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+1325A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455193 | |||||||
| chr3:9455208 | G | A | 1 | a0001c0001t0022g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2476+1340G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455208 | |||||||
| chr3:9455230 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2476+1362C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455230 | |||||||
| chr3:9455297 | G | A | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2476+1429G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455297 | |||||||
| chr3:9455359 | G | T | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+1491G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455359 | |||||||
| chr3:9455665 | GT | G | 91 | a0001c0001t0002g0190 a0001c0001t0003g0209 a0001c0001t0003g0210 others(88): Show |
92 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.2476+1799delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9455665 | ||||||
| chr3:9455709 | G | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0045 others(2): Show |
5 | HG01346.hp2 NA18968.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2476+1841G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455709 | |||||||
| chr3:9455737 | T | C | 3 | a0003c0005t0009g0201 a0003c0005t0009g0202 a0003c0005t0011g0200 |
3 | HG01069.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2476+1869T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455737 | |||||||
| chr3:9455915 | A | G | 3 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0044g0178 |
3 | HG02145.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2476+2047A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9455915 | |||||||
| chr3:9456198 | G | A | 30 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(27): Show |
30 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.2476+2330G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456198 | |||||||
| chr3:9456200 | C | T | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2332C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456200 | |||||||
| chr3:9456201 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2476+2333G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456201 | |||||||
| chr3:9456201 | GT | G | 76 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(73): Show |
77 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.2476+2335delT | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9456201 | ||||||
| chr3:9456211 | C | G | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2476+2343C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456211 | |||||||
| chr3:9456251 | G | A | 3 | a0001c0003t0009g0194 a0001c0003t0011g0195 a0001c0003t0011g0204 |
3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2476+2383G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456251 | |||||||
| chr3:9456286 | G | A | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2476+2418G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456286 | |||||||
| chr3:9456336 | C | T | 1 | a0002c0002t0006g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2476+2468C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456336 | |||||||
| chr3:9456344 | C | T | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+2476C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456344 | |||||||
| chr3:9456346 | T | C | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+2478T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456346 | |||||||
| chr3:9456458 | G | A | 12 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2590G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456458 | |||||||
| chr3:9456459 | G | A | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2591G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456459 | |||||||
| chr3:9456480 | T | TA | 65 | a0001c0001t0002g0142 a0001c0001t0003g0209 a0001c0001t0003g0210 others(62): Show |
65 | HG00621.hp1 HG00639.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.2476+2629dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9456480 | ||||||
| chr3:9456480 | T | TAA | 14 | a0001c0001t0016g0153 a0001c0001t0016g0154 a0001c0001t0035g0206 others(11): Show |
15 | HG00735.hp1 HG00741.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.2476+2628_2476+262 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9456480 | ||||||
| chr3:9456562 | A | G | 1 | a0001c0001t0033g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2476+2694A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456562 | |||||||
| chr3:9456617 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2476+2749T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456617 | |||||||
| chr3:9456751 | G | T | 1 | a0001c0001t0022g0225 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2476+2883G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456751 | |||||||
| chr3:9456835 | G | A | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+2967G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456835 | |||||||
| chr3:9456970 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0002g0124 |
2 | HG01192.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2476+3102G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9456970 | |||||||
| chr3:9457030 | G | GAAGA | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+3169_2476+317 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9457030 | ||||||
| chr3:9457117 | T | A | 1 | a0004c0004t0021g0078 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2476+3249T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457117 | |||||||
| chr3:9457149 | A | G | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+3281A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457149 | |||||||
| chr3:9457190 | TTAA | T | 2 | a0001c0001t0001g0106 a0001c0001t0002g0105 |
2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2476+3329_2476+333 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9457190 | ||||||
| chr3:9457372 | C | A | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2476+3504C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457372 | |||||||
| chr3:9457373 | G | A | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2476+3505G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457373 | |||||||
| chr3:9457376 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2476+3508A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457376 | |||||||
| chr3:9457444 | G | A | 32 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2476+3576G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457444 | |||||||
| chr3:9457566 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2476+3698G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457566 | |||||||
| chr3:9457578 | T | A | 1 | a0001c0001t0018g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2476+3710T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457578 | |||||||
| chr3:9457579 | A | T | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2476+3711A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457579 | |||||||
| chr3:9457636 | C | T | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+3768C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457636 | |||||||
| chr3:9457764 | A | G | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2476+3896A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457764 | |||||||
| chr3:9457991 | T | C | 1 | a0001c0001t0002g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2476+4123T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9457991 | |||||||
| chr3:9458066 | G | A | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2476+4198G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458066 | |||||||
| chr3:9458108 | T | C | 2 | a0002c0002t0013g0179 a0002c0002t0013g0183 |
2 | HG03688.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2476+4240T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458108 | |||||||
| chr3:9458514 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2476+4646G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458514 | |||||||
| chr3:9458517 | G | A | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2476+4649G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458517 | |||||||
| chr3:9458606 | C | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2476+4738C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458606 | |||||||
| chr3:9458661 | A | G | 1 | a0001c0001t0020g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2476+4793A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9458661 | |||||||
| chr3:9459164 | G | A | 9 | a0001c0001t0001g0083 a0001c0001t0014g0031 a0001c0001t0014g0032 others(6): Show |
9 | HG02040.hp2 HG02080.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.2477-5261G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459164 | |||||||
| chr3:9459263 | G | C | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2477-5162G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459263 | |||||||
| chr3:9459304 | T | G | 1 | a0002c0002t0013g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2477-5121T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459304 | |||||||
| chr3:9459419 | G | A | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2477-5006G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459419 | |||||||
| chr3:9459476 | A | C | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-4949A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459476 | |||||||
| chr3:9459629 | A | C | 33 | a0001c0001t0002g0010 a0001c0001t0004g0114 a0001c0001t0004g0115 others(30): Show |
34 | HG00673.hp2 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.2477-4796A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459629 | |||||||
| chr3:9459638 | C | A | 1 | a0001c0001t0028g0025 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2477-4787C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459638 | |||||||
| chr3:9459712 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2477-4713A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459712 | |||||||
| chr3:9459714 | C | CA | 46 | a0001c0001t0001g0085 a0001c0001t0003g0209 a0001c0001t0003g0211 others(43): Show |
46 | HG00621.hp1 HG00639.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.2477-4693dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9459714 | ||||||
| chr3:9459714 | C | CAA | 15 | a0001c0001t0003g0210 a0001c0001t0003g0230 a0001c0001t0004g0114 others(12): Show |
15 | HG01081.hp2 HG01978.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-4694_2477-469 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9459714 | ||||||
| chr3:9459941 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2477-4484C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9459941 | |||||||
| chr3:9460025 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2477-4400A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460025 | |||||||
| chr3:9460027 | C | G | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2477-4398C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460027 | |||||||
| chr3:9460089 | C | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-4336C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460089 | |||||||
| chr3:9460145 | T | C | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-4280T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460145 | |||||||
| chr3:9460170 | A | G | 11 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2477-4255A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460170 | |||||||
| chr3:9460204 | T | C | 1 | a0001c0001t0008g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2477-4221T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460204 | |||||||
| chr3:9460210 | A | T | 1 | a0001c0001t0008g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2477-4215A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460210 | |||||||
| chr3:9460245 | A | G | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-4180A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460245 | |||||||
| chr3:9460263 | T | TA | 10 | a0001c0001t0026g0189 a0002c0002t0006g0004 a0002c0002t0006g0181 others(7): Show |
11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2477-4150dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9460263 | ||||||
| chr3:9460395 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2477-4030C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460395 | |||||||
| chr3:9460524 | C | T | 35 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(32): Show |
35 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2477-3901C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460524 | |||||||
| chr3:9460643 | A | G | 1 | a0001c0001t0017g0018 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2477-3782A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460643 | |||||||
| chr3:9460779 | T | C | 92 | a0001c0001t0002g0190 a0001c0001t0003g0209 a0001c0001t0003g0210 others(89): Show |
93 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.2477-3646T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460779 | |||||||
| chr3:9460813 | C | T | 1 | a0002c0002t0006g0184 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2477-3612C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9460813 | |||||||
| chr3:9461269 | A | G | 1 | a0001c0001t0024g0019 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2477-3156A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9461269 | |||||||
| chr3:9461510 | G | T | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-2915G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9461510 | |||||||
| chr3:9461575 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-2850A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9461575 | |||||||
| chr3:9462359 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2477-2066G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462359 | |||||||
| chr3:9462415 | G | A | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2477-2010G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462415 | |||||||
| chr3:9462432 | A | G | 1 | a0001c0001t0007g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2477-1993A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462432 | |||||||
| chr3:9462575 | A | G | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2477-1850A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462575 | |||||||
| chr3:9462586 | CA | C | 13 | a0001c0001t0006g0205 a0001c0003t0011g0195 a0001c0003t0042g0198 others(10): Show |
14 | HG00735.hp1 HG00741.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.2477-1824delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9462586 | ||||||
| chr3:9462823 | T | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-1602T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462823 | |||||||
| chr3:9462838 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2477-1587A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462838 | |||||||
| chr3:9462905 | G | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-1520G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462905 | |||||||
| chr3:9462948 | T | A | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2477-1477T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9462948 | |||||||
| chr3:9463021 | C | A | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-1404C>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463021 | |||||||
| chr3:9463163 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0060 a0001c0001t0001g0061 others(5): Show |
8 | HG01109.hp1 HG02809.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2477-1262G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463163 | |||||||
| chr3:9463201 | T | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0109 others(3): Show |
6 | HG02258.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-1224T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463201 | |||||||
| chr3:9463275 | G | C | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2477-1150G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463275 | |||||||
| chr3:9463554 | C | T | 93 | a0001c0001t0002g0190 a0001c0001t0003g0209 a0001c0001t0003g0210 others(90): Show |
94 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.2477-871C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463554 | |||||||
| chr3:9463665 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0002g0012 |
2 | HG01258.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2477-760A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463665 | |||||||
| chr3:9463778 | T | C | 18 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(15): Show |
18 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.2477-647T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463778 | |||||||
| chr3:9463787 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0002g0010 a0001c0001t0008g0002 others(1): Show |
4 | HG00673.hp2 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2477-638A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463787 | |||||||
| chr3:9463803 | A | G | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-622A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463803 | |||||||
| chr3:9463823 | T | C | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2477-602T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9463823 | |||||||
| chr3:9464107 | G | A | 1 | a0001c0001t0026g0189 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2477-318G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9464107 | |||||||
| chr3:9464127 | CATAAATA others(1): Show |
C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2477-291_2477-284d others(10): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr3 | 9464127 | ||||||
| chr3:9464367 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0002g0010 others(3): Show |
6 | HG00438.hp1 HG00673.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.2477-58G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 17/22 | chr3 | 9464367 | |||||||
| chr3:9464770 | T | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2724+98T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464770 | |||||||
| chr3:9464889 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2724+217A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464889 | |||||||
| chr3:9464943 | A | G | 1 | a0001c0001t0027g0028 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2724+271A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464943 | |||||||
| chr3:9464966 | G | A | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2724+294G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9464966 | |||||||
| chr3:9465024 | A | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2724+352A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465024 | |||||||
| chr3:9465054 | T | C | 15 | a0001c0001t0002g0190 a0001c0003t0009g0193 a0001c0003t0009g0194 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2724+382T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465054 | |||||||
| chr3:9465086 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2724+414A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465086 | |||||||
| chr3:9465309 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2724+637A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465309 | |||||||
| chr3:9465341 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2724+669T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465341 | |||||||
| chr3:9465573 | C | T | 10 | a0002c0002t0006g0004 a0002c0002t0006g0181 a0002c0002t0006g0182 others(7): Show |
11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2724+901C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465573 | |||||||
| chr3:9465587 | C | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0023 others(29): Show |
32 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.2724+915C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465587 | |||||||
| chr3:9465630 | T | A | 10 | a0002c0002t0006g0004 a0002c0002t0006g0181 a0002c0002t0006g0182 others(7): Show |
11 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2724+958T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465630 | |||||||
| chr3:9465695 | C | T | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2724+1023C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465695 | |||||||
| chr3:9465715 | T | C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2724+1043T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9465715 | |||||||
| chr3:9466170 | C | G | 1 | a0001c0001t0006g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2724+1498C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466170 | |||||||
| chr3:9466171 | C | G | 1 | a0001c0001t0025g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2724+1499C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466171 | |||||||
| chr3:9466224 | C | G | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2724+1552C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466224 | |||||||
| chr3:9466283 | G | C | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2724+1611G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466283 | |||||||
| chr3:9466287 | C | CA | 13 | a0001c0001t0001g0048 a0001c0001t0002g0046 a0001c0001t0002g0055 others(10): Show |
13 | HG00621.hp1 HG01934.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2724+1637dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9466287 | ||||||
| chr3:9466287 | CA | C | 52 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0072 others(49): Show |
53 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.2724+1637delA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9466287 | ||||||
| chr3:9466287 | CAA | C | 23 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0002g0024 others(20): Show |
23 | HG01070.hp1 HG01109.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2724+1636_2724+163 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9466287 | ||||||
| chr3:9466304 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2724+1632A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466304 | |||||||
| chr3:9466306 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2724+1634A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466306 | |||||||
| chr3:9466473 | A | C | 33 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2724+1801A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466473 | |||||||
| chr3:9466581 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2724+1909A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466581 | |||||||
| chr3:9466613 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2724+1941T>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466613 | |||||||
| chr3:9466640 | C | T | 10 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(7): Show |
10 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2724+1968C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466640 | |||||||
| chr3:9466672 | G | C | 6 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0119 others(3): Show |
6 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2724+2000G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466672 | |||||||
| chr3:9466708 | A | G | 10 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(7): Show |
10 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2724+2036A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466708 | |||||||
| chr3:9466854 | A | G | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2724+2182A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466854 | |||||||
| chr3:9466994 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2724+2322A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9466994 | |||||||
| chr3:9467039 | A | C | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2724+2367A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467039 | |||||||
| chr3:9467120 | G | A | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2724+2448G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467120 | |||||||
| chr3:9467199 | C | CA | 34 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0021 others(31): Show |
35 | HG00438.hp2 HG00597.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.2724+2552dupA | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | ||||||
| chr3:9467199 | C | CAA | 11 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0054 others(8): Show |
11 | HG00621.hp2 HG00741.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2724+2551_2724+255 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | ||||||
| chr3:9467199 | C | CAAA | 5 | a0001c0003t0009g0197 a0001c0003t0011g0204 a0003c0005t0009g0201 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2724+2550_2724+255 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | ||||||
| chr3:9467199 | C | CAAAA | 6 | a0001c0003t0009g0193 a0001c0003t0009g0194 a0001c0003t0009g0203 others(3): Show |
6 | HG01175.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2724+2549_2724+255 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | ||||||
| chr3:9467199 | CAA | C | 11 | a0001c0001t0003g0210 a0001c0001t0003g0215 a0001c0001t0004g0166 others(8): Show |
11 | HG00621.hp1 HG01978.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2724+2551_2724+255 others(6): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | ||||||
| chr3:9467199 | CAAA | C | 43 | a0001c0001t0003g0209 a0001c0001t0003g0211 a0001c0001t0003g0213 others(40): Show |
43 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.2724+2550_2724+255 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467199 | ||||||
| chr3:9467214 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0003g0228 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2724+2545_2724+255 others(15): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467214 | ||||||
| chr3:9467215 | AAAAAAAA others(3): Show |
A | 7 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0230 others(4): Show |
7 | HG01070.hp1 HG01255.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.2724+2546_2724+255 others(14): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr3 | 9467215 | ||||||
| chr3:9467263 | G | A | 10 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(7): Show |
10 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2724+2591G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467263 | |||||||
| chr3:9467451 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2724+2779A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467451 | |||||||
| chr3:9467496 | G | A | 15 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(12): Show |
15 | HG01081.hp2 HG02055.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2724+2824G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467496 | |||||||
| chr3:9467514 | C | T | 1 | a0001c0001t0041g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2724+2842C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467514 | |||||||
| chr3:9467744 | C | T | 15 | a0001c0001t0002g0190 a0001c0003t0009g0193 a0001c0003t0009g0194 others(12): Show |
15 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2725-2715C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467744 | |||||||
| chr3:9467795 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2725-2664C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467795 | |||||||
| chr3:9467799 | C | T | 7 | a0001c0001t0012g0170 a0001c0001t0012g0172 a0001c0001t0012g0173 others(4): Show |
7 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2725-2660C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467799 | |||||||
| chr3:9467869 | G | C | 1 | a0001c0001t0038g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2725-2590G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467869 | |||||||
| chr3:9467962 | C | G | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2725-2497C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9467962 | |||||||
| chr3:9468392 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2725-2067C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468392 | |||||||
| chr3:9468404 | C | T | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2725-2055C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468404 | |||||||
| chr3:9468405 | C | T | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2725-2054C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468405 | |||||||
| chr3:9468702 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2725-1757A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468702 | |||||||
| chr3:9468788 | G | A | 1 | a0002c0002t0034g0187 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2725-1671G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468788 | |||||||
| chr3:9468806 | G | A | 1 | a0001c0001t0025g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2725-1653G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468806 | |||||||
| chr3:9468938 | A | G | 3 | a0001c0001t0004g0117 a0001c0001t0007g0116 a0001c0001t0015g0120 |
3 | HG02886.hp2 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2725-1521A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9468938 | |||||||
| chr3:9469480 | T | A | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2725-979T>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469480 | |||||||
| chr3:9469525 | G | C | 1 | a0001c0001t0002g0012 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2725-934G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469525 | |||||||
| chr3:9469627 | C | T | 25 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(22): Show |
25 | HG00621.hp1 HG00639.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2725-832C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469627 | |||||||
| chr3:9469682 | C | T | 1 | a0002c0002t0006g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2725-777C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469682 | |||||||
| chr3:9469709 | G | A | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2725-750G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469709 | |||||||
| chr3:9469871 | C | T | 1 | a0001c0001t0044g0178 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2725-588C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469871 | |||||||
| chr3:9469916 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2725-543G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9469916 | |||||||
| chr3:9470008 | C | T | 1 | a0001c0001t0040g0231 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2725-451C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470008 | |||||||
| chr3:9470011 | C | T | 32 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(29): Show |
32 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.2725-448C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470011 | |||||||
| chr3:9470045 | C | T | 2 | a0001c0001t0025g0077 a0001c0001t0046g0177 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2725-414C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470045 | |||||||
| chr3:9470052 | C | T | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2725-407C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470052 | |||||||
| chr3:9470291 | G | A | 11 | a0001c0001t0006g0205 a0002c0002t0006g0004 a0002c0002t0006g0181 others(8): Show |
12 | HG00735.hp1 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.2725-168G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 18/22 | chr3 | 9470291 | |||||||
| chr3:9470978 | G | A | 1 | a0001c0001t0004g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3195+49G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9470978 | |||||||
| chr3:9471023 | A | G | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3195+94A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471023 | |||||||
| chr3:9471098 | T | C | 1 | a0004c0004t0019g0059 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3195+169T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471098 | |||||||
| chr3:9471435 | G | C | 6 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 others(3): Show |
6 | HG01070.hp1 HG01255.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3195+506G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471435 | |||||||
| chr3:9471728 | G | A | 5 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0213 others(2): Show |
5 | HG01074.hp1 HG01192.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.3195+799G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471728 | |||||||
| chr3:9471785 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0002g0131 |
3 | HG00099.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.3195+856G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471785 | |||||||
| chr3:9471877 | G | T | 1 | a0001c0001t0038g0044 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3195+948G>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9471877 | |||||||
| chr3:9472013 | TAGA | T | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.3195+1087_3195+108 others(7): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | 9472013 | ||||||
| chr3:9472067 | C | T | 1 | a0001c0001t0004g0119 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3195+1138C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472067 | |||||||
| chr3:9472173 | T | C | 9 | a0001c0001t0002g0190 a0001c0003t0009g0194 a0001c0003t0009g0197 others(6): Show |
9 | HG01099.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3196-1063T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472173 | |||||||
| chr3:9472190 | A | ACACT | 3 | a0001c0001t0001g0146 a0001c0001t0002g0069 a0004c0004t0021g0078 |
3 | HG02132.hp1 NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3196-1046_3196-104 others(8): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472190 | |||||||
| chr3:9472191 | A | ACACTT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(35): Show |
38 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.3196-1043_3196-103 others(9): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | 9472191 | ||||||
| chr3:9472191 | A | T | 3 | a0001c0001t0001g0146 a0001c0001t0002g0069 a0004c0004t0021g0078 |
3 | HG02132.hp1 NA18998.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3196-1045A>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472191 | |||||||
| chr3:9472332 | G | A | 61 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(58): Show |
62 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.3196-904G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472332 | |||||||
| chr3:9472544 | A | G | 2 | a0001c0007t0029g0005 a0001c0007t0047g0006 |
2 | HG02129.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.3196-692A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472544 | |||||||
| chr3:9472644 | A | G | 1 | a0002c0002t0006g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3196-592A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472644 | |||||||
| chr3:9472724 | C | CCACCTCC others(7): Show |
3 | a0001c0001t0035g0206 a0001c0007t0029g0005 a0001c0007t0047g0006 |
3 | HG02129.hp2 HG02723.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3196-510_3196-497d others(16): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr3 | 9472724 | ||||||
| chr3:9472752 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3196-484C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472752 | |||||||
| chr3:9472791 | G | A | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3196-445G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472791 | |||||||
| chr3:9472896 | G | A | 76 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(73): Show |
77 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.3196-340G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472896 | |||||||
| chr3:9472907 | C | T | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3196-329C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9472907 | |||||||
| chr3:9473024 | A | G | 1 | a0001c0001t0020g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3196-212A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473024 | |||||||
| chr3:9473153 | T | C | 3 | a0001c0001t0035g0206 a0001c0007t0029g0005 a0001c0007t0047g0006 |
3 | HG02129.hp2 HG02723.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3196-83T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473153 | |||||||
| chr3:9473172 | G | A | 91 | a0001c0001t0002g0190 a0001c0001t0003g0209 a0001c0001t0003g0210 others(88): Show |
92 | HG00621.hp1 HG00639.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.3196-64G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473172 | |||||||
| chr3:9473204 | C | T | 1 | a0001c0001t0007g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3196-32C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 19/22 | chr3 | 9473204 | |||||||
| chr3:9473551 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3497+14T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473551 | |||||||
| chr3:9473608 | G | C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3497+71G>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473608 | |||||||
| chr3:9473711 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3497+174C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473711 | |||||||
| chr3:9473910 | C | T | 1 | a0001c0001t0046g0177 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3497+373C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9473910 | |||||||
| chr3:9474101 | A | C | 1 | a0001c0001t0035g0206 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3498-348A>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | chr3 | 9474101 | |||||||
| chr3:9474260 | GGTT | G | 9 | a0001c0001t0004g0114 a0001c0001t0004g0115 a0001c0001t0004g0117 others(6): Show |
9 | HG01081.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3498-181_3498-179d others(5): Show |
SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr3 | 9474260 | ||||||
| chr3:9474656 | G | A | 7 | a0001c0001t0001g0072 a0001c0001t0010g0071 a0001c0001t0017g0018 others(4): Show |
7 | HG00735.hp2 HG02559.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.3631+74G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474656 | |||||||
| chr3:9474700 | G | A | 1 | a0001c0001t0025g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3631+118G>A | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474700 | |||||||
| chr3:9474840 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3632-228C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474840 | |||||||
| chr3:9474902 | T | C | 12 | a0001c0001t0004g0158 a0001c0001t0004g0159 a0001c0001t0004g0160 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.3632-166T>C | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 21/22 | chr3 | 9474902 | |||||||
| chr3:9475245 | C | G | 1 | a0001c0001t0004g0176 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3720+89C>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475245 | |||||||
| chr3:9475389 | A | G | 2 | a0001c0001t0016g0153 a0001c0001t0016g0154 |
2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3721-94A>G | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475389 | |||||||
| chr3:9475448 | C | T | 1 | a0001c0003t0009g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3721-35C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475448 | |||||||
| chr3:9475450 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3721-33C>T | SETD5 | ENSG00000168137.20 | transcript | ENST00000402198.7 | protein_coding | 22/22 | chr3 | 9475450 |