Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 56341 |
|---|---|
| ensemblid | ENSG00000111218.12 |
| hgncid | 5188 |
| symbol | PRMT8 |
| name | protein arginine methyltransferase 8 |
| refseq_nuc | NM_019854.5 |
| refseq_prot | NP_062828.3 |
| ensembl_nuc | ENST00000382622.4 |
| ensembl_prot | ENSP00000372067.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 3491203 |
| end | 3593973 |
| strand | + |
| ver | v1.2 |
| region | chr12:3491203-3593973 |
| region5000 | chr12:3486203-3598973 |
| regionname0 | PRMT8_chr12_3491203_3593973 |
| regionname5000 | PRMT8_chr12_3486203_3598973 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 394 | 363 | 89 | 68 | 154 | 16 | 34 | 112 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0002 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1185 | 311 | 70 | 60 | 131 | 16 | 32 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0002 | 0/0 | 1185 | 36 | 14 | 5 | 15 | 0 | 2 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0003 | 0/0 | 1185 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0004 | 0/0 | 1185 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0005 | 0/0 | 1185 | 4 | 3 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0006 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0007 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0008 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0009 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| c0010 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1215 | 303 | 65 | 55 | 134 | 16 | 31 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0002 | 0/0 | 1215 | 37 | 16 | 4 | 15 | 0 | 2 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0003 | 0/0 | 1215 | 8 | 0 | 8 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0004 | 0/0 | 1221 | 3 | 0 | 0 | 3 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0005 | 0/0 | 1221 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0006 | 0/0 | 1215 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0007 | 0/0 | 1215 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0008 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0009 | 0/0 | 1215 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0010 | 0/0 | 1215 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0011 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0012 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0013 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| t0014 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1185 | 311 | 70 | 60 | 131 | 16 | 32 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0002 | 0/0 | 1185 | 36 | 14 | 5 | 15 | 0 | 2 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0003 | 0/0 | 1185 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0004 | 0/0 | 1185 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0005 | 0/0 | 1185 | 4 | 3 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0006 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0007 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0009 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0010 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0002c0008 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2399 | 288 | 60 | 52 | 127 | 16 | 31 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0002 | 0/0 | 2399 | 4 | 3 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0003 | 0/0 | 2399 | 8 | 0 | 8 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0004 | 0/0 | 2405 | 3 | 0 | 0 | 3 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0006 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0007 | 0/0 | 2399 | 2 | 2 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0008 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0010 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0012 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0013 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0001t0014 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0002t0002 | 0/0 | 2399 | 32 | 13 | 4 | 13 | 0 | 2 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0002t0005 | 0/0 | 2405 | 2 | 0 | 0 | 2 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0002t0009 | 0/0 | 2399 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0002t0011 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0003t0001 | 0/0 | 2399 | 4 | 0 | 0 | 4 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0004t0001 | 0/0 | 2399 | 4 | 2 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0005t0001 | 0/0 | 2399 | 3 | 2 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0005t0006 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0006t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0007t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0009t0001 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0001c0010t0002 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| a0002c0008t0001 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | copy fasta | chr12 | 3486203 | 3598973 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0010g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0012g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0001t0014g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0002t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0004t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0005t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0005t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0005t0006g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0007t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0009t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0001c0010t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| a0002c0008t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0321 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01069 | hp1 | a0001 | c0002 | t0009 | g0094 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0334 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01346 | hp2 | a0001 | c0005 | t0001 | g0344 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0277 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0338 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0282 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0270 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0309 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0348 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0314 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02647 | hp1 | a0001 | c0005 | t0006 | g0359 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0322 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0346 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02895 | hp1 | a0001 | c0002 | t0011 | g0208 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0002 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03098 | hp1 | a0002 | c0008 | t0001 | g0355 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0097 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0313 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0296 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0302 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0345 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18951 | hp1 | a0001 | c0007 | t0001 | g0226 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18981 | hp1 | a0001 | c0006 | t0001 | g0043 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18990 | hp2 | a0001 | c0010 | t0002 | g0216 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18992 | hp1 | a0001 | c0002 | t0005 | g0194 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18995 | hp1 | a0001 | c0009 | t0001 | g0250 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0102 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19043 | hp1 | a0001 | c0001 | t0012 | g0316 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0354 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0155 | AFR | YRI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0018 | AFR | ASW | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0308 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | GIH | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0300 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA18955 | hp2 | a0001 | c0002 | t0005 | g0195 | EAS | JPT | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | LWK | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0357 | REF | REF | PRMT8_chr12_3486203_3598973 | PRMT8 | chr12 | 3486203 | 3598973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3592301
|
G | C | 1 | a0002 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1050G>C | p.Arg350Ser | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/10 | 1473/2399 | 1050/1185 | 350/394 | chr12 | 3592301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3540614
|
C | T | 1 | a0001c0010 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.84C>T | p.Ser28Ser | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 507/2399 | 84/1185 | 28/394 | chr12 | 3540614 | ||
| chr12:3540632
|
C | G | 1 | a0001c0005 | 4 | HG01346.hp2 HG02145.hp2 HG02559.hp1 others(1): Show |
synonymous_variant | LOW | c.102C>G | p.Pro34Pro | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 525/2399 | 102/1185 | 34/394 | chr12 | 3540632 | ||
| chr12:3540641
|
C | T | 1 | a0001c0009 | 1 | NA18995.hp1 | synonymous_variant | LOW | c.111C>T | p.Val37Val | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 534/2399 | 111/1185 | 37/394 | chr12 | 3540641 | ||
| chr12:3540764
|
C | T | 1 | a0001c0004 | 4 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(1): Show |
synonymous_variant | LOW | c.234C>T | p.Asp78Asp | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 657/2399 | 234/1185 | 78/394 | chr12 | 3540764 | ||
| chr12:3540788
|
C | T | 1 | a0001c0010 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.258C>T | p.His86His | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/10 | 681/2399 | 258/1185 | 86/394 | chr12 | 3540788 | ||
| chr12:3568821
|
G | A | 2 | a0001c0006a0001c0007 | 2 | NA18951.hp1 NA18981.hp1 |
synonymous_variant | LOW | c.597G>A | p.Thr199Thr | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/10 | 1020/2399 | 597/1185 | 199/394 | chr12 | 3568821 | ||
| chr12:3592298
|
G | A | 2 | a0001c0002a0001c0010 | 37 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(34): Show |
synonymous_variant | LOW | c.1047G>A | p.Arg349Arg | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/10 | 1470/2399 | 1047/1185 | 349/394 | chr12 | 3592298 | ||
| chr12:3592301
|
G | A | 2 | a0001c0003a0001c0006 | 5 | NA18967.hp1 NA18981.hp1 NA18984.hp1 others(2): Show |
synonymous_variant | LOW | c.1050G>A | p.Arg350Arg | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/10 | 1473/2399 | 1050/1185 | 350/394 | chr12 | 3592301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3491220
|
G | T | 1 | a0001c0001t0014 | 1 | HG02976.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-406G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/10 | chr12 | 3491220 | ||||||
| chr12:3491269
|
C | A | 1 | a0001c0001t0003 | 8 | HG01167.hp1 HG01169.hp2 HG01256.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-357C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/10 | 357 | chr12 | 3491269 | |||||
| chr12:3491293
|
A | ACCGCCG | 2 | a0001c0001t0004a0001c0002t0005 | 5 | NA18955.hp2 NA18968.hp1 NA18987.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-319_-314dupCGCCGC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/10 | 313 | INFO_REALIGN_3_PRIME | chr12 | 3491293 | ||||
| chr12:3593210
|
G | A | 1 | a0001c0001t0008 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 28 | chr12 | 3593210 | |||||
| chr12:3593259
|
G | C | 1 | a0001c0002t0009 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 77 | chr12 | 3593259 | |||||
| chr12:3593389
|
C | G | 1 | a0001c0001t0013 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 207 | chr12 | 3593389 | |||||
| chr12:3593423
|
G | A | 1 | a0001c0001t0010 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 241 | chr12 | 3593423 | |||||
| chr12:3593453
|
G | T | 1 | a0001c0001t0007 | 2 | HG02615.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*271G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 271 | chr12 | 3593453 | |||||
| chr12:3593623
|
C | A | 7 | a0001c0001t0002a0001c0001t0007a0001c0002t0002others(4): Show | 43 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*441C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 441 | chr12 | 3593623 | |||||
| chr12:3593626
|
G | A | 1 | a0001c0002t0011 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 444 | chr12 | 3593626 | |||||
| chr12:3593662
|
C | T | 1 | a0001c0001t0012 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 480 | chr12 | 3593662 | |||||
| chr12:3593736
|
G | A | 2 | a0001c0001t0006a0001c0005t0006 | 2 | HG02647.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*554G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 10/10 | 554 | chr12 | 3593736 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:3491729
|
G | C | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+29G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491729 | ||||||
| chr12:3491749
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+49G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491749 | ||||||
| chr12:3491801
|
T | C | 354 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.75+101T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491801 | ||||||
| chr12:3491831
|
CCTGT | C | 5 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0001g0352others(2): Show | 5 | NA18951.hp2 NA18970.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+132_75+135delCT others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491831 | ||||||
| chr12:3491832
|
C | CTG | 25 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 25 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.75+188_75+189dupGT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
C | CTGTG | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 8 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+186_75+189dupGT others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0006 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+180_75+189dupGT others(8): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0005 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.75+178_75+189dupGT others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
C | G | 1 | a0001c0001t0001g0349 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.75+132C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491832 | ||||||
| chr12:3491832
|
CTG | C | 55 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.75+188_75+189delGT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTG | C | 49 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(46): Show | 49 | HG00280.hp2 HG00597.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+186_75+189delGT others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTG | C | 56 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0191others(53): Show | 56 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.75+184_75+189delGT others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTGT others(1): Show |
C | 36 | a0001c0001t0001g0004a0001c0001t0001g0243a0001c0001t0001g0244others(33): Show | 36 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.75+182_75+189delGT others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTGT others(3): Show |
C | 38 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0001g0281others(35): Show | 38 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+180_75+189delGT others(8): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTGT others(5): Show |
C | 8 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(5): Show | 8 | HG00642.hp1 HG00673.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+178_75+189delGT others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTGT others(7): Show |
C | 11 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0327others(8): Show | 11 | HG01175.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+176_75+189delGT others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0337 | 3 | HG02148.hp1 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.75+174_75+189delGT others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491832
|
CTGTGTGT others(11): Show |
C | 11 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341others(8): Show | 11 | HG01346.hp2 HG01891.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+172_75+189delGT others(16): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3491832 | |||||
| chr12:3491833
|
TGTGTGTG others(4): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+134_75+144delGT others(9): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491833 | ||||||
| chr12:3491845
|
T | C | 1 | a0001c0001t0001g0003 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+145T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491845 | ||||||
| chr12:3491864
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.75+164G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3491864 | ||||||
| chr12:3492006
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+306C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492006 | ||||||
| chr12:3492175
|
C | G | 5 | a0001c0001t0001g0187a0001c0001t0001g0242a0001c0001t0001g0276others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+475C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492175 | ||||||
| chr12:3492210
|
C | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(51): Show | 54 | HG00280.hp2 HG00558.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.75+510C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492210 | ||||||
| chr12:3492250
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0037 | 2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.75+550A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492250 | ||||||
| chr12:3492374
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0241 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+674C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492374 | ||||||
| chr12:3492507
|
C | G | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+807C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492507 | ||||||
| chr12:3492655
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+955A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492655 | ||||||
| chr12:3492903
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.75+1203C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492903 | ||||||
| chr12:3492910
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.75+1210C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3492910 | ||||||
| chr12:3493203
|
C | G | 2 | a0001c0001t0002g0347a0001c0002t0002g0348 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.75+1503C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493203 | ||||||
| chr12:3493347
|
G | C | 1 | a0001c0001t0001g0350 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.75+1647G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493347 | ||||||
| chr12:3493370
|
T | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(55): Show | 58 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.75+1670T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493370 | ||||||
| chr12:3493535
|
C | G | 55 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(52): Show | 55 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+1835C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493535 | ||||||
| chr12:3493561
|
G | GGTGCAGA others(20): Show |
1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+1868_75+1894dup others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3493561 | |||||
| chr12:3493581
|
T | A | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+1881T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493581 | ||||||
| chr12:3493636
|
G | C | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0317others(4): Show | 7 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+1936G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493636 | ||||||
| chr12:3493818
|
G | C | 1 | a0001c0001t0001g0339 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+2118G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493818 | ||||||
| chr12:3493997
|
C | T | 16 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(13): Show | 16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+2297C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3493997 | ||||||
| chr12:3494300
|
C | G | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0006g0346 | 3 | HG02723.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+2600C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494300 | ||||||
| chr12:3494382
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+2682T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494382 | ||||||
| chr12:3494461
|
A | G | 5 | a0001c0001t0004g0013a0001c0001t0004g0038a0001c0001t0004g0193others(2): Show | 5 | NA18955.hp2 NA18968.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2761A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494461 | ||||||
| chr12:3494645
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.75+2945C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494645 | ||||||
| chr12:3494718
|
C | T | 3 | a0001c0001t0001g0317a0001c0002t0002g0345a0001c0005t0001g0344 | 3 | HG01346.hp2 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.75+3018C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494718 | ||||||
| chr12:3494727
|
C | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+3027C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494727 | ||||||
| chr12:3494822
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.75+3122G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494822 | ||||||
| chr12:3494951
|
G | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+3251G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3494951 | ||||||
| chr12:3495098
|
G | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.75+3398G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495098 | ||||||
| chr12:3495110
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+3410T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495110 | ||||||
| chr12:3495309
|
G | A | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+3609G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495309 | ||||||
| chr12:3495438
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+3738C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495438 | ||||||
| chr12:3495468
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0241 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+3768C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495468 | ||||||
| chr12:3495524
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+3824C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495524 | ||||||
| chr12:3495583
|
C | G | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+3883C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495583 | ||||||
| chr12:3495643
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG02165.hp2 NA18949.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.75+3943A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495643 | ||||||
| chr12:3495738
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+4038T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495738 | ||||||
| chr12:3495743
|
G | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0152a0001c0001t0001g0153 | 3 | HG00280.hp1 HG01099.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.75+4043G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495743 | ||||||
| chr12:3495840
|
G | T | 11 | a0001c0001t0001g0105a0001c0001t0001g0151a0001c0001t0001g0201others(8): Show | 11 | HG00597.hp2 NA18939.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4140G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3495840 | ||||||
| chr12:3496085
|
C | G | 2 | a0001c0001t0001g0353a0001c0003t0001g0354 | 2 | NA18951.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.75+4385C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496085 | ||||||
| chr12:3496199
|
G | GATATAT | 4 | a0001c0001t0001g0110a0001c0001t0001g0139a0001c0001t0001g0252others(1): Show | 4 | HG01169.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4510_75+4515dup others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(3): Show |
15 | a0001c0001t0001g0025a0001c0001t0001g0104a0001c0001t0001g0109others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+4506_75+4515dup others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(5): Show |
8 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0285others(5): Show | 8 | HG01346.hp2 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+4504_75+4515dup others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(7): Show |
1 | a0001c0001t0001g0230 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.75+4502_75+4515dup others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(9): Show |
3 | a0001c0001t0001g0083a0001c0001t0001g0180a0001c0001t0001g0242 | 3 | HG01192.hp2 HG01433.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75+4500_75+4515dup others(16): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(11): Show |
4 | a0001c0001t0001g0004a0001c0001t0001g0081a0001c0001t0003g0136others(1): Show | 4 | HG01256.hp1 HG01361.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(13): Show |
5 | a0001c0001t0001g0179a0001c0001t0001g0237a0001c0001t0001g0238others(2): Show | 5 | HG02083.hp1 HG02451.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(20): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(15): Show |
4 | a0001c0001t0001g0275a0001c0001t0001g0310a0001c0001t0001g0326others(1): Show | 4 | HG00639.hp2 HG02615.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(17): Show |
1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(24): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(19): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0324 | 2 | HG03139.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496199
|
G | GATATATA others(23): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0091 | 2 | HG00423.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496199 | |||||
| chr12:3496212
|
A | ATTT | 7 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0062others(4): Show | 8 | HG01256.hp2 HG01258.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+4513_75+4514ins others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496212 | |||||
| chr12:3496212
|
A | ATTTT | 18 | a0001c0001t0001g0032a0001c0001t0001g0064a0001c0001t0001g0066others(15): Show | 18 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+4513_75+4514ins others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496212 | |||||
| chr12:3496212
|
A | ATTTTT | 14 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0071others(11): Show | 14 | HG00280.hp1 HG01081.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+4513_75+4514ins others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496212 | |||||
| chr12:3496214
|
A | ATATATAT others(4): Show |
11 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 11 | HG00140.hp2 HG01109.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0159a0001c0001t0001g0257a0001c0001t0001g0286 | 3 | HG01074.hp2 HG01891.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(13): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0142 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0328 | 2 | HG02818.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(26): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0177 | 2 | HG00558.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(33): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(45): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(40): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(43): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(44): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(36): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(32): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(27): Show |
1 | a0001c0002t0011g0208 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(34): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(38): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0003 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(46): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0141 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(31): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(39): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(24): Show |
2 | a0001c0002t0002g0041a0001c0002t0002g0097 | 2 | HG03139.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(31): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(34): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0017 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(39): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0330 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(33): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0098 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(40): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0186 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0201 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(25): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(14): Show |
1 | a0001c0009t0001g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0202 | 2 | NA18971.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0021a0001c0001t0001g0241a0001c0002t0002g0210 | 3 | HG01071.hp1 HG02055.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(25): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0203 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0154a0001c0001t0001g0211a0001c0001t0001g0251 | 3 | HG01261.hp1 NA18959.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(15): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0204a0001c0002t0002g0106 | 3 | HG01069.hp2 NA18942.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0196a0001c0001t0001g0244a0001c0002t0002g0212 | 3 | HG01070.hp1 HG03579.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0245 | 2 | HG01071.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(24): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(21): Show |
1 | a0001c0002t0002g0102 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(28): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0205 | 2 | HG02080.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0151 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(20): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0254a0001c0005t0006g0359 | 2 | HG02135.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(16): Show |
4 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0213others(1): Show | 4 | HG02055.hp2 HG02896.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0049 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0248 | 2 | NA18939.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0288 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(20): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0217a0001c0010t0002g0216 | 3 | NA18963.hp1 NA18990.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0246 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0160a0001c0002t0002g0218 | 2 | HG01358.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(24): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0266a0001c0002t0002g0249 | 3 | HG02886.hp1 HG02970.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0222a0001c0001t0001g0342 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0007g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(3): Show |
6 | a0001c0001t0001g0055a0001c0001t0001g0150a0001c0001t0001g0199others(3): Show | 6 | HG01934.hp1 HG02451.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0268a0001c0001t0001g0298a0001c0001t0001g0318others(1): Show | 4 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0200a0001c0001t0001g0247a0001c0001t0001g0319 | 3 | HG00438.hp1 HG00558.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0010g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
A | T | 49 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(46): Show | 50 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.75+4514A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496214 | ||||||
| chr12:3496214
|
AT | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0349a0001c0001t0001g0352others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+4540delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
ATTT | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0351a0001c0002t0002g0007others(3): Show | 6 | HG00642.hp1 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4538_75+4540del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496214
|
ATTTTT | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4536_75+4540del others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496214 | |||||
| chr12:3496215
|
T | TATATATA others(2): Show |
9 | a0001c0001t0001g0111a0001c0001t0001g0197a0001c0001t0001g0258others(6): Show | 9 | HG00099.hp2 HG02056.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(9): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(4): Show |
8 | a0001c0001t0001g0053a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 8 | HG01070.hp2 HG01981.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0253 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(13): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(8): Show |
4 | a0001c0001t0001g0085a0001c0001t0001g0108a0001c0001t0001g0138others(1): Show | 4 | HG02523.hp1 HG03195.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(15): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(10): Show |
8 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0182others(5): Show | 8 | HG01074.hp1 HG01175.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(17): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(12): Show |
6 | a0001c0001t0001g0082a0001c0001t0001g0137a0001c0001t0001g0231others(3): Show | 6 | HG00099.hp1 HG01123.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(19): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(14): Show |
7 | a0001c0001t0001g0235a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00639.hp1 HG00673.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(21): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(16): Show |
2 | a0001c0001t0001g0232a0001c0001t0001g0236 | 2 | NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(23): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(18): Show |
2 | a0001c0001t0001g0135a0001c0001t0001g0233 | 2 | NA18959.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(25): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(20): Show |
3 | a0001c0002t0002g0134a0001c0002t0002g0228a0001c0003t0001g0076 | 3 | NA18967.hp1 NA18994.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(27): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(22): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0227 | 2 | NA18747.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.75+4515_75+4516ins others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496215
|
T | TATATATA others(24): Show |
1 | a0001c0001t0001g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75+4515_75+4516ins others(31): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496215 | ||||||
| chr12:3496216
|
T | A | 29 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0081others(26): Show | 29 | HG00438.hp2 HG00639.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+4516T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496216 | ||||||
| chr12:3496217
|
T | A | 32 | a0001c0001t0001g0044a0001c0001t0001g0080a0001c0001t0001g0082others(29): Show | 32 | HG00639.hp1 HG01123.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.75+4517T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496217 | ||||||
| chr12:3496218
|
T | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0081a0001c0001t0001g0091others(12): Show | 15 | HG00438.hp2 HG01169.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+4518T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496218 | ||||||
| chr12:3496219
|
T | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0080a0001c0001t0001g0135others(21): Show | 24 | HG00639.hp1 HG00642.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+4519T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496219 | ||||||
| chr12:3496220
|
T | A | 9 | a0001c0001t0001g0139a0001c0001t0001g0230a0001c0001t0001g0252others(6): Show | 9 | HG01169.hp1 HG01256.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+4520T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496220 | ||||||
| chr12:3496221
|
T | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0137others(20): Show | 23 | HG00642.hp1 HG01123.hp1 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+4521T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496221 | ||||||
| chr12:3496222
|
T | A | 11 | a0001c0001t0001g0139a0001c0001t0001g0148a0001c0001t0001g0230others(8): Show | 11 | HG01169.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4522T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496222 | ||||||
| chr12:3496223
|
T | A | 21 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(18): Show | 21 | HG00642.hp1 HG01517.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.75+4523T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496223 | ||||||
| chr12:3496224
|
T | A | 7 | a0001c0001t0001g0148a0001c0001t0001g0230a0001c0001t0001g0339others(4): Show | 7 | HG01175.hp1 HG01891.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+4524T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496224 | ||||||
| chr12:3496225
|
T | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(15): Show | 18 | HG00642.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+4525T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496225 | ||||||
| chr12:3496226
|
T | A | 6 | a0001c0001t0001g0148a0001c0001t0001g0230a0001c0001t0001g0339others(3): Show | 6 | HG01891.hp2 HG02723.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+4526T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496226 | ||||||
| chr12:3496227
|
T | A | 4 | a0001c0001t0001g0337a0001c0001t0001g0343a0001c0001t0002g0347others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+4527T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496227 | ||||||
| chr12:3496228
|
T | A | 3 | a0001c0001t0001g0339a0001c0001t0006g0346a0001c0002t0002g0338 | 3 | HG01891.hp2 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.75+4528T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496228 | ||||||
| chr12:3496229
|
T | A | 3 | a0001c0001t0001g0343a0001c0001t0002g0347a0001c0002t0002g0348 | 3 | HG02258.hp2 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.75+4529T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496229 | ||||||
| chr12:3496241
|
G | T | 3 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0206 | 3 | NA18969.hp2 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.75+4541G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496241 | ||||||
| chr12:3496301
|
T | C | 1 | a0001c0001t0013g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.75+4601T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496301 | ||||||
| chr12:3496386
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+4686G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496386 | ||||||
| chr12:3496392
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.75+4692T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496392 | ||||||
| chr12:3496659
|
T | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(13): Show | 16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+4959T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496659 | ||||||
| chr12:3496742
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0241 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+5042T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496742 | ||||||
| chr12:3496747
|
G | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(13): Show | 16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+5047G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496747 | ||||||
| chr12:3496848
|
T | C | 13 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0177others(10): Show | 13 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+5148T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496848 | ||||||
| chr12:3496914
|
A | AT | 18 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0158others(15): Show | 18 | HG01175.hp1 HG01433.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+5233dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | |||||
| chr12:3496914
|
AT | A | 67 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0078others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.75+5233delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | |||||
| chr12:3496914
|
ATT | A | 44 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(41): Show | 44 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.75+5232_75+5233del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | |||||
| chr12:3496914
|
ATTT | A | 8 | a0001c0001t0001g0140a0001c0001t0001g0207a0001c0001t0001g0224others(5): Show | 8 | HG02258.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+5231_75+5233del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3496914 | |||||
| chr12:3496939
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+5239G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3496939 | ||||||
| chr12:3497310
|
C | T | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+5610C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497310 | ||||||
| chr12:3497452
|
T | G | 19 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0023others(16): Show | 19 | HG00597.hp2 HG00733.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+5752T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497452 | ||||||
| chr12:3497476
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75+5776T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497476 | ||||||
| chr12:3497720
|
TC | T | 37 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0044others(34): Show | 37 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+6023delC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3497720 | |||||
| chr12:3497741
|
T | C | 4 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0287others(1): Show | 4 | HG01261.hp1 HG02135.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+6041T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3497741 | ||||||
| chr12:3498175
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+6475C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498175 | ||||||
| chr12:3498176
|
A | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+6476A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498176 | ||||||
| chr12:3498402
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75+6702G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498402 | ||||||
| chr12:3498523
|
A | G | 6 | a0001c0001t0001g0070a0001c0001t0001g0121a0001c0001t0001g0129others(3): Show | 6 | HG00733.hp2 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+6823A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498523 | ||||||
| chr12:3498573
|
C | T | 1 | a0001c0002t0002g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+6873C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498573 | ||||||
| chr12:3498606
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+6906G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498606 | ||||||
| chr12:3498845
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+7145C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498845 | ||||||
| chr12:3498974
|
C | G | 3 | a0001c0001t0003g0001a0001c0001t0003g0028a0001c0001t0003g0060 | 4 | HG01256.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+7274C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3498974 | ||||||
| chr12:3499041
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.75+7341T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499041 | ||||||
| chr12:3499159
|
A | AT | 60 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(57): Show | 60 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.75+7464dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499159 | |||||
| chr12:3499165
|
A | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(12): Show | 15 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+7465A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499165 | ||||||
| chr12:3499177
|
A | AT | 50 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(47): Show | 50 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.75+7487dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499177 | |||||
| chr12:3499177
|
ATT | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(13): Show | 16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+7486_75+7487del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499177 | |||||
| chr12:3499181
|
T | A | 9 | a0001c0001t0001g0192a0001c0001t0001g0224a0001c0001t0001g0337others(6): Show | 9 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+7481T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499181 | ||||||
| chr12:3499193
|
CT | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 76 | HG00099.hp1 HG00558.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.75+7508delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499193 | |||||
| chr12:3499193
|
CTT | C | 20 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0088others(17): Show | 20 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.75+7507_75+7508del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3499193 | |||||
| chr12:3499215
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(50): Show | 53 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.75+7515C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499215 | ||||||
| chr12:3499346
|
C | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.75+7646C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499346 | ||||||
| chr12:3499354
|
G | A | 72 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.75+7654G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499354 | ||||||
| chr12:3499377
|
G | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0154a0001c0001t0001g0158others(10): Show | 13 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.75+7677G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499377 | ||||||
| chr12:3499399
|
C | T | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0002g0345others(1): Show | 4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+7699C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499399 | ||||||
| chr12:3499450
|
A | T | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+7750A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499450 | ||||||
| chr12:3499683
|
C | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0137a0001c0001t0001g0235 | 3 | NA18612.hp2 NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.75+7983C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3499683 | ||||||
| chr12:3500016
|
A | C | 12 | a0001c0001t0001g0105a0001c0001t0001g0151a0001c0001t0001g0201others(9): Show | 12 | HG00597.hp2 NA18939.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+8316A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500016 | ||||||
| chr12:3500024
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(79): Show | 83 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.75+8324C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500024 | ||||||
| chr12:3500025
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0098 | 2 | HG00733.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.75+8325G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500025 | ||||||
| chr12:3500122
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(50): Show | 53 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.75+8422C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500122 | ||||||
| chr12:3500136
|
C | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.75+8436C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500136 | ||||||
| chr12:3500141
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+8441T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500141 | ||||||
| chr12:3500238
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA18980.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.75+8538A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500238 | ||||||
| chr12:3500258
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.75+8558C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500258 | ||||||
| chr12:3500345
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.75+8645A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500345 | ||||||
| chr12:3500408
|
T | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0105others(13): Show | 16 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+8708T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500408 | ||||||
| chr12:3500414
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.75+8714T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500414 | ||||||
| chr12:3500516
|
C | T | 1 | a0001c0001t0006g0346 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.75+8816C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500516 | ||||||
| chr12:3500517
|
G | A | 71 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.75+8817G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500517 | ||||||
| chr12:3500518
|
G | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0002g0345others(1): Show | 4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+8818G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500518 | ||||||
| chr12:3500723
|
C | G | 6 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0004t0001g0314others(3): Show | 6 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+9023C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500723 | ||||||
| chr12:3500945
|
T | G | 6 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0004t0001g0314others(3): Show | 6 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+9245T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500945 | ||||||
| chr12:3500980
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+9280C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3500980 | ||||||
| chr12:3501059
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.75+9359G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501059 | ||||||
| chr12:3501107
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.75+9407G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501107 | ||||||
| chr12:3501137
|
G | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0317others(5): Show | 8 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+9437G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501137 | ||||||
| chr12:3501206
|
G | A | 29 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0088others(26): Show | 29 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+9506G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501206 | ||||||
| chr12:3501248
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0251a0001c0001t0001g0254others(3): Show | 6 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+9548C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501248 | ||||||
| chr12:3501249
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75+9549G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501249 | ||||||
| chr12:3501368
|
C | T | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0002g0345others(1): Show | 4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+9668C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501368 | ||||||
| chr12:3501538
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+9838C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501538 | ||||||
| chr12:3501596
|
G | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(50): Show | 53 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.75+9896G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501596 | ||||||
| chr12:3501671
|
T | G | 1 | a0001c0001t0001g0305 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.75+9971T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501671 | ||||||
| chr12:3501683
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01952.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.75+9983C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501683 | ||||||
| chr12:3501693
|
G | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+9993G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501693 | ||||||
| chr12:3501744
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(128): Show | 131 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.75+10044C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501744 | ||||||
| chr12:3501951
|
G | T | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10251G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501951 | ||||||
| chr12:3501958
|
T | C | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10258T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3501958 | ||||||
| chr12:3502026
|
T | C | 30 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0088others(27): Show | 30 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.75+10326T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502026 | ||||||
| chr12:3502036
|
C | T | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10336C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502036 | ||||||
| chr12:3502069
|
T | C | 56 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(53): Show | 56 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.75+10369T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502069 | ||||||
| chr12:3502150
|
A | G | 1 | a0001c0001t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.75+10450A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502150 | ||||||
| chr12:3502282
|
A | C | 1 | a0001c0001t0001g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.75+10582A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502282 | ||||||
| chr12:3502336
|
T | G | 3 | a0001c0001t0001g0240a0001c0001t0007g0313a0001c0002t0011g0208 | 3 | HG02895.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+10636T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502336 | ||||||
| chr12:3502397
|
G | T | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+10697G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502397 | ||||||
| chr12:3502411
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+10711C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502411 | ||||||
| chr12:3502412
|
G | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0324others(3): Show | 6 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+10712G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502412 | ||||||
| chr12:3502428
|
A | G | 1 | a0001c0001t0001g0362 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.75+10728A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502428 | ||||||
| chr12:3502543
|
T | C | 2 | a0001c0001t0001g0105a0001c0002t0002g0106 | 2 | NA18942.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.75+10843T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502543 | ||||||
| chr12:3502570
|
T | C | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0002g0345others(1): Show | 4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+10870T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502570 | ||||||
| chr12:3502584
|
G | C | 1 | a0001c0001t0007g0325 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.75+10884G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502584 | ||||||
| chr12:3502609
|
C | T | 2 | a0001c0001t0002g0157a0001c0002t0002g0218 | 2 | HG02896.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.75+10909C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502609 | ||||||
| chr12:3502718
|
T | C | 2 | a0001c0001t0001g0214a0001c0002t0002g0282 | 2 | HG01070.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.75+11018T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502718 | ||||||
| chr12:3502823
|
T | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+11123T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502823 | ||||||
| chr12:3502856
|
G | C | 1 | a0001c0001t0001g0342 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75+11156G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502856 | ||||||
| chr12:3502954
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75+11254A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3502954 | ||||||
| chr12:3503037
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.75+11337T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503037 | ||||||
| chr12:3503102
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+11402C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503102 | ||||||
| chr12:3503103
|
G | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+11403G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503103 | ||||||
| chr12:3503156
|
A | C | 5 | a0001c0001t0001g0105a0001c0001t0001g0151a0001c0001t0001g0203others(2): Show | 5 | HG00597.hp2 NA18942.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+11456A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503156 | ||||||
| chr12:3503183
|
A | G | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+11483A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503183 | ||||||
| chr12:3503297
|
C | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0017others(48): Show | 51 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.75+11597C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503297 | ||||||
| chr12:3503397
|
G | A | 2 | a0001c0001t0004g0013a0001c0001t0004g0038 | 2 | NA18968.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.75+11697G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503397 | ||||||
| chr12:3503562
|
A | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+11862A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503562 | ||||||
| chr12:3503591
|
T | C | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+11891T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503591 | ||||||
| chr12:3503598
|
A | T | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+11898A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503598 | ||||||
| chr12:3503608
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.75+11908G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503608 | ||||||
| chr12:3503670
|
A | G | 62 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0104others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.75+11970A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503670 | ||||||
| chr12:3503848
|
G | A | 5 | a0001c0001t0001g0323a0001c0004t0001g0314a0001c0004t0001g0321others(2): Show | 5 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+12148G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503848 | ||||||
| chr12:3503900
|
T | G | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+12200T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503900 | ||||||
| chr12:3503935
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0317a0001c0002t0011g0208 | 3 | HG00733.hp2 HG02895.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.75+12235G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503935 | ||||||
| chr12:3503961
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+12261A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503961 | ||||||
| chr12:3503989
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.75+12289C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503989 | ||||||
| chr12:3503990
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+12290G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503990 | ||||||
| chr12:3503993
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(52): Show | 55 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+12293T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503993 | ||||||
| chr12:3503994
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.75+12294C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503994 | ||||||
| chr12:3503995
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0128a0001c0001t0001g0168 | 3 | HG02040.hp1 HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.75+12295G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3503995 | ||||||
| chr12:3504097
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+12397A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504097 | ||||||
| chr12:3504157
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+12457G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504157 | ||||||
| chr12:3504178
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+12478G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504178 | ||||||
| chr12:3504233
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+12533T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504233 | ||||||
| chr12:3504248
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(82): Show | 86 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.75+12548A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504248 | ||||||
| chr12:3504273
|
A | G | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.75+12573A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504273 | ||||||
| chr12:3504361
|
G | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0241 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.75+12661G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504361 | ||||||
| chr12:3504379
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0126a0001c0001t0001g0132others(4): Show | 7 | HG02055.hp1 HG02056.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+12679C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504379 | ||||||
| chr12:3504385
|
A | G | 8 | a0001c0001t0001g0032a0001c0001t0001g0126a0001c0001t0001g0132others(5): Show | 8 | HG02055.hp1 HG02056.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+12685A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504385 | ||||||
| chr12:3504399
|
G | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0186a0001c0001t0001g0241others(3): Show | 6 | HG02055.hp1 HG02056.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+12699G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504399 | ||||||
| chr12:3504401
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.75+12701T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504401 | ||||||
| chr12:3504412
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.75+12712C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504412 | ||||||
| chr12:3504434
|
G | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0132 | 2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.75+12734G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504434 | ||||||
| chr12:3504441
|
G | A | 12 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+12741G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504441 | ||||||
| chr12:3504443
|
C | G | 12 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+12743C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504443 | ||||||
| chr12:3504446
|
C | T | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(97): Show | 101 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.75+12746C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504446 | ||||||
| chr12:3504451
|
A | G | 4 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0356others(1): Show | 4 | HG01884.hp1 HG02056.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+12751A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504451 | ||||||
| chr12:3504455
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0042 | 2 | HG02056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12755C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504455 | ||||||
| chr12:3504456
|
C | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0042 | 2 | HG02056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12756C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504456 | ||||||
| chr12:3504457
|
T | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0042 | 2 | HG02056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12757T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504457 | ||||||
| chr12:3504460
|
C | T | 2 | a0001c0001t0001g0356a0001c0001t0001g0361 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.75+12760C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504460 | ||||||
| chr12:3504461
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.75+12761G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504461 | ||||||
| chr12:3504476
|
G | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0139 | 3 | HG01169.hp1 NA18997.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.75+12776G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504476 | ||||||
| chr12:3504478
|
G | A | 1 | a0001c0005t0001g0300 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75+12778G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504478 | ||||||
| chr12:3504485
|
G | C | 76 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0025others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.75+12785G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504485 | ||||||
| chr12:3504487
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.75+12787G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504487 | ||||||
| chr12:3504493
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.75+12793T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504493 | ||||||
| chr12:3504514
|
G | A | 15 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(12): Show | 15 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+12814G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504514 | ||||||
| chr12:3504540
|
G | A | 2 | a0001c0001t0001g0356a0001c0001t0001g0361 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.75+12840G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504540 | ||||||
| chr12:3504556
|
C | G | 4 | a0001c0001t0001g0196a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+12856C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504556 | ||||||
| chr12:3504574
|
T | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0091others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+12874T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504574 | ||||||
| chr12:3504576
|
T | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0089others(10): Show | 13 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.75+12876T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504576 | ||||||
| chr12:3504577
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.75+12877G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504577 | ||||||
| chr12:3504592
|
C | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(52): Show | 55 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.75+12892C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504592 | ||||||
| chr12:3504616
|
A | T | 71 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.75+12916A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504616 | ||||||
| chr12:3504623
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0154 | 3 | HG01069.hp2 HG01071.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.75+12923C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504623 | ||||||
| chr12:3504653
|
T | C | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+12953T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504653 | ||||||
| chr12:3504671
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.75+12971C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504671 | ||||||
| chr12:3504721
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0002g0127 | 2 | HG02083.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.75+13021G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504721 | ||||||
| chr12:3504728
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.75+13028A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504728 | ||||||
| chr12:3504745
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.75+13045C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504745 | ||||||
| chr12:3504746
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.75+13046G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504746 | ||||||
| chr12:3504765
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0255 | 2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13065G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504765 | ||||||
| chr12:3504772
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0255a0001c0005t0001g0300 | 3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13072T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504772 | ||||||
| chr12:3504777
|
A | T | 1 | a0001c0001t0001g0047 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.75+13077A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504777 | ||||||
| chr12:3504783
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.75+13083G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504783 | ||||||
| chr12:3504783
|
G | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0255a0001c0005t0001g0300 | 3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13083G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504783 | ||||||
| chr12:3504786
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.75+13086C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504786 | ||||||
| chr12:3504805
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0255others(2): Show | 5 | HG01099.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+13105T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504805 | ||||||
| chr12:3504809
|
C | G | 2 | a0001c0001t0001g0197a0001c0002t0002g0280 | 2 | HG02129.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.75+13109C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504809 | ||||||
| chr12:3504855
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0255a0001c0005t0001g0300 | 3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13155T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504855 | ||||||
| chr12:3504876
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0255a0001c0005t0001g0300 | 3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13176T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504876 | ||||||
| chr12:3504891
|
A | T | 53 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.75+13191A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504891 | ||||||
| chr12:3504901
|
G | A | 16 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(13): Show | 16 | HG00642.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+13201G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504901 | ||||||
| chr12:3504915
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0255a0001c0005t0001g0300 | 3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13215C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504915 | ||||||
| chr12:3504922
|
C | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+13222C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504922 | ||||||
| chr12:3504961
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0255a0001c0005t0001g0300 | 3 | HG02280.hp1 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.75+13261T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504961 | ||||||
| chr12:3504977
|
G | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0177others(11): Show | 14 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.75+13277G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3504977 | ||||||
| chr12:3505056
|
C | T | 2 | a0001c0001t0001g0254a0001c0002t0002g0212 | 2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.75+13356C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505056 | ||||||
| chr12:3505067
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+13367C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505067 | ||||||
| chr12:3505334
|
C | T | 1 | a0001c0004t0001g0334 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.75+13634C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505334 | ||||||
| chr12:3505389
|
C | T | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.75+13689C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505389 | ||||||
| chr12:3505390
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0251a0001c0001t0001g0254others(2): Show | 5 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+13690G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505390 | ||||||
| chr12:3505403
|
C | G | 8 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0167others(5): Show | 8 | HG02523.hp2 NA18959.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+13703C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505403 | ||||||
| chr12:3505601
|
G | A | 68 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(65): Show | 68 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.75+13901G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505601 | ||||||
| chr12:3505653
|
A | G | 9 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0317others(6): Show | 9 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+13953A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505653 | ||||||
| chr12:3505911
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+14211C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505911 | ||||||
| chr12:3505998
|
G | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0154a0001c0001t0001g0158others(11): Show | 14 | HG01261.hp1 HG02080.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+14298G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3505998 | ||||||
| chr12:3506013
|
A | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+14313A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506013 | ||||||
| chr12:3506039
|
G | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0173a0001c0002t0002g0174 | 3 | NA18967.hp2 NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.75+14339G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506039 | ||||||
| chr12:3506398
|
C | T | 7 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0002t0002g0249others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+14698C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506398 | ||||||
| chr12:3506489
|
T | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+14789T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506489 | ||||||
| chr12:3506725
|
G | T | 1 | a0001c0001t0010g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+15025G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506725 | ||||||
| chr12:3506902
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+15202T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506902 | ||||||
| chr12:3506931
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.75+15231A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506931 | ||||||
| chr12:3506981
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0248 | 2 | NA18939.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.75+15281G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3506981 | ||||||
| chr12:3507118
|
C | CT | 32 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0069others(29): Show | 32 | HG02129.hp1 HG02257.hp2 HG02273.hp2 others(29): Show |
intron_variant | MODIFIER | c.75+15439dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507118 | |||||
| chr12:3507118
|
CT | C | 18 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0165others(15): Show | 18 | HG00642.hp1 HG01169.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.75+15439delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507118 | |||||
| chr12:3507182
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+15482C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507182 | ||||||
| chr12:3507314
|
C | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(67): Show | 70 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.75+15614C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507314 | ||||||
| chr12:3507367
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.75+15667C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507367 | ||||||
| chr12:3507446
|
C | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0002g0345others(1): Show | 4 | HG01346.hp2 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+15746C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507446 | ||||||
| chr12:3507613
|
G | A | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0317others(4): Show | 7 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+15913G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507613 | ||||||
| chr12:3507644
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.75+15944C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507644 | ||||||
| chr12:3507646
|
C | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0070others(6): Show | 9 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+15946C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507646 | ||||||
| chr12:3507758
|
C | CT | 16 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0167others(13): Show | 16 | HG02258.hp1 HG02258.hp2 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.75+16076dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507758 | |||||
| chr12:3507758
|
CT | C | 40 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(37): Show | 40 | HG00558.hp2 HG01070.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.75+16076delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3507758 | |||||
| chr12:3507804
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0311a0001c0002t0002g0312 | 3 | HG00673.hp1 HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.75+16104G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507804 | ||||||
| chr12:3507819
|
T | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(74): Show | 77 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.75+16119T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507819 | ||||||
| chr12:3507962
|
C | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0002t0002g0102 | 3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.75+16262C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3507962 | ||||||
| chr12:3508145
|
A | AT | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+16452dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3508145 | |||||
| chr12:3508149
|
T | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0105others(13): Show | 16 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+16449T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508149 | ||||||
| chr12:3508300
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0332 | 2 | HG02486.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.75+16600C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508300 | ||||||
| chr12:3508311
|
C | A | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+16611C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508311 | ||||||
| chr12:3508321
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.75+16621G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508321 | ||||||
| chr12:3508380
|
T | C | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+16680T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508380 | ||||||
| chr12:3508458
|
G | A | 12 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0177others(9): Show | 12 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+16758G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508458 | ||||||
| chr12:3508473
|
T | G | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+16773T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508473 | ||||||
| chr12:3508566
|
T | A | 12 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0177others(9): Show | 12 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+16866T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508566 | ||||||
| chr12:3508683
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(28): Show | 31 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.75+16983C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3508683 | ||||||
| chr12:3509058
|
C | G | 1 | a0001c0001t0001g0332 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75+17358C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509058 | ||||||
| chr12:3509103
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(61): Show | 64 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.75+17403A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509103 | ||||||
| chr12:3509129
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0281 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.75+17429G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509129 | ||||||
| chr12:3509199
|
G | A | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+17499G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509199 | ||||||
| chr12:3509302
|
T | C | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+17602T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509302 | ||||||
| chr12:3509519
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+17819A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509519 | ||||||
| chr12:3509681
|
G | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0305a0001c0003t0001g0076 | 3 | NA18967.hp1 NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.75+17981G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509681 | ||||||
| chr12:3509784
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.75+18084G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509784 | ||||||
| chr12:3509876
|
A | G | 7 | a0001c0001t0001g0058a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 7 | HG02071.hp1 HG02735.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+18176A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509876 | ||||||
| chr12:3509941
|
G | A | 1 | a0001c0002t0002g0007 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.75+18241G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3509941 | ||||||
| chr12:3510023
|
C | T | 52 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(49): Show | 52 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.75+18323C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510023 | ||||||
| chr12:3510098
|
T | C | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+18398T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510098 | ||||||
| chr12:3510103
|
G | T | 70 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(67): Show | 70 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.75+18403G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510103 | ||||||
| chr12:3510372
|
A | G | 23 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 23 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+18672A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510372 | ||||||
| chr12:3510433
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0141others(1): Show | 4 | HG00558.hp2 HG02027.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+18733A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510433 | ||||||
| chr12:3510580
|
C | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(116): Show | 119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.75+18880C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510580 | ||||||
| chr12:3510758
|
C | T | 2 | a0001c0002t0002g0345a0001c0005t0001g0344 | 2 | HG01346.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.75+19058C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3510758 | ||||||
| chr12:3511048
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+19348C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511048 | ||||||
| chr12:3511322
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.75+19622G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511322 | ||||||
| chr12:3511759
|
C | A | 37 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0044others(34): Show | 37 | HG00280.hp2 HG01069.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.75+20059C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511759 | ||||||
| chr12:3511849
|
A | G | 3 | a0001c0001t0001g0091a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG01192.hp1 HG02818.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.75+20149A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511849 | ||||||
| chr12:3511867
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0007g0313 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+20167C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3511867 | ||||||
| chr12:3512006
|
C | G | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+20306C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512006 | ||||||
| chr12:3512009
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0252a0001c0001t0001g0281 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.75+20309G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512009 | ||||||
| chr12:3512054
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+20354A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512054 | ||||||
| chr12:3512185
|
G | A | 1 | a0001c0002t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.75+20485G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512185 | ||||||
| chr12:3512326
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG01952.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.75+20626T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512326 | ||||||
| chr12:3512536
|
T | C | 1 | a0001c0004t0001g0334 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.75+20836T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512536 | ||||||
| chr12:3512576
|
C | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+20876C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512576 | ||||||
| chr12:3512722
|
C | T | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21022C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512722 | ||||||
| chr12:3512803
|
G | A | 12 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0177others(9): Show | 12 | HG01261.hp2 HG01346.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.75+21103G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512803 | ||||||
| chr12:3512819
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.75+21119T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512819 | ||||||
| chr12:3512892
|
A | T | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21192A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3512892 | ||||||
| chr12:3513058
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+21358C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513058 | ||||||
| chr12:3513098
|
G | A | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+21398G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513098 | ||||||
| chr12:3513104
|
C | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0260a0001c0001t0001g0263others(2): Show | 5 | NA18940.hp2 NA18949.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+21404C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513104 | ||||||
| chr12:3513168
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0129 | 2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.75+21468G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513168 | ||||||
| chr12:3513231
|
C | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(76): Show | 80 | HG00140.hp1 HG00642.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.75+21531C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513231 | ||||||
| chr12:3513348
|
G | T | 7 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0002t0002g0249others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21648G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513348 | ||||||
| chr12:3513350
|
T | A | 7 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0002t0002g0249others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21650T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513350 | ||||||
| chr12:3513444
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.75+21744G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513444 | ||||||
| chr12:3513558
|
T | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0203a0001c0001t0001g0205 | 3 | HG00597.hp2 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.75+21858T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513558 | ||||||
| chr12:3513610
|
G | A | 12 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+21910G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513610 | ||||||
| chr12:3513634
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75+21934A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513634 | ||||||
| chr12:3513651
|
G | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+21951G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513651 | ||||||
| chr12:3513993
|
T | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(48): Show | 51 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.75+22293T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3513993 | ||||||
| chr12:3514124
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22424G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514124 | ||||||
| chr12:3514211
|
C | CT | 8 | a0001c0001t0001g0068a0001c0001t0001g0110a0001c0001t0001g0177others(5): Show | 8 | HG00735.hp1 HG00735.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+22525dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3514211 | |||||
| chr12:3514211
|
C | CTTT | 45 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(42): Show | 45 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.75+22523_75+22525d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3514211 | |||||
| chr12:3514211
|
CT | C | 6 | a0001c0001t0001g0301a0001c0001t0001g0328a0001c0001t0001g0329others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+22525delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3514211 | |||||
| chr12:3514222
|
T | C | 1 | a0001c0001t0008g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.75+22522T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514222 | ||||||
| chr12:3514298
|
C | T | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75+22598C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514298 | ||||||
| chr12:3514389
|
G | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0167others(5): Show | 8 | HG02523.hp2 NA18959.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+22689G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514389 | ||||||
| chr12:3514406
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.75+22706G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514406 | ||||||
| chr12:3514429
|
G | A | 7 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0002t0002g0249others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+22729G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514429 | ||||||
| chr12:3514508
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22808G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514508 | ||||||
| chr12:3514510
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.75+22810T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514510 | ||||||
| chr12:3514518
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22818C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514518 | ||||||
| chr12:3514547
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22847G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514547 | ||||||
| chr12:3514673
|
T | C | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0001t0006g0346 | 3 | HG02723.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75+22973T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514673 | ||||||
| chr12:3514678
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+22978G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514678 | ||||||
| chr12:3514776
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA18980.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.75+23076C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514776 | ||||||
| chr12:3514792
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75+23092C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514792 | ||||||
| chr12:3514807
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23107G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514807 | ||||||
| chr12:3514968
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23268G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3514968 | ||||||
| chr12:3515006
|
C | T | 12 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+23306C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515006 | ||||||
| chr12:3515018
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.75+23318C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515018 | ||||||
| chr12:3515041
|
T | TA | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23348dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3515041 | |||||
| chr12:3515102
|
A | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+23402A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515102 | ||||||
| chr12:3515140
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75+23440A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515140 | ||||||
| chr12:3515158
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23458C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515158 | ||||||
| chr12:3515191
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.75+23491G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515191 | ||||||
| chr12:3515244
|
T | G | 4 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+23544T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515244 | ||||||
| chr12:3515342
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23642A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515342 | ||||||
| chr12:3515506
|
A | G | 4 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0003g0063others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+23806A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515506 | ||||||
| chr12:3515589
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.75+23889C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515589 | ||||||
| chr12:3515590
|
G | A | 7 | a0001c0001t0001g0323a0001c0001t0012g0316a0001c0002t0002g0249others(4): Show | 7 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+23890G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515590 | ||||||
| chr12:3515591
|
G | A | 4 | a0001c0001t0001g0064a0001c0001t0001g0071a0001c0001t0003g0063others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+23891G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515591 | ||||||
| chr12:3515640
|
C | A | 4 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+23940C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515640 | ||||||
| chr12:3515652
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23952A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515652 | ||||||
| chr12:3515698
|
T | C | 49 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(46): Show | 49 | HG00558.hp2 HG00597.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.75+23998T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515698 | ||||||
| chr12:3515755
|
G | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.75+24055G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515755 | ||||||
| chr12:3515787
|
G | A | 8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0317others(5): Show | 8 | HG01261.hp2 HG01358.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+24087G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515787 | ||||||
| chr12:3515879
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.75+24179C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515879 | ||||||
| chr12:3515931
|
T | C | 204 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.75+24231T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3515931 | ||||||
| chr12:3516007
|
T | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.75+24307T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516007 | ||||||
| chr12:3516198
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0089 | 2 | HG02071.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.76-24408G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516198 | ||||||
| chr12:3516295
|
T | C | 1 | a0001c0002t0002g0027 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-24311T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516295 | ||||||
| chr12:3516315
|
GTTCA | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0251a0001c0001t0001g0292others(6): Show | 9 | HG00423.hp1 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-24267_76-24264d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3516315 | |||||
| chr12:3516315
|
GTTCATTC others(1): Show |
G | 8 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0167others(5): Show | 8 | HG02523.hp2 NA18959.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-24271_76-24264d others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3516315 | |||||
| chr12:3516315
|
GTTCATTC others(5): Show |
G | 1 | a0001c0001t0001g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.76-24275_76-24264d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3516315 | |||||
| chr12:3516612
|
G | A | 4 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-23994G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516612 | ||||||
| chr12:3516762
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.76-23844G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3516762 | ||||||
| chr12:3517159
|
G | T | 4 | a0001c0001t0001g0323a0001c0004t0001g0314a0001c0004t0001g0321others(1): Show | 4 | HG00642.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-23447G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517159 | ||||||
| chr12:3517222
|
A | G | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-23384A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517222 | ||||||
| chr12:3517240
|
G | A | 2 | a0001c0001t0003g0001a0001c0001t0003g0060 | 3 | HG01256.hp2 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.76-23366G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517240 | ||||||
| chr12:3517330
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.76-23276G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517330 | ||||||
| chr12:3517356
|
G | A | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-23250G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517356 | ||||||
| chr12:3517560
|
G | A | 9 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0070others(6): Show | 9 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-23046G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517560 | ||||||
| chr12:3517595
|
C | T | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-23011C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517595 | ||||||
| chr12:3517933
|
C | G | 19 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0105others(16): Show | 19 | HG00597.hp2 HG01257.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-22673C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3517933 | ||||||
| chr12:3518041
|
GA | G | 360 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.76-22553delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518041 | |||||
| chr12:3518077
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(69): Show | 72 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.76-22529G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518077 | ||||||
| chr12:3518113
|
C | T | 12 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-22493C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518113 | ||||||
| chr12:3518130
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-22476C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518130 | ||||||
| chr12:3518170
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-22436G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518170 | ||||||
| chr12:3518189
|
G | T | 1 | a0001c0001t0013g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.76-22417G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518189 | ||||||
| chr12:3518237
|
T | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0128a0001c0001t0001g0251others(3): Show | 6 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-22369T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518237 | ||||||
| chr12:3518285
|
C | A | 284 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.76-22321C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518285 | ||||||
| chr12:3518397
|
C | CT | 19 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0024others(16): Show | 19 | HG01099.hp2 HG01169.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-22197dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518397 | |||||
| chr12:3518397
|
C | CTT | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 190 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.76-22198_76-22197d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518397 | |||||
| chr12:3518397
|
C | CTTT | 9 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0217others(6): Show | 9 | HG02818.hp1 HG02922.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-22199_76-22197d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518397 | |||||
| chr12:3518400
|
T | G | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.76-22206T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518400 | ||||||
| chr12:3518409
|
T | TTA | 68 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.76-22197_76-22196i others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518409 | ||||||
| chr12:3518410
|
A | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG01069.hp1 HG01515.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-22196A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518410 | ||||||
| chr12:3518427
|
T | C | 286 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.76-22179T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518427 | ||||||
| chr12:3518476
|
C | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.76-22130C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518476 | ||||||
| chr12:3518483
|
T | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG00741.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.76-22123T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518483 | ||||||
| chr12:3518509
|
C | G | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-22097C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518509 | ||||||
| chr12:3518667
|
G | A | 2 | a0001c0001t0001g0144a0001c0002t0009g0094 | 2 | HG01069.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.76-21939G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518667 | ||||||
| chr12:3518835
|
G | A | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.76-21771G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3518835 | ||||||
| chr12:3518992
|
GA | G | 8 | a0001c0001t0001g0088a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-21607delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3518992 | |||||
| chr12:3519012
|
A | G | 5 | a0001c0001t0001g0177a0001c0001t0001g0340a0001c0001t0001g0341others(2): Show | 5 | HG01346.hp2 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-21594A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519012 | ||||||
| chr12:3519138
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.76-21468A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519138 | ||||||
| chr12:3519307
|
T | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0001t0001g0077others(55): Show | 58 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.76-21299T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519307 | ||||||
| chr12:3519399
|
T | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0141others(1): Show | 4 | HG00558.hp2 HG02027.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-21207T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519399 | ||||||
| chr12:3519403
|
G | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0089a0001c0001t0001g0092others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-21203G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519403 | ||||||
| chr12:3519480
|
T | C | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-21126T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519480 | ||||||
| chr12:3519540
|
T | C | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-21066T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519540 | ||||||
| chr12:3519639
|
T | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0070others(4): Show | 7 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-20967T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519639 | ||||||
| chr12:3519765
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0069 | 2 | NA19066.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.76-20841G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519765 | ||||||
| chr12:3519795
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76-20811G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3519795 | ||||||
| chr12:3520020
|
T | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0128a0001c0001t0001g0251others(4): Show | 7 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-20586T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520020 | ||||||
| chr12:3520083
|
C | G | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-20523C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520083 | ||||||
| chr12:3520110
|
C | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0335 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-20496C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520110 | ||||||
| chr12:3520163
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.76-20443G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520163 | ||||||
| chr12:3520200
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-20406G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520200 | ||||||
| chr12:3520200
|
G | T | 56 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(53): Show | 56 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.76-20406G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520200 | ||||||
| chr12:3520203
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-20403G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520203 | ||||||
| chr12:3520246
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.76-20360A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520246 | ||||||
| chr12:3520247
|
C | T | 227 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(224): Show | 228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.76-20359C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520247 | ||||||
| chr12:3520248
|
G | A | 84 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.76-20358G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520248 | ||||||
| chr12:3520509
|
A | G | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-20097A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520509 | ||||||
| chr12:3520680
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.76-19926A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520680 | ||||||
| chr12:3520712
|
A | G | 1 | a0001c0002t0002g0234 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.76-19894A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520712 | ||||||
| chr12:3520757
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0335 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-19849G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520757 | ||||||
| chr12:3520899
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.76-19707T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520899 | ||||||
| chr12:3520913
|
G | C | 258 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(255): Show | 259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.76-19693G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3520913 | ||||||
| chr12:3521180
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-19426G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521180 | ||||||
| chr12:3521267
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.76-19339A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521267 | ||||||
| chr12:3521340
|
G | A | 7 | a0001c0001t0001g0107a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00280.hp1 HG02698.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-19266G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521340 | ||||||
| chr12:3521348
|
C | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(59): Show | 63 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.76-19258C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521348 | ||||||
| chr12:3521349
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.76-19257G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521349 | ||||||
| chr12:3521371
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0133a0001c0001t0001g0175others(1): Show | 4 | HG02165.hp2 NA18949.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-19235C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521371 | ||||||
| chr12:3521389
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19217C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521389 | ||||||
| chr12:3521390
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19216A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521390 | ||||||
| chr12:3521400
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19206C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521400 | ||||||
| chr12:3521401
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19205C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521401 | ||||||
| chr12:3521402
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-19204C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521402 | ||||||
| chr12:3521448
|
C | T | 1 | a0001c0002t0002g0228 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.76-19158C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521448 | ||||||
| chr12:3521492
|
T | G | 2 | a0001c0001t0001g0211a0001c0001t0001g0217 | 2 | NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.76-19114T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521492 | ||||||
| chr12:3521575
|
A | C | 2 | a0001c0002t0002g0249a0001c0002t0002g0345 | 2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.76-19031A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521575 | ||||||
| chr12:3521607
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0335 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-18999G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521607 | ||||||
| chr12:3521676
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0061others(2): Show | 5 | NA18951.hp1 NA18965.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-18930G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521676 | ||||||
| chr12:3521833
|
A | G | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-18773A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521833 | ||||||
| chr12:3521931
|
TA | T | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.76-18673delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3521931 | |||||
| chr12:3521947
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0335 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-18659A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3521947 | ||||||
| chr12:3522128
|
GC | G | 76 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(73): Show | 76 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.76-18473delC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522128 | |||||
| chr12:3522202
|
C | A | 82 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0055others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.76-18404C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522202 | ||||||
| chr12:3522233
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.76-18373A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522233 | ||||||
| chr12:3522265
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.76-18341C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522265 | ||||||
| chr12:3522405
|
C | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0040others(14): Show | 17 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-18201C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522405 | ||||||
| chr12:3522449
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0305 | 2 | NA18969.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.76-18157A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522449 | ||||||
| chr12:3522479
|
G | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0173a0001c0002t0002g0174 | 3 | NA18967.hp2 NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.76-18127G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522479 | ||||||
| chr12:3522596
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.76-18010G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522596 | ||||||
| chr12:3522648
|
TA | T | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.76-17938delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522648 | |||||
| chr12:3522648
|
TAA | T | 26 | a0001c0001t0001g0033a0001c0001t0001g0050a0001c0001t0001g0051others(23): Show | 26 | HG00733.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.76-17939_76-17938d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522648 | |||||
| chr12:3522662
|
A | C | 6 | a0001c0001t0001g0109a0001c0001t0001g0243a0001c0001t0001g0335others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-17944A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522662 | ||||||
| chr12:3522665
|
A | C | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.76-17941A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522665 | ||||||
| chr12:3522726
|
G | A | 10 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0167others(7): Show | 10 | HG02523.hp2 HG02976.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-17880G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522726 | ||||||
| chr12:3522778
|
AAAAC | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0117a0001c0005t0001g0300 | 3 | HG00280.hp1 HG02559.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.76-17816_76-17813d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522778 | |||||
| chr12:3522790
|
C | CA | 4 | a0001c0001t0001g0196a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-17810dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522790 | |||||
| chr12:3522793
|
AAAAC | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-17801_76-17798d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522793 | |||||
| chr12:3522801
|
C | CA | 5 | a0001c0001t0001g0243a0001c0001t0001g0335a0001c0001t0001g0340others(2): Show | 5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-17802dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522801 | |||||
| chr12:3522805
|
C | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0243a0001c0001t0001g0335others(3): Show | 6 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-17801C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522805 | ||||||
| chr12:3522805
|
CA | C | 10 | a0001c0001t0001g0154a0001c0001t0001g0158a0001c0001t0001g0167others(7): Show | 10 | HG02523.hp2 HG02976.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-17792delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3522805 | |||||
| chr12:3522926
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-17680C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522926 | ||||||
| chr12:3522944
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.76-17662C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3522944 | ||||||
| chr12:3523007
|
GA | G | 225 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.76-17589delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3523007 | |||||
| chr12:3523369
|
T | C | 82 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.76-17237T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523369 | ||||||
| chr12:3523436
|
G | A | 6 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-17170G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523436 | ||||||
| chr12:3523556
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.76-17050A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523556 | ||||||
| chr12:3523797
|
T | C | 12 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 12 | HG02523.hp2 HG02630.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-16809T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523797 | ||||||
| chr12:3523880
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.76-16726G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3523880 | ||||||
| chr12:3524332
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-16274C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524332 | ||||||
| chr12:3524642
|
T | TA | 17 | a0001c0001t0001g0014a0001c0001t0001g0089a0001c0001t0001g0092others(14): Show | 17 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-15944dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3524642 | |||||
| chr12:3524642
|
TA | T | 139 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(136): Show | 139 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.76-15944delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3524642 | |||||
| chr12:3524678
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-15928A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524678 | ||||||
| chr12:3524712
|
G | A | 1 | a0001c0001t0001g0353 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.76-15894G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524712 | ||||||
| chr12:3524960
|
T | C | 7 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-15646T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3524960 | ||||||
| chr12:3525076
|
G | C | 17 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0040others(14): Show | 17 | HG00558.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-15530G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525076 | ||||||
| chr12:3525117
|
G | A | 1 | a0001c0002t0002g0048 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.76-15489G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525117 | ||||||
| chr12:3525165
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-15441T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525165 | ||||||
| chr12:3525522
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.76-15084A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525522 | ||||||
| chr12:3525805
|
A | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0128a0001c0001t0001g0251others(9): Show | 12 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-14801A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525805 | ||||||
| chr12:3525908
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.76-14698A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525908 | ||||||
| chr12:3525926
|
A | T | 99 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0055others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.76-14680A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3525926 | ||||||
| chr12:3526491
|
G | A | 6 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-14115G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526491 | ||||||
| chr12:3526513
|
T | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(1): Show | 4 | NA18747.hp1 NA18959.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-14093T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526513 | ||||||
| chr12:3526515
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-14091C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526515 | ||||||
| chr12:3526565
|
T | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(21): Show | 24 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-14041T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526565 | ||||||
| chr12:3526616
|
T | C | 2 | a0001c0001t0002g0347a0001c0002t0002g0348 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.76-13990T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526616 | ||||||
| chr12:3526743
|
C | A | 2 | a0001c0001t0001g0324a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-13863C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526743 | ||||||
| chr12:3526919
|
A | G | 7 | a0001c0001t0001g0104a0001c0001t0001g0266a0001c0001t0001g0283others(4): Show | 7 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-13687A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526919 | ||||||
| chr12:3526921
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.76-13685T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526921 | ||||||
| chr12:3526958
|
A | C | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-13648A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526958 | ||||||
| chr12:3526994
|
G | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0213others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-13612G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3526994 | ||||||
| chr12:3527335
|
G | GGCGGGCA others(13): Show |
1 | a0001c0002t0002g0264 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-13269_76-13250d others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3527335 | |||||
| chr12:3527350
|
C | T | 1 | a0001c0002t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-13256C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3527350 | ||||||
| chr12:3527475
|
G | A | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.76-13131G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3527475 | ||||||
| chr12:3527565
|
T | C | 1 | a0001c0001t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.76-13041T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3527565 | ||||||
| chr12:3528062
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-12544C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528062 | ||||||
| chr12:3528195
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.76-12411T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528195 | ||||||
| chr12:3528231
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0335 | 3 | HG01257.hp2 HG01258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.76-12375C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528231 | ||||||
| chr12:3528232
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-12374G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528232 | ||||||
| chr12:3528284
|
G | A | 80 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(77): Show | 80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.76-12322G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528284 | ||||||
| chr12:3528499
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-12107C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528499 | ||||||
| chr12:3528501
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.76-12105G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528501 | ||||||
| chr12:3528503
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.76-12103C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528503 | ||||||
| chr12:3528633
|
G | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0049others(14): Show | 17 | HG00597.hp2 HG00733.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-11973G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528633 | ||||||
| chr12:3528653
|
AT | A | 6 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0108others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-11945delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3528653 | |||||
| chr12:3528679
|
T | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0002t0002g0102 | 3 | HG02922.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.76-11927T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528679 | ||||||
| chr12:3528706
|
AT | A | 11 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(8): Show | 11 | HG02523.hp2 HG02976.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-11895delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3528706 | |||||
| chr12:3528852
|
T | A | 24 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(21): Show | 24 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.76-11754T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3528852 | ||||||
| chr12:3529114
|
C | G | 12 | a0001c0001t0001g0023a0001c0001t0001g0128a0001c0001t0001g0251others(9): Show | 12 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-11492C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529114 | ||||||
| chr12:3529153
|
C | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0151a0001c0001t0001g0203others(2): Show | 5 | HG00597.hp2 NA18942.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-11453C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529153 | ||||||
| chr12:3529251
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-11355C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529251 | ||||||
| chr12:3529267
|
TGG | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0128a0001c0001t0001g0251others(3): Show | 6 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-11336_76-11335d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3529267 | |||||
| chr12:3529352
|
C | G | 75 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0086others(72): Show | 75 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.76-11254C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529352 | ||||||
| chr12:3529362
|
C | A | 2 | a0001c0001t0004g0013a0001c0001t0004g0038 | 2 | NA18968.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.76-11244C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529362 | ||||||
| chr12:3529396
|
G | T | 7 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(4): Show | 7 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-11210G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529396 | ||||||
| chr12:3529835
|
A | C | 1 | a0001c0001t0001g0033 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.76-10771A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529835 | ||||||
| chr12:3529836
|
C | A | 1 | a0001c0001t0001g0033 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.76-10770C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529836 | ||||||
| chr12:3529849
|
A | G | 5 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0213others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-10757A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529849 | ||||||
| chr12:3529849
|
A | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-10757A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529849 | ||||||
| chr12:3529919
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.76-10687C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529919 | ||||||
| chr12:3529922
|
G | A | 11 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(8): Show | 11 | HG02523.hp2 HG02976.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-10684G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529922 | ||||||
| chr12:3529988
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-10618T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3529988 | ||||||
| chr12:3530393
|
G | T | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-10213G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530393 | ||||||
| chr12:3530591
|
A | G | 12 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 12 | HG02523.hp2 HG02630.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.76-10015A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530591 | ||||||
| chr12:3530643
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-9963C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530643 | ||||||
| chr12:3530683
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.76-9923G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530683 | ||||||
| chr12:3530743
|
C | G | 104 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0055others(101): Show | 104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.76-9863C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530743 | ||||||
| chr12:3530774
|
C | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 7 | HG00639.hp2 HG01074.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.76-9832C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530774 | ||||||
| chr12:3530798
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0177 | 2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.76-9808G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530798 | ||||||
| chr12:3530898
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0146a0001c0001t0001g0147others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-9708C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3530898 | ||||||
| chr12:3531128
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0049others(15): Show | 18 | HG00597.hp2 HG00733.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-9478C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531128 | ||||||
| chr12:3531175
|
G | GT | 25 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(22): Show | 25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-9430dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3531175 | |||||
| chr12:3531187
|
A | G | 2 | a0001c0001t0001g0339a0001c0001t0006g0346 | 2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.76-9419A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531187 | ||||||
| chr12:3531324
|
A | T | 10 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(7): Show | 10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-9282A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531324 | ||||||
| chr12:3531572
|
G | T | 1 | a0001c0002t0002g0027 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.76-9034G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531572 | ||||||
| chr12:3531582
|
A | G | 26 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0117others(23): Show | 26 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.76-9024A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531582 | ||||||
| chr12:3531648
|
T | C | 25 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(22): Show | 25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-8958T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531648 | ||||||
| chr12:3531674
|
C | T | 1 | a0001c0003t0001g0291 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.76-8932C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531674 | ||||||
| chr12:3531716
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0007g0313 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.76-8890C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531716 | ||||||
| chr12:3531717
|
G | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(52): Show | 56 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.76-8889G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531717 | ||||||
| chr12:3531789
|
T | G | 25 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(22): Show | 25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-8817T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531789 | ||||||
| chr12:3531879
|
G | C | 2 | a0001c0001t0001g0317a0001c0001t0001g0319 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.76-8727G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3531879 | ||||||
| chr12:3532050
|
A | G | 2 | a0001c0002t0002g0249a0001c0002t0002g0345 | 2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.76-8556A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532050 | ||||||
| chr12:3532060
|
G | A | 9 | a0001c0001t0001g0036a0001c0001t0001g0115a0001c0001t0001g0142others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-8546G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532060 | ||||||
| chr12:3532071
|
G | C | 1 | a0001c0002t0002g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-8535G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532071 | ||||||
| chr12:3532091
|
C | A | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-8515C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532091 | ||||||
| chr12:3532109
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG00438.hp1 HG00558.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-8497A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532109 | ||||||
| chr12:3532111
|
C | T | 4 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(1): Show | 4 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-8495C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532111 | ||||||
| chr12:3532151
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-8455G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532151 | ||||||
| chr12:3532396
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.76-8210G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532396 | ||||||
| chr12:3532478
|
G | T | 32 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0044others(29): Show | 32 | HG00735.hp1 HG01069.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.76-8128G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532478 | ||||||
| chr12:3532506
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.76-8100G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532506 | ||||||
| chr12:3532552
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.76-8054C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532552 | ||||||
| chr12:3532569
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0241 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.76-8037G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532569 | ||||||
| chr12:3532611
|
C | CA | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(44): Show | 47 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.76-7965dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532611
|
C | CAA | 19 | a0001c0001t0001g0141a0001c0001t0001g0154a0001c0001t0001g0158others(16): Show | 19 | HG01358.hp2 HG02109.hp1 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.76-7966_76-7965dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532611
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0254 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.76-7974_76-7965dup others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532611
|
CA | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0077others(61): Show | 65 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.76-7965delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532611
|
CAA | C | 14 | a0001c0001t0001g0113a0001c0001t0001g0215a0001c0001t0001g0224others(11): Show | 14 | HG00597.hp1 HG01123.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-7966_76-7965del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532611
|
CAAA | C | 68 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0055others(65): Show | 68 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.76-7967_76-7965del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532611
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-7974_76-7965del others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 3532611 | |||||
| chr12:3532763
|
A | C | 78 | a0001c0001t0001g0032a0001c0001t0001g0053a0001c0001t0001g0055others(75): Show | 78 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.76-7843A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532763 | ||||||
| chr12:3532970
|
G | A | 10 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(7): Show | 10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-7636G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3532970 | ||||||
| chr12:3533053
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.76-7553T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533053 | ||||||
| chr12:3533103
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.76-7503T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533103 | ||||||
| chr12:3533181
|
A | G | 6 | a0001c0001t0001g0323a0001c0004t0001g0314a0001c0004t0001g0321others(3): Show | 6 | HG00642.hp1 HG01175.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-7425A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533181 | ||||||
| chr12:3533260
|
G | A | 1 | a0001c0001t0007g0325 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.76-7346G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533260 | ||||||
| chr12:3533512
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.76-7094T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533512 | ||||||
| chr12:3533571
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.76-7035C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533571 | ||||||
| chr12:3533842
|
A | T | 1 | a0001c0001t0001g0266 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.76-6764A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3533842 | ||||||
| chr12:3534008
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6598C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534008 | ||||||
| chr12:3534118
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6488C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534118 | ||||||
| chr12:3534123
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6483T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534123 | ||||||
| chr12:3534221
|
T | C | 2 | a0001c0001t0001g0317a0001c0001t0001g0319 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.76-6385T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534221 | ||||||
| chr12:3534403
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-6203C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534403 | ||||||
| chr12:3534406
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76-6200C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534406 | ||||||
| chr12:3534467
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.76-6139C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534467 | ||||||
| chr12:3534516
|
C | G | 11 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(8): Show | 11 | HG02523.hp2 HG02976.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-6090C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534516 | ||||||
| chr12:3534524
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.76-6082C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534524 | ||||||
| chr12:3534752
|
G | A | 10 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(7): Show | 10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-5854G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534752 | ||||||
| chr12:3534823
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-5783G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534823 | ||||||
| chr12:3534876
|
G | A | 8 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.76-5730G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534876 | ||||||
| chr12:3534975
|
G | T | 1 | a0001c0001t0001g0349 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.76-5631G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3534975 | ||||||
| chr12:3535002
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.76-5604A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535002 | ||||||
| chr12:3535004
|
C | T | 6 | a0001c0001t0001g0224a0001c0001t0001g0337a0001c0001t0001g0339others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-5602C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535004 | ||||||
| chr12:3535026
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-5580T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535026 | ||||||
| chr12:3535174
|
C | T | 1 | a0001c0005t0001g0344 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.76-5432C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535174 | ||||||
| chr12:3535225
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-5381C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535225 | ||||||
| chr12:3535261
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.76-5345G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535261 | ||||||
| chr12:3535367
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-5239G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535367 | ||||||
| chr12:3535433
|
T | G | 20 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(17): Show | 20 | HG00735.hp1 HG01069.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-5173T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535433 | ||||||
| chr12:3535481
|
G | A | 115 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0053others(112): Show | 115 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-5125G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535481 | ||||||
| chr12:3535527
|
C | T | 19 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0117others(16): Show | 19 | HG00642.hp1 HG01175.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.76-5079C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535527 | ||||||
| chr12:3535608
|
G | C | 3 | a0001c0001t0001g0240a0001c0001t0007g0313a0001c0002t0011g0208 | 3 | HG02895.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.76-4998G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535608 | ||||||
| chr12:3535787
|
C | T | 5 | a0001c0001t0001g0323a0001c0004t0001g0314a0001c0004t0001g0321others(2): Show | 5 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4819C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535787 | ||||||
| chr12:3535862
|
C | T | 4 | a0001c0001t0001g0243a0001c0001t0001g0340a0001c0005t0001g0270others(1): Show | 4 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-4744C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535862 | ||||||
| chr12:3535908
|
C | G | 2 | a0001c0001t0001g0254a0001c0002t0002g0212 | 2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.76-4698C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535908 | ||||||
| chr12:3535948
|
A | G | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.76-4658A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535948 | ||||||
| chr12:3535963
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.76-4643C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535963 | ||||||
| chr12:3535980
|
C | A | 1 | a0001c0001t0010g0302 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.76-4626C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3535980 | ||||||
| chr12:3536008
|
T | C | 3 | a0001c0001t0001g0341a0001c0002t0002g0097a0001c0002t0002g0348 | 3 | HG02572.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.76-4598T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536008 | ||||||
| chr12:3536186
|
C | T | 9 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-4420C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536186 | ||||||
| chr12:3536265
|
T | C | 31 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0051others(28): Show | 31 | HG00642.hp1 HG01175.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-4341T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536265 | ||||||
| chr12:3536267
|
T | C | 31 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0051others(28): Show | 31 | HG00642.hp1 HG01175.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.76-4339T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536267 | ||||||
| chr12:3536480
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-4126G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536480 | ||||||
| chr12:3536504
|
G | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0335a0001c0001t0001g0340others(2): Show | 5 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-4102G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536504 | ||||||
| chr12:3536522
|
C | T | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.76-4084C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3536522 | ||||||
| chr12:3537046
|
T | C | 7 | a0001c0001t0001g0081a0001c0001t0001g0179a0001c0001t0001g0229others(4): Show | 7 | HG00438.hp2 NA18612.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-3560T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537046 | ||||||
| chr12:3537076
|
T | A | 25 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(22): Show | 25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-3530T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537076 | ||||||
| chr12:3537102
|
A | T | 25 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0128others(22): Show | 25 | HG01261.hp1 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.76-3504A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537102 | ||||||
| chr12:3537282
|
G | T | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.76-3324G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537282 | ||||||
| chr12:3537284
|
T | G | 9 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0330others(6): Show | 9 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-3322T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537284 | ||||||
| chr12:3537402
|
G | C | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.76-3204G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537402 | ||||||
| chr12:3537452
|
C | A | 10 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(7): Show | 10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-3154C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537452 | ||||||
| chr12:3537540
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.76-3066T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537540 | ||||||
| chr12:3537758
|
A | G | 10 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0158others(7): Show | 10 | HG02523.hp2 NA18747.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-2848A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537758 | ||||||
| chr12:3537996
|
T | C | 4 | a0001c0001t0001g0243a0001c0001t0001g0340a0001c0005t0001g0270others(1): Show | 4 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-2610T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3537996 | ||||||
| chr12:3538102
|
T | C | 142 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0050others(139): Show | 142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.76-2504T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538102 | ||||||
| chr12:3538117
|
C | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-2489C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538117 | ||||||
| chr12:3538239
|
A | T | 10 | a0001c0001t0001g0255a0001c0001t0001g0328a0001c0001t0001g0329others(7): Show | 10 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-2367A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538239 | ||||||
| chr12:3538365
|
C | T | 9 | a0001c0001t0001g0023a0001c0001t0001g0128a0001c0001t0001g0251others(6): Show | 9 | HG01109.hp2 HG01261.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-2241C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538365 | ||||||
| chr12:3538471
|
C | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0213others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.76-2135C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538471 | ||||||
| chr12:3538600
|
C | T | 152 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0032others(149): Show | 152 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.76-2006C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538600 | ||||||
| chr12:3538625
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.76-1981C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538625 | ||||||
| chr12:3538669
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.76-1937G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538669 | ||||||
| chr12:3538704
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0001g0327 | 2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.76-1902A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538704 | ||||||
| chr12:3538876
|
G | C | 4 | a0001c0001t0001g0243a0001c0001t0001g0340a0001c0005t0001g0270others(1): Show | 4 | HG01346.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-1730G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538876 | ||||||
| chr12:3538926
|
G | A | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.76-1680G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538926 | ||||||
| chr12:3538985
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.76-1621C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3538985 | ||||||
| chr12:3539080
|
T | C | 3 | a0001c0001t0001g0358a0001c0002t0002g0249a0002c0008t0001g0355 | 3 | HG01109.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.76-1526T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539080 | ||||||
| chr12:3539233
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-1373A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539233 | ||||||
| chr12:3539368
|
C | G | 309 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(306): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.76-1238C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539368 | ||||||
| chr12:3539929
|
C | T | 1 | a0001c0001t0001g0350 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.76-677C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3539929 | ||||||
| chr12:3540160
|
A | G | 78 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.76-446A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540160 | ||||||
| chr12:3540215
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.76-391G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540215 | ||||||
| chr12:3540245
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0059a0001c0001t0001g0119 | 3 | HG00140.hp1 HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.76-361C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540245 | ||||||
| chr12:3540392
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.76-214T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540392 | ||||||
| chr12:3540392
|
T | G | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.76-214T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540392 | ||||||
| chr12:3540447
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.76-159G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540447 | ||||||
| chr12:3540522
|
G | C | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.76-84G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 1/9 | chr12 | 3540522 | ||||||
| chr12:3540798
|
T | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01261.hp2 HG01358.hp1 |
splice_region_variant&intron_variant | LOW | c.261+7T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540798 | ||||||
| chr12:3540804
|
G | A | 1 | a0001c0002t0002g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.261+13G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540804 | ||||||
| chr12:3540967
|
C | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0111 | 2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.261+176C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540967 | ||||||
| chr12:3540990
|
T | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(355): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.261+199T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3540990 | ||||||
| chr12:3541120
|
G | A | 1 | a0001c0001t0001g0353 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.261+329G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541120 | ||||||
| chr12:3541197
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0111 | 2 | HG00099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.261+406G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541197 | ||||||
| chr12:3541215
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.261+424T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541215 | ||||||
| chr12:3541226
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.261+435G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541226 | ||||||
| chr12:3541277
|
C | T | 108 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.261+486C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541277 | ||||||
| chr12:3541337
|
A | C | 1 | a0001c0001t0001g0284 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.261+546A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541337 | ||||||
| chr12:3541529
|
T | C | 89 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(86): Show | 89 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.261+738T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541529 | ||||||
| chr12:3541566
|
G | A | 3 | a0001c0004t0001g0314a0001c0004t0001g0321a0001c0004t0001g0322 | 3 | HG00642.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.261+775G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541566 | ||||||
| chr12:3541665
|
C | T | 4 | a0001c0004t0001g0314a0001c0004t0001g0321a0001c0004t0001g0322others(1): Show | 4 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+874C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541665 | ||||||
| chr12:3541783
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+992G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541783 | ||||||
| chr12:3541909
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.261+1118C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541909 | ||||||
| chr12:3541953
|
G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0188others(1): Show | 4 | HG01192.hp1 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1162G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541953 | ||||||
| chr12:3541994
|
A | C | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.261+1203A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3541994 | ||||||
| chr12:3542021
|
A | AT | 111 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+1231dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3542021 | |||||
| chr12:3542061
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.261+1270C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542061 | ||||||
| chr12:3542222
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.261+1431G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542222 | ||||||
| chr12:3542225
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.261+1434C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542225 | ||||||
| chr12:3542232
|
T | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+1441T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542232 | ||||||
| chr12:3542283
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+1492G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542283 | ||||||
| chr12:3542438
|
G | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0337 | 3 | HG01261.hp2 HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.261+1647G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542438 | ||||||
| chr12:3542470
|
C | T | 2 | a0001c0001t0001g0173a0001c0002t0002g0174 | 2 | NA18967.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.261+1679C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542470 | ||||||
| chr12:3542528
|
A | G | 3 | a0001c0001t0001g0240a0001c0001t0007g0313a0001c0002t0002g0345 | 3 | HG03209.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.261+1737A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542528 | ||||||
| chr12:3542542
|
T | C | 2 | a0001c0001t0001g0100a0001c0002t0002g0007 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.261+1751T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542542 | ||||||
| chr12:3542586
|
G | C | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.261+1795G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542586 | ||||||
| chr12:3542615
|
C | T | 1 | a0001c0001t0001g0350 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.261+1824C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542615 | ||||||
| chr12:3542727
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.261+1936G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3542727 | ||||||
| chr12:3543045
|
A | G | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.261+2254A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543045 | ||||||
| chr12:3543135
|
C | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0278a0001c0001t0001g0307 | 3 | HG03490.hp1 HG03669.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.261+2344C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543135 | ||||||
| chr12:3543201
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.261+2410C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543201 | ||||||
| chr12:3543248
|
G | A | 1 | a0001c0001t0001g0356 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.261+2457G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543248 | ||||||
| chr12:3543460
|
T | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(104): Show | 107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+2669T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543460 | ||||||
| chr12:3543470
|
C | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(104): Show | 107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+2679C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543470 | ||||||
| chr12:3543590
|
G | C | 107 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(104): Show | 107 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261+2799G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543590 | ||||||
| chr12:3543592
|
C | T | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.261+2801C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543592 | ||||||
| chr12:3543600
|
G | A | 3 | a0001c0001t0001g0341a0001c0002t0002g0097a0001c0002t0002g0348 | 3 | HG02572.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.261+2809G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543600 | ||||||
| chr12:3543723
|
A | G | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.261+2932A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543723 | ||||||
| chr12:3543767
|
A | G | 358 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(355): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.261+2976A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543767 | ||||||
| chr12:3543834
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.261+3043G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543834 | ||||||
| chr12:3543854
|
A | G | 111 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.261+3063A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543854 | ||||||
| chr12:3543892
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.261+3101A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3543892 | ||||||
| chr12:3544141
|
G | A | 324 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.261+3350G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544141 | ||||||
| chr12:3544612
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0337 | 3 | HG01261.hp2 HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.261+3821C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544612 | ||||||
| chr12:3544613
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.261+3822G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544613 | ||||||
| chr12:3544670
|
A | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0172others(5): Show | 8 | HG00099.hp1 HG00741.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+3879A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544670 | ||||||
| chr12:3544752
|
A | T | 1 | a0001c0001t0001g0342 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261+3961A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544752 | ||||||
| chr12:3544784
|
C | T | 2 | a0001c0001t0001g0254a0001c0002t0002g0212 | 2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.261+3993C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544784 | ||||||
| chr12:3544812
|
C | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(322): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.261+4021C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3544812 | ||||||
| chr12:3545190
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.261+4399C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545190 | ||||||
| chr12:3545285
|
C | T | 351 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(348): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.261+4494C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545285 | ||||||
| chr12:3545321
|
A | G | 1 | a0001c0005t0001g0344 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.261+4530A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545321 | ||||||
| chr12:3545608
|
G | A | 31 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.262-4328G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545608 | ||||||
| chr12:3545648
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-4288C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545648 | ||||||
| chr12:3545682
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0049 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.262-4254C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545682 | ||||||
| chr12:3545685
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.262-4251G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545685 | ||||||
| chr12:3545929
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(95): Show | 99 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.262-4007G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3545929 | ||||||
| chr12:3546016
|
T | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0001t0001g0213others(3): Show | 6 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-3920T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546016 | ||||||
| chr12:3546096
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.262-3840C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546096 | ||||||
| chr12:3546486
|
G | A | 3 | a0001c0001t0001g0358a0001c0002t0002g0249a0002c0008t0001g0355 | 3 | HG01109.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.262-3450G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546486 | ||||||
| chr12:3546519
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.262-3417C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546519 | ||||||
| chr12:3546595
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0263 | 2 | NA18940.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.262-3341C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546595 | ||||||
| chr12:3546739
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.262-3197C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546739 | ||||||
| chr12:3546812
|
G | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0340a0001c0001t0001g0358others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-3124G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546812 | ||||||
| chr12:3546834
|
G | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-3102G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546834 | ||||||
| chr12:3546953
|
A | G | 23 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(20): Show | 23 | HG00597.hp2 HG00733.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.262-2983A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3546953 | ||||||
| chr12:3547050
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-2886A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547050 | ||||||
| chr12:3547184
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.262-2752G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547184 | ||||||
| chr12:3547261
|
G | A | 86 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0016others(83): Show | 87 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.262-2675G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547261 | ||||||
| chr12:3547407
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0089others(1): Show | 4 | HG02071.hp2 HG02165.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-2529A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547407 | ||||||
| chr12:3547481
|
A | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0002g0157others(1): Show | 4 | HG01358.hp2 HG02055.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-2455A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547481 | ||||||
| chr12:3547496
|
G | A | 1 | a0001c0002t0002g0027 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.262-2440G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547496 | ||||||
| chr12:3547504
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0098 | 2 | HG00733.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.262-2432A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547504 | ||||||
| chr12:3547568
|
C | T | 33 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(30): Show | 33 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.262-2368C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547568 | ||||||
| chr12:3547615
|
C | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-2321C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547615 | ||||||
| chr12:3547659
|
A | G | 33 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(30): Show | 33 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.262-2277A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547659 | ||||||
| chr12:3547764
|
A | G | 1 | a0001c0001t0001g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.262-2172A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3547764 | ||||||
| chr12:3547934
|
AG | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0328a0001c0001t0001g0329others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1999delG | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3547934 | |||||
| chr12:3548238
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.262-1698T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548238 | ||||||
| chr12:3548470
|
G | T | 1 | a0001c0001t0001g0343 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.262-1466G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548470 | ||||||
| chr12:3548520
|
A | G | 113 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0075others(110): Show | 113 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.262-1416A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548520 | ||||||
| chr12:3548574
|
G | GA | 26 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(23): Show | 26 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.262-1354dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3548574 | |||||
| chr12:3548574
|
GA | G | 10 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0201others(7): Show | 10 | NA18939.hp2 NA18942.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-1354delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3548574 | |||||
| chr12:3548692
|
T | C | 358 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(355): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.262-1244T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548692 | ||||||
| chr12:3548721
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.262-1215A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548721 | ||||||
| chr12:3548741
|
A | G | 11 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0001t0001g0213others(8): Show | 11 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.262-1195A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3548741 | ||||||
| chr12:3549186
|
T | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0044others(143): Show | 146 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.262-750T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549186 | ||||||
| chr12:3549497
|
CT | C | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.262-426delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3549497 | |||||
| chr12:3549497
|
CTT | C | 10 | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0001g0057others(7): Show | 10 | HG00099.hp1 HG00639.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-427_262-426del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3549497 | |||||
| chr12:3549510
|
T | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0128others(6): Show | 9 | HG00597.hp2 HG01069.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.262-426T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549510 | ||||||
| chr12:3549510
|
TA | T | 39 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0042others(36): Show | 39 | HG00280.hp1 HG00558.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.262-418delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 3549510 | |||||
| chr12:3549511
|
A | T | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0323others(1): Show | 4 | HG01261.hp2 HG01358.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-425A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549511 | ||||||
| chr12:3549565
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-371G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549565 | ||||||
| chr12:3549608
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.262-328C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549608 | ||||||
| chr12:3549609
|
G | A | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262-327G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549609 | ||||||
| chr12:3549719
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.262-217G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549719 | ||||||
| chr12:3549723
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.262-213T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 2/9 | chr12 | 3549723 | ||||||
| chr12:3550159
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(15): Show | 18 | HG00733.hp1 HG02055.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.417+68C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550159 | ||||||
| chr12:3550310
|
C | T | 16 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0001g0183others(13): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.417+219C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550310 | ||||||
| chr12:3550399
|
G | T | 1 | a0001c0001t0014g0002 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.417+308G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550399 | ||||||
| chr12:3550410
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.417+319G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550410 | ||||||
| chr12:3550496
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0119 | 2 | HG00140.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.417+405C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550496 | ||||||
| chr12:3550597
|
A | G | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+506A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550597 | ||||||
| chr12:3550611
|
C | T | 11 | a0001c0001t0001g0198a0001c0001t0001g0240a0001c0001t0001g0317others(8): Show | 11 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+520C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550611 | ||||||
| chr12:3550727
|
G | T | 3 | a0001c0001t0001g0240a0001c0001t0007g0313a0001c0002t0002g0345 | 3 | HG03209.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.417+636G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550727 | ||||||
| chr12:3550818
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0003g0060 | 2 | HG01346.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.417+727G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3550818 | ||||||
| chr12:3551004
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.417+913C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551004 | ||||||
| chr12:3551048
|
T | C | 3 | a0001c0004t0001g0314a0001c0004t0001g0321a0001c0004t0001g0322 | 3 | HG00642.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.417+957T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551048 | ||||||
| chr12:3551076
|
A | AC | 98 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0034others(95): Show | 98 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.417+994dupC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 3551076 | |||||
| chr12:3551076
|
A | ACC | 42 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0077others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.417+993_417+994dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 3551076 | |||||
| chr12:3551076
|
A | ACCC | 20 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(17): Show | 20 | HG00642.hp1 HG01071.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.417+992_417+994dup others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 3551076 | |||||
| chr12:3551080
|
C | G | 1 | a0001c0001t0001g0205 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.417+989C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551080 | ||||||
| chr12:3551085
|
C | T | 5 | a0001c0001t0001g0243a0001c0001t0001g0340a0001c0001t0001g0358others(2): Show | 5 | HG01109.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+994C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551085 | ||||||
| chr12:3551226
|
C | T | 11 | a0001c0001t0001g0198a0001c0001t0001g0240a0001c0001t0001g0317others(8): Show | 11 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+1135C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551226 | ||||||
| chr12:3551227
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+1136G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551227 | ||||||
| chr12:3551369
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.417+1278C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551369 | ||||||
| chr12:3551459
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.417+1368G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551459 | ||||||
| chr12:3551489
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.417+1398C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551489 | ||||||
| chr12:3551632
|
C | T | 2 | a0001c0001t0001g0353a0001c0003t0001g0354 | 2 | NA18951.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.417+1541C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551632 | ||||||
| chr12:3551788
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.417+1697C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551788 | ||||||
| chr12:3551813
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(95): Show | 99 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.417+1722G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3551813 | ||||||
| chr12:3552183
|
C | T | 1 | a0001c0002t0002g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.418-1468C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552183 | ||||||
| chr12:3552372
|
C | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-1279C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552372 | ||||||
| chr12:3552393
|
T | C | 174 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0024others(171): Show | 174 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.418-1258T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552393 | ||||||
| chr12:3552419
|
AC | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0016others(24): Show | 27 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418-1231delC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552419 | ||||||
| chr12:3552450
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0001t0001g0213 | 3 | HG02280.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.418-1201C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552450 | ||||||
| chr12:3552463
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.418-1188A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552463 | ||||||
| chr12:3552530
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.418-1121C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552530 | ||||||
| chr12:3552795
|
C | T | 4 | a0001c0001t0001g0251a0001c0001t0001g0276a0001c0001t0001g0277others(1): Show | 4 | HG00639.hp1 HG01261.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-856C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552795 | ||||||
| chr12:3552846
|
C | CTTAGCA | 4 | a0001c0001t0001g0324a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.418-805_418-804ins others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552846 | ||||||
| chr12:3552875
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.418-776A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552875 | ||||||
| chr12:3552902
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.418-749G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552902 | ||||||
| chr12:3552956
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-695G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3552956 | ||||||
| chr12:3553060
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.418-591C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553060 | ||||||
| chr12:3553078
|
C | T | 86 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0014others(83): Show | 87 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.418-573C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553078 | ||||||
| chr12:3553088
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.418-563A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553088 | ||||||
| chr12:3553118
|
G | T | 1 | a0001c0001t0001g0251 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.418-533G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553118 | ||||||
| chr12:3553217
|
C | T | 2 | a0001c0001t0001g0214a0001c0002t0002g0282 | 2 | HG01070.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.418-434C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553217 | ||||||
| chr12:3553265
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0273a0001c0001t0001g0320 | 3 | HG02300.hp1 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.418-386C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553265 | ||||||
| chr12:3553305
|
C | T | 1 | a0001c0001t0013g0018 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.418-346C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553305 | ||||||
| chr12:3553315
|
G | C | 18 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG00280.hp1 HG01123.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.418-336G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553315 | ||||||
| chr12:3553444
|
C | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0274others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-207C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553444 | ||||||
| chr12:3553488
|
G | T | 2 | a0001c0001t0001g0088a0001c0001t0002g0347 | 2 | HG02258.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.418-163G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553488 | ||||||
| chr12:3553489
|
G | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0037 | 2 | NA18961.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.418-162G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553489 | ||||||
| chr12:3553590
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0146others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.418-61G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 3/9 | chr12 | 3553590 | ||||||
| chr12:3553756
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.481+42C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553756 | ||||||
| chr12:3553799
|
G | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0274others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+85G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553799 | ||||||
| chr12:3553800
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.481+86C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553800 | ||||||
| chr12:3553808
|
A | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+94A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553808 | ||||||
| chr12:3553835
|
A | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(7): Show | 10 | HG01891.hp1 HG02056.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+121A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553835 | ||||||
| chr12:3553984
|
C | G | 9 | a0001c0001t0001g0003a0001c0001t0001g0139a0001c0001t0001g0172others(6): Show | 9 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.481+270C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3553984 | ||||||
| chr12:3554676
|
AG | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+967delG | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3554676 | |||||
| chr12:3554681
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.481+967G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554681 | ||||||
| chr12:3554699
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+985G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554699 | ||||||
| chr12:3554774
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+1060C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554774 | ||||||
| chr12:3554832
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481+1118A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554832 | ||||||
| chr12:3554918
|
T | G | 4 | a0001c0001t0004g0013a0001c0001t0004g0038a0001c0001t0004g0193others(1): Show | 4 | NA18955.hp2 NA18968.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+1204T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554918 | ||||||
| chr12:3554949
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+1235G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554949 | ||||||
| chr12:3554952
|
C | A | 2 | a0001c0001t0001g0100a0001c0002t0002g0007 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.481+1238C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3554952 | ||||||
| chr12:3555271
|
C | T | 58 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0032others(55): Show | 58 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.481+1557C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555271 | ||||||
| chr12:3555468
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.481+1754G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555468 | ||||||
| chr12:3555538
|
C | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+1824C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555538 | ||||||
| chr12:3555617
|
A | G | 6 | a0001c0001t0001g0100a0001c0001t0001g0156a0001c0001t0001g0160others(3): Show | 6 | HG01358.hp2 HG01952.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.481+1903A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555617 | ||||||
| chr12:3555780
|
AGGACCTG others(157): Show |
A | 126 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0032others(123): Show | 126 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.481+2077_481+2240d others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3555780 | |||||
| chr12:3555791
|
GTGCATTG others(157): Show |
G | 52 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0042others(49): Show | 52 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.481+2150_481+2313d others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3555791 | |||||
| chr12:3555931
|
A | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(97): Show | 101 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.481+2217A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555931 | ||||||
| chr12:3555967
|
T | C | 126 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0032others(123): Show | 126 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.481+2253T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3555967 | ||||||
| chr12:3556013
|
C | A | 7 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0358others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+2299C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556013 | ||||||
| chr12:3556040
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+2326G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556040 | ||||||
| chr12:3556150
|
A | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0054 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.481+2436A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556150 | ||||||
| chr12:3556520
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0055others(16): Show | 19 | HG01361.hp2 HG01934.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.481+2806G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556520 | ||||||
| chr12:3556635
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+2921G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556635 | ||||||
| chr12:3556673
|
T | A | 1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.481+2959T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556673 | ||||||
| chr12:3556673
|
TA | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0003g0063others(6): Show | 9 | HG00642.hp1 HG01169.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+2969delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3556673 | |||||
| chr12:3556674
|
A | T | 95 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0014others(92): Show | 96 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.481+2960A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556674 | ||||||
| chr12:3556675
|
A | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0057a0001c0001t0001g0240others(2): Show | 5 | HG03209.hp2 NA18906.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+2961A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556675 | ||||||
| chr12:3556739
|
G | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0017others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.481+3025G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556739 | ||||||
| chr12:3556747
|
G | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0017others(174): Show | 177 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.481+3033G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556747 | ||||||
| chr12:3556826
|
AGTGGAGG others(21): Show |
A | 1 | a0001c0001t0001g0224 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+3145_481+3172d others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3556826 | |||||
| chr12:3556861
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.481+3147G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556861 | ||||||
| chr12:3556920
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.481+3206C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556920 | ||||||
| chr12:3556923
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481+3209C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3556923 | ||||||
| chr12:3557376
|
G | A | 2 | a0001c0001t0001g0254a0001c0002t0002g0212 | 2 | HG02135.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.481+3662G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557376 | ||||||
| chr12:3557384
|
A | G | 358 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(355): Show | 359 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.481+3670A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557384 | ||||||
| chr12:3557412
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481+3698C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557412 | ||||||
| chr12:3557460
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0007g0313a0001c0002t0002g0345 | 3 | HG03209.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.481+3746G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557460 | ||||||
| chr12:3557539
|
G | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0328a0001c0001t0001g0329others(2): Show | 5 | HG02559.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+3825G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557539 | ||||||
| chr12:3557584
|
C | A | 1 | a0001c0010t0002g0216 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.481+3870C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557584 | ||||||
| chr12:3557643
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+3929G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557643 | ||||||
| chr12:3557652
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.481+3938C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557652 | ||||||
| chr12:3557819
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0336 | 2 | HG00738.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.481+4105G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557819 | ||||||
| chr12:3557994
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.481+4280C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3557994 | ||||||
| chr12:3558225
|
T | TCTCCCCT others(2): Show |
10 | a0001c0001t0001g0198a0001c0001t0001g0240a0001c0001t0001g0317others(7): Show | 10 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.481+4532_481+4540d others(11): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558225 | |||||
| chr12:3558225
|
T | TCTCCCCT others(20): Show |
1 | a0001c0002t0002g0345 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.481+4514_481+4540d others(29): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558225 | |||||
| chr12:3558301
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+4587A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558301 | ||||||
| chr12:3558302
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+4588T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558302 | ||||||
| chr12:3558371
|
C | T | 2 | a0001c0001t0001g0192a0001c0002t0002g0190 | 2 | HG02698.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.481+4657C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558371 | ||||||
| chr12:3558463
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.481+4749G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558463 | ||||||
| chr12:3558464
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.481+4750T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558464 | ||||||
| chr12:3558658
|
T | C | 17 | a0001c0001t0001g0047a0001c0001t0001g0085a0001c0001t0001g0100others(14): Show | 17 | HG01099.hp1 HG01109.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.481+4944T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558658 | ||||||
| chr12:3558683
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+4969T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558683 | ||||||
| chr12:3558930
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+5216C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558930 | ||||||
| chr12:3558949
|
T | G | 119 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(116): Show | 119 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.481+5235T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558949 | ||||||
| chr12:3558949
|
TCTATCTA others(5): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+5247_481+5258d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558949 | |||||
| chr12:3558961
|
C | CCTAT | 92 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0053others(89): Show | 92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.481+5274_481+5277d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | CCTATCTA others(21): Show |
1 | a0001c0001t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.481+5254_481+5255i others(30): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | CCTATCTA others(1): Show |
61 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0016others(58): Show | 61 | HG00597.hp1 HG00597.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.481+5270_481+5277d others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | CCTATCTA others(5): Show |
61 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0040others(58): Show | 62 | HG00558.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.481+5266_481+5277d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | CCTATCTA others(9): Show |
14 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(11): Show | 14 | HG00099.hp1 HG01074.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.481+5262_481+5277d others(18): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | CCTATCTA others(13): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0049others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+5258_481+5277d others(22): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | CCTATCTA others(17): Show |
2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.481+5254_481+5277d others(26): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.481+5247C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558961 | ||||||
| chr12:3558961
|
CCTAT | C | 8 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0093others(5): Show | 8 | HG01175.hp1 HG01261.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.481+5274_481+5277d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558961
|
CCTATCTA others(5): Show |
C | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.481+5266_481+5277d others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558961 | |||||
| chr12:3558984
|
ATCTATCT others(1): Show |
A | 4 | a0001c0001t0001g0196a0001c0001t0001g0244a0001c0001t0001g0245others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+5278_481+5285d others(10): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3558984 | |||||
| chr12:3558992
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.481+5278G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3558992 | ||||||
| chr12:3559048
|
T | G | 1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.481+5334T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559048 | ||||||
| chr12:3559235
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.481+5521G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559235 | ||||||
| chr12:3559489
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.481+5775G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559489 | ||||||
| chr12:3559503
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.481+5789G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559503 | ||||||
| chr12:3559584
|
T | A | 4 | a0001c0004t0001g0314a0001c0004t0001g0321a0001c0004t0001g0322others(1): Show | 4 | HG00642.hp1 HG01175.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+5870T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559584 | ||||||
| chr12:3559823
|
G | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(119): Show | 122 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.481+6109G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559823 | ||||||
| chr12:3559835
|
G | A | 3 | a0001c0001t0001g0341a0001c0002t0002g0097a0001c0002t0002g0348 | 3 | HG02572.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.481+6121G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559835 | ||||||
| chr12:3559938
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481+6224C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3559938 | ||||||
| chr12:3560036
|
C | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+6322C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560036 | ||||||
| chr12:3560088
|
C | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0337 | 3 | HG01261.hp2 HG01358.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.481+6374C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560088 | ||||||
| chr12:3560172
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.481+6458G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560172 | ||||||
| chr12:3560458
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.481+6744G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560458 | ||||||
| chr12:3560665
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(5): Show | 8 | NA18966.hp2 NA18977.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+6951A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560665 | ||||||
| chr12:3560873
|
C | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(108): Show | 111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.481+7159C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560873 | ||||||
| chr12:3560979
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.481+7265G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560979 | ||||||
| chr12:3560985
|
T | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(114): Show | 117 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.481+7271T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3560985 | ||||||
| chr12:3561167
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0333 | 2 | HG01074.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.481+7453C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561167 | ||||||
| chr12:3561186
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481+7472G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561186 | ||||||
| chr12:3561252
|
G | A | 4 | a0001c0001t0001g0356a0001c0001t0001g0360a0001c0001t0001g0361others(1): Show | 4 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-7454G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561252 | ||||||
| chr12:3561500
|
C | T | 1 | a0001c0005t0001g0300 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.482-7206C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561500 | ||||||
| chr12:3561559
|
C | G | 1 | a0001c0002t0002g0041 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.482-7147C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561559 | ||||||
| chr12:3561688
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0171 | 2 | HG00733.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.482-7018G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3561688 | ||||||
| chr12:3562125
|
A | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0236 | 2 | NA18944.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.482-6581A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562125 | ||||||
| chr12:3562149
|
G | A | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482-6557G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562149 | ||||||
| chr12:3562340
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482-6366G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562340 | ||||||
| chr12:3562357
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.482-6349G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562357 | ||||||
| chr12:3562390
|
G | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(17): Show | 20 | HG00597.hp2 HG00733.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.482-6316G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562390 | ||||||
| chr12:3562506
|
G | A | 58 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0032others(55): Show | 58 | HG00280.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.482-6200G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562506 | ||||||
| chr12:3562547
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.482-6159G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562547 | ||||||
| chr12:3562747
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0339a0001c0001t0006g0346 | 3 | HG02723.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.482-5959T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562747 | ||||||
| chr12:3562752
|
T | C | 1 | a0001c0002t0002g0264 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.482-5954T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3562752 | ||||||
| chr12:3563024
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.482-5682G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563024 | ||||||
| chr12:3563258
|
C | T | 3 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0315 | 3 | HG00639.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.482-5448C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563258 | ||||||
| chr12:3563259
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0001g0340 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.482-5447G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563259 | ||||||
| chr12:3563287
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0273a0001c0001t0001g0320 | 3 | HG02300.hp1 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.482-5419G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563287 | ||||||
| chr12:3563290
|
C | T | 2 | a0001c0003t0001g0076a0001c0003t0001g0291 | 2 | NA18967.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.482-5416C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563290 | ||||||
| chr12:3563374
|
T | A | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482-5332T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563374 | ||||||
| chr12:3563433
|
G | C | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.482-5273G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563433 | ||||||
| chr12:3563553
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0108a0001c0001t0001g0139others(10): Show | 13 | HG00099.hp1 HG00741.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.482-5153G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563553 | ||||||
| chr12:3563554
|
CAGG | C | 16 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0001g0183others(13): Show | 17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-5149_482-5147d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3563554 | |||||
| chr12:3563563
|
G | T | 30 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(27): Show | 30 | HG00280.hp1 HG00642.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.482-5143G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563563 | ||||||
| chr12:3563609
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482-5097C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563609 | ||||||
| chr12:3563617
|
T | G | 1 | a0001c0002t0002g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.482-5089T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563617 | ||||||
| chr12:3563695
|
G | A | 2 | a0001c0001t0001g0100a0001c0002t0002g0007 | 2 | HG01952.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.482-5011G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563695 | ||||||
| chr12:3563811
|
G | C | 3 | a0001c0004t0001g0314a0001c0004t0001g0321a0001c0004t0001g0322 | 3 | HG00642.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.482-4895G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563811 | ||||||
| chr12:3563928
|
G | GC | 112 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(109): Show | 112 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.482-4772dupC | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3563928 | |||||
| chr12:3563935
|
A | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-4771A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563935 | ||||||
| chr12:3563935
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(176): Show | 180 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.482-4771A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3563935 | ||||||
| chr12:3564172
|
C | T | 21 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(18): Show | 21 | HG00597.hp2 HG00733.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.482-4534C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564172 | ||||||
| chr12:3564204
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0349a0001c0001t0001g0351others(1): Show | 4 | NA18980.hp1 NA19064.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-4502G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564204 | ||||||
| chr12:3564271
|
G | C | 1 | a0001c0001t0001g0343 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.482-4435G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564271 | ||||||
| chr12:3564333
|
C | T | 115 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(112): Show | 115 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.482-4373C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564333 | ||||||
| chr12:3564334
|
G | A | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-4372G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564334 | ||||||
| chr12:3564377
|
G | C | 1 | a0001c0007t0001g0226 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.482-4329G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564377 | ||||||
| chr12:3564429
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.482-4277A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564429 | ||||||
| chr12:3564526
|
CAGG | C | 4 | a0001c0001t0001g0261a0001c0001t0001g0290a0001c0001t0001g0294others(1): Show | 4 | HG02056.hp2 HG02080.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4177_482-4175d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3564526 | |||||
| chr12:3564590
|
T | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(4): Show | 7 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-4116T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564590 | ||||||
| chr12:3564602
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.482-4104C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564602 | ||||||
| chr12:3564626
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.482-4080G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564626 | ||||||
| chr12:3564676
|
G | A | 116 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(113): Show | 116 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.482-4030G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564676 | ||||||
| chr12:3564759
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.482-3947G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564759 | ||||||
| chr12:3564907
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(3): Show | 6 | NA18966.hp2 NA18977.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-3799T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3564907 | ||||||
| chr12:3565292
|
G | A | 1 | a0001c0004t0001g0334 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.482-3414G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565292 | ||||||
| chr12:3565336
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.482-3370G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565336 | ||||||
| chr12:3565397
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.482-3309C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565397 | ||||||
| chr12:3565507
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(115): Show | 118 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.482-3199G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565507 | ||||||
| chr12:3565665
|
A | G | 117 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0044others(114): Show | 117 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.482-3041A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565665 | ||||||
| chr12:3565697
|
C | T | 3 | a0001c0001t0001g0159a0001c0001t0008g0052a0001c0002t0002g0155 | 3 | HG01891.hp1 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.482-3009C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565697 | ||||||
| chr12:3565710
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.482-2996A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565710 | ||||||
| chr12:3565714
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0012g0316 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.482-2992A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565714 | ||||||
| chr12:3565931
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0311 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.482-2775A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3565931 | ||||||
| chr12:3566054
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.482-2652C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566054 | ||||||
| chr12:3566102
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(21): Show | 24 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-2604A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566102 | ||||||
| chr12:3566178
|
GT | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0349a0001c0001t0001g0351others(1): Show | 4 | NA18980.hp1 NA19064.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-2527delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566178 | ||||||
| chr12:3566586
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.482-2120T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566586 | ||||||
| chr12:3566637
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482-2069A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566637 | ||||||
| chr12:3566660
|
G | A | 1 | a0001c0001t0008g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.482-2046G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566660 | ||||||
| chr12:3566675
|
C | A | 1 | a0001c0001t0001g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.482-2031C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566675 | ||||||
| chr12:3566824
|
A | T | 6 | a0001c0001t0001g0032a0001c0001t0001g0117a0001c0001t0001g0154others(3): Show | 6 | HG02056.hp1 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-1882A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566824 | ||||||
| chr12:3566941
|
A | G | 1 | a0001c0001t0008g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.482-1765A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566941 | ||||||
| chr12:3566955
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.482-1751A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3566955 | ||||||
| chr12:3567080
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.482-1626C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567080 | ||||||
| chr12:3567160
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.482-1546A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567160 | ||||||
| chr12:3567664
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.482-1042G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567664 | ||||||
| chr12:3567679
|
C | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0339a0001c0001t0006g0346 | 3 | HG02723.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.482-1027C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567679 | ||||||
| chr12:3567756
|
C | A | 6 | a0001c0001t0001g0198a0001c0001t0001g0356a0001c0001t0001g0360others(3): Show | 6 | HG01167.hp2 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-950C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567756 | ||||||
| chr12:3567811
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0281 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.482-895T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567811 | ||||||
| chr12:3567851
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0099others(14): Show | 17 | HG00741.hp2 HG01123.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.482-855A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567851 | ||||||
| chr12:3567871
|
T | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0273a0001c0001t0001g0320 | 3 | HG02300.hp1 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.482-835T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567871 | ||||||
| chr12:3567929
|
C | T | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.482-777C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3567929 | ||||||
| chr12:3568003
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.482-703C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568003 | ||||||
| chr12:3568028
|
C | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0328a0001c0001t0001g0329others(5): Show | 8 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-678C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568028 | ||||||
| chr12:3568033
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.482-673C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568033 | ||||||
| chr12:3568072
|
C | CA | 86 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(83): Show | 87 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.482-618dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | |||||
| chr12:3568072
|
C | CAA | 7 | a0001c0001t0001g0255a0001c0001t0001g0328a0001c0001t0001g0329others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-619_482-618dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | |||||
| chr12:3568072
|
CAA | C | 13 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0147others(10): Show | 13 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.482-619_482-618del others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | |||||
| chr12:3568072
|
CAAA | C | 29 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0058others(26): Show | 29 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-620_482-618del others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568072 | |||||
| chr12:3568162
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.482-544A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568162 | ||||||
| chr12:3568186
|
T | C | 3 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0001t0007g0325 | 3 | HG01167.hp2 HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.482-520T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568186 | ||||||
| chr12:3568306
|
C | CAGAGGTG others(7): Show |
1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.482-400_482-399ins others(14): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568306 | ||||||
| chr12:3568320
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0363 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.482-386A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568320 | ||||||
| chr12:3568332
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.482-374C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568332 | ||||||
| chr12:3568339
|
G | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0054others(4): Show | 7 | HG02896.hp2 HG02897.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.482-367G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568339 | ||||||
| chr12:3568347
|
T | TA | 6 | a0001c0001t0001g0053a0001c0001t0001g0100a0001c0001t0001g0358others(3): Show | 6 | HG01109.hp2 HG01952.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.482-347dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568347 | |||||
| chr12:3568347
|
TA | T | 170 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.482-347delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568347 | |||||
| chr12:3568352
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0340 | 2 | HG02258.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.482-354A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568352 | ||||||
| chr12:3568395
|
G | GGTT | 207 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(204): Show | 207 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.482-307_482-305dup others(3): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568395 | |||||
| chr12:3568461
|
G | A | 8 | a0001c0001t0001g0103a0001c0001t0001g0140a0001c0001t0001g0207others(5): Show | 8 | HG03209.hp2 HG06807.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-245G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568461 | ||||||
| chr12:3568478
|
C | T | 18 | a0001c0001t0001g0069a0001c0001t0001g0086a0001c0001t0001g0087others(15): Show | 18 | HG00673.hp2 HG02258.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.482-228C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568478 | ||||||
| chr12:3568610
|
AG | A | 9 | a0001c0001t0001g0055a0001c0001t0001g0068a0001c0001t0001g0135others(6): Show | 9 | HG00735.hp2 HG00738.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.482-93delG | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 3568610 | |||||
| chr12:3568628
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482-78T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 4/9 | chr12 | 3568628 | ||||||
| chr12:3568872
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.624+24C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3568872 | ||||||
| chr12:3568914
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.624+66G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3568914 | ||||||
| chr12:3568954
|
G | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0103a0001c0001t0001g0328others(3): Show | 6 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.624+106G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3568954 | ||||||
| chr12:3569023
|
C | T | 9 | a0001c0001t0001g0091a0001c0001t0001g0146a0001c0001t0001g0147others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+175C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569023 | ||||||
| chr12:3569085
|
A | G | 18 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 19 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.624+237A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569085 | ||||||
| chr12:3569207
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-270G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569207 | ||||||
| chr12:3569214
|
C | G | 1 | a0001c0001t0001g0292 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.625-263C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569214 | ||||||
| chr12:3569355
|
C | G | 3 | a0001c0001t0001g0351a0001c0003t0001g0354a0001c0007t0001g0226 | 3 | NA18951.hp1 NA19065.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.625-122C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569355 | ||||||
| chr12:3569386
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.625-91C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569386 | ||||||
| chr12:3569402
|
A | G | 26 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0031others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.625-75A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 5/9 | chr12 | 3569402 | ||||||
| chr12:3569579
|
G | A | 79 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0020others(76): Show | 80 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.712+15G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569579 | ||||||
| chr12:3569586
|
C | T | 5 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(2): Show | 5 | HG01261.hp2 HG01358.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.712+22C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569586 | ||||||
| chr12:3569752
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.712+188A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569752 | ||||||
| chr12:3569776
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0003g0181 | 2 | HG01192.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.712+212C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3569776 | ||||||
| chr12:3570020
|
T | C | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0069others(4): Show | 7 | HG01361.hp2 HG02273.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.712+456T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570020 | ||||||
| chr12:3570108
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.712+544G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570108 | ||||||
| chr12:3570233
|
G | C | 50 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(47): Show | 50 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.712+669G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570233 | ||||||
| chr12:3570388
|
A | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0171a0001c0001t0001g0200others(8): Show | 12 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.712+824A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570388 | ||||||
| chr12:3570412
|
A | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0055others(9): Show | 12 | HG00438.hp1 HG00741.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.712+848A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570412 | ||||||
| chr12:3570452
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.712+888G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570452 | ||||||
| chr12:3570489
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0243a0001c0001t0001g0340 | 3 | HG02109.hp1 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.712+925G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570489 | ||||||
| chr12:3570557
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(67): Show | 70 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.712+993G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570557 | ||||||
| chr12:3570613
|
T | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(67): Show | 70 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.712+1049T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570613 | ||||||
| chr12:3570672
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.712+1108C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570672 | ||||||
| chr12:3570693
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(65): Show | 68 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.712+1129G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570693 | ||||||
| chr12:3570861
|
A | T | 22 | a0001c0001t0001g0079a0001c0001t0001g0202a0001c0001t0001g0203others(19): Show | 22 | HG00621.hp2 HG00673.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.712+1297A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3570861 | ||||||
| chr12:3571014
|
C | T | 80 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0030others(77): Show | 81 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.712+1450C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571014 | ||||||
| chr12:3571169
|
G | C | 1 | a0001c0006t0001g0043 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.712+1605G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571169 | ||||||
| chr12:3571189
|
A | C | 11 | a0001c0001t0001g0090a0001c0001t0002g0157a0001c0001t0002g0209others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.712+1625A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571189 | ||||||
| chr12:3571396
|
G | A | 2 | a0001c0001t0002g0157a0001c0002t0011g0208 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.712+1832G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571396 | ||||||
| chr12:3571404
|
C | G | 1 | a0001c0001t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.712+1840C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571404 | ||||||
| chr12:3571493
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0268 | 2 | HG00621.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.712+1929G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571493 | ||||||
| chr12:3571700
|
C | T | 1 | a0001c0001t0003g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.712+2136C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571700 | ||||||
| chr12:3571902
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.712+2338A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571902 | ||||||
| chr12:3571913
|
T | G | 2 | a0001c0001t0001g0214a0001c0002t0009g0094 | 2 | HG01069.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.712+2349T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3571913 | ||||||
| chr12:3572186
|
A | G | 1 | a0001c0001t0001g0331 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.712+2622A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572186 | ||||||
| chr12:3572241
|
C | T | 2 | a0001c0002t0002g0048a0001c0002t0002g0348 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.712+2677C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572241 | ||||||
| chr12:3572345
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712+2781T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572345 | ||||||
| chr12:3572503
|
A | C | 1 | a0001c0001t0001g0030 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.712+2939A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572503 | ||||||
| chr12:3572633
|
C | T | 7 | a0001c0001t0001g0129a0001c0001t0001g0171a0001c0001t0001g0200others(4): Show | 8 | HG00558.hp1 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.712+3069C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572633 | ||||||
| chr12:3572658
|
C | G | 95 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0049others(92): Show | 95 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.712+3094C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572658 | ||||||
| chr12:3572667
|
A | C | 7 | a0001c0001t0001g0129a0001c0001t0001g0171a0001c0001t0001g0200others(4): Show | 8 | HG00558.hp1 HG00733.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.712+3103A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3572667 | ||||||
| chr12:3573150
|
A | T | 9 | a0001c0001t0002g0209a0001c0002t0002g0015a0001c0002t0002g0096others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.712+3586A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573150 | ||||||
| chr12:3573317
|
A | G | 78 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(75): Show | 79 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.713-3554A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573317 | ||||||
| chr12:3573467
|
T | C | 2 | a0001c0001t0001g0108a0001c0005t0001g0344 | 2 | HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.713-3404T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573467 | ||||||
| chr12:3573591
|
G | A | 1 | a0001c0002t0002g0027 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.713-3280G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573591 | ||||||
| chr12:3573781
|
C | G | 1 | a0001c0001t0001g0005 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.713-3090C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573781 | ||||||
| chr12:3573923
|
C | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA19074.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.713-2948C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3573923 | ||||||
| chr12:3574078
|
A | G | 1 | a0001c0001t0007g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.713-2793A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574078 | ||||||
| chr12:3574221
|
A | G | 66 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(63): Show | 66 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.713-2650A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574221 | ||||||
| chr12:3574398
|
A | G | 10 | a0001c0001t0001g0143a0001c0001t0002g0209a0001c0001t0007g0325others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.713-2473A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574398 | ||||||
| chr12:3574528
|
C | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA18980.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.713-2343C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574528 | ||||||
| chr12:3574630
|
G | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(61): Show | 64 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.713-2241G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574630 | ||||||
| chr12:3574760
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.713-2111C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574760 | ||||||
| chr12:3574876
|
A | G | 61 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(58): Show | 61 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.713-1995A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574876 | ||||||
| chr12:3574944
|
A | G | 1 | a0001c0004t0001g0321 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.713-1927A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3574944 | ||||||
| chr12:3575006
|
A | C | 1 | a0001c0001t0001g0324 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.713-1865A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575006 | ||||||
| chr12:3575632
|
A | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0343others(2): Show | 5 | HG01346.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-1239A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575632 | ||||||
| chr12:3575876
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.713-995C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575876 | ||||||
| chr12:3575890
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0002g0157a0001c0001t0002g0347 | 3 | HG01891.hp1 HG02258.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.713-981G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575890 | ||||||
| chr12:3575908
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.713-963A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575908 | ||||||
| chr12:3575912
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0047others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.713-959G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575912 | ||||||
| chr12:3575934
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(137): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.713-937A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3575934 | ||||||
| chr12:3576323
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.713-548T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576323 | ||||||
| chr12:3576338
|
T | A | 28 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.713-533T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576338 | ||||||
| chr12:3576424
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.713-447G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576424 | ||||||
| chr12:3576543
|
G | C | 2 | a0001c0001t0001g0343a0001c0001t0014g0002 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.713-328G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576543 | ||||||
| chr12:3576544
|
AAGGAAGA others(26): Show |
A | 2 | a0001c0001t0001g0343a0001c0001t0014g0002 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.713-326_713-294del others(33): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576544 | ||||||
| chr12:3576597
|
A | G | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(61): Show | 64 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.713-274A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576597 | ||||||
| chr12:3576700
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.713-171A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576700 | ||||||
| chr12:3576714
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.713-157A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576714 | ||||||
| chr12:3576829
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.713-42G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576829 | ||||||
| chr12:3576850
|
C | A | 2 | a0001c0001t0001g0143a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.713-21C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 6/9 | chr12 | 3576850 | ||||||
| chr12:3577031
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0128a0001c0001t0001g0301 | 3 | HG02074.hp1 NA18977.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.828+45C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577031 | ||||||
| chr12:3577151
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.828+165C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577151 | ||||||
| chr12:3577228
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.828+242G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577228 | ||||||
| chr12:3577229
|
C | T | 21 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0027others(18): Show | 21 | HG00673.hp1 HG00738.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.828+243C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577229 | ||||||
| chr12:3577281
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0014g0002 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.828+295C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577281 | ||||||
| chr12:3577302
|
C | T | 9 | a0001c0001t0002g0209a0001c0002t0002g0015a0001c0002t0002g0096others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+316C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577302 | ||||||
| chr12:3577316
|
T | G | 21 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0064others(18): Show | 21 | HG00558.hp2 HG00735.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.828+330T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577316 | ||||||
| chr12:3577405
|
A | T | 1 | a0001c0001t0002g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.828+419A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577405 | ||||||
| chr12:3577406
|
CACACCTT others(76): Show |
C | 2 | a0001c0001t0001g0343a0001c0001t0014g0002 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.828+485_828+567del others(83): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3577406 | |||||
| chr12:3577462
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.828+476G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577462 | ||||||
| chr12:3577479
|
C | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0196a0001c0001t0001g0198others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.828+493C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577479 | ||||||
| chr12:3577488
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.828+502A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577488 | ||||||
| chr12:3577678
|
AT | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(149): Show | 153 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.828+702delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3577678 | |||||
| chr12:3577684
|
T | C | 49 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0064others(46): Show | 49 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.828+698T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577684 | ||||||
| chr12:3577754
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.828+768G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577754 | ||||||
| chr12:3577776
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.828+790T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577776 | ||||||
| chr12:3577891
|
C | T | 4 | a0001c0001t0001g0159a0001c0001t0002g0157a0001c0001t0002g0347others(1): Show | 4 | HG01891.hp1 HG02258.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.828+905C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577891 | ||||||
| chr12:3577953
|
C | G | 9 | a0001c0001t0002g0209a0001c0002t0002g0015a0001c0002t0002g0096others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.828+967C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3577953 | ||||||
| chr12:3578055
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.828+1069A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578055 | ||||||
| chr12:3578086
|
T | TAAAG | 94 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(91): Show | 95 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.828+1101_828+1102i others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3578086 | |||||
| chr12:3578221
|
C | G | 6 | a0001c0001t0001g0143a0001c0001t0001g0159a0001c0001t0002g0157others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.828+1235C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578221 | ||||||
| chr12:3578331
|
T | C | 94 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(91): Show | 95 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.828+1345T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578331 | ||||||
| chr12:3578340
|
T | C | 77 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(74): Show | 77 | HG00099.hp1 HG00558.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.828+1354T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578340 | ||||||
| chr12:3578347
|
C | A | 2 | a0001c0001t0001g0337a0001c0001t0012g0316 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.828+1361C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578347 | ||||||
| chr12:3578391
|
A | AT | 18 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0083others(15): Show | 19 | HG00558.hp1 HG00597.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.828+1418dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3578391 | |||||
| chr12:3578623
|
A | G | 28 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.828+1637A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578623 | ||||||
| chr12:3578668
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0323 | 2 | HG01358.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.828+1682G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578668 | ||||||
| chr12:3578700
|
G | T | 1 | a0001c0001t0001g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.828+1714G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3578700 | ||||||
| chr12:3579018
|
T | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0289 | 2 | NA18992.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.828+2032T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579018 | ||||||
| chr12:3579151
|
T | C | 1 | a0001c0001t0007g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.828+2165T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579151 | ||||||
| chr12:3579245
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.828+2259G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579245 | ||||||
| chr12:3579262
|
A | G | 14 | a0001c0001t0001g0080a0001c0001t0001g0141a0001c0001t0001g0206others(11): Show | 14 | HG00423.hp1 HG00438.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.828+2276A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579262 | ||||||
| chr12:3579282
|
G | T | 1 | a0001c0002t0002g0345 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.828+2296G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579282 | ||||||
| chr12:3579532
|
G | A | 10 | a0001c0001t0002g0209a0001c0002t0002g0015a0001c0002t0002g0096others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.828+2546G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579532 | ||||||
| chr12:3579551
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.828+2565C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579551 | ||||||
| chr12:3579577
|
C | T | 2 | a0001c0001t0001g0337a0001c0001t0012g0316 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.828+2591C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579577 | ||||||
| chr12:3579677
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.828+2691T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579677 | ||||||
| chr12:3579678
|
G | A | 2 | a0001c0001t0001g0337a0001c0001t0012g0316 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.828+2692G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579678 | ||||||
| chr12:3579727
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.828+2741G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579727 | ||||||
| chr12:3579821
|
A | G | 93 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0030others(90): Show | 94 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.828+2835A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3579821 | ||||||
| chr12:3580036
|
T | A | 163 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(160): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.829-3022T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580036 | ||||||
| chr12:3580094
|
G | C | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.829-2964G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580094 | ||||||
| chr12:3580113
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0152others(2): Show | 5 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.829-2945C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580113 | ||||||
| chr12:3580217
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.829-2841G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580217 | ||||||
| chr12:3580335
|
T | TGC | 3 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0342 | 3 | HG01261.hp2 HG01358.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.829-2721_829-2720d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580335 | |||||
| chr12:3580337
|
C | CGT | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.829-2692_829-2691d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | |||||
| chr12:3580337
|
C | CGTGT | 50 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0046others(47): Show | 51 | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.829-2694_829-2691d others(6): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | |||||
| chr12:3580337
|
C | CGTGTGT | 4 | a0001c0001t0001g0156a0001c0001t0007g0313a0001c0001t0008g0052others(1): Show | 4 | HG02055.hp2 HG02135.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-2696_829-2691d others(8): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | |||||
| chr12:3580337
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0159 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.829-2700_829-2691d others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | |||||
| chr12:3580337
|
CGT | C | 8 | a0001c0001t0001g0030a0001c0001t0001g0099a0001c0001t0001g0108others(5): Show | 8 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.829-2692_829-2691d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580337 | |||||
| chr12:3580354
|
G | GTA | 9 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0107others(6): Show | 9 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.829-2703_829-2702i others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 3580354 | |||||
| chr12:3580371
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0049a0001c0001t0001g0185others(3): Show | 6 | HG00099.hp1 HG01081.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.829-2687C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580371 | ||||||
| chr12:3580379
|
T | C | 81 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(78): Show | 82 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.829-2679T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580379 | ||||||
| chr12:3580396
|
A | C | 1 | a0001c0001t0007g0313 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.829-2662A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580396 | ||||||
| chr12:3580450
|
A | G | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-2608A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580450 | ||||||
| chr12:3580484
|
G | A | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-2574G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580484 | ||||||
| chr12:3580518
|
A | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(23): Show | 26 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.829-2540A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580518 | ||||||
| chr12:3580679
|
C | T | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.829-2379C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580679 | ||||||
| chr12:3580737
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.829-2321A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580737 | ||||||
| chr12:3580869
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-2189C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580869 | ||||||
| chr12:3580998
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.829-2060G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3580998 | ||||||
| chr12:3581083
|
A | G | 251 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(248): Show | 252 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.829-1975A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581083 | ||||||
| chr12:3581225
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0159 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.829-1833G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581225 | ||||||
| chr12:3581322
|
C | T | 1 | a0001c0001t0001g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829-1736C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581322 | ||||||
| chr12:3581388
|
A | G | 68 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(65): Show | 68 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.829-1670A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581388 | ||||||
| chr12:3581418
|
C | T | 1 | a0001c0001t0001g0333 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.829-1640C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581418 | ||||||
| chr12:3581533
|
G | T | 2 | a0001c0001t0001g0337a0001c0001t0012g0316 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.829-1525G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581533 | ||||||
| chr12:3581647
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.829-1411C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581647 | ||||||
| chr12:3581711
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.829-1347A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581711 | ||||||
| chr12:3581791
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.829-1267G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581791 | ||||||
| chr12:3581866
|
A | G | 1 | a0001c0002t0002g0120 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.829-1192A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581866 | ||||||
| chr12:3581917
|
A | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(3): Show | 6 | HG00642.hp1 HG01346.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.829-1141A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581917 | ||||||
| chr12:3581966
|
T | C | 9 | a0001c0002t0002g0015a0001c0002t0002g0096a0001c0002t0002g0097others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-1092T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3581966 | ||||||
| chr12:3582053
|
C | G | 2 | a0001c0001t0001g0337a0001c0001t0012g0316 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.829-1005C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582053 | ||||||
| chr12:3582070
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.829-988A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582070 | ||||||
| chr12:3582198
|
G | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0295 | 2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.829-860G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582198 | ||||||
| chr12:3582271
|
G | A | 38 | a0001c0001t0001g0055a0001c0002t0002g0007a0001c0002t0002g0008others(35): Show | 38 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.829-787G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582271 | ||||||
| chr12:3582272
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.829-786C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582272 | ||||||
| chr12:3582328
|
A | G | 28 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.829-730A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582328 | ||||||
| chr12:3582393
|
T | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0050others(10): Show | 13 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.829-665T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582393 | ||||||
| chr12:3582443
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0206a0001c0001t0001g0310others(1): Show | 4 | NA18968.hp2 NA18969.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-615C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582443 | ||||||
| chr12:3582590
|
G | A | 8 | a0001c0001t0001g0083a0001c0001t0001g0129a0001c0001t0001g0171others(5): Show | 9 | HG00558.hp1 HG00733.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.829-468G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582590 | ||||||
| chr12:3582630
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.829-428C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582630 | ||||||
| chr12:3582662
|
A | C | 1 | a0001c0001t0001g0306 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.829-396A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582662 | ||||||
| chr12:3582766
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.829-292T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582766 | ||||||
| chr12:3582799
|
A | C | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.829-259A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582799 | ||||||
| chr12:3582813
|
G | A | 1 | a0001c0002t0002g0264 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.829-245G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582813 | ||||||
| chr12:3582876
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.829-182C>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582876 | ||||||
| chr12:3582940
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.829-118A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582940 | ||||||
| chr12:3582947
|
T | A | 3 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0268 | 3 | HG00621.hp2 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.829-111T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 7/9 | chr12 | 3582947 | ||||||
| chr12:3583237
|
C | T | 5 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(2): Show | 5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+29C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583237 | ||||||
| chr12:3583370
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(4): Show | 7 | HG01346.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+162T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583370 | ||||||
| chr12:3583540
|
T | A | 2 | a0001c0001t0001g0143a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.979+332T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583540 | ||||||
| chr12:3583544
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.979+336G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583544 | ||||||
| chr12:3583741
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.979+533G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583741 | ||||||
| chr12:3583746
|
C | T | 7 | a0001c0002t0002g0048a0001c0002t0002g0120a0001c0002t0002g0190others(4): Show | 7 | HG00735.hp1 HG01069.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+538C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583746 | ||||||
| chr12:3583848
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.979+640C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583848 | ||||||
| chr12:3583861
|
G | A | 1 | a0001c0002t0002g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.979+653G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583861 | ||||||
| chr12:3583936
|
T | C | 1 | a0001c0002t0002g0106 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.979+728T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3583936 | ||||||
| chr12:3584380
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.979+1172G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584380 | ||||||
| chr12:3584477
|
G | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0196a0001c0001t0001g0241others(3): Show | 6 | HG02055.hp1 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.979+1269G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584477 | ||||||
| chr12:3584487
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979+1279C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584487 | ||||||
| chr12:3584511
|
A | G | 1 | a0001c0001t0001g0353 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.979+1303A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584511 | ||||||
| chr12:3584645
|
A | C | 2 | a0001c0001t0001g0169a0001c0001t0004g0193 | 2 | HG02040.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.979+1437A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584645 | ||||||
| chr12:3584718
|
A | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(154): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.979+1510A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584718 | ||||||
| chr12:3584730
|
G | A | 1 | a0001c0003t0001g0072 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.979+1522G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584730 | ||||||
| chr12:3584816
|
C | T | 2 | a0001c0001t0001g0337a0001c0001t0012g0316 | 2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.979+1608C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3584816 | ||||||
| chr12:3585301
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(151): Show | 154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.979+2093G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585301 | ||||||
| chr12:3585322
|
C | T | 7 | a0001c0002t0002g0048a0001c0002t0002g0120a0001c0002t0002g0190others(4): Show | 7 | HG00735.hp1 HG01069.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+2114C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585322 | ||||||
| chr12:3585345
|
C | CT | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.979+2164dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | |||||
| chr12:3585345
|
C | CTT | 99 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0016others(96): Show | 100 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.979+2163_979+2164d others(4): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | |||||
| chr12:3585345
|
C | CTTT | 9 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0129others(6): Show | 9 | HG01934.hp1 HG01993.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.979+2162_979+2164d others(5): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | |||||
| chr12:3585345
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0009t0001g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.979+2155_979+2164d others(12): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | |||||
| chr12:3585345
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.979+2154_979+2164d others(13): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | |||||
| chr12:3585345
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0004t0001g0321 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.979+2152_979+2164d others(15): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585345 | |||||
| chr12:3585436
|
G | T | 1 | a0001c0001t0001g0129 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.979+2228G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585436 | ||||||
| chr12:3585532
|
A | AT | 262 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.979+2339dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3585532 | |||||
| chr12:3585650
|
G | T | 14 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0095others(11): Show | 14 | HG01109.hp2 HG01192.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.979+2442G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585650 | ||||||
| chr12:3585704
|
G | A | 2 | a0001c0001t0002g0347a0001c0004t0001g0321 | 2 | HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.979+2496G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585704 | ||||||
| chr12:3585714
|
C | T | 5 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(2): Show | 5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2506C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585714 | ||||||
| chr12:3585722
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0310a0001c0009t0001g0250 | 3 | NA18968.hp2 NA18995.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.979+2514G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585722 | ||||||
| chr12:3585728
|
T | G | 2 | a0001c0001t0004g0013a0001c0001t0004g0038 | 2 | NA18968.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.979+2520T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585728 | ||||||
| chr12:3585964
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.979+2756C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3585964 | ||||||
| chr12:3586078
|
T | A | 1 | a0001c0001t0001g0326 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.979+2870T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586078 | ||||||
| chr12:3586179
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.979+2971A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586179 | ||||||
| chr12:3586279
|
G | A | 1 | a0001c0004t0001g0334 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.979+3071G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586279 | ||||||
| chr12:3586315
|
T | C | 5 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(2): Show | 5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+3107T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586315 | ||||||
| chr12:3586354
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0098 | 2 | HG00733.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.979+3146G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586354 | ||||||
| chr12:3586452
|
C | T | 2 | a0001c0001t0007g0313a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.979+3244C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586452 | ||||||
| chr12:3586468
|
A | T | 4 | a0001c0001t0001g0079a0001c0001t0001g0118a0001c0001t0001g0217others(1): Show | 4 | NA18969.hp1 NA19009.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+3260A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586468 | ||||||
| chr12:3586635
|
A | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0328a0001c0001t0001g0329others(2): Show | 5 | HG02615.hp2 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.979+3427A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586635 | ||||||
| chr12:3586840
|
T | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(2): Show | 5 | HG01346.hp2 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+3632T>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586840 | ||||||
| chr12:3586858
|
C | T | 1 | a0001c0002t0011g0208 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.979+3650C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586858 | ||||||
| chr12:3586946
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.979+3738C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586946 | ||||||
| chr12:3586947
|
G | A | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.979+3739G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3586947 | ||||||
| chr12:3587052
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.979+3844C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587052 | ||||||
| chr12:3587202
|
T | G | 1 | a0001c0001t0001g0340 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.979+3994T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587202 | ||||||
| chr12:3587463
|
G | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0203a0001c0001t0001g0268 | 3 | HG00621.hp2 NA18998.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.979+4255G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587463 | ||||||
| chr12:3587512
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0278a0001c0001t0001g0284 | 3 | HG02300.hp1 HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.979+4304C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587512 | ||||||
| chr12:3587515
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0049 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.979+4307G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587515 | ||||||
| chr12:3587541
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0108a0001c0001t0001g0337others(4): Show | 7 | HG01346.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+4333T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587541 | ||||||
| chr12:3587781
|
T | C | 1 | a0001c0004t0001g0321 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.980-4450T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587781 | ||||||
| chr12:3587787
|
C | T | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.980-4444C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587787 | ||||||
| chr12:3587804
|
G | A | 1 | a0001c0002t0009g0094 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.980-4427G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587804 | ||||||
| chr12:3587875
|
C | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-4356C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3587875 | ||||||
| chr12:3588203
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0159 | 3 | HG01891.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.980-4028T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588203 | ||||||
| chr12:3588244
|
A | C | 9 | a0001c0001t0001g0083a0001c0001t0001g0129a0001c0001t0001g0171others(6): Show | 10 | HG00558.hp1 HG00733.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.980-3987A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588244 | ||||||
| chr12:3588593
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-3638C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588593 | ||||||
| chr12:3588673
|
A | G | 85 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(82): Show | 86 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.980-3558A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3588673 | ||||||
| chr12:3589086
|
G | A | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-3145G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589086 | ||||||
| chr12:3589140
|
A | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0159 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.980-3091A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589140 | ||||||
| chr12:3589186
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.980-3045A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589186 | ||||||
| chr12:3589307
|
C | T | 6 | a0001c0001t0001g0177a0001c0001t0001g0243a0001c0001t0001g0337others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.980-2924C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589307 | ||||||
| chr12:3589312
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.980-2919C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589312 | ||||||
| chr12:3589671
|
G | T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.980-2560G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589671 | ||||||
| chr12:3589677
|
C | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.980-2554C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589677 | ||||||
| chr12:3589681
|
G | A | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-2550G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589681 | ||||||
| chr12:3589755
|
A | C | 11 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(8): Show | 11 | HG00741.hp2 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.980-2476A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589755 | ||||||
| chr12:3589761
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.980-2470G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589761 | ||||||
| chr12:3589815
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.980-2416C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589815 | ||||||
| chr12:3589860
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0001g0220others(1): Show | 4 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-2371G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589860 | ||||||
| chr12:3589877
|
A | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0159others(3): Show | 6 | HG01891.hp1 HG02896.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-2354A>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3589877 | ||||||
| chr12:3590027
|
G | C | 76 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(73): Show | 76 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.980-2204G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590027 | ||||||
| chr12:3590048
|
G | A | 28 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.980-2183G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590048 | ||||||
| chr12:3590097
|
G | A | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-2134G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590097 | ||||||
| chr12:3590142
|
A | G | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-2089A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590142 | ||||||
| chr12:3590396
|
G | A | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.980-1835G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590396 | ||||||
| chr12:3590495
|
C | G | 1 | a0001c0001t0012g0316 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.980-1736C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590495 | ||||||
| chr12:3590497
|
T | C | 2 | a0001c0001t0002g0157a0001c0001t0002g0209 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.980-1734T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590497 | ||||||
| chr12:3590520
|
T | G | 5 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0159others(2): Show | 5 | HG01891.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-1711T>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590520 | ||||||
| chr12:3590522
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0001g0159 | 3 | HG01891.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.980-1709C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590522 | ||||||
| chr12:3590632
|
T | TA | 17 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0050others(14): Show | 17 | HG00642.hp2 HG01071.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.980-1583dupA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3590632 | |||||
| chr12:3590632
|
TA | T | 60 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(57): Show | 60 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.980-1583delA | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3590632 | |||||
| chr12:3590781
|
T | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0124a0001c0001t0001g0164others(3): Show | 6 | NA18612.hp1 NA18943.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.980-1450T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590781 | ||||||
| chr12:3590871
|
G | A | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.980-1360G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590871 | ||||||
| chr12:3590912
|
G | A | 28 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.980-1319G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590912 | ||||||
| chr12:3590921
|
G | A | 37 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0015others(34): Show | 37 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.980-1310G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3590921 | ||||||
| chr12:3591217
|
G | A | 2 | a0001c0001t0007g0313a0001c0001t0007g0325 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.980-1014G>A | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591217 | ||||||
| chr12:3591407
|
C | CT | 138 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.980-803dupT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3591407 | |||||
| chr12:3591407
|
C | CTT | 21 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0088others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.980-804_980-803dup others(2): Show |
PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3591407 | |||||
| chr12:3591407
|
CT | C | 41 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0131others(38): Show | 41 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.980-803delT | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 3591407 | |||||
| chr12:3591608
|
G | T | 1 | a0001c0004t0001g0321 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.980-623G>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591608 | ||||||
| chr12:3591621
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.980-610T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591621 | ||||||
| chr12:3591896
|
A | C | 1 | a0001c0001t0001g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.980-335A>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591896 | ||||||
| chr12:3591975
|
G | C | 4 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0001g0220others(1): Show | 4 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.980-256G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3591975 | ||||||
| chr12:3592224
|
C | T | 28 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0049others(25): Show | 28 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(25): Show |
splice_region_variant&intron_variant | LOW | c.980-7C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 8/9 | chr12 | 3592224 | ||||||
| chr12:3592503
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1101+151G>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592503 | ||||||
| chr12:3592531
|
C | G | 1 | a0001c0001t0002g0347 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1101+179C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592531 | ||||||
| chr12:3592725
|
C | G | 6 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0001g0220others(3): Show | 6 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+373C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592725 | ||||||
| chr12:3592743
|
A | G | 6 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0001g0220others(3): Show | 6 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102-356A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592743 | ||||||
| chr12:3592748
|
C | G | 3 | a0001c0002t0002g0096a0001c0002t0002g0249a0001c0002t0002g0338 | 3 | HG01884.hp2 HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1102-351C>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592748 | ||||||
| chr12:3592783
|
A | G | 51 | a0001c0001t0001g0083a0001c0001t0001g0090a0001c0001t0001g0143others(48): Show | 51 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1102-316A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592783 | ||||||
| chr12:3592823
|
T | C | 6 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0001g0220others(3): Show | 6 | HG00558.hp1 HG01192.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1102-276T>C | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592823 | ||||||
| chr12:3592852
|
C | T | 44 | a0001c0001t0001g0083a0001c0001t0001g0200a0001c0001t0001g0220others(41): Show | 44 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1102-247C>T | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3592852 | ||||||
| chr12:3593053
|
A | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1102-46A>G | PRMT8 | ENSG00000111218.12 | transcript | ENST00000382622.4 | protein_coding | 9/9 | chr12 | 3593053 |