Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9403 |
|---|---|
| ensemblid | ENSG00000183291.18 |
| hgncid | 17705 |
| symbol | SELENOF |
| name | selenoprotein F |
| refseq_nuc | NM_004261.5 |
| refseq_prot | NP_004252.2 |
| ensembl_nuc | ENST00000331835.10 |
| ensembl_prot | ENSP00000328729.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 86862445 |
| end | 86914126 |
| strand | - |
| ver | v1.2 |
| region | chr1:86862445-86914126 |
| region5000 | chr1:86857445-86919126 |
| regionname0 | SELENOF_chr1_86862445_86914126 |
| regionname5000 | SELENOF_chr1_86857445_86919126 |
| 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 | 95 | 226 | 94 | 32 | 56 | 8 | 34 | 38 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| 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 | 498 | 224 | 92 | 32 | 56 | 8 | 34 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| c0002 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| c0003 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| 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 | 1/0 | 1045 | 124 | 30 | 21 | 48 | 3 | 21 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0002 | 0/1 | 1045 | 71 | 38 | 10 | 8 | 5 | 9 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0003 | 0/0 | 1045 | 16 | 15 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0004 | 0/0 | 1045 | 5 | 4 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0005 | 0/0 | 1045 | 5 | 5 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0006 | 0/0 | 1045 | 3 | 0 | 0 | 0 | 0 | 3 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0007 | 0/0 | 1045 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| t0008 | 0/0 | 1045 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| 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 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0007 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| 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 | 498 | 224 | 92 | 32 | 56 | 8 | 34 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0002 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0003 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1542 | 123 | 29 | 21 | 48 | 3 | 21 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0002 | 0/1 | 1542 | 70 | 37 | 10 | 8 | 5 | 9 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0003 | 0/0 | 1542 | 16 | 15 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0004 | 0/0 | 1542 | 5 | 4 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0005 | 0/0 | 1542 | 5 | 5 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0006 | 0/0 | 1542 | 3 | 0 | 0 | 0 | 0 | 3 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0007 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0001t0008 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0002t0002 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| a0001c0003t0001 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | copy fasta | chr1 | 86857445 | 86919126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0007 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0006g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | GBR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | FIN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0008 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0093 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0008 | SAS | STU | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | LWK | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | YRI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | YRI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0089 | EUR | TSI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | USA | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | USA | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0007 | REF | REF | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0153 | REF | REF | SELENOF_chr1_86857445_86919126 | SELENOF | chr1 | 86857445 | 86919126 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:86863567
|
G | A | 1 | a0001c0003 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.405C>T | p.Asp135Asp | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 420/1542 | 405/498 | 135/165 | chr1 | 86863567 | ||
| chr1:86914061
|
C | T | 1 | a0001c0002 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.51G>A | p.Gly17Gly | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/5 | 66/1542 | 51/498 | 17/165 | chr1 | 86914061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:86862596
|
A | G | 1 | a0001c0001t0006 | 3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*878T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 878 | chr1 | 86862596 | |||||
| chr1:86862625
|
C | T | 4 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(1): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*849G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 849 | chr1 | 86862625 | |||||
| chr1:86862842
|
C | T | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*632G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 632 | chr1 | 86862842 | |||||
| chr1:86862941
|
A | G | 2 | a0001c0001t0004a0001c0001t0005 | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*533T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 533 | chr1 | 86862941 | |||||
| chr1:86863115
|
G | A | 1 | a0001c0001t0005 | 5 | HG02630.hp1 HG03453.hp2 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*359C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 359 | chr1 | 86863115 | |||||
| chr1:86863156
|
G | A | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*318C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 318 | chr1 | 86863156 | |||||
| chr1:86863215
|
C | T | 1 | a0001c0001t0007 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 259 | chr1 | 86863215 | |||||
| chr1:86863244
|
T | C | 1 | a0001c0001t0008 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 5/5 | 230 | chr1 | 86863244 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:86863619
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.367-14C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86863619 | ||||||
| chr1:86863628
|
C | T | 8 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0038others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-23G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86863628 | ||||||
| chr1:86863808
|
CTCAT | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.367-207_367-204del others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86863808 | ||||||
| chr1:86864441
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.367-836A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864441 | ||||||
| chr1:86864458
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.367-853T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864458 | ||||||
| chr1:86864661
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.367-1056C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864661 | ||||||
| chr1:86864707
|
G | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.367-1102C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864707 | ||||||
| chr1:86864767
|
G | C | 1 | a0001c0001t0002g0010 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.367-1162C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864767 | ||||||
| chr1:86864782
|
C | G | 1 | a0001c0001t0002g0084 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.367-1177G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864782 | ||||||
| chr1:86864811
|
T | C | 1 | a0001c0002t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.367-1206A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864811 | ||||||
| chr1:86864915
|
T | G | 5 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(2): Show | 5 | HG02717.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-1310A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864915 | ||||||
| chr1:86864961
|
A | AT | 33 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0002g0007others(30): Show | 37 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.367-1357dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864961 | ||||||
| chr1:86864985
|
TTTGAGAT others(5): Show |
T | 1 | a0001c0001t0001g0162 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.367-1392_367-1381d others(14): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86864985 | ||||||
| chr1:86865094
|
T | A | 1 | a0001c0001t0001g0183 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.367-1489A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865094 | ||||||
| chr1:86865096
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.367-1491T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865096 | ||||||
| chr1:86865099
|
A | G | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-1494T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865099 | ||||||
| chr1:86865212
|
C | CCAAA | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.367-1611_367-1608d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865212 | ||||||
| chr1:86865212
|
CCAAA | C | 52 | a0001c0001t0001g0160a0001c0001t0001g0179a0001c0001t0002g0002others(49): Show | 57 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.367-1611_367-1608d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865212 | ||||||
| chr1:86865212
|
CCAAACAA others(1): Show |
C | 16 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0031others(13): Show | 17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.367-1615_367-1608d others(10): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865212 | ||||||
| chr1:86865520
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.367-1915T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865520 | ||||||
| chr1:86865528
|
C | T | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.367-1923G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865528 | ||||||
| chr1:86865861
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.366+2192T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865861 | ||||||
| chr1:86865978
|
C | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.366+2075G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865978 | ||||||
| chr1:86865979
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.366+2074C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86865979 | ||||||
| chr1:86866010
|
C | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+2043G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866010 | ||||||
| chr1:86866057
|
C | A | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.366+1996G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866057 | ||||||
| chr1:86866195
|
C | CA | 49 | a0001c0001t0001g0104a0001c0001t0001g0116a0001c0001t0001g0117others(46): Show | 52 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.366+1857dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866195 | ||||||
| chr1:86866195
|
C | CAA | 11 | a0001c0001t0002g0023a0001c0001t0002g0028a0001c0001t0002g0031others(8): Show | 12 | HG00741.hp2 HG01891.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.366+1856_366+1857d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866195 | ||||||
| chr1:86866195
|
C | CAAA | 6 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.366+1855_366+1857d others(5): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866195 | ||||||
| chr1:86866195
|
CA | C | 9 | a0001c0001t0001g0127a0001c0001t0001g0152a0001c0001t0001g0177others(6): Show | 9 | HG01169.hp2 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.366+1857delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866195 | ||||||
| chr1:86866195
|
CAAAAAAA | C | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+1851_366+1857d others(9): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866195 | ||||||
| chr1:86866228
|
C | CTG | 2 | a0001c0001t0002g0076a0001c0001t0002g0079 | 2 | HG00323.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.366+1824_366+1825i others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866228 | ||||||
| chr1:86866228
|
C | CTGTGTG | 3 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0077 | 3 | HG01884.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.366+1824_366+1825i others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866228 | ||||||
| chr1:86866228
|
CTCTGTGT others(3): Show |
C | 1 | a0001c0001t0002g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.366+1815_366+1824d others(12): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866228 | ||||||
| chr1:86866230
|
C | CTCTG | 13 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0081others(10): Show | 16 | HG00323.hp1 HG00408.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.366+1822_366+1823i others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTCTGTG | 2 | a0001c0001t0002g0083a0001c0001t0002g0092 | 2 | HG03017.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.366+1822_366+1823i others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.366+1822_366+1823i others(12): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTG | 19 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0001g0167others(16): Show | 21 | HG01081.hp2 HG01255.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.366+1821_366+1822d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTGTG | 18 | a0001c0001t0001g0098a0001c0001t0001g0174a0001c0001t0001g0190others(15): Show | 19 | HG00639.hp1 HG01106.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.366+1819_366+1822d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTGTGTG | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0102others(15): Show | 21 | HG00741.hp2 HG01255.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.366+1817_366+1822d others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTGTGTGT others(1): Show |
22 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0099others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.366+1815_366+1822d others(10): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTGTGTGT others(3): Show |
17 | a0001c0001t0001g0015a0001c0001t0001g0103a0001c0001t0001g0104others(14): Show | 17 | HG00741.hp1 HG01167.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.366+1813_366+1822d others(12): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | CTGTGTGT others(5): Show |
17 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0112others(14): Show | 17 | HG00639.hp2 HG02080.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.366+1811_366+1822d others(14): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
C | G | 7 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0075others(4): Show | 7 | HG00323.hp2 HG01884.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+1823G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
CTG | C | 28 | a0001c0001t0001g0123a0001c0001t0001g0151a0001c0001t0001g0152others(25): Show | 30 | HG00609.hp2 HG01169.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.366+1821_366+1822d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866230
|
CTGTGTGT others(11): Show |
C | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+1805_366+1822d others(20): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866230 | ||||||
| chr1:86866232
|
G | C | 1 | a0001c0001t0002g0010 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.366+1821C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866232 | ||||||
| chr1:86866234
|
G | C | 1 | a0001c0001t0002g0010 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.366+1819C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866234 | ||||||
| chr1:86866236
|
G | C | 1 | a0001c0001t0002g0010 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.366+1817C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866236 | ||||||
| chr1:86866278
|
T | C | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.366+1775A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866278 | ||||||
| chr1:86866364
|
C | G | 1 | a0001c0001t0004g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.366+1689G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866364 | ||||||
| chr1:86866364
|
C | T | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.366+1689G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866364 | ||||||
| chr1:86866387
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+1666C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866387 | ||||||
| chr1:86866493
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.366+1560T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866493 | ||||||
| chr1:86866499
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.366+1554C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866499 | ||||||
| chr1:86866614
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.366+1439A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866614 | ||||||
| chr1:86866696
|
A | C | 210 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(207): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.366+1357T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866696 | ||||||
| chr1:86866716
|
A | T | 1 | a0001c0002t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.366+1337T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866716 | ||||||
| chr1:86866848
|
C | G | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.366+1205G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866848 | ||||||
| chr1:86866920
|
T | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0112others(2): Show | 6 | HG02486.hp2 HG02886.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+1133A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866920 | ||||||
| chr1:86866934
|
C | T | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.366+1119G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866934 | ||||||
| chr1:86866942
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.366+1111A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86866942 | ||||||
| chr1:86867053
|
G | T | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.366+1000C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867053 | ||||||
| chr1:86867083
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+970C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867083 | ||||||
| chr1:86867087
|
A | G | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.366+966T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867087 | ||||||
| chr1:86867119
|
T | G | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+934A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867119 | ||||||
| chr1:86867424
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.366+629T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867424 | ||||||
| chr1:86867486
|
C | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+567G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867486 | ||||||
| chr1:86867490
|
T | TCAA | 56 | a0001c0001t0001g0111a0001c0001t0001g0114a0001c0001t0001g0117others(53): Show | 59 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.366+560_366+562dup others(3): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867490 | ||||||
| chr1:86867490
|
T | TCAACAA | 10 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0078others(7): Show | 11 | HG01433.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.366+557_366+562dup others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867490 | ||||||
| chr1:86867490
|
T | TCAACAAC others(2): Show |
4 | a0001c0001t0005g0003a0001c0001t0005g0052a0001c0001t0006g0008others(1): Show | 6 | HG03453.hp2 HG03486.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+554_366+562dup others(9): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867490 | ||||||
| chr1:86867490
|
T | TCAACAAC others(5): Show |
2 | a0001c0001t0004g0053a0001c0001t0005g0050 | 2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.366+551_366+562dup others(12): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867490 | ||||||
| chr1:86867490
|
TCAA | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0039a0001c0001t0007g0063 | 4 | HG01884.hp1 HG02109.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+560_366+562del others(3): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867490 | ||||||
| chr1:86867642
|
T | C | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(14): Show | 17 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.366+411A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867642 | ||||||
| chr1:86867756
|
A | T | 3 | a0001c0001t0002g0073a0001c0001t0002g0079a0001c0001t0002g0109 | 3 | HG00323.hp2 HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.366+297T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867756 | ||||||
| chr1:86867821
|
A | T | 1 | a0001c0001t0003g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.366+232T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 4/4 | chr1 | 86867821 | ||||||
| chr1:86868162
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.317-60C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86868162 | ||||||
| chr1:86868192
|
A | G | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-90T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86868192 | ||||||
| chr1:86868259
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.317-157A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86868259 | ||||||
| chr1:86868389
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.317-287A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86868389 | ||||||
| chr1:86868790
|
C | A | 4 | a0001c0001t0002g0017a0001c0001t0002g0021a0001c0001t0002g0024others(1): Show | 4 | HG00639.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-688G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86868790 | ||||||
| chr1:86869233
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.317-1131G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869233 | ||||||
| chr1:86869277
|
C | T | 16 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0081others(13): Show | 19 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.317-1175G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869277 | ||||||
| chr1:86869307
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.317-1205G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869307 | ||||||
| chr1:86869631
|
ATACTT | A | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-1534_317-1530d others(7): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869631 | ||||||
| chr1:86869696
|
C | T | 9 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0075others(6): Show | 9 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.317-1594G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869696 | ||||||
| chr1:86869708
|
TTTCC | T | 10 | a0001c0001t0001g0187a0001c0001t0002g0017a0001c0001t0002g0024others(7): Show | 11 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.317-1610_317-1607d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869708 | ||||||
| chr1:86869734
|
T | C | 9 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0075others(6): Show | 9 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.317-1632A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869734 | ||||||
| chr1:86869785
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.317-1683G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869785 | ||||||
| chr1:86869909
|
T | G | 210 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(207): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.317-1807A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86869909 | ||||||
| chr1:86870077
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.317-1975A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870077 | ||||||
| chr1:86870268
|
T | A | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-2166A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870268 | ||||||
| chr1:86870360
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.317-2258G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870360 | ||||||
| chr1:86870617
|
T | TA | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.317-2516dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870617 | ||||||
| chr1:86870622
|
T | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0068 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.317-2520A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870622 | ||||||
| chr1:86870623
|
A | AT | 67 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(64): Show | 74 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.317-2522dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870623 | ||||||
| chr1:86870623
|
A | T | 4 | a0001c0001t0002g0081a0001c0001t0002g0094a0001c0001t0003g0067others(1): Show | 4 | HG01891.hp2 HG02615.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-2521T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870623 | ||||||
| chr1:86870624
|
T | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0068 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.317-2522A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870624 | ||||||
| chr1:86870741
|
A | C | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.317-2639T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870741 | ||||||
| chr1:86870821
|
G | A | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.317-2719C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870821 | ||||||
| chr1:86870822
|
C | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.317-2720G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870822 | ||||||
| chr1:86870841
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.317-2739T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870841 | ||||||
| chr1:86870854
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.317-2752G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870854 | ||||||
| chr1:86870861
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.317-2759A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870861 | ||||||
| chr1:86870928
|
A | AT | 22 | a0001c0001t0001g0102a0001c0001t0001g0151a0001c0001t0002g0001others(19): Show | 23 | HG02055.hp1 HG02056.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.317-2827dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86870928 | ||||||
| chr1:86871367
|
A | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0067a0001c0001t0003g0068others(1): Show | 5 | HG00741.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-3265T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871367 | ||||||
| chr1:86871422
|
A | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.317-3320T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871422 | ||||||
| chr1:86871425
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0046 | 2 | NA18973.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.317-3323T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871425 | ||||||
| chr1:86871545
|
A | G | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(14): Show | 17 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.317-3443T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871545 | ||||||
| chr1:86871625
|
A | G | 1 | a0001c0002t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.317-3523T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871625 | ||||||
| chr1:86871654
|
T | C | 16 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0031others(13): Show | 17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.317-3552A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871654 | ||||||
| chr1:86871811
|
ATTAT | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(62): Show | 71 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.317-3713_317-3710d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86871811 | ||||||
| chr1:86872151
|
TAGTG | T | 5 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(2): Show | 5 | HG02717.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-4053_317-4050d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872151 | ||||||
| chr1:86872173
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0211 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.317-4071G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872173 | ||||||
| chr1:86872181
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.317-4079A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872181 | ||||||
| chr1:86872270
|
G | T | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.317-4168C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872270 | ||||||
| chr1:86872537
|
G | GT | 33 | a0001c0001t0001g0015a0001c0001t0001g0117a0001c0001t0001g0119others(30): Show | 37 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.317-4436dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872537 | ||||||
| chr1:86872537
|
G | GTT | 32 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(29): Show | 34 | HG00323.hp2 HG00639.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.317-4437_317-4436d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872537 | ||||||
| chr1:86872537
|
G | GTTT | 12 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0024others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.317-4438_317-4436d others(5): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872537 | ||||||
| chr1:86872573
|
G | A | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.317-4471C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872573 | ||||||
| chr1:86872645
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.317-4543A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872645 | ||||||
| chr1:86872919
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0061 | 3 | HG02965.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.317-4817A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872919 | ||||||
| chr1:86872926
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.317-4824C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872926 | ||||||
| chr1:86872934
|
G | A | 1 | a0001c0001t0003g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.317-4832C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872934 | ||||||
| chr1:86872994
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.317-4892G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86872994 | ||||||
| chr1:86873012
|
A | G | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.317-4910T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873012 | ||||||
| chr1:86873044
|
A | AAAAT | 23 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(20): Show | 23 | HG00408.hp1 HG00741.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.317-4946_317-4943d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873044 | ||||||
| chr1:86873044
|
A | AAAATAAA others(1): Show |
8 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0172others(5): Show | 8 | HG00673.hp2 HG02257.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-4950_317-4943d others(10): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873044 | ||||||
| chr1:86873044
|
AAAAT | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0169a0001c0001t0001g0183others(9): Show | 12 | HG00140.hp2 HG02145.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-4946_317-4943d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873044 | ||||||
| chr1:86873044
|
AAAATAAA others(5): Show |
A | 23 | a0001c0001t0001g0011a0001c0001t0001g0107a0001c0001t0001g0111others(20): Show | 24 | HG00609.hp2 HG00639.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.317-4954_317-4943d others(14): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873044 | ||||||
| chr1:86873044
|
AAAATAAA others(9): Show |
A | 18 | a0001c0001t0001g0012a0001c0001t0001g0095a0001c0001t0001g0102others(15): Show | 21 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.317-4958_317-4943d others(18): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873044 | ||||||
| chr1:86873044
|
AAAATAAA others(21): Show |
A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.317-4970_317-4943d others(30): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873044 | ||||||
| chr1:86873078
|
AATAAATA others(7): Show |
A | 1 | a0001c0001t0004g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.317-4990_317-4977d others(16): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873078 | ||||||
| chr1:86873093
|
A | T | 1 | a0001c0001t0004g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.317-4991T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873093 | ||||||
| chr1:86873214
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.317-5112C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873214 | ||||||
| chr1:86873354
|
A | ATATT | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(62): Show | 71 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.317-5256_317-5253d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873354 | ||||||
| chr1:86873809
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.317-5707C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873809 | ||||||
| chr1:86873852
|
CA | C | 162 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(159): Show | 173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.317-5751delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873852 | ||||||
| chr1:86873852
|
CAA | C | 36 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0002g0001others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.317-5752_317-5751d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86873852 | ||||||
| chr1:86874074
|
T | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.317-5972A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874074 | ||||||
| chr1:86874130
|
A | AT | 5 | a0001c0001t0002g0002a0001c0001t0002g0042a0001c0001t0002g0048others(2): Show | 6 | HG01496.hp2 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-6029dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874130 | ||||||
| chr1:86874130
|
AT | A | 6 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-6029delA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874130 | ||||||
| chr1:86874229
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.317-6127T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874229 | ||||||
| chr1:86874485
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316+6177A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874485 | ||||||
| chr1:86874558
|
A | T | 16 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0081others(13): Show | 19 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.316+6104T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874558 | ||||||
| chr1:86874588
|
A | C | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316+6074T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874588 | ||||||
| chr1:86874730
|
G | A | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+5932C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874730 | ||||||
| chr1:86874766
|
C | T | 1 | a0001c0001t0007g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.316+5896G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874766 | ||||||
| chr1:86874838
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.316+5824A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874838 | ||||||
| chr1:86874877
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.316+5785A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86874877 | ||||||
| chr1:86875110
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0209a0001c0001t0002g0047 | 3 | HG02145.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.316+5552C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875110 | ||||||
| chr1:86875135
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.316+5527C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875135 | ||||||
| chr1:86875189
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.316+5473G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875189 | ||||||
| chr1:86875241
|
GA | G | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.316+5420delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875241 | ||||||
| chr1:86875272
|
T | G | 19 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(16): Show | 23 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.316+5390A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875272 | ||||||
| chr1:86875451
|
T | C | 1 | a0001c0001t0004g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.316+5211A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875451 | ||||||
| chr1:86875561
|
A | G | 7 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0023others(4): Show | 7 | HG01106.hp2 HG01433.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+5101T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875561 | ||||||
| chr1:86875945
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.316+4717G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875945 | ||||||
| chr1:86875996
|
C | T | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+4666G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86875996 | ||||||
| chr1:86876132
|
C | G | 8 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0161others(5): Show | 8 | HG00673.hp1 NA18945.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4530G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876132 | ||||||
| chr1:86876184
|
G | T | 1 | a0001c0001t0002g0034 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.316+4478C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876184 | ||||||
| chr1:86876190
|
G | A | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.316+4472C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876190 | ||||||
| chr1:86876201
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.316+4461A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876201 | ||||||
| chr1:86876474
|
G | A | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.316+4188C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876474 | ||||||
| chr1:86876549
|
A | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+4113T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876549 | ||||||
| chr1:86876627
|
T | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.316+4035A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876627 | ||||||
| chr1:86876787
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.316+3875C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86876787 | ||||||
| chr1:86877018
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.316+3644A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877018 | ||||||
| chr1:86877127
|
G | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.316+3535C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877127 | ||||||
| chr1:86877212
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.316+3450G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877212 | ||||||
| chr1:86877549
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.316+3113T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877549 | ||||||
| chr1:86877579
|
T | C | 3 | a0001c0001t0002g0073a0001c0001t0002g0079a0001c0001t0002g0109 | 3 | HG00323.hp2 HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.316+3083A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877579 | ||||||
| chr1:86877610
|
C | T | 2 | a0001c0001t0004g0056a0001c0001t0004g0057 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.316+3052G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877610 | ||||||
| chr1:86877613
|
A | G | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+3049T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877613 | ||||||
| chr1:86877662
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316+3000A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877662 | ||||||
| chr1:86877687
|
C | A | 1 | a0001c0001t0002g0021 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.316+2975G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877687 | ||||||
| chr1:86877696
|
G | GT | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+2965dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877696 | ||||||
| chr1:86877800
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG02056.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.316+2862G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877800 | ||||||
| chr1:86877851
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.316+2811T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86877851 | ||||||
| chr1:86878204
|
A | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.316+2458T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878204 | ||||||
| chr1:86878508
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02895.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.316+2154G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878508 | ||||||
| chr1:86878590
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.316+2072C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878590 | ||||||
| chr1:86878622
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.316+2040G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878622 | ||||||
| chr1:86878634
|
A | G | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.316+2028T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878634 | ||||||
| chr1:86878721
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.316+1941T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878721 | ||||||
| chr1:86878854
|
C | T | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.316+1808G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878854 | ||||||
| chr1:86878992
|
A | G | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.316+1670T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86878992 | ||||||
| chr1:86879021
|
T | C | 1 | a0001c0001t0002g0076 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.316+1641A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879021 | ||||||
| chr1:86879158
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.316+1504G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879158 | ||||||
| chr1:86879209
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.316+1453A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879209 | ||||||
| chr1:86879386
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.316+1276A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879386 | ||||||
| chr1:86879810
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.316+852G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879810 | ||||||
| chr1:86879818
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0048a0001c0001t0002g0049 | 4 | HG01496.hp2 HG03098.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+844A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879818 | ||||||
| chr1:86879990
|
C | A | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+672G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86879990 | ||||||
| chr1:86880045
|
T | TGTAAA | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.316+616_316+617ins others(5): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880045 | ||||||
| chr1:86880118
|
T | C | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+544A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880118 | ||||||
| chr1:86880175
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+487C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880175 | ||||||
| chr1:86880250
|
C | A | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.316+412G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880250 | ||||||
| chr1:86880404
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0204 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.316+258C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880404 | ||||||
| chr1:86880482
|
T | C | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.316+180A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880482 | ||||||
| chr1:86880492
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.316+170G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880492 | ||||||
| chr1:86880524
|
A | AC | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.316+137_316+138ins others(1): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880524 | ||||||
| chr1:86880528
|
T | C | 16 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0031others(13): Show | 17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.316+134A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880528 | ||||||
| chr1:86880606
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.316+56T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 3/4 | chr1 | 86880606 | ||||||
| chr1:86880802
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.253-77G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86880802 | ||||||
| chr1:86880896
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-171C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86880896 | ||||||
| chr1:86881034
|
G | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-309C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881034 | ||||||
| chr1:86881047
|
A | G | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-322T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881047 | ||||||
| chr1:86881096
|
A | G | 8 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0038others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-371T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881096 | ||||||
| chr1:86881184
|
TTATAGAA others(5): Show |
T | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.253-471_253-460del others(12): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881184 | ||||||
| chr1:86881211
|
A | G | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-486T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881211 | ||||||
| chr1:86881363
|
C | T | 6 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-638G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881363 | ||||||
| chr1:86881522
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.253-797C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881522 | ||||||
| chr1:86881631
|
A | AAAC | 9 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0019others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-909_253-907dup others(3): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881631 | ||||||
| chr1:86881631
|
AAAC | A | 4 | a0001c0001t0001g0096a0001c0001t0001g0125a0001c0001t0001g0131others(1): Show | 4 | HG02080.hp2 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-909_253-907del others(3): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881631 | ||||||
| chr1:86881684
|
T | G | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-959A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881684 | ||||||
| chr1:86881694
|
C | G | 2 | a0001c0001t0004g0056a0001c0001t0004g0057 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.253-969G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881694 | ||||||
| chr1:86881828
|
GAT | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0126 | 2 | NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.253-1105_253-1104d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881828 | ||||||
| chr1:86881839
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG01928.hp1 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.253-1114C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86881839 | ||||||
| chr1:86882024
|
G | C | 1 | a0001c0001t0008g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.253-1299C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882024 | ||||||
| chr1:86882062
|
T | A | 1 | a0001c0001t0004g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.253-1337A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882062 | ||||||
| chr1:86882195
|
G | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-1470C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882195 | ||||||
| chr1:86882244
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-1519A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882244 | ||||||
| chr1:86882247
|
C | CA | 15 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 15 | HG00621.hp1 HG01169.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.253-1523dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882247 | ||||||
| chr1:86882247
|
CAA | C | 6 | a0001c0001t0002g0004a0001c0001t0002g0034a0001c0001t0002g0035others(3): Show | 7 | HG02647.hp1 HG02717.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-1524_253-1523d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882247 | ||||||
| chr1:86882247
|
CAAA | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(47): Show | 56 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.253-1525_253-1523d others(5): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882247 | ||||||
| chr1:86882247
|
CAAAA | C | 14 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(11): Show | 14 | HG00323.hp2 HG00639.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-1526_253-1523d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882247 | ||||||
| chr1:86882247
|
CAAAAAAA | C | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-1529_253-1523d others(9): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882247 | ||||||
| chr1:86882247
|
CAAAAAAA others(7): Show |
C | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-1536_253-1523d others(16): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882247 | ||||||
| chr1:86882273
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0177a0001c0001t0001g0178 | 4 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-1548T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882273 | ||||||
| chr1:86882414
|
G | C | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.253-1689C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882414 | ||||||
| chr1:86882482
|
G | A | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-1757C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882482 | ||||||
| chr1:86882494
|
T | TA | 6 | a0001c0001t0001g0154a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 6 | HG02004.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-1770dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882494 | ||||||
| chr1:86882494
|
TA | T | 7 | a0001c0001t0001g0139a0001c0001t0001g0141a0001c0001t0001g0160others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-1770delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882494 | ||||||
| chr1:86882536
|
AC | A | 7 | a0001c0001t0002g0016a0001c0001t0002g0022a0001c0001t0002g0023others(4): Show | 7 | HG01106.hp2 HG01433.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-1812delG | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882536 | ||||||
| chr1:86882589
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.253-1864C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882589 | ||||||
| chr1:86882596
|
C | G | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-1871G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882596 | ||||||
| chr1:86882603
|
G | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-1878C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882603 | ||||||
| chr1:86882882
|
T | C | 2 | a0001c0001t0002g0004a0001c0001t0002g0061 | 3 | HG02965.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.253-2157A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882882 | ||||||
| chr1:86882927
|
ACCAG | A | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.253-2206_253-2203d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882927 | ||||||
| chr1:86882963
|
T | C | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-2238A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882963 | ||||||
| chr1:86882980
|
G | A | 209 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(206): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.253-2255C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86882980 | ||||||
| chr1:86883003
|
T | A | 10 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-2278A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883003 | ||||||
| chr1:86883125
|
C | CA | 9 | a0001c0001t0001g0149a0001c0001t0001g0202a0001c0001t0001g0204others(6): Show | 10 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-2401dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883125 | ||||||
| chr1:86883125
|
CA | C | 63 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0130others(60): Show | 69 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.253-2401delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883125 | ||||||
| chr1:86883270
|
A | T | 1 | a0001c0001t0002g0016 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.253-2545T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883270 | ||||||
| chr1:86883271
|
T | G | 1 | a0001c0001t0002g0016 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.253-2546A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883271 | ||||||
| chr1:86883273
|
G | T | 1 | a0001c0001t0002g0016 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.253-2548C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883273 | ||||||
| chr1:86883384
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.253-2659C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883384 | ||||||
| chr1:86883447
|
TTACACTA others(39): Show |
T | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.253-2768_253-2723d others(48): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883447 | ||||||
| chr1:86883456
|
ATAGTGTA others(14): Show |
A | 2 | a0001c0001t0001g0013a0001c0001t0001g0155 | 3 | HG03490.hp1 HG03492.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.253-2752_253-2732d others(23): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883456 | ||||||
| chr1:86883471
|
T | C | 14 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0112others(11): Show | 15 | HG00323.hp2 HG01884.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.253-2746A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883471 | ||||||
| chr1:86883576
|
A | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.253-2851T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883576 | ||||||
| chr1:86883860
|
C | T | 3 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060 | 3 | HG02486.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.253-3135G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883860 | ||||||
| chr1:86883963
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.253-3238A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883963 | ||||||
| chr1:86883964
|
C | A | 1 | a0001c0001t0002g0016 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.253-3239G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86883964 | ||||||
| chr1:86884125
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.253-3400T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884125 | ||||||
| chr1:86884140
|
G | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-3415C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884140 | ||||||
| chr1:86884331
|
G | A | 1 | a0001c0001t0002g0010 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.253-3606C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884331 | ||||||
| chr1:86884346
|
T | TAC | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0103others(11): Show | 15 | HG01081.hp2 HG01106.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.253-3623_253-3622d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884346 | ||||||
| chr1:86884346
|
T | TACACAC | 2 | a0001c0001t0003g0064a0001c0001t0003g0066 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.253-3627_253-3622d others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884346 | ||||||
| chr1:86884346
|
TAC | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0135a0001c0001t0001g0175others(15): Show | 18 | HG01106.hp2 HG01433.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-3623_253-3622d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884346 | ||||||
| chr1:86884346
|
TACAC | T | 57 | a0001c0001t0001g0157a0001c0001t0001g0174a0001c0001t0002g0001others(54): Show | 62 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.253-3625_253-3622d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884346 | ||||||
| chr1:86884346
|
TACACAC | T | 7 | a0001c0001t0002g0084a0001c0001t0004g0053a0001c0001t0004g0054others(4): Show | 8 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-3627_253-3622d others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884346 | ||||||
| chr1:86884346
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-3633_253-3622d others(14): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884346 | ||||||
| chr1:86884378
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.253-3653A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884378 | ||||||
| chr1:86884380
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(62): Show | 71 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.253-3655A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884380 | ||||||
| chr1:86884408
|
CAT | C | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-3685_253-3684d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884408 | ||||||
| chr1:86884467
|
ATAACT | A | 2 | a0001c0001t0002g0004a0001c0001t0002g0061 | 3 | HG02965.hp1 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.253-3747_253-3743d others(7): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884467 | ||||||
| chr1:86884783
|
A | G | 11 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0172others(8): Show | 11 | HG00408.hp1 HG00621.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.253-4058T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884783 | ||||||
| chr1:86884884
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.253-4159G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884884 | ||||||
| chr1:86884993
|
A | G | 7 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0038others(4): Show | 8 | HG02055.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-4268T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86884993 | ||||||
| chr1:86885238
|
C | G | 210 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(207): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.253-4513G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885238 | ||||||
| chr1:86885299
|
G | T | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-4574C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885299 | ||||||
| chr1:86885391
|
CCAGATAG | C | 70 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(67): Show | 77 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.253-4673_253-4667d others(9): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885391 | ||||||
| chr1:86885439
|
G | A | 69 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(66): Show | 76 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.253-4714C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885439 | ||||||
| chr1:86885458
|
C | G | 3 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060 | 3 | HG02486.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.253-4733G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885458 | ||||||
| chr1:86885506
|
CCAT | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02895.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.253-4784_253-4782d others(5): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885506 | ||||||
| chr1:86885590
|
C | T | 14 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(11): Show | 14 | HG00323.hp2 HG01884.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-4865G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885590 | ||||||
| chr1:86885708
|
A | G | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-4983T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885708 | ||||||
| chr1:86885789
|
G | A | 8 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-5064C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885789 | ||||||
| chr1:86885951
|
C | A | 1 | a0001c0001t0003g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.253-5226G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86885951 | ||||||
| chr1:86886028
|
G | T | 1 | a0001c0001t0003g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-5303C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886028 | ||||||
| chr1:86886120
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-5395C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886120 | ||||||
| chr1:86886265
|
T | C | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-5540A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886265 | ||||||
| chr1:86886267
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.253-5542C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886267 | ||||||
| chr1:86886354
|
C | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-5629G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886354 | ||||||
| chr1:86886433
|
C | CTT | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.253-5710_253-5709d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886433 | ||||||
| chr1:86886433
|
CT | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.253-5709delA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886433 | ||||||
| chr1:86886445
|
T | C | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-5720A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886445 | ||||||
| chr1:86886517
|
G | C | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-5792C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886517 | ||||||
| chr1:86886717
|
A | C | 1 | a0001c0001t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.253-5992T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886717 | ||||||
| chr1:86886785
|
T | C | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-6060A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886785 | ||||||
| chr1:86886815
|
G | T | 5 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(2): Show | 5 | HG02717.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-6090C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886815 | ||||||
| chr1:86886876
|
T | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-6151A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886876 | ||||||
| chr1:86886980
|
T | C | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-6255A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86886980 | ||||||
| chr1:86887177
|
T | C | 4 | a0001c0001t0003g0006a0001c0001t0003g0067a0001c0001t0003g0068others(1): Show | 5 | HG00741.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-6452A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887177 | ||||||
| chr1:86887453
|
A | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.253-6728T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887453 | ||||||
| chr1:86887516
|
G | C | 1 | a0001c0001t0002g0021 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253-6791C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887516 | ||||||
| chr1:86887597
|
A | T | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-6872T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887597 | ||||||
| chr1:86887691
|
T | A | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-6966A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887691 | ||||||
| chr1:86887742
|
T | G | 2 | a0001c0001t0002g0072a0001c0001t0002g0077 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.253-7017A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887742 | ||||||
| chr1:86887786
|
C | G | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033 | 3 | HG02970.hp1 HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.253-7061G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887786 | ||||||
| chr1:86887823
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-7098C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887823 | ||||||
| chr1:86887943
|
C | T | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-7218G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887943 | ||||||
| chr1:86887978
|
C | A | 21 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(18): Show | 22 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.253-7253G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86887978 | ||||||
| chr1:86888007
|
T | A | 1 | a0001c0001t0002g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253-7282A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888007 | ||||||
| chr1:86888171
|
A | G | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-7446T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888171 | ||||||
| chr1:86888262
|
C | CA | 14 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0048others(11): Show | 16 | HG01496.hp2 HG02257.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-7538dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888262 | ||||||
| chr1:86888439
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.253-7714A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888439 | ||||||
| chr1:86888445
|
T | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-7720A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888445 | ||||||
| chr1:86888446
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.253-7721T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888446 | ||||||
| chr1:86888468
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.253-7743A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888468 | ||||||
| chr1:86888582
|
T | C | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-7857A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888582 | ||||||
| chr1:86888667
|
A | G | 16 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0081others(13): Show | 19 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.253-7942T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888667 | ||||||
| chr1:86888671
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.253-7946T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888671 | ||||||
| chr1:86888883
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.253-8158C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86888883 | ||||||
| chr1:86889013
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-8288C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889013 | ||||||
| chr1:86889031
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.253-8306A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889031 | ||||||
| chr1:86889068
|
C | G | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.253-8343G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889068 | ||||||
| chr1:86889089
|
C | G | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-8364G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889089 | ||||||
| chr1:86889289
|
A | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.253-8564T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889289 | ||||||
| chr1:86889638
|
G | C | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.253-8913C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889638 | ||||||
| chr1:86889752
|
A | C | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.253-9027T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889752 | ||||||
| chr1:86889835
|
T | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0208 | 4 | HG01167.hp2 HG01255.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-9110A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889835 | ||||||
| chr1:86889955
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-9230G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889955 | ||||||
| chr1:86889959
|
C | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-9234G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86889959 | ||||||
| chr1:86890086
|
T | C | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-9361A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890086 | ||||||
| chr1:86890257
|
A | G | 9 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0075others(6): Show | 9 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-9532T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890257 | ||||||
| chr1:86890433
|
G | T | 1 | a0001c0001t0002g0075 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.253-9708C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890433 | ||||||
| chr1:86890485
|
ACT | A | 5 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0076others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-9762_253-9761d others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890485 | ||||||
| chr1:86890567
|
G | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.253-9842C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890567 | ||||||
| chr1:86890656
|
C | CT | 30 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(27): Show | 31 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.253-9932dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890656 | ||||||
| chr1:86890691
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.253-9966C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890691 | ||||||
| chr1:86890813
|
G | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0026others(1): Show | 4 | HG01106.hp2 HG01433.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-10088C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86890813 | ||||||
| chr1:86891007
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(62): Show | 71 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.253-10282A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891007 | ||||||
| chr1:86891009
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.253-10284T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891009 | ||||||
| chr1:86891053
|
C | CT | 9 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG00609.hp1 HG00621.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-10329dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891053 | ||||||
| chr1:86891053
|
C | CTT | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-10330_253-1032 others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891053 | ||||||
| chr1:86891113
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.253-10388C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891113 | ||||||
| chr1:86891140
|
C | A | 1 | a0001c0001t0004g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.253-10415G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891140 | ||||||
| chr1:86891174
|
C | T | 1 | a0001c0001t0007g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.253-10449G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891174 | ||||||
| chr1:86891181
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.253-10456G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891181 | ||||||
| chr1:86891240
|
G | A | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.253-10515C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891240 | ||||||
| chr1:86891342
|
C | T | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-10617G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891342 | ||||||
| chr1:86891932
|
GT | G | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.253-11208delA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891932 | ||||||
| chr1:86891961
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-11236G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86891961 | ||||||
| chr1:86892122
|
C | T | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+11159G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892122 | ||||||
| chr1:86892175
|
AC | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(73): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.252+11105delG | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892175 | ||||||
| chr1:86892193
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.252+11088G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892193 | ||||||
| chr1:86892252
|
G | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+11029C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892252 | ||||||
| chr1:86892449
|
A | G | 8 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0038others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+10832T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892449 | ||||||
| chr1:86892648
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0007g0063 | 2 | HG02735.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.252+10633G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892648 | ||||||
| chr1:86892855
|
G | A | 3 | a0001c0001t0002g0017a0001c0001t0002g0024a0001c0001t0002g0025 | 3 | HG01167.hp1 HG01169.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.252+10426C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86892855 | ||||||
| chr1:86893088
|
G | A | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+10193C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893088 | ||||||
| chr1:86893300
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.252+9981G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893300 | ||||||
| chr1:86893321
|
C | T | 1 | a0001c0001t0007g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.252+9960G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893321 | ||||||
| chr1:86893328
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.252+9953C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893328 | ||||||
| chr1:86893425
|
G | A | 2 | a0001c0001t0004g0056a0001c0001t0004g0057 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.252+9856C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893425 | ||||||
| chr1:86893450
|
C | CA | 18 | a0001c0001t0001g0102a0001c0001t0001g0131a0001c0001t0001g0191others(15): Show | 19 | HG01255.hp2 HG01257.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+9830dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893450 | ||||||
| chr1:86893450
|
CA | C | 56 | a0001c0001t0001g0015a0001c0001t0002g0001a0001c0001t0002g0002others(53): Show | 63 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.252+9830delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893450 | ||||||
| chr1:86893458
|
A | G | 1 | a0001c0001t0003g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.252+9823T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893458 | ||||||
| chr1:86893474
|
C | T | 10 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+9807G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893474 | ||||||
| chr1:86893481
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0135others(1): Show | 5 | HG02886.hp2 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+9800C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893481 | ||||||
| chr1:86893518
|
TGAGGCTG others(25): Show |
T | 10 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+9731_252+9762d others(34): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893518 | ||||||
| chr1:86893614
|
C | CATAA | 5 | a0001c0001t0001g0132a0001c0001t0001g0195a0001c0001t0001g0196others(2): Show | 5 | HG02071.hp1 HG02071.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+9663_252+9666d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893614 | ||||||
| chr1:86893632
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0002g0004a0001c0001t0002g0061 | 4 | HG02965.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+9649A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893632 | ||||||
| chr1:86893695
|
G | T | 1 | a0001c0001t0001g0012 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.252+9586C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893695 | ||||||
| chr1:86893795
|
T | TA | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+9485dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893795 | ||||||
| chr1:86893855
|
G | C | 8 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0038others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+9426C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893855 | ||||||
| chr1:86893891
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.252+9390T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86893891 | ||||||
| chr1:86894170
|
G | GT | 48 | a0001c0001t0001g0112a0001c0001t0002g0001a0001c0001t0002g0007others(45): Show | 51 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.252+9110dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894170 | ||||||
| chr1:86894188
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0209 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.252+9093A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894188 | ||||||
| chr1:86894272
|
T | C | 1 | a0001c0002t0002g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.252+9009A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894272 | ||||||
| chr1:86894298
|
T | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.252+8983A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894298 | ||||||
| chr1:86894373
|
A | G | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+8908T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894373 | ||||||
| chr1:86894666
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.252+8615A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894666 | ||||||
| chr1:86894667
|
T | C | 9 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0075others(6): Show | 9 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.252+8614A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894667 | ||||||
| chr1:86894839
|
A | AAAC | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+8439_252+8441d others(5): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894839 | ||||||
| chr1:86894839
|
A | AAACAAC | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+8436_252+8441d others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894839 | ||||||
| chr1:86894839
|
AAACAACA others(5): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+8430_252+8441d others(14): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894839 | ||||||
| chr1:86894879
|
C | A | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+8402G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894879 | ||||||
| chr1:86894986
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG01256.hp1 HG01257.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+8295G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86894986 | ||||||
| chr1:86895212
|
C | T | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+8069G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895212 | ||||||
| chr1:86895396
|
C | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+7885G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895396 | ||||||
| chr1:86895397
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.252+7884C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895397 | ||||||
| chr1:86895416
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.252+7865A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895416 | ||||||
| chr1:86895490
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+7791T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895490 | ||||||
| chr1:86895732
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+7549C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895732 | ||||||
| chr1:86895824
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0204 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.252+7457G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895824 | ||||||
| chr1:86895956
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+7325C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86895956 | ||||||
| chr1:86896084
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0028 | 2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.252+7197G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86896084 | ||||||
| chr1:86896167
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.252+7114A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86896167 | ||||||
| chr1:86896227
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0135others(1): Show | 5 | HG02886.hp2 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+7054C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86896227 | ||||||
| chr1:86896590
|
A | C | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+6691T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86896590 | ||||||
| chr1:86897003
|
TA | T | 35 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(32): Show | 37 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.252+6277delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897003 | ||||||
| chr1:86897072
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.252+6209C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897072 | ||||||
| chr1:86897097
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.252+6184C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897097 | ||||||
| chr1:86897215
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+6066T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897215 | ||||||
| chr1:86897282
|
C | T | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+5999G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897282 | ||||||
| chr1:86897335
|
G | A | 7 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+5946C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897335 | ||||||
| chr1:86897532
|
T | C | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+5749A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897532 | ||||||
| chr1:86897548
|
T | C | 12 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(9): Show | 12 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+5733A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897548 | ||||||
| chr1:86897556
|
C | A | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+5725G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897556 | ||||||
| chr1:86897651
|
GCAGCTAA | G | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+5623_252+5629d others(9): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897651 | ||||||
| chr1:86897829
|
A | T | 1 | a0001c0001t0002g0016 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.252+5452T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897829 | ||||||
| chr1:86897958
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.252+5323T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86897958 | ||||||
| chr1:86898016
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.252+5265C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898016 | ||||||
| chr1:86898107
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+5174T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898107 | ||||||
| chr1:86898232
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.252+5049A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898232 | ||||||
| chr1:86898359
|
C | T | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(85): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.252+4922G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898359 | ||||||
| chr1:86898473
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.252+4808T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898473 | ||||||
| chr1:86898546
|
A | C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.252+4735T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898546 | ||||||
| chr1:86898580
|
C | CT | 8 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+4700dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898580 | ||||||
| chr1:86898580
|
CT | C | 69 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(66): Show | 77 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.252+4700delA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898580 | ||||||
| chr1:86898582
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.252+4699A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898582 | ||||||
| chr1:86898603
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.252+4678T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898603 | ||||||
| chr1:86898628
|
T | A | 1 | a0001c0001t0007g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.252+4653A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898628 | ||||||
| chr1:86898760
|
TTTTTTTT others(1): Show |
T | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+4513_252+4520d others(10): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898760 | ||||||
| chr1:86898763
|
TTTTTG | T | 10 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+4513_252+4517d others(7): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898763 | ||||||
| chr1:86898764
|
T | G | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+4517A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898764 | ||||||
| chr1:86898764
|
TTTTG | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.252+4513_252+4516d others(6): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898764 | ||||||
| chr1:86898776
|
G | T | 1 | a0001c0001t0003g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+4505C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898776 | ||||||
| chr1:86898780
|
T | G | 13 | a0001c0001t0001g0144a0001c0001t0002g0061a0001c0001t0003g0062others(10): Show | 14 | HG02280.hp2 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.252+4501A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898780 | ||||||
| chr1:86898791
|
C | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 5 | HG01496.hp2 HG02451.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+4490G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898791 | ||||||
| chr1:86898848
|
G | C | 1 | a0001c0001t0001g0137 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252+4433C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898848 | ||||||
| chr1:86898938
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+4343C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86898938 | ||||||
| chr1:86899044
|
T | C | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+4237A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899044 | ||||||
| chr1:86899060
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.252+4221C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899060 | ||||||
| chr1:86899098
|
T | G | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(74): Show | 85 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.252+4183A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899098 | ||||||
| chr1:86899303
|
T | C | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.252+3978A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899303 | ||||||
| chr1:86899321
|
GTGGCCGG others(121): Show |
G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+3832_252+3959d others(2): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899321 | ||||||
| chr1:86899397
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.252+3884C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899397 | ||||||
| chr1:86899416
|
C | T | 24 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0058others(21): Show | 27 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.252+3865G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899416 | ||||||
| chr1:86899424
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.252+3857G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899424 | ||||||
| chr1:86899431
|
CCCTCCCG others(71): Show |
C | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+3772_252+3849d others(80): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899431 | ||||||
| chr1:86899455
|
G | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.252+3826C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899455 | ||||||
| chr1:86899462
|
G | C | 1 | a0001c0001t0002g0088 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.252+3819C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899462 | ||||||
| chr1:86899463
|
G | A | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+3818C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899463 | ||||||
| chr1:86899464
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.252+3817C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899464 | ||||||
| chr1:86899488
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+3793C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899488 | ||||||
| chr1:86899501
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.252+3780G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899501 | ||||||
| chr1:86899508
|
C | T | 16 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0081others(13): Show | 19 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.252+3773G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899508 | ||||||
| chr1:86899532
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+3749G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899532 | ||||||
| chr1:86899636
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.252+3645C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899636 | ||||||
| chr1:86899683
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.252+3598C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899683 | ||||||
| chr1:86899692
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+3589G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899692 | ||||||
| chr1:86899707
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252+3574G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899707 | ||||||
| chr1:86899767
|
C | T | 1 | a0001c0001t0005g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.252+3514G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899767 | ||||||
| chr1:86899768
|
G | A | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+3513C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899768 | ||||||
| chr1:86899817
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.252+3464G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899817 | ||||||
| chr1:86899831
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.252+3450G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899831 | ||||||
| chr1:86899844
|
A | G | 209 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(206): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.252+3437T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899844 | ||||||
| chr1:86899862
|
C | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(62): Show | 71 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.252+3419G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899862 | ||||||
| chr1:86899879
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.252+3402G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899879 | ||||||
| chr1:86899906
|
G | C | 3 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060 | 3 | HG02486.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.252+3375C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899906 | ||||||
| chr1:86899908
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(62): Show | 71 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.252+3373G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899908 | ||||||
| chr1:86899924
|
C | G | 5 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0076others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+3357G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899924 | ||||||
| chr1:86899992
|
CG | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG01256.hp1 HG01257.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+3288delC | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86899992 | ||||||
| chr1:86900007
|
ACTCCTCA others(33): Show |
A | 1 | a0001c0001t0002g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252+3234_252+3273d others(42): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900007 | ||||||
| chr1:86900073
|
G | A | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.252+3208C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900073 | ||||||
| chr1:86900075
|
C | A | 1 | a0001c0001t0001g0201 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.252+3206G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900075 | ||||||
| chr1:86900077
|
G | A | 1 | a0001c0001t0002g0010 | 2 | HG01884.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.252+3204C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900077 | ||||||
| chr1:86900192
|
T | C | 99 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(96): Show | 109 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.252+3089A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900192 | ||||||
| chr1:86900201
|
G | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18963.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.252+3080C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900201 | ||||||
| chr1:86900237
|
G | A | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+3044C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900237 | ||||||
| chr1:86900344
|
T | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+2937A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900344 | ||||||
| chr1:86900351
|
C | T | 29 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(26): Show | 33 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.252+2930G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900351 | ||||||
| chr1:86900423
|
CA | C | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+2857delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900423 | ||||||
| chr1:86900454
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.252+2827C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900454 | ||||||
| chr1:86900599
|
C | A | 1 | a0001c0001t0001g0145 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.252+2682G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900599 | ||||||
| chr1:86900647
|
A | AAGGGAG | 7 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108others(4): Show | 9 | HG00741.hp2 HG01891.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+2628_252+2633d others(8): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900647 | ||||||
| chr1:86900667
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(9): Show | 12 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+2614G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900667 | ||||||
| chr1:86900832
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.252+2449G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900832 | ||||||
| chr1:86900866
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.252+2415C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900866 | ||||||
| chr1:86900897
|
T | G | 1 | a0001c0001t0003g0069 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.252+2384A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900897 | ||||||
| chr1:86900914
|
T | A | 211 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(208): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.252+2367A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900914 | ||||||
| chr1:86900991
|
C | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.252+2290G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86900991 | ||||||
| chr1:86901024
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.252+2257G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901024 | ||||||
| chr1:86901052
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0207 | 3 | HG01928.hp2 HG02071.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.252+2229A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901052 | ||||||
| chr1:86901094
|
C | T | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+2187G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901094 | ||||||
| chr1:86901424
|
TA | T | 5 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0094others(2): Show | 6 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1856delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901424 | ||||||
| chr1:86901582
|
A | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1699T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901582 | ||||||
| chr1:86901708
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+1573C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901708 | ||||||
| chr1:86901734
|
G | C | 1 | a0001c0001t0002g0089 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.252+1547C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901734 | ||||||
| chr1:86901950
|
C | T | 10 | a0001c0001t0002g0072a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG00323.hp2 HG01884.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+1331G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901950 | ||||||
| chr1:86901995
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.252+1286A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86901995 | ||||||
| chr1:86902252
|
T | C | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | NA18946.hp1 NA18949.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.252+1029A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902252 | ||||||
| chr1:86902412
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(74): Show | 85 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.252+869G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902412 | ||||||
| chr1:86902440
|
A | G | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+841T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902440 | ||||||
| chr1:86902552
|
T | C | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+729A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902552 | ||||||
| chr1:86902611
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(74): Show | 85 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.252+670G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902611 | ||||||
| chr1:86902684
|
A | G | 4 | a0001c0001t0003g0006a0001c0001t0003g0067a0001c0001t0003g0068others(1): Show | 5 | HG00741.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+597T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902684 | ||||||
| chr1:86902792
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+489C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902792 | ||||||
| chr1:86902831
|
AAACT | A | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+446_252+449del others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902831 | ||||||
| chr1:86902860
|
G | C | 1 | a0001c0001t0002g0028 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+421C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902860 | ||||||
| chr1:86902872
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.252+409G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902872 | ||||||
| chr1:86902970
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.252+311G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86902970 | ||||||
| chr1:86903024
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+257C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86903024 | ||||||
| chr1:86903025
|
G | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0064a0001c0001t0003g0066others(2): Show | 6 | HG02258.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+256C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86903025 | ||||||
| chr1:86903113
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.252+168G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86903113 | ||||||
| chr1:86903186
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.252+95C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86903186 | ||||||
| chr1:86903234
|
A | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.252+47T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86903234 | ||||||
| chr1:86903270
|
G | C | 3 | a0001c0001t0004g0055a0001c0001t0004g0056a0001c0001t0004g0057 | 3 | HG02630.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+11C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 2/4 | chr1 | 86903270 | ||||||
| chr1:86903493
|
C | T | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.85-45G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86903493 | ||||||
| chr1:86903542
|
T | C | 8 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0038others(5): Show | 9 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-94A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86903542 | ||||||
| chr1:86903641
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.85-193G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86903641 | ||||||
| chr1:86903654
|
G | A | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-206C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86903654 | ||||||
| chr1:86903661
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.85-213G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86903661 | ||||||
| chr1:86904085
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.85-637T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904085 | ||||||
| chr1:86904182
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.85-734G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904182 | ||||||
| chr1:86904311
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.85-863A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904311 | ||||||
| chr1:86904364
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.85-916A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904364 | ||||||
| chr1:86904367
|
T | C | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-919A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904367 | ||||||
| chr1:86904380
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85-932T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904380 | ||||||
| chr1:86904391
|
A | T | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(89): Show | 102 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.85-943T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904391 | ||||||
| chr1:86904697
|
A | T | 1 | a0001c0001t0001g0110 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.85-1249T>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904697 | ||||||
| chr1:86904791
|
G | A | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-1343C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904791 | ||||||
| chr1:86904844
|
A | G | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-1396T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904844 | ||||||
| chr1:86904999
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.85-1551A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86904999 | ||||||
| chr1:86905059
|
A | G | 29 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(26): Show | 33 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.85-1611T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905059 | ||||||
| chr1:86905180
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.85-1732A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905180 | ||||||
| chr1:86905516
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.85-2068G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905516 | ||||||
| chr1:86905562
|
T | C | 1 | a0001c0001t0004g0053 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.85-2114A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905562 | ||||||
| chr1:86905683
|
C | G | 68 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(65): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.85-2235G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905683 | ||||||
| chr1:86905773
|
G | A | 1 | a0001c0001t0007g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85-2325C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905773 | ||||||
| chr1:86905880
|
A | ATGAG | 77 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(74): Show | 85 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.85-2433_85-2432ins others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905880 | ||||||
| chr1:86905943
|
G | A | 11 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0062others(8): Show | 13 | HG00741.hp2 HG01891.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.85-2495C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86905943 | ||||||
| chr1:86906022
|
A | G | 3 | a0001c0001t0002g0004a0001c0001t0002g0061a0001c0001t0002g0108 | 4 | HG02647.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-2574T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86906022 | ||||||
| chr1:86906079
|
C | T | 150 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(147): Show | 162 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.85-2631G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86906079 | ||||||
| chr1:86906476
|
ATG | A | 4 | a0001c0001t0003g0058a0001c0001t0003g0059a0001c0001t0003g0060others(1): Show | 4 | HG02486.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.85-3030_85-3029del others(2): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86906476 | ||||||
| chr1:86906590
|
T | C | 4 | a0001c0001t0002g0001a0001c0001t0002g0040a0001c0001t0002g0041others(1): Show | 5 | HG02055.hp1 HG02257.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-3142A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86906590 | ||||||
| chr1:86906707
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.85-3259C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86906707 | ||||||
| chr1:86906944
|
C | T | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.85-3496G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86906944 | ||||||
| chr1:86907053
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.85-3605C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907053 | ||||||
| chr1:86907060
|
A | G | 1 | a0001c0001t0003g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.85-3612T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907060 | ||||||
| chr1:86907306
|
T | A | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-3858A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907306 | ||||||
| chr1:86907460
|
G | C | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.85-4012C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907460 | ||||||
| chr1:86907655
|
A | C | 1 | a0001c0001t0008g0030 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-4207T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907655 | ||||||
| chr1:86907736
|
T | C | 91 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(88): Show | 101 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.85-4288A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907736 | ||||||
| chr1:86907755
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.85-4307C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907755 | ||||||
| chr1:86907859
|
A | C | 1 | a0001c0001t0002g0074 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.85-4411T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907859 | ||||||
| chr1:86907932
|
G | A | 9 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0055others(6): Show | 10 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.85-4484C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907932 | ||||||
| chr1:86907950
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85-4502G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907950 | ||||||
| chr1:86907997
|
AC | A | 5 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0076others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-4550delG | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907997 | ||||||
| chr1:86907998
|
C | A | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.85-4550G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907998 | ||||||
| chr1:86907998
|
C | CA | 12 | a0001c0001t0001g0206a0001c0001t0003g0006a0001c0001t0003g0067others(9): Show | 14 | HG00741.hp2 HG01891.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85-4551dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907998 | ||||||
| chr1:86907998
|
CA | C | 39 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0009others(36): Show | 44 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.85-4551delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907998 | ||||||
| chr1:86907999
|
A | C | 3 | a0001c0001t0001g0107a0001c0001t0002g0082a0001c0001t0002g0094 | 3 | HG01256.hp2 HG02615.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.85-4551T>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907999 | ||||||
| chr1:86907999
|
A | G | 5 | a0001c0001t0002g0072a0001c0001t0002g0075a0001c0001t0002g0076others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-4551T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86907999 | ||||||
| chr1:86908033
|
C | G | 1 | a0001c0001t0001g0106 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.85-4585G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86908033 | ||||||
| chr1:86908103
|
A | G | 1 | a0001c0001t0002g0044 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.85-4655T>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86908103 | ||||||
| chr1:86908387
|
C | G | 8 | a0001c0001t0003g0005a0001c0001t0003g0058a0001c0001t0003g0059others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-4939G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86908387 | ||||||
| chr1:86908580
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85-5132G>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86908580 | ||||||
| chr1:86908943
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.84+5085G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86908943 | ||||||
| chr1:86909255
|
T | A | 2 | a0001c0001t0004g0056a0001c0001t0004g0057 | 2 | HG02630.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.84+4773A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909255 | ||||||
| chr1:86909684
|
T | A | 1 | a0001c0001t0007g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.84+4344A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909684 | ||||||
| chr1:86909745
|
T | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(61): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.84+4283A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909745 | ||||||
| chr1:86909859
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.84+4169C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909859 | ||||||
| chr1:86909865
|
C | T | 4 | a0001c0001t0003g0006a0001c0001t0003g0067a0001c0001t0003g0068others(1): Show | 5 | HG00741.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+4163G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909865 | ||||||
| chr1:86909874
|
G | A | 4 | a0001c0001t0003g0006a0001c0001t0003g0067a0001c0001t0003g0068others(1): Show | 5 | HG00741.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+4154C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909874 | ||||||
| chr1:86909889
|
T | A | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+4139A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909889 | ||||||
| chr1:86909929
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.84+4099G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86909929 | ||||||
| chr1:86910185
|
T | G | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.84+3843A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910185 | ||||||
| chr1:86910470
|
C | G | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84+3558G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910470 | ||||||
| chr1:86910591
|
CT | C | 16 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0031others(13): Show | 17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.84+3436delA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910591 | ||||||
| chr1:86910595
|
T | TTGGGAGG others(18): Show |
48 | a0001c0001t0002g0002a0001c0001t0002g0007a0001c0001t0002g0009others(45): Show | 53 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.84+3408_84+3432dup others(25): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910595 | ||||||
| chr1:86910595
|
T | TTTGGGAG others(152): Show |
16 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0031others(13): Show | 17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.84+3432_84+3433ins others(159): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910595 | ||||||
| chr1:86910660
|
T | C | 1 | a0001c0001t0003g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.84+3368A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910660 | ||||||
| chr1:86910702
|
C | CA | 14 | a0001c0001t0001g0015a0001c0001t0001g0208a0001c0001t0001g0209others(11): Show | 15 | HG00408.hp1 HG02071.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.84+3325dupT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910702 | ||||||
| chr1:86910702
|
C | CAAAA | 4 | a0001c0001t0005g0003a0001c0001t0005g0050a0001c0001t0005g0051others(1): Show | 5 | HG02630.hp1 HG03453.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+3322_84+3325dup others(4): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910702 | ||||||
| chr1:86910702
|
CA | C | 62 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(59): Show | 69 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.84+3325delT | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910702 | ||||||
| chr1:86910862
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.84+3166C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910862 | ||||||
| chr1:86910866
|
T | A | 1 | a0001c0001t0002g0080 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.84+3162A>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86910866 | ||||||
| chr1:86911149
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.84+2879A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911149 | ||||||
| chr1:86911169
|
C | T | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(77): Show | 89 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.84+2859G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911169 | ||||||
| chr1:86911324
|
G | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(61): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.84+2704C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911324 | ||||||
| chr1:86911354
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.84+2674G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911354 | ||||||
| chr1:86911705
|
T | C | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.84+2323A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911705 | ||||||
| chr1:86911784
|
A | AT | 12 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(9): Show | 13 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.84+2243dupA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911784 | ||||||
| chr1:86911784
|
A | ATT | 5 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+2242_84+2243dup others(2): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911784 | ||||||
| chr1:86911784
|
AT | A | 66 | a0001c0001t0001g0096a0001c0001t0002g0001a0001c0001t0002g0002others(63): Show | 73 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.84+2243delA | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911784 | ||||||
| chr1:86911879
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18963.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.84+2149C>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911879 | ||||||
| chr1:86911947
|
T | G | 64 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0007others(61): Show | 70 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.84+2081A>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86911947 | ||||||
| chr1:86912257
|
G | C | 1 | a0001c0001t0003g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.84+1771C>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86912257 | ||||||
| chr1:86912377
|
T | C | 17 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(14): Show | 21 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.84+1651A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86912377 | ||||||
| chr1:86912726
|
C | T | 6 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0005g0003others(3): Show | 7 | HG02451.hp2 HG02630.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+1302G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86912726 | ||||||
| chr1:86912837
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.84+1191A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86912837 | ||||||
| chr1:86912944
|
T | C | 28 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(25): Show | 32 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.84+1084A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86912944 | ||||||
| chr1:86913093
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.84+935C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86913093 | ||||||
| chr1:86913119
|
C | G | 4 | a0001c0001t0005g0003a0001c0001t0005g0050a0001c0001t0005g0051others(1): Show | 5 | HG02630.hp1 HG03453.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+909G>C | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86913119 | ||||||
| chr1:86913144
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0048a0001c0001t0002g0049 | 4 | HG01496.hp2 HG03098.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+884A>G | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86913144 | ||||||
| chr1:86913402
|
C | CTTATT | 90 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(87): Show | 100 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.84+625_84+626insAA others(3): Show |
SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86913402 | ||||||
| chr1:86913626
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0016others(33): Show | 38 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.84+402C>T | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86913626 | ||||||
| chr1:86913954
|
C | T | 37 | a0001c0001t0001g0015a0001c0001t0002g0001a0001c0001t0002g0002others(34): Show | 39 | HG00639.hp1 HG01106.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.84+74G>A | SELENOF | ENSG00000183291.18 | transcript | ENST00000331835.10 | protein_coding | 1/4 | chr1 | 86913954 |