Search by Gene
| geneid | 166968 |
|---|---|
| ensemblid | ENSG00000155545.20 |
| hgncid | 26678 |
| symbol | MIER3 |
| name | MIER family member 3 |
| refseq_nuc | NM_001297599.2 |
| refseq_prot | NP_001284528.1 |
| ensembl_nuc | ENST00000381199.8 |
| ensembl_prot | ENSP00000370596.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 56919603 |
| end | 56952123 |
| strand | - |
| ver | v1.2 |
| region | chr5:56919603-56952123 |
| region5000 | chr5:56914603-56957123 |
| regionname0 | MIER3_chr5_56919603_56952123 |
| regionname5000 | MIER3_chr5_56914603_56957123 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 550 | 373 | 62 | 67 | 186 | 10 | 46 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0002 | 0/0 | 550 | 21 | 20 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1653 | 176 | 25 | 36 | 84 | 6 | 23 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0002 | 0/0 | 1653 | 174 | 23 | 26 | 100 | 4 | 21 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0003 | 0/0 | 1653 | 21 | 20 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0004 | 0/0 | 1653 | 7 | 7 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0005 | 0/0 | 1653 | 6 | 1 | 4 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0006 | 0/0 | 1653 | 5 | 4 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0007 | 0/0 | 1653 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0008 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0009 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| c0010 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3547 | 205 | 39 | 30 | 109 | 4 | 23 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0002 | 0/1 | 3547 | 112 | 30 | 31 | 31 | 4 | 15 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0003 | 0/0 | 3547 | 47 | 3 | 5 | 32 | 2 | 5 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0004 | 1/0 | 3547 | 11 | 0 | 0 | 10 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0005 | 0/0 | 3543 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0006 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0007 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0008 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0009 | 0/0 | 3547 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0010 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0011 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0012 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0013 | 0/0 | 3547 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0014 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0015 | 0/0 | 3543 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0016 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0017 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0018 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0019 | 0/0 | 3547 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| t0020 | 0/0 | 3547 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 31 | 0 | 2 | 29 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0002 | 0/0 | 30 | 5 | 8 | 13 | 1 | 3 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0003 | 0/0 | 22 | 0 | 5 | 13 | 0 | 4 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0004 | 0/1 | 14 | 2 | 3 | 7 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0005 | 0/0 | 13 | 0 | 3 | 6 | 2 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0007 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0008 | 0/0 | 9 | 0 | 0 | 7 | 2 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0010 | 0/0 | 8 | 0 | 3 | 3 | 1 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0011 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0012 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0015 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0022 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 176 | 25 | 36 | 84 | 6 | 23 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 174 | 23 | 26 | 100 | 4 | 21 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0005 | a0001 | c0005 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0007 | a0001 | c0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0009 | a0001 | c0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 21 | 20 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 72 | 1 | 9 | 52 | 2 | 8 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/1 | 94 | 19 | 26 | 31 | 4 | 13 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 111 | 19 | 20 | 55 | 2 | 15 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 47 | 3 | 5 | 32 | 2 | 5 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0004 | a0001 | c0002 | t0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0007 | a0001 | c0002 | t0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0010 | a0001 | c0002 | t0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0011 | a0001 | c0002 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0012 | a0001 | c0002 | t0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0013 | a0001 | c0002 | t0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0002t0020 | a0001 | c0002 | t0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0004t0002 | a0001 | c0004 | t0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0005t0002 | a0001 | c0005 | t0002 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0006t0008 | a0001 | c0006 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0007t0001 | a0001 | c0007 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0008t0016 | a0001 | c0008 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0009t0002 | a0001 | c0009 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0001c0010t0001 | a0001 | c0010 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 19 | 18 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0002c0003t0014 | a0002 | c0003 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| a0002c0003t0018 | a0002 | c0003 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 31 | 0 | 2 | 29 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 13 | 0 | 3 | 6 | 2 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/1 | 14 | 2 | 3 | 7 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0010 | a0001 | c0001 | t0002 | g0010 | 0/0 | 8 | 0 | 3 | 3 | 1 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0017 | a0001 | c0001 | t0002 | g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0128 | a0001 | c0001 | t0002 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0135 | a0001 | c0001 | t0002 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0137 | a0001 | c0001 | t0002 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0138 | a0001 | c0001 | t0002 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0142 | a0001 | c0001 | t0002 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0144 | a0001 | c0001 | t0002 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0145 | a0001 | c0001 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0146 | a0001 | c0001 | t0002 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0147 | a0001 | c0001 | t0002 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0149 | a0001 | c0001 | t0002 | g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0152 | a0001 | c0001 | t0002 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0153 | a0001 | c0001 | t0002 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0155 | a0001 | c0001 | t0002 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0156 | a0001 | c0001 | t0002 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0157 | a0001 | c0001 | t0002 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0160 | a0001 | c0001 | t0002 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0161 | a0001 | c0001 | t0002 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0162 | a0001 | c0001 | t0002 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0163 | a0001 | c0001 | t0002 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0164 | a0001 | c0001 | t0002 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0165 | a0001 | c0001 | t0002 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0166 | a0001 | c0001 | t0002 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0175 | a0001 | c0001 | t0002 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0176 | a0001 | c0001 | t0002 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0177 | a0001 | c0001 | t0002 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0002g0186 | a0001 | c0001 | t0002 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0004g0130 | a0001 | c0001 | t0004 | g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0005g0023 | a0001 | c0001 | t0005 | g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0006g0141 | a0001 | c0001 | t0006 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0006g0154 | a0001 | c0001 | t0006 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0009g0140 | a0001 | c0001 | t0009 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0015g0118 | a0001 | c0001 | t0015 | g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0017g0115 | a0001 | c0001 | t0017 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0001t0019g0143 | a0001 | c0001 | t0019 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0002 | a0001 | c0002 | t0001 | g0002 | 0/0 | 30 | 5 | 8 | 13 | 1 | 3 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0003 | a0001 | c0002 | t0001 | g0003 | 0/0 | 22 | 0 | 5 | 13 | 0 | 4 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0007 | a0001 | c0002 | t0001 | g0007 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0013 | a0001 | c0002 | t0001 | g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0014 | a0001 | c0002 | t0001 | g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0019 | a0001 | c0002 | t0001 | g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0025 | a0001 | c0002 | t0001 | g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0026 | a0001 | c0002 | t0001 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0027 | a0001 | c0002 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0028 | a0001 | c0002 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0029 | a0001 | c0002 | t0001 | g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0048 | a0001 | c0002 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0049 | a0001 | c0002 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0050 | a0001 | c0002 | t0001 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0051 | a0001 | c0002 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0053 | a0001 | c0002 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0054 | a0001 | c0002 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0055 | a0001 | c0002 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0056 | a0001 | c0002 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0057 | a0001 | c0002 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0058 | a0001 | c0002 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0059 | a0001 | c0002 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0060 | a0001 | c0002 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0061 | a0001 | c0002 | t0001 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0062 | a0001 | c0002 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0063 | a0001 | c0002 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0064 | a0001 | c0002 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0066 | a0001 | c0002 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0068 | a0001 | c0002 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0069 | a0001 | c0002 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0070 | a0001 | c0002 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0071 | a0001 | c0002 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0072 | a0001 | c0002 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0073 | a0001 | c0002 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0074 | a0001 | c0002 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0075 | a0001 | c0002 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0076 | a0001 | c0002 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0001g0077 | a0001 | c0002 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0008 | a0001 | c0002 | t0003 | g0008 | 0/0 | 9 | 0 | 0 | 7 | 2 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0015 | a0001 | c0002 | t0003 | g0015 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0020 | a0001 | c0002 | t0003 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0021 | a0001 | c0002 | t0003 | g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0030 | a0001 | c0002 | t0003 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0031 | a0001 | c0002 | t0003 | g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0032 | a0001 | c0002 | t0003 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0033 | a0001 | c0002 | t0003 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0079 | a0001 | c0002 | t0003 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0080 | a0001 | c0002 | t0003 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0081 | a0001 | c0002 | t0003 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0082 | a0001 | c0002 | t0003 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0083 | a0001 | c0002 | t0003 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0084 | a0001 | c0002 | t0003 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0085 | a0001 | c0002 | t0003 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0086 | a0001 | c0002 | t0003 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0087 | a0001 | c0002 | t0003 | g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0088 | a0001 | c0002 | t0003 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0089 | a0001 | c0002 | t0003 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0091 | a0001 | c0002 | t0003 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0092 | a0001 | c0002 | t0003 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0094 | a0001 | c0002 | t0003 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0095 | a0001 | c0002 | t0003 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0096 | a0001 | c0002 | t0003 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0097 | a0001 | c0002 | t0003 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0099 | a0001 | c0002 | t0003 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0125 | a0001 | c0002 | t0003 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0003g0126 | a0001 | c0002 | t0003 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0004g0006 | a0001 | c0002 | t0004 | g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0007g0090 | a0001 | c0002 | t0007 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0010g0100 | a0001 | c0002 | t0010 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0011g0098 | a0001 | c0002 | t0011 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0012g0067 | a0001 | c0002 | t0012 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0013g0065 | a0001 | c0002 | t0013 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0002t0020g0093 | a0001 | c0002 | t0020 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0004t0002g0024 | a0001 | c0004 | t0002 | g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0004t0002g0119 | a0001 | c0004 | t0002 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0004t0002g0122 | a0001 | c0004 | t0002 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0004t0002g0123 | a0001 | c0004 | t0002 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0004t0002g0124 | a0001 | c0004 | t0002 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0005t0002g0037 | a0001 | c0005 | t0002 | g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0005t0002g0045 | a0001 | c0005 | t0002 | g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0005t0002g0134 | a0001 | c0005 | t0002 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0005t0002g0174 | a0001 | c0005 | t0002 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0006t0002g0180 | a0001 | c0006 | t0002 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0006t0002g0182 | a0001 | c0006 | t0002 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0006t0002g0183 | a0001 | c0006 | t0002 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0006t0002g0184 | a0001 | c0006 | t0002 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0006t0008g0181 | a0001 | c0006 | t0008 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0007t0001g0112 | a0001 | c0007 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0007t0001g0113 | a0001 | c0007 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0008t0016g0167 | a0001 | c0008 | t0016 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0009t0002g0139 | a0001 | c0009 | t0002 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0001c0010t0001g0052 | a0001 | c0010 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0009 | a0002 | c0003 | t0001 | g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0044 | a0002 | c0003 | t0001 | g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0102 | a0002 | c0003 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0103 | a0002 | c0003 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0169 | a0002 | c0003 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0170 | a0002 | c0003 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0171 | a0002 | c0003 | t0001 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0172 | a0002 | c0003 | t0001 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0173 | a0002 | c0003 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0178 | a0002 | c0003 | t0001 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0001g0179 | a0002 | c0003 | t0001 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0014g0104 | a0002 | c0003 | t0014 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| a0002c0003t0018g0168 | a0002 | c0003 | t0018 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIER3_chr5_56914603_56957123 | MIER3 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | FIN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | FIN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0115 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0084 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00544 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00558 | hp2 | a0001 | c0002 | t0012 | g0067 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0118 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01109 | hp1 | a0001 | c0006 | t0002 | g0184 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01257 | hp2 | a0001 | c0005 | t0002 | g0037 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01346 | hp1 | a0001 | c0005 | t0002 | g0037 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0031 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01361 | hp2 | a0001 | c0005 | t0002 | g0134 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0169 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0145 | EUR | IBS | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01891 | hp1 | a0001 | c0006 | t0002 | g0182 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01943 | hp1 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01952 | hp1 | a0001 | c0005 | t0002 | g0045 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0141 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02056 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02155 | hp1 | a0001 | c0007 | t0001 | g0112 | EAS | CDX | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | CDX | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02300 | hp2 | a0001 | c0002 | t0013 | g0065 | AMR | PEL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02523 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | KHV | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0172 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02622 | hp1 | a0001 | c0010 | t0001 | g0052 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02622 | hp2 | a0001 | c0006 | t0002 | g0183 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0170 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02698 | hp1 | a0001 | c0001 | t0019 | g0143 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02698 | hp2 | a0001 | c0002 | t0020 | g0093 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02723 | hp2 | a0001 | c0004 | t0002 | g0122 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0119 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0102 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02896 | hp2 | a0001 | c0006 | t0008 | g0181 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0124 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0171 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03098 | hp2 | a0002 | c0003 | t0018 | g0168 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0044 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03195 | hp2 | a0002 | c0003 | t0014 | g0104 | AFR | ESN | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03453 | hp2 | a0001 | c0006 | t0002 | g0180 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0178 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03491 | hp2 | a0001 | c0009 | t0002 | g0139 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | GWD | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03579 | hp1 | a0001 | c0002 | t0010 | g0100 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0086 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0140 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0094 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0126 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0088 | SAS | BEB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0087 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | STU | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0173 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18953 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18976 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18976 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18981 | hp1 | a0001 | c0002 | t0007 | g0090 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18990 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19005 | hp2 | a0001 | c0007 | t0001 | g0113 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19006 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19043 | hp2 | a0001 | c0004 | t0002 | g0123 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19059 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19076 | hp1 | a0001 | c0002 | t0011 | g0098 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0006 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19240 | hp1 | a0001 | c0008 | t0016 | g0167 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0179 | AFR | YRI | MIER3_chr5_56914603_56957123 | MIER3 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MIER3_chr5_56914603_56957123 | MIER3 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | MIER3_chr5_56914603_56957123 | MIER3 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | GIH | MIER3_chr5_56914603_56957123 | MIER3 |
| NA20905 | hp2 | a0001 | c0005 | t0002 | g0045 | SAS | GIH | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0030 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0125 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0044 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0009 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0024 | AFR | MSL | MIER3_chr5_56914603_56957123 | MIER3 |
| HG06807 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | MIER3_chr5_56914603_56957123 | MIER3 |
| NA20300 | hp1 | a0001 | c0005 | t0002 | g0174 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0009 | AFR | USA | MIER3_chr5_56914603_56957123 | MIER3 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | LWK | MIER3_chr5_56914603_56957123 | MIER3 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0004 | REF | REF | MIER3_chr5_56914603_56957123 | MIER3 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0130 | REF | REF | MIER3_chr5_56914603_56957123 | MIER3 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56923192
|
T | C | 1 | a0002 | 21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
missense_variant | MODERATE | c.1589A>G | p.Asn530Ser | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1610/5199 | 1589/1653 | 530/550 | chr5 | 56923192 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56923227
|
A | T | 1 | a0001c0004 | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
synonymous_variant | LOW | c.1554T>A | p.Ala518Ala | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1575/5199 | 1554/1653 | 518/550 | chr5 | 56923227 | ||
| chr5:56923266
|
A | G | 1 | a0001c0009 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.1515T>C | p.Phe505Phe | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1536/5199 | 1515/1653 | 505/550 | chr5 | 56923266 | ||
| chr5:56923827
|
A | G | 1 | a0001c0010 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1059T>C | p.Tyr353Tyr | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 12/13 | 1080/5199 | 1059/1653 | 353/550 | chr5 | 56923827 | ||
| chr5:56930698
|
G | T | 1 | a0001c0007 | 2 | HG02155.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.795C>A | p.Ile265Ile | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/13 | 816/5199 | 795/1653 | 265/550 | chr5 | 56930698 | ||
| chr5:56935714
|
A | G | 2 | a0001c0006a0001c0008 | 6 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.474T>C | p.Val158Val | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 6/13 | 495/5199 | 474/1653 | 158/550 | chr5 | 56935714 | ||
| chr5:56937663
|
G | A | 1 | a0001c0005 | 6 | HG01257.hp2 HG01346.hp1 HG01361.hp2 others(3): Show |
synonymous_variant | LOW | c.351C>T | p.Asp117Asp | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/13 | 372/5199 | 351/1653 | 117/550 | chr5 | 56937663 | ||
| chr5:56946947
|
T | C | 3 | a0001c0002a0001c0006a0001c0010 | 180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
synonymous_variant | LOW | c.159A>G | p.Ser53Ser | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/13 | 180/5199 | 159/1653 | 53/550 | chr5 | 56946947 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56919926
|
G | A | 5 | a0001c0002t0003a0001c0002t0007a0001c0002t0010others(2): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3202C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 3202 | chr5 | 56919926 | |||||
| chr5:56920049
|
T | G | 1 | a0001c0002t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3079A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 3079 | chr5 | 56920049 | |||||
| chr5:56920083
|
G | T | 1 | a0001c0002t0011 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3045C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 3045 | chr5 | 56920083 | |||||
| chr5:56920282
|
A | G | 1 | a0001c0002t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2846T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2846 | chr5 | 56920282 | |||||
| chr5:56920448
|
G | A | 1 | a0001c0001t0015 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2680C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2680 | chr5 | 56920448 | |||||
| chr5:56920547
|
C | T | 1 | a0001c0002t0013 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2581G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2581 | chr5 | 56920547 | |||||
| chr5:56920610
|
T | C | 1 | a0002c0003t0014 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2518A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2518 | chr5 | 56920610 | |||||
| chr5:56920762
|
A | G | 1 | a0001c0008t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2366 | chr5 | 56920762 | |||||
| chr5:56920940
|
AATTT | A | 2 | a0001c0001t0005a0001c0001t0015 | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2184_*2187delAAAT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 2184 | chr5 | 56920940 | |||||
| chr5:56921265
|
T | C | 1 | a0001c0008t0016 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1863A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1863 | chr5 | 56921265 | |||||
| chr5:56921362
|
A | C | 1 | a0001c0001t0009 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1766 | chr5 | 56921362 | |||||
| chr5:56921369
|
A | G | 5 | a0001c0002t0003a0001c0002t0007a0001c0002t0010others(2): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1759T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1759 | chr5 | 56921369 | |||||
| chr5:56921418
|
A | C | 1 | a0001c0006t0008 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1710T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1710 | chr5 | 56921418 | |||||
| chr5:56921514
|
C | T | 1 | a0001c0006t0008 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1614G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1614 | chr5 | 56921514 | |||||
| chr5:56921663
|
A | G | 1 | a0001c0002t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1465 | chr5 | 56921663 | |||||
| chr5:56921702
|
T | C | 5 | a0001c0002t0003a0001c0002t0007a0001c0002t0010others(2): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1426A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1426 | chr5 | 56921702 | |||||
| chr5:56921756
|
G | C | 1 | a0001c0001t0006 | 2 | HG01891.hp2 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1372 | chr5 | 56921756 | |||||
| chr5:56922037
|
T | C | 1 | a0001c0001t0017 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1091A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 1091 | chr5 | 56922037 | |||||
| chr5:56922202
|
C | T | 14 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(11): Show | 168 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*926G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 926 | chr5 | 56922202 | |||||
| chr5:56922297
|
G | A | 1 | a0002c0003t0018 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 831 | chr5 | 56922297 | |||||
| chr5:56922340
|
T | C | 1 | a0001c0001t0019 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 788 | chr5 | 56922340 | |||||
| chr5:56922452
|
C | T | 1 | a0001c0002t0007 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*676G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 676 | chr5 | 56922452 | |||||
| chr5:56922453
|
G | A | 1 | a0001c0002t0020 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 675 | chr5 | 56922453 | |||||
| chr5:56922724
|
C | G | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(24): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
3_prime_UTR_variant | MODIFIER | c.*404G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 13/13 | 404 | chr5 | 56922724 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:56923871
|
T | C | 32 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(29): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1053-38A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 11/12 | chr5 | 56923871 | ||||||
| chr5:56924211
|
T | C | 1 | a0001c0005t0002g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.925-169A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924211 | ||||||
| chr5:56924253
|
G | GT | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.925-212dupA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924253 | ||||||
| chr5:56924263
|
T | A | 4 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.925-221A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924263 | ||||||
| chr5:56924264
|
A | T | 4 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0163others(1): Show | 6 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.925-222T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924264 | ||||||
| chr5:56924320
|
C | T | 1 | a0001c0002t0001g0064 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.925-278G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924320 | ||||||
| chr5:56924376
|
G | A | 1 | a0001c0002t0001g0057 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.925-334C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924376 | ||||||
| chr5:56924555
|
T | C | 60 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(57): Show | 106 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.925-513A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924555 | ||||||
| chr5:56924577
|
A | G | 1 | a0001c0002t0003g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.925-535T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924577 | ||||||
| chr5:56924635
|
A | G | 6 | a0002c0003t0001g0044a0002c0003t0001g0169a0002c0003t0001g0170others(3): Show | 7 | HG01433.hp1 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.925-593T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924635 | ||||||
| chr5:56924887
|
T | C | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.925-845A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924887 | ||||||
| chr5:56924975
|
T | G | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.925-933A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924975 | ||||||
| chr5:56924990
|
T | G | 6 | a0002c0003t0001g0009a0002c0003t0001g0102a0002c0003t0001g0103others(3): Show | 13 | HG02145.hp1 HG02572.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.925-948A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56924990 | ||||||
| chr5:56925171
|
C | T | 13 | a0002c0003t0001g0009a0002c0003t0001g0044a0002c0003t0001g0102others(10): Show | 21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.925-1129G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925171 | ||||||
| chr5:56925172
|
G | A | 32 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(29): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.925-1130C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925172 | ||||||
| chr5:56925216
|
A | C | 2 | a0001c0002t0001g0072a0001c0002t0001g0074 | 2 | HG00621.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.925-1174T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925216 | ||||||
| chr5:56925350
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.925-1308C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925350 | ||||||
| chr5:56925369
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.925-1327G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925369 | ||||||
| chr5:56925501
|
A | G | 70 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(67): Show | 118 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.925-1459T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925501 | ||||||
| chr5:56925579
|
T | C | 1 | a0001c0002t0003g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.925-1537A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925579 | ||||||
| chr5:56925710
|
A | G | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.925-1668T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925710 | ||||||
| chr5:56925857
|
T | C | 1 | a0002c0003t0001g0172 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.925-1815A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925857 | ||||||
| chr5:56925961
|
T | A | 1 | a0001c0001t0015g0118 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.925-1919A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56925961 | ||||||
| chr5:56926017
|
G | T | 2 | a0001c0002t0003g0089a0001c0002t0003g0092 | 2 | NA18981.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.925-1975C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926017 | ||||||
| chr5:56926053
|
G | A | 2 | a0001c0002t0003g0015a0002c0003t0001g0179 | 5 | HG01928.hp1 HG01943.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-2011C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926053 | ||||||
| chr5:56926065
|
T | A | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.925-2023A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926065 | ||||||
| chr5:56926111
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(140): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.925-2069A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926111 | ||||||
| chr5:56926260
|
TA | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(19): Show | 70 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.925-2219delT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926260 | ||||||
| chr5:56926293
|
G | A | 19 | a0001c0001t0001g0151a0001c0001t0002g0010a0001c0001t0002g0011others(16): Show | 37 | HG00280.hp1 HG00609.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.925-2251C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926293 | ||||||
| chr5:56926317
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.925-2275A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926317 | ||||||
| chr5:56926413
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.924+2354T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926413 | ||||||
| chr5:56926413
|
A | T | 1 | a0001c0002t0001g0053 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.924+2354T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926413 | ||||||
| chr5:56926478
|
A | G | 1 | a0001c0001t0002g0011 | 7 | HG01257.hp1 HG01258.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.924+2289T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926478 | ||||||
| chr5:56926531
|
A | T | 65 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(62): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.924+2236T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926531 | ||||||
| chr5:56926626
|
T | C | 1 | a0001c0002t0001g0059 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.924+2141A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926626 | ||||||
| chr5:56926645
|
A | ATGGTACA others(7): Show |
5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+2121_924+2122i others(16): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926645 | ||||||
| chr5:56926718
|
C | T | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.924+2049G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926718 | ||||||
| chr5:56926719
|
G | A | 7 | a0001c0002t0001g0066a0002c0003t0001g0044a0002c0003t0001g0169others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.924+2048C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926719 | ||||||
| chr5:56926859
|
C | A | 2 | a0001c0001t0005g0023a0001c0001t0015g0118 | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.924+1908G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926859 | ||||||
| chr5:56926884
|
A | AT | 18 | a0001c0001t0002g0004a0001c0001t0002g0127a0001c0001t0002g0128others(15): Show | 33 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.924+1882dupA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926884 | ||||||
| chr5:56926912
|
C | T | 36 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(33): Show | 55 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.924+1855G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926912 | ||||||
| chr5:56926938
|
C | A | 1 | a0002c0003t0001g0044 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.924+1829G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56926938 | ||||||
| chr5:56927040
|
C | T | 3 | a0001c0002t0001g0050a0001c0002t0001g0055a0001c0010t0001g0052 | 3 | HG02572.hp2 HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.924+1727G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927040 | ||||||
| chr5:56927118
|
CAT | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(21): Show | 72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+1647_924+1648d others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927118 | ||||||
| chr5:56927173
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(107): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.924+1594C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927173 | ||||||
| chr5:56927296
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.924+1471G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927296 | ||||||
| chr5:56927478
|
T | G | 1 | a0001c0002t0003g0096 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.924+1289A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927478 | ||||||
| chr5:56927607
|
G | C | 2 | a0001c0004t0002g0024a0001c0004t0002g0119 | 4 | HG02809.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.924+1160C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927607 | ||||||
| chr5:56927671
|
G | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(26): Show | 79 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.924+1096C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927671 | ||||||
| chr5:56927678
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(180): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.924+1089C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927678 | ||||||
| chr5:56927965
|
C | G | 1 | a0001c0002t0003g0085 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.924+802G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56927965 | ||||||
| chr5:56928051
|
A | AT | 30 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(27): Show | 49 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.924+715dupA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928051 | ||||||
| chr5:56928234
|
A | T | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.924+533T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928234 | ||||||
| chr5:56928297
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(159): Show | 311 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.924+470T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928297 | ||||||
| chr5:56928351
|
C | T | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.924+416G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928351 | ||||||
| chr5:56928365
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.924+402C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928365 | ||||||
| chr5:56928512
|
G | T | 52 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(49): Show | 96 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.924+255C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928512 | ||||||
| chr5:56928581
|
T | C | 1 | a0001c0002t0003g0091 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.924+186A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928581 | ||||||
| chr5:56928621
|
G | A | 1 | a0001c0002t0003g0083 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.924+146C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928621 | ||||||
| chr5:56928623
|
A | C | 3 | a0001c0004t0002g0122a0001c0004t0002g0123a0001c0004t0002g0124 | 3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.924+144T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928623 | ||||||
| chr5:56928658
|
T | TTGGC | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(108): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.924+108_924+109ins others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 10/12 | chr5 | 56928658 | ||||||
| chr5:56928887
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(108): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.830-26A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928887 | ||||||
| chr5:56928893
|
C | T | 12 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0030others(9): Show | 24 | HG00423.hp1 HG01516.hp2 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.830-32G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928893 | ||||||
| chr5:56928932
|
G | T | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.830-71C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928932 | ||||||
| chr5:56928955
|
ACTCT | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(40): Show | 102 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.830-98_830-95delAG others(2): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928955 | ||||||
| chr5:56928967
|
T | A | 68 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(65): Show | 116 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.830-106A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928967 | ||||||
| chr5:56928969
|
T | A | 68 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(65): Show | 116 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.830-108A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928969 | ||||||
| chr5:56928979
|
A | T | 9 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(6): Show | 11 | HG01109.hp1 HG02723.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.830-118T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928979 | ||||||
| chr5:56928981
|
A | T | 68 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(65): Show | 116 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.830-120T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928981 | ||||||
| chr5:56928982
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.830-121G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928982 | ||||||
| chr5:56928989
|
T | TCACACA | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.830-129_830-128ins others(6): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928989 | ||||||
| chr5:56928991
|
T | A | 9 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(6): Show | 11 | HG01109.hp1 HG02723.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.830-130A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | ||||||
| chr5:56928991
|
T | TCACACA | 30 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(27): Show | 48 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.830-136_830-131dup others(6): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | ||||||
| chr5:56928991
|
T | TCACACAC others(1): Show |
59 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(56): Show | 105 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.830-138_830-131dup others(8): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | ||||||
| chr5:56928991
|
T | TCACACAC others(3): Show |
11 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0107others(8): Show | 30 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.830-140_830-131dup others(10): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | ||||||
| chr5:56928991
|
T | TCACACAC others(5): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0034others(23): Show | 63 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.830-142_830-131dup others(12): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | ||||||
| chr5:56928991
|
T | TCACACAC others(7): Show |
4 | a0001c0001t0001g0022a0001c0001t0001g0035a0001c0001t0001g0078others(1): Show | 7 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.830-144_830-131dup others(14): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56928991 | ||||||
| chr5:56929005
|
A | ACACACAC others(7): Show |
2 | a0001c0006t0002g0183a0002c0003t0018g0168 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.830-145_830-144ins others(14): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | ||||||
| chr5:56929005
|
A | ACACACAC others(5): Show |
1 | a0001c0006t0002g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.830-145_830-144ins others(12): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | ||||||
| chr5:56929005
|
A | ACACACAC others(3): Show |
1 | a0001c0006t0008g0181 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.830-145_830-144ins others(10): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | ||||||
| chr5:56929005
|
A | ACACACAC others(1): Show |
3 | a0001c0006t0002g0180a0001c0006t0002g0184a0001c0008t0016g0167 | 3 | HG01109.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.830-145_830-144ins others(8): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929005 | ||||||
| chr5:56929007
|
T | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(93): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.830-146A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929007 | ||||||
| chr5:56929009
|
T | A | 2 | a0001c0002t0003g0032a0002c0003t0001g0173 | 3 | NA18522.hp1 NA18960.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.830-148A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929009 | ||||||
| chr5:56929172
|
T | TA | 17 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0032others(14): Show | 23 | HG00673.hp1 HG02080.hp1 HG02698.hp2 others(20): Show |
intron_variant | MODIFIER | c.830-312dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929172 | ||||||
| chr5:56929181
|
T | A | 2 | a0001c0002t0003g0079a0001c0002t0003g0096 | 2 | NA18968.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.830-320A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929181 | ||||||
| chr5:56929198
|
C | T | 2 | a0001c0001t0005g0023a0001c0001t0015g0118 | 4 | HG01081.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.830-337G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929198 | ||||||
| chr5:56929449
|
C | T | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.830-588G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929449 | ||||||
| chr5:56929462
|
A | C | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.830-601T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929462 | ||||||
| chr5:56929591
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(108): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.830-730C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929591 | ||||||
| chr5:56929760
|
T | C | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.830-899A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929760 | ||||||
| chr5:56929942
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(108): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.829+722A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56929942 | ||||||
| chr5:56930060
|
A | T | 1 | a0001c0001t0002g0038 | 2 | HG00609.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.829+604T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930060 | ||||||
| chr5:56930281
|
C | T | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.829+383G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930281 | ||||||
| chr5:56930384
|
A | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(38): Show | 99 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.829+280T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930384 | ||||||
| chr5:56930502
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.829+162T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930502 | ||||||
| chr5:56930583
|
T | C | 65 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(62): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.829+81A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 9/12 | chr5 | 56930583 | ||||||
| chr5:56930778
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(36): Show | 97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.748-33C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930778 | ||||||
| chr5:56930816
|
G | A | 1 | a0001c0001t0002g0039 | 2 | HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.748-71C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930816 | ||||||
| chr5:56930962
|
A | G | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.748-217T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930962 | ||||||
| chr5:56930997
|
CT | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(140): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.748-253delA | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56930997 | ||||||
| chr5:56931053
|
A | C | 1 | a0001c0002t0001g0051 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.748-308T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931053 | ||||||
| chr5:56931150
|
C | T | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.748-405G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931150 | ||||||
| chr5:56931201
|
G | C | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-456C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931201 | ||||||
| chr5:56931242
|
C | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(108): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.748-497G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931242 | ||||||
| chr5:56931463
|
T | G | 1 | a0001c0002t0003g0084 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-718A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931463 | ||||||
| chr5:56931466
|
G | A | 1 | a0001c0002t0003g0084 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-721C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931466 | ||||||
| chr5:56931467
|
T | C | 1 | a0001c0002t0003g0084 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-722A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931467 | ||||||
| chr5:56931499
|
T | A | 53 | a0001c0001t0001g0151a0001c0001t0002g0004a0001c0001t0002g0010others(50): Show | 97 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.748-754A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931499 | ||||||
| chr5:56931510
|
C | T | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(182): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.748-765G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931510 | ||||||
| chr5:56931552
|
G | GATAA | 32 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(29): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.748-808_748-807ins others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931552 | ||||||
| chr5:56931630
|
C | T | 1 | a0001c0004t0002g0122 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.748-885G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931630 | ||||||
| chr5:56931632
|
G | A | 2 | a0002c0003t0001g0170a0002c0003t0001g0171 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.748-887C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931632 | ||||||
| chr5:56931642
|
G | A | 1 | a0001c0002t0003g0088 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.748-897C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931642 | ||||||
| chr5:56931744
|
T | C | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.748-999A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931744 | ||||||
| chr5:56931797
|
A | G | 13 | a0002c0003t0001g0009a0002c0003t0001g0044a0002c0003t0001g0102others(10): Show | 21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.748-1052T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56931797 | ||||||
| chr5:56932006
|
T | C | 1 | a0001c0001t0002g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.747+1241A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932006 | ||||||
| chr5:56932074
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.747+1173G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932074 | ||||||
| chr5:56932164
|
G | A | 1 | a0001c0002t0003g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.747+1083C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932164 | ||||||
| chr5:56932173
|
G | A | 3 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0152 | 3 | NA18963.hp1 NA19078.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.747+1074C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932173 | ||||||
| chr5:56932213
|
T | C | 14 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0030others(11): Show | 27 | HG00423.hp1 HG00642.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.747+1034A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932213 | ||||||
| chr5:56932344
|
A | G | 1 | a0001c0001t0002g0036 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.747+903T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932344 | ||||||
| chr5:56932482
|
G | A | 1 | a0001c0001t0002g0040 | 2 | HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.747+765C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932482 | ||||||
| chr5:56932574
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(108): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.747+673T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932574 | ||||||
| chr5:56932598
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(182): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.747+649G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932598 | ||||||
| chr5:56932618
|
G | A | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.747+629C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932618 | ||||||
| chr5:56932640
|
G | A | 32 | a0001c0001t0002g0149a0001c0002t0003g0008a0001c0002t0003g0015others(29): Show | 51 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.747+607C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932640 | ||||||
| chr5:56932644
|
T | C | 1 | a0001c0004t0002g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.747+603A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932644 | ||||||
| chr5:56932668
|
T | C | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.747+579A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932668 | ||||||
| chr5:56932678
|
A | T | 1 | a0001c0002t0001g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.747+569T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932678 | ||||||
| chr5:56932686
|
G | A | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.747+561C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932686 | ||||||
| chr5:56932780
|
T | C | 1 | a0001c0001t0002g0150 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.747+467A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56932780 | ||||||
| chr5:56933151
|
A | G | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.747+96T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 8/12 | chr5 | 56933151 | ||||||
| chr5:56933461
|
C | T | 64 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(61): Show | 112 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.596-63G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933461 | ||||||
| chr5:56933826
|
A | G | 41 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(38): Show | 99 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.596-428T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933826 | ||||||
| chr5:56933841
|
T | C | 1 | a0001c0002t0001g0074 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.596-443A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933841 | ||||||
| chr5:56933913
|
T | C | 1 | a0001c0002t0003g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.596-515A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933913 | ||||||
| chr5:56933953
|
GGA | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0011others(56): Show | 105 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.596-557_596-556del others(2): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56933953 | ||||||
| chr5:56934142
|
G | C | 6 | a0002c0003t0001g0009a0002c0003t0001g0102a0002c0003t0001g0103others(3): Show | 13 | HG02145.hp1 HG02572.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.596-744C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934142 | ||||||
| chr5:56934269
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.596-871A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934269 | ||||||
| chr5:56934343
|
A | G | 2 | a0002c0003t0001g0178a0002c0003t0001g0179 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.596-945T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934343 | ||||||
| chr5:56934408
|
A | C | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-1010T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934408 | ||||||
| chr5:56934461
|
T | C | 1 | a0001c0005t0002g0134 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.595+967A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934461 | ||||||
| chr5:56934544
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0163 | 3 | HG02109.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.595+884C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934544 | ||||||
| chr5:56934724
|
GA | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(76): Show | 180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.595+703delT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934724 | ||||||
| chr5:56934821
|
T | C | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.595+607A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934821 | ||||||
| chr5:56934829
|
T | C | 1 | a0001c0001t0002g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.595+599A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934829 | ||||||
| chr5:56934895
|
T | C | 1 | a0001c0002t0003g0085 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.595+533A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56934895 | ||||||
| chr5:56935207
|
C | A | 2 | a0001c0002t0001g0013a0001c0002t0012g0067 | 6 | HG00558.hp2 NA18991.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+221G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56935207 | ||||||
| chr5:56935227
|
G | T | 3 | a0001c0002t0003g0020a0001c0002t0003g0091a0001c0002t0007g0090 | 5 | HG00673.hp1 NA18959.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+201C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56935227 | ||||||
| chr5:56935309
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.595+119G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 7/12 | chr5 | 56935309 | ||||||
| chr5:56935593
|
A | G | 1 | a0001c0002t0001g0071 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.522+73T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 6/12 | chr5 | 56935593 | ||||||
| chr5:56935782
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0185 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.437-31G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56935782 | ||||||
| chr5:56935855
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437-104T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56935855 | ||||||
| chr5:56936216
|
CA | C | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.437-466delT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56936216 | ||||||
| chr5:56936721
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.436+857A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56936721 | ||||||
| chr5:56936768
|
T | C | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.436+810A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56936768 | ||||||
| chr5:56937149
|
G | A | 2 | a0001c0002t0001g0014a0001c0002t0001g0060 | 6 | HG01884.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+429C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937149 | ||||||
| chr5:56937201
|
A | T | 1 | a0001c0002t0001g0061 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.436+377T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937201 | ||||||
| chr5:56937329
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.436+249C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937329 | ||||||
| chr5:56937400
|
A | G | 1 | a0001c0002t0001g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.436+178T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 5/12 | chr5 | 56937400 | ||||||
| chr5:56937714
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-16C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937714 | ||||||
| chr5:56937724
|
C | G | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-26G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937724 | ||||||
| chr5:56937861
|
T | G | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-163A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937861 | ||||||
| chr5:56937910
|
C | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(36): Show | 97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.316-212G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56937910 | ||||||
| chr5:56938104
|
A | G | 1 | a0001c0002t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.316-406T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938104 | ||||||
| chr5:56938186
|
G | A | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.316-488C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938186 | ||||||
| chr5:56938206
|
T | C | 1 | a0001c0001t0001g0116 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.316-508A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938206 | ||||||
| chr5:56938631
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.315+252A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 4/12 | chr5 | 56938631 | ||||||
| chr5:56939251
|
G | C | 1 | a0001c0001t0002g0153 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.181-234C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939251 | ||||||
| chr5:56939477
|
C | T | 1 | a0001c0002t0003g0030 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.181-460G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939477 | ||||||
| chr5:56939615
|
T | G | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-598A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939615 | ||||||
| chr5:56939685
|
C | T | 5 | a0001c0001t0002g0133a0001c0005t0002g0037a0001c0005t0002g0045others(2): Show | 7 | HG00735.hp2 HG01257.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-668G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939685 | ||||||
| chr5:56939721
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(122): Show | 287 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.181-704G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939721 | ||||||
| chr5:56939794
|
C | A | 1 | a0001c0002t0001g0075 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.181-777G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939794 | ||||||
| chr5:56939860
|
T | A | 1 | a0001c0001t0006g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.181-843A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939860 | ||||||
| chr5:56939863
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.181-846A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939863 | ||||||
| chr5:56939992
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0131a0001c0001t0002g0162 | 4 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-975T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56939992 | ||||||
| chr5:56940149
|
G | A | 1 | a0002c0003t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-1132C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940149 | ||||||
| chr5:56940186
|
C | T | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-1169G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940186 | ||||||
| chr5:56940240
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.181-1223A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940240 | ||||||
| chr5:56940301
|
T | C | 6 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1284A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940301 | ||||||
| chr5:56940349
|
T | C | 80 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(77): Show | 181 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.181-1332A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940349 | ||||||
| chr5:56940540
|
T | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.181-1523A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940540 | ||||||
| chr5:56940724
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.181-1707C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940724 | ||||||
| chr5:56940828
|
G | C | 1 | a0001c0002t0003g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.181-1811C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940828 | ||||||
| chr5:56940901
|
C | G | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.181-1884G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56940901 | ||||||
| chr5:56941073
|
T | G | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.181-2056A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941073 | ||||||
| chr5:56941108
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.181-2091A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941108 | ||||||
| chr5:56941151
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.181-2134C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941151 | ||||||
| chr5:56941203
|
T | C | 3 | a0001c0004t0002g0122a0001c0004t0002g0123a0001c0004t0002g0124 | 3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.181-2186A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941203 | ||||||
| chr5:56941239
|
A | G | 1 | a0001c0001t0001g0016 | 4 | NA18979.hp2 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-2222T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941239 | ||||||
| chr5:56941267
|
T | C | 1 | a0001c0002t0003g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.181-2250A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941267 | ||||||
| chr5:56941308
|
T | A | 42 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(39): Show | 124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.181-2291A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941308 | ||||||
| chr5:56941328
|
G | A | 42 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(39): Show | 124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.181-2311C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941328 | ||||||
| chr5:56941467
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.181-2450G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941467 | ||||||
| chr5:56941838
|
C | A | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-2821G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941838 | ||||||
| chr5:56941870
|
A | G | 1 | a0001c0001t0002g0017 | 4 | HG00438.hp1 HG03239.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-2853T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941870 | ||||||
| chr5:56941880
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.181-2863A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941880 | ||||||
| chr5:56941932
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0107others(2): Show | 17 | HG00099.hp2 HG00408.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-2915A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941932 | ||||||
| chr5:56941973
|
C | G | 6 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-2956G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56941973 | ||||||
| chr5:56942000
|
G | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0131a0001c0001t0002g0162 | 4 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-2983C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942000 | ||||||
| chr5:56942018
|
G | GA | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-3002dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942018 | ||||||
| chr5:56942055
|
CAGTTAAG others(4): Show |
C | 9 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0080others(6): Show | 20 | HG00423.hp1 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.181-3049_181-3039d others(13): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942055 | ||||||
| chr5:56942299
|
G | C | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-3282C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942299 | ||||||
| chr5:56942313
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.181-3296T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942313 | ||||||
| chr5:56942335
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0185 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.181-3318A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942335 | ||||||
| chr5:56942377
|
G | A | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.181-3360C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942377 | ||||||
| chr5:56942578
|
T | C | 1 | a0001c0002t0001g0076 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.181-3561A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942578 | ||||||
| chr5:56942712
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.181-3695A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942712 | ||||||
| chr5:56942770
|
A | G | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(76): Show | 180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.181-3753T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942770 | ||||||
| chr5:56942812
|
G | C | 2 | a0001c0002t0001g0027a0001c0002t0001g0068 | 3 | HG02559.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.181-3795C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942812 | ||||||
| chr5:56942984
|
A | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(65): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.180+3942T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56942984 | ||||||
| chr5:56943335
|
T | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(20): Show | 71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.180+3591A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943335 | ||||||
| chr5:56943335
|
T | TA | 68 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(65): Show | 169 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.180+3590dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943335 | ||||||
| chr5:56943350
|
TAGA | T | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+3573_180+3575d others(5): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943350 | ||||||
| chr5:56943500
|
C | T | 1 | a0001c0002t0003g0089 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.180+3426G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943500 | ||||||
| chr5:56943542
|
C | G | 73 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(70): Show | 174 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.180+3384G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943542 | ||||||
| chr5:56943558
|
G | A | 3 | a0002c0003t0001g0044a0002c0003t0001g0172a0002c0003t0001g0173 | 4 | HG02559.hp1 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+3368C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943558 | ||||||
| chr5:56943644
|
T | A | 2 | a0001c0002t0003g0033a0001c0002t0011g0098 | 3 | NA18948.hp2 NA19060.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.180+3282A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943644 | ||||||
| chr5:56943745
|
A | G | 2 | a0001c0001t0001g0111a0001c0001t0001g0121 | 2 | NA18955.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.180+3181T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943745 | ||||||
| chr5:56943771
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.180+3155C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943771 | ||||||
| chr5:56943800
|
G | A | 13 | a0002c0003t0001g0009a0002c0003t0001g0044a0002c0003t0001g0102others(10): Show | 21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.180+3126C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943800 | ||||||
| chr5:56943850
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+3076C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943850 | ||||||
| chr5:56943887
|
C | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+3039G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56943887 | ||||||
| chr5:56944088
|
C | T | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+2838G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944088 | ||||||
| chr5:56944099
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+2827T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944099 | ||||||
| chr5:56944117
|
AG | A | 16 | a0001c0002t0003g0020a0001c0002t0003g0021a0001c0002t0003g0032others(13): Show | 22 | HG00673.hp1 HG02080.hp1 HG02698.hp2 others(19): Show |
intron_variant | MODIFIER | c.180+2808delC | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944117 | ||||||
| chr5:56944152
|
G | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0022others(14): Show | 53 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.180+2774C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944152 | ||||||
| chr5:56944238
|
G | A | 2 | a0002c0003t0001g0178a0002c0003t0001g0179 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.180+2688C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944238 | ||||||
| chr5:56944253
|
C | T | 1 | a0001c0002t0003g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.180+2673G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944253 | ||||||
| chr5:56944288
|
G | A | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.180+2638C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944288 | ||||||
| chr5:56944425
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(118): Show | 282 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.180+2501T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944425 | ||||||
| chr5:56944460
|
G | A | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180+2466C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944460 | ||||||
| chr5:56944475
|
C | G | 15 | a0001c0001t0005g0023a0001c0001t0015g0118a0002c0003t0001g0009others(12): Show | 25 | HG01081.hp2 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.180+2451G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944475 | ||||||
| chr5:56944480
|
C | CA | 5 | a0001c0001t0002g0157a0001c0001t0002g0177a0001c0001t0005g0023others(2): Show | 8 | HG01081.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+2445dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944480 | ||||||
| chr5:56944526
|
C | T | 1 | a0001c0002t0003g0079 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.180+2400G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944526 | ||||||
| chr5:56944799
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.180+2127T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944799 | ||||||
| chr5:56944913
|
T | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0158 | 3 | HG01256.hp2 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.180+2013A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944913 | ||||||
| chr5:56944921
|
T | TCC | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.180+2003_180+2004d others(4): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944921 | ||||||
| chr5:56944957
|
A | G | 2 | a0001c0002t0001g0026a0001c0002t0001g0069 | 3 | HG02280.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.180+1969T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56944957 | ||||||
| chr5:56945174
|
G | A | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+1752C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945174 | ||||||
| chr5:56945192
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.180+1734C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945192 | ||||||
| chr5:56945457
|
C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(21): Show | 72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.180+1469G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945457 | ||||||
| chr5:56945492
|
G | C | 1 | a0001c0001t0002g0159 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.180+1434C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945492 | ||||||
| chr5:56945665
|
C | T | 1 | a0001c0002t0001g0029 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.180+1261G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945665 | ||||||
| chr5:56945851
|
T | A | 15 | a0001c0001t0005g0023a0001c0001t0015g0118a0002c0003t0001g0009others(12): Show | 25 | HG01081.hp2 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.180+1075A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945851 | ||||||
| chr5:56945862
|
A | G | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.180+1064T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945862 | ||||||
| chr5:56945882
|
T | C | 15 | a0001c0001t0005g0023a0001c0001t0015g0118a0002c0003t0001g0009others(12): Show | 25 | HG01081.hp2 HG01433.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.180+1044A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56945882 | ||||||
| chr5:56946041
|
G | T | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+885C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946041 | ||||||
| chr5:56946132
|
A | G | 5 | a0001c0002t0001g0007a0001c0002t0001g0028a0001c0002t0001g0056others(2): Show | 23 | HG00544.hp1 HG00597.hp2 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.180+794T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946132 | ||||||
| chr5:56946206
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.180+720C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946206 | ||||||
| chr5:56946246
|
T | A | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.180+680A>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946246 | ||||||
| chr5:56946271
|
T | C | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180+655A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946271 | ||||||
| chr5:56946406
|
C | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0163 | 3 | HG02109.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.180+520G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946406 | ||||||
| chr5:56946496
|
C | T | 42 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(39): Show | 124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.180+430G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946496 | ||||||
| chr5:56946546
|
C | A | 1 | a0001c0001t0002g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.180+380G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946546 | ||||||
| chr5:56946721
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(179): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.180+205A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946721 | ||||||
| chr5:56946787
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.180+139G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946787 | ||||||
| chr5:56946816
|
G | GA | 7 | a0001c0001t0005g0023a0001c0001t0015g0118a0001c0006t0002g0180others(4): Show | 9 | HG01081.hp2 HG01109.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+109dupT | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946816 | ||||||
| chr5:56946838
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.180+88G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 3/12 | chr5 | 56946838 | ||||||
| chr5:56947301
|
T | C | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.35-230A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947301 | ||||||
| chr5:56947319
|
A | T | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.35-248T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947319 | ||||||
| chr5:56947353
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.35-282C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947353 | ||||||
| chr5:56947427
|
A | T | 1 | a0002c0003t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.35-356T>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947427 | ||||||
| chr5:56947453
|
T | C | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-382A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947453 | ||||||
| chr5:56947476
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(36): Show | 97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.35-405G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947476 | ||||||
| chr5:56947519
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.35-448T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947519 | ||||||
| chr5:56947735
|
C | A | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.35-664G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947735 | ||||||
| chr5:56947858
|
T | C | 42 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(39): Show | 124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.35-787A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947858 | ||||||
| chr5:56947939
|
T | C | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-868A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56947939 | ||||||
| chr5:56948138
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.35-1067G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948138 | ||||||
| chr5:56948139
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(37): Show | 98 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.35-1068T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948139 | ||||||
| chr5:56948429
|
C | T | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.35-1358G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948429 | ||||||
| chr5:56948464
|
G | A | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.35-1393C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948464 | ||||||
| chr5:56948481
|
T | G | 4 | a0001c0001t0002g0043a0001c0001t0002g0163a0001c0001t0002g0164others(1): Show | 5 | HG02109.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-1410A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948481 | ||||||
| chr5:56948560
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0176 | 3 | HG02683.hp1 HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.35-1489C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948560 | ||||||
| chr5:56948565
|
A | G | 1 | a0001c0002t0001g0070 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.35-1494T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948565 | ||||||
| chr5:56948576
|
G | A | 1 | a0001c0002t0003g0099 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.35-1505C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948576 | ||||||
| chr5:56948704
|
A | G | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.35-1633T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948704 | ||||||
| chr5:56948777
|
G | A | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.35-1706C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948777 | ||||||
| chr5:56948936
|
T | C | 1 | a0001c0002t0001g0028 | 2 | HG03669.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.34+1692A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948936 | ||||||
| chr5:56948973
|
A | C | 1 | a0001c0001t0001g0105 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.34+1655T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56948973 | ||||||
| chr5:56949104
|
C | T | 2 | a0001c0005t0002g0045a0001c0005t0002g0174 | 3 | HG01952.hp1 NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.34+1524G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949104 | ||||||
| chr5:56949121
|
C | T | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.34+1507G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949121 | ||||||
| chr5:56949148
|
G | C | 1 | a0001c0002t0010g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.34+1480C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949148 | ||||||
| chr5:56949217
|
G | C | 74 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(71): Show | 175 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.34+1411C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949217 | ||||||
| chr5:56949268
|
G | GAAC | 5 | a0001c0004t0002g0024a0001c0004t0002g0119a0001c0004t0002g0122others(2): Show | 7 | HG02723.hp2 HG02809.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+1357_34+1359dup others(3): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949268 | ||||||
| chr5:56949313
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(21): Show | 72 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.34+1315T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949313 | ||||||
| chr5:56949351
|
C | T | 13 | a0002c0003t0001g0009a0002c0003t0001g0044a0002c0003t0001g0102others(10): Show | 21 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+1277G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949351 | ||||||
| chr5:56949442
|
C | G | 31 | a0001c0002t0003g0008a0001c0002t0003g0015a0001c0002t0003g0020others(28): Show | 50 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.34+1186G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949442 | ||||||
| chr5:56949501
|
T | C | 1 | a0001c0001t0002g0018 | 4 | HG00735.hp1 HG01516.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+1127A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949501 | ||||||
| chr5:56949547
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.34+1081C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949547 | ||||||
| chr5:56949556
|
A | G | 1 | a0001c0002t0001g0019 | 3 | HG00423.hp2 NA18612.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.34+1072T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949556 | ||||||
| chr5:56949776
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.34+852A>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949776 | ||||||
| chr5:56949816
|
C | T | 1 | a0001c0002t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.34+812G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949816 | ||||||
| chr5:56949838
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.34+790G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949838 | ||||||
| chr5:56949933
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.34+695C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949933 | ||||||
| chr5:56949976
|
C | G | 75 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(72): Show | 176 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.34+652G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56949976 | ||||||
| chr5:56950021
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.34+607C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950021 | ||||||
| chr5:56950265
|
TACTC | T | 3 | a0001c0004t0002g0122a0001c0004t0002g0123a0001c0004t0002g0124 | 3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.34+359_34+362delGA others(2): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950265 | ||||||
| chr5:56950338
|
C | G | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+290G>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950338 | ||||||
| chr5:56950449
|
A | AAAC | 79 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(76): Show | 180 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.34+176_34+178dupGT others(1): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950449 | ||||||
| chr5:56950516
|
C | A | 1 | a0001c0006t0002g0184 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.34+112G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950516 | ||||||
| chr5:56950551
|
G | C | 3 | a0001c0004t0002g0122a0001c0004t0002g0123a0001c0004t0002g0124 | 3 | HG02723.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.34+77C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 2/12 | chr5 | 56950551 | ||||||
| chr5:56950663
|
G | C | 1 | a0001c0002t0003g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10-11C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950663 | ||||||
| chr5:56950758
|
T | G | 1 | a0001c0002t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.10-106A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950758 | ||||||
| chr5:56950763
|
A | G | 1 | a0001c0002t0001g0048 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.10-111T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950763 | ||||||
| chr5:56950783
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(122): Show | 287 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.10-131T>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950783 | ||||||
| chr5:56950893
|
G | A | 1 | a0001c0008t0016g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10-241C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56950893 | ||||||
| chr5:56951008
|
A | C | 1 | a0001c0001t0001g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.10-356T>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951008 | ||||||
| chr5:56951025
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.10-373C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951025 | ||||||
| chr5:56951075
|
G | A | 1 | a0001c0001t0002g0043 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.10-423C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951075 | ||||||
| chr5:56951196
|
C | A | 7 | a0002c0003t0001g0044a0002c0003t0001g0169a0002c0003t0001g0170others(4): Show | 8 | HG01433.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-544G>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951196 | ||||||
| chr5:56951209
|
G | A | 2 | a0001c0005t0002g0045a0001c0005t0002g0174 | 3 | HG01952.hp1 NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.10-557C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951209 | ||||||
| chr5:56951446
|
T | G | 1 | a0001c0001t0002g0175 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.9+648A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951446 | ||||||
| chr5:56951516
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.9+578A>C | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951516 | ||||||
| chr5:56951552
|
C | T | 23 | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0013others(20): Show | 82 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.9+542G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951552 | ||||||
| chr5:56951701
|
G | A | 1 | a0001c0001t0002g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.9+393C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951701 | ||||||
| chr5:56951701
|
G | T | 42 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0007others(39): Show | 124 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.9+393C>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951701 | ||||||
| chr5:56951702
|
GGGGGCTC others(25): Show |
G | 9 | a0001c0002t0001g0025a0001c0002t0001g0048a0001c0002t0001g0049others(6): Show | 10 | HG00280.hp2 HG00738.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.9+360_9+391delGGGC others(28): Show |
MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951702 | ||||||
| chr5:56951831
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.9+263G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951831 | ||||||
| chr5:56951931
|
G | A | 2 | a0002c0003t0001g0178a0002c0003t0001g0179 | 2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.9+163C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951931 | ||||||
| chr5:56951981
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.9+113G>A | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951981 | ||||||
| chr5:56951988
|
G | A | 5 | a0001c0006t0002g0180a0001c0006t0002g0182a0001c0006t0002g0183others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+106C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56951988 | ||||||
| chr5:56952075
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9+19C>T | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56952075 | ||||||
| chr5:56952080
|
G | C | 1 | a0001c0001t0002g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9+14C>G | MIER3 | ENSG00000155545.20 | transcript | ENST00000381199.8 | protein_coding | 1/12 | chr5 | 56952080 |