Search by Gene
| geneid | 150365 |
|---|---|
| ensemblid | ENSG00000167077.13 |
| hgncid | 28613 |
| symbol | MEI1 |
| name | meiotic double-stranded break formation protein 1 |
| refseq_nuc | NM_152513.4 |
| refseq_prot | NP_689726.3 |
| ensembl_nuc | ENST00000401548.8 |
| ensembl_prot | ENSP00000384115.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 41699503 |
| end | 41799454 |
| strand | + |
| ver | v1.2 |
| region | chr22:41699503-41799454 |
| region5000 | chr22:41694503-41804454 |
| regionname0 | MEI1_chr22_41699503_41799454 |
| regionname5000 | MEI1_chr22_41694503_41804454 |
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 | 1274 | 219 | 61 | 46 | 73 | 12 | 25 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0002 | 0/0 | 1274 | 13 | 1 | 4 | 7 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0003 | 0/0 | 1274 | 9 | 8 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0004 | 0/0 | 1274 | 5 | 4 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0005 | 0/0 | 1274 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0006 | 0/0 | 1274 | 3 | 2 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0007 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0008 | 0/0 | 1274 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0009 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0010 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0011 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0012 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | 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 | 0/1 | 3825 | 121 | 15 | 22 | 58 | 9 | 16 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0002 | 1/0 | 3825 | 49 | 2 | 21 | 13 | 3 | 9 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0003 | 0/0 | 3825 | 20 | 17 | 3 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0004 | 0/0 | 3825 | 16 | 16 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0005 | 0/0 | 3825 | 13 | 1 | 4 | 7 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0006 | 0/0 | 3825 | 9 | 8 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0007 | 0/0 | 3825 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0008 | 0/0 | 3825 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0009 | 0/0 | 3825 | 5 | 4 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0010 | 0/0 | 3825 | 3 | 2 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0011 | 0/0 | 3825 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0012 | 0/0 | 3825 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0013 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0014 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0015 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0016 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0017 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0018 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0019 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0020 | 0/0 | 3825 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0021 | 0/0 | 3825 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| c0022 | 0/0 | 3825 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | 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 | 1/1 | 192 | 160 | 36 | 29 | 67 | 9 | 17 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| t0002 | 0/0 | 192 | 49 | 2 | 22 | 13 | 3 | 9 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| t0003 | 0/0 | 194 | 24 | 24 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| t0004 | 0/0 | 189 | 23 | 20 | 3 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| t0005 | 0/0 | 192 | 3 | 3 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| t0006 | 0/0 | 191 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | 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 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| 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 | 0/1 | 121 | 15 | 22 | 58 | 9 | 16 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0002 | a0001 | c0002 | 1/0 | 49 | 2 | 21 | 13 | 3 | 9 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 20 | 17 | 3 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 16 | 16 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0008 | a0001 | c0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0011 | a0001 | c0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0017 | a0001 | c0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0018 | a0001 | c0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0022 | a0001 | c0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0002c0005 | a0002 | c0005 | 0/0 | 13 | 1 | 4 | 7 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0003c0006 | a0003 | c0006 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0004c0009 | a0004 | c0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0005c0007 | a0005 | c0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0006c0010 | a0006 | c0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0007c0021 | a0007 | c0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0008c0020 | a0008 | c0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0009c0016 | a0009 | c0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0010c0019 | a0010 | c0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0011c0014 | a0011 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0012c0013 | a0012 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | 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 | 0/1 | 117 | 12 | 21 | 58 | 9 | 16 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0002t0001 | a0001 | c0002 | t0001 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 48 | 2 | 21 | 13 | 3 | 9 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0003t0004 | a0001 | c0003 | t0004 | 0/0 | 17 | 14 | 3 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0004t0003 | a0001 | c0004 | t0003 | 0/0 | 15 | 15 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0004t0006 | a0001 | c0004 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0008t0003 | a0001 | c0008 | t0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0011t0003 | a0001 | c0011 | t0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0012t0001 | a0001 | c0012 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0015t0003 | a0001 | c0015 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0017t0001 | a0001 | c0017 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0018t0001 | a0001 | c0018 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0001c0022t0001 | a0001 | c0022 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0002c0005t0001 | a0002 | c0005 | t0001 | 0/0 | 13 | 1 | 4 | 7 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0003c0006t0001 | a0003 | c0006 | t0001 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0004c0009t0001 | a0004 | c0009 | t0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0005c0007t0004 | a0005 | c0007 | t0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0006c0010t0001 | a0006 | c0010 | t0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0007c0021t0001 | a0007 | c0021 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0008c0020t0001 | a0008 | c0020 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0009c0016t0003 | a0009 | c0016 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0010c0019t0001 | a0010 | c0019 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0011c0014t0004 | a0011 | c0014 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | copy fasta |
| a0012c0013t0001 | a0012 | c0013 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | 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 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0201 | a0001 | c0001 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0212 | a0001 | c0001 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0223 | a0001 | c0001 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0238 | a0001 | c0001 | t0001 | g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0247 | a0001 | c0001 | t0001 | g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0249 | a0001 | c0001 | t0001 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0254 | a0001 | c0001 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0255 | a0001 | c0001 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0005g0183 | a0001 | c0001 | t0005 | g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0005g0190 | a0001 | c0001 | t0005 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0001t0005g0191 | a0001 | c0001 | t0005 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0001g0090 | a0001 | c0002 | t0001 | g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0054 | a0001 | c0002 | t0002 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0055 | a0001 | c0002 | t0002 | g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0056 | a0001 | c0002 | t0002 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0057 | a0001 | c0002 | t0002 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0058 | a0001 | c0002 | t0002 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0059 | a0001 | c0002 | t0002 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0060 | a0001 | c0002 | t0002 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0061 | a0001 | c0002 | t0002 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0062 | a0001 | c0002 | t0002 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0063 | a0001 | c0002 | t0002 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0064 | a0001 | c0002 | t0002 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0065 | a0001 | c0002 | t0002 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0066 | a0001 | c0002 | t0002 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0067 | a0001 | c0002 | t0002 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0068 | a0001 | c0002 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0069 | a0001 | c0002 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0070 | a0001 | c0002 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0071 | a0001 | c0002 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0072 | a0001 | c0002 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0073 | a0001 | c0002 | t0002 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0074 | a0001 | c0002 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0075 | a0001 | c0002 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0076 | a0001 | c0002 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0077 | a0001 | c0002 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0078 | a0001 | c0002 | t0002 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0079 | a0001 | c0002 | t0002 | g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0080 | a0001 | c0002 | t0002 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0081 | a0001 | c0002 | t0002 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0082 | a0001 | c0002 | t0002 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0083 | a0001 | c0002 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0084 | a0001 | c0002 | t0002 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0085 | a0001 | c0002 | t0002 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0086 | a0001 | c0002 | t0002 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0087 | a0001 | c0002 | t0002 | g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0088 | a0001 | c0002 | t0002 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0089 | a0001 | c0002 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0091 | a0001 | c0002 | t0002 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0092 | a0001 | c0002 | t0002 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0093 | a0001 | c0002 | t0002 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0094 | a0001 | c0002 | t0002 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0095 | a0001 | c0002 | t0002 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0096 | a0001 | c0002 | t0002 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0097 | a0001 | c0002 | t0002 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0102 | a0001 | c0002 | t0002 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0103 | a0001 | c0002 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0104 | a0001 | c0002 | t0002 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0105 | a0001 | c0002 | t0002 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0002t0002g0107 | a0001 | c0002 | t0002 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0001g0099 | a0001 | c0003 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0001g0100 | a0001 | c0003 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0001g0101 | a0001 | c0003 | t0001 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0003 | a0001 | c0003 | t0004 | g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0004 | a0001 | c0003 | t0004 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0005 | a0001 | c0003 | t0004 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0006 | a0001 | c0003 | t0004 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0007 | a0001 | c0003 | t0004 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0008 | a0001 | c0003 | t0004 | g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0015 | a0001 | c0003 | t0004 | g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0016 | a0001 | c0003 | t0004 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0017 | a0001 | c0003 | t0004 | g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0018 | a0001 | c0003 | t0004 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0019 | a0001 | c0003 | t0004 | g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0020 | a0001 | c0003 | t0004 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0021 | a0001 | c0003 | t0004 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0022 | a0001 | c0003 | t0004 | g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0023 | a0001 | c0003 | t0004 | g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0024 | a0001 | c0003 | t0004 | g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0003t0004g0025 | a0001 | c0003 | t0004 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0039 | a0001 | c0004 | t0003 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0040 | a0001 | c0004 | t0003 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0041 | a0001 | c0004 | t0003 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0042 | a0001 | c0004 | t0003 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0043 | a0001 | c0004 | t0003 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0114 | a0001 | c0004 | t0003 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0115 | a0001 | c0004 | t0003 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0116 | a0001 | c0004 | t0003 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0118 | a0001 | c0004 | t0003 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0120 | a0001 | c0004 | t0003 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0121 | a0001 | c0004 | t0003 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0122 | a0001 | c0004 | t0003 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0124 | a0001 | c0004 | t0003 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0125 | a0001 | c0004 | t0003 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0003g0127 | a0001 | c0004 | t0003 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0004t0006g0126 | a0001 | c0004 | t0006 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0008t0003g0108 | a0001 | c0008 | t0003 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0008t0003g0110 | a0001 | c0008 | t0003 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0008t0003g0111 | a0001 | c0008 | t0003 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0008t0003g0112 | a0001 | c0008 | t0003 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0008t0003g0113 | a0001 | c0008 | t0003 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0011t0003g0117 | a0001 | c0011 | t0003 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0011t0003g0123 | a0001 | c0011 | t0003 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0012t0001g0184 | a0001 | c0012 | t0001 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0012t0001g0192 | a0001 | c0012 | t0001 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0015t0003g0109 | a0001 | c0015 | t0003 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0017t0001g0200 | a0001 | c0017 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0018t0001g0098 | a0001 | c0018 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0001c0022t0001g0240 | a0001 | c0022 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0026 | a0002 | c0005 | t0001 | g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0027 | a0002 | c0005 | t0001 | g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0028 | a0002 | c0005 | t0001 | g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0029 | a0002 | c0005 | t0001 | g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0030 | a0002 | c0005 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0031 | a0002 | c0005 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0032 | a0002 | c0005 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0033 | a0002 | c0005 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0034 | a0002 | c0005 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0035 | a0002 | c0005 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0036 | a0002 | c0005 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0037 | a0002 | c0005 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0002c0005t0001g0038 | a0002 | c0005 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0044 | a0003 | c0006 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0045 | a0003 | c0006 | t0001 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0046 | a0003 | c0006 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0047 | a0003 | c0006 | t0001 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0048 | a0003 | c0006 | t0001 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0049 | a0003 | c0006 | t0001 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0050 | a0003 | c0006 | t0001 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0051 | a0003 | c0006 | t0001 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0003c0006t0001g0052 | a0003 | c0006 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0004c0009t0001g0002 | a0004 | c0009 | t0001 | g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0004c0009t0001g0144 | a0004 | c0009 | t0001 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0004c0009t0001g0239 | a0004 | c0009 | t0001 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0004c0009t0001g0258 | a0004 | c0009 | t0001 | g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0005c0007t0004g0009 | a0005 | c0007 | t0004 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0005c0007t0004g0010 | a0005 | c0007 | t0004 | g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0005c0007t0004g0011 | a0005 | c0007 | t0004 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0005c0007t0004g0013 | a0005 | c0007 | t0004 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0005c0007t0004g0014 | a0005 | c0007 | t0004 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0006c0010t0001g0179 | a0006 | c0010 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0006c0010t0001g0220 | a0006 | c0010 | t0001 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0006c0010t0001g0236 | a0006 | c0010 | t0001 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0007c0021t0001g0131 | a0007 | c0021 | t0001 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0008c0020t0001g0210 | a0008 | c0020 | t0001 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0009c0016t0003g0119 | a0009 | c0016 | t0003 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0010c0019t0001g0106 | a0010 | c0019 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0011c0014t0004g0012 | a0011 | c0014 | t0004 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| a0012c0013t0001g0053 | a0012 | c0013 | t0001 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0084 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0083 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00408 | hp1 | a0002 | c0005 | t0001 | g0036 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00423 | hp2 | a0002 | c0005 | t0001 | g0034 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00639 | hp1 | a0001 | c0003 | t0004 | g0024 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00673 | hp2 | a0002 | c0005 | t0001 | g0037 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01109 | hp1 | a0003 | c0006 | t0001 | g0046 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01109 | hp2 | a0002 | c0005 | t0001 | g0029 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0017 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01243 | hp2 | a0006 | c0010 | t0001 | g0179 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0079 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01496 | hp1 | a0001 | c0003 | t0004 | g0019 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01884 | hp1 | a0001 | c0004 | t0003 | g0116 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0191 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01934 | hp1 | a0004 | c0009 | t0001 | g0002 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01934 | hp2 | a0002 | c0005 | t0001 | g0027 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01943 | hp2 | a0002 | c0005 | t0001 | g0026 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG01981 | hp2 | a0008 | c0020 | t0001 | g0210 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02004 | hp1 | a0002 | c0005 | t0001 | g0028 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02145 | hp1 | a0007 | c0021 | t0001 | g0131 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02258 | hp2 | a0003 | c0006 | t0001 | g0044 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02280 | hp1 | a0001 | c0004 | t0003 | g0042 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02280 | hp2 | a0004 | c0009 | t0001 | g0002 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02451 | hp2 | a0005 | c0007 | t0004 | g0010 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02572 | hp1 | a0001 | c0008 | t0003 | g0111 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02572 | hp2 | a0001 | c0003 | t0004 | g0016 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0094 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02615 | hp1 | a0001 | c0012 | t0001 | g0184 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02615 | hp2 | a0001 | c0003 | t0004 | g0005 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02622 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0100 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02630 | hp1 | a0010 | c0019 | t0001 | g0106 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02717 | hp1 | a0001 | c0003 | t0004 | g0021 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02717 | hp2 | a0001 | c0012 | t0001 | g0192 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02723 | hp1 | a0001 | c0004 | t0003 | g0041 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02723 | hp2 | a0001 | c0004 | t0003 | g0114 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02809 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02809 | hp2 | a0005 | c0007 | t0004 | g0009 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02818 | hp1 | a0009 | c0016 | t0003 | g0119 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02886 | hp2 | a0001 | c0004 | t0003 | g0115 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02895 | hp2 | a0001 | c0004 | t0003 | g0125 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0124 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02896 | hp2 | a0001 | c0008 | t0003 | g0110 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02897 | hp1 | a0001 | c0008 | t0003 | g0108 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02965 | hp1 | a0003 | c0006 | t0001 | g0047 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02965 | hp2 | a0004 | c0009 | t0001 | g0144 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02970 | hp1 | a0001 | c0003 | t0004 | g0023 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02970 | hp2 | a0003 | c0006 | t0001 | g0045 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02976 | hp1 | a0001 | c0004 | t0003 | g0120 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02976 | hp2 | a0001 | c0011 | t0003 | g0117 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03041 | hp1 | a0001 | c0004 | t0003 | g0040 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03041 | hp2 | a0001 | c0003 | t0004 | g0003 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03098 | hp2 | a0011 | c0014 | t0004 | g0012 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03130 | hp1 | a0003 | c0006 | t0001 | g0051 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03130 | hp2 | a0004 | c0009 | t0001 | g0258 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0018 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0007 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0015 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03225 | hp1 | a0001 | c0004 | t0003 | g0121 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03225 | hp2 | a0002 | c0005 | t0001 | g0038 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0101 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03453 | hp2 | a0012 | c0013 | t0001 | g0053 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03486 | hp1 | a0004 | c0009 | t0001 | g0239 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03486 | hp2 | a0001 | c0004 | t0006 | g0126 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03540 | hp2 | a0001 | c0004 | t0003 | g0043 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03579 | hp1 | a0005 | c0007 | t0004 | g0014 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03704 | hp1 | a0002 | c0005 | t0001 | g0030 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0095 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0093 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0087 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18522 | hp1 | a0003 | c0006 | t0001 | g0052 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0118 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHB | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | CHB | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18906 | hp1 | a0005 | c0007 | t0004 | g0013 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18906 | hp2 | a0001 | c0018 | t0001 | g0098 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18969 | hp2 | a0001 | c0017 | t0001 | g0200 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18975 | hp2 | a0002 | c0005 | t0001 | g0031 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18991 | hp1 | a0001 | c0022 | t0001 | g0240 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18994 | hp1 | a0002 | c0005 | t0001 | g0035 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19000 | hp2 | a0002 | c0005 | t0001 | g0033 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19030 | hp1 | a0001 | c0008 | t0003 | g0113 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19030 | hp2 | a0006 | c0010 | t0001 | g0236 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0022 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19088 | hp2 | a0002 | c0005 | t0001 | g0032 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19240 | hp1 | a0003 | c0006 | t0001 | g0049 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA19240 | hp2 | a0001 | c0011 | t0003 | g0123 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20129 | hp1 | a0001 | c0004 | t0003 | g0122 | AFR | ASW | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20129 | hp2 | a0003 | c0006 | t0001 | g0048 | AFR | ASW | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0089 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | GIH | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | GIH | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02109 | hp1 | a0006 | c0010 | t0001 | g0220 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0004 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02559 | hp1 | a0001 | c0015 | t0003 | g0109 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG02559 | hp2 | a0001 | c0003 | t0004 | g0025 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03471 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG03471 | hp2 | a0001 | c0008 | t0003 | g0112 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 |
| HG06807 | hp2 | a0003 | c0006 | t0001 | g0050 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 |
| NA21309 | hp1 | a0001 | c0004 | t0003 | g0127 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 |
| NA21309 | hp2 | a0005 | c0007 | t0004 | g0011 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0243 | REF | REF | MEI1_chr22_41694503_41804454 | MEI1 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0090 | REF | REF | MEI1_chr22_41694503_41804454 | MEI1 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41699535
|
G | GGA | 2 | a0001a0009 | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
frameshift_variant&start_lost | HIGH | c.-1_1dupGA | p.Met1fs | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 38/4016 | 2/3825 | 1/1274 | INFO_REALIGN_3_PRIME | chr22 | 41699535 | |
| chr22:41699599
|
G | A | 2 | a0003a0012 | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
missense_variant | MODERATE | c.61G>A | p.Ala21Thr | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 97/4016 | 61/3825 | 21/1274 | chr22 | 41699599 | ||
| chr22:41699651
|
C | T | 1 | a0007 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.113C>T | p.Pro38Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 149/4016 | 113/3825 | 38/1274 | chr22 | 41699651 | ||
| chr22:41699707
|
G | C | 1 | a0002 | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
missense_variant | MODERATE | c.169G>C | p.Val57Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 205/4016 | 169/3825 | 57/1274 | chr22 | 41699707 | ||
| chr22:41753975
|
C | G | 1 | a0008 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1880C>G | p.Ser627Cys | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/31 | 1916/4016 | 1880/3825 | 627/1274 | chr22 | 41753975 | ||
| chr22:41758382
|
G | C | 2 | a0005a0011 | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.1969G>C | p.Glu657Gln | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2005/4016 | 1969/3825 | 657/1274 | chr22 | 41758382 | ||
| chr22:41758467
|
G | T | 1 | a0010 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2054G>T | p.Gly685Val | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2090/4016 | 2054/3825 | 685/1274 | chr22 | 41758467 | ||
| chr22:41763250
|
C | T | 1 | a0009 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.2197C>T | p.Pro733Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/31 | 2233/4016 | 2197/3825 | 733/1274 | chr22 | 41763250 | ||
| chr22:41770720
|
G | A | 2 | a0003a0012 | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
missense_variant | MODERATE | c.2303G>A | p.Gly768Asp | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/31 | 2339/4016 | 2303/3825 | 768/1274 | chr22 | 41770720 | ||
| chr22:41776114
|
T | A | 1 | a0004 | 5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.2557T>A | p.Ser853Thr | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/31 | 2593/4016 | 2557/3825 | 853/1274 | chr22 | 41776114 | ||
| chr22:41781313
|
A | G | 1 | a0002 | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
missense_variant | MODERATE | c.2845A>G | p.Thr949Ala | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 23/31 | 2881/4016 | 2845/3825 | 949/1274 | chr22 | 41781313 | ||
| chr22:41784640
|
C | G | 1 | a0012 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.3202C>G | p.Arg1068Gly | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/31 | 3238/4016 | 3202/3825 | 1068/1274 | chr22 | 41784640 | ||
| chr22:41795817
|
C | T | 1 | a0011 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3749C>T | p.Ser1250Phe | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/31 | 3785/4016 | 3749/3825 | 1250/1274 | chr22 | 41795817 | ||
| chr22:41795840
|
G | T | 1 | a0006 | 3 | HG01243.hp2 HG02109.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.3772G>T | p.Asp1258Tyr | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/31 | 3808/4016 | 3772/3825 | 1258/1274 | chr22 | 41795840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41699640
|
C | T | 1 | a0001c0022 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.102C>T | p.Arg34Arg | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 138/4016 | 102/3825 | 34/1274 | chr22 | 41699640 | ||
| chr22:41732339
|
G | C | 2 | a0003c0006a0012c0013 | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
synonymous_variant | LOW | c.1191G>C | p.Leu397Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 10/31 | 1227/4016 | 1191/3825 | 397/1274 | chr22 | 41732339 | ||
| chr22:41758405
|
C | G | 1 | a0001c0012 | 2 | HG02615.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.1992C>G | p.Pro664Pro | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2028/4016 | 1992/3825 | 664/1274 | chr22 | 41758405 | ||
| chr22:41758426
|
T | C | 5 | a0001c0004a0001c0008a0001c0011others(2): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
synonymous_variant | LOW | c.2013T>C | p.Pro671Pro | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2049/4016 | 2013/3825 | 671/1274 | chr22 | 41758426 | ||
| chr22:41758456
|
G | A | 1 | a0001c0015 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.2043G>A | p.Gln681Gln | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2079/4016 | 2043/3825 | 681/1274 | chr22 | 41758456 | ||
| chr22:41763225
|
G | T | 21 | a0001c0001a0001c0003a0001c0004others(18): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
synonymous_variant | LOW | c.2172G>T | p.Ser724Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/31 | 2208/4016 | 2172/3825 | 724/1274 | chr22 | 41763225 | ||
| chr22:41770952
|
C | T | 1 | a0001c0018 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2535C>T | p.Leu845Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/31 | 2571/4016 | 2535/3825 | 845/1274 | chr22 | 41770952 | ||
| chr22:41776125
|
G | A | 1 | a0010c0019 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2568G>A | p.Val856Val | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/31 | 2604/4016 | 2568/3825 | 856/1274 | chr22 | 41776125 | ||
| chr22:41776224
|
C | A | 1 | a0010c0019 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2667C>A | p.Ile889Ile | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/31 | 2703/4016 | 2667/3825 | 889/1274 | chr22 | 41776224 | ||
| chr22:41778775
|
A | G | 1 | a0001c0011 | 2 | HG02976.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2778A>G | p.Gln926Gln | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/31 | 2814/4016 | 2778/3825 | 926/1274 | chr22 | 41778775 | ||
| chr22:41781812
|
C | A | 9 | a0001c0003a0001c0004a0001c0011others(6): Show | 60 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
synonymous_variant | LOW | c.3054C>A | p.Ser1018Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/31 | 3090/4016 | 3054/3825 | 1018/1274 | chr22 | 41781812 | ||
| chr22:41795503
|
G | A | 1 | a0001c0017 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.3627G>A | p.Ser1209Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 29/31 | 3663/4016 | 3627/3825 | 1209/1274 | chr22 | 41795503 | ||
| chr22:41795536
|
C | T | 9 | a0001c0003a0001c0004a0001c0011others(6): Show | 60 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
synonymous_variant | LOW | c.3660C>T | p.Phe1220Phe | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 29/31 | 3696/4016 | 3660/3825 | 1220/1274 | chr22 | 41795536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41699513
|
C | T | 1 | a0001c0001t0005 | 3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | chr22 | 41699513 | ||||||
| chr22:41799360
|
ATTG | A | 4 | a0001c0003t0004a0001c0004t0006a0005c0007t0004others(1): Show | 24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*65_*67delTTG | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 31/31 | 65 | INFO_REALIGN_3_PRIME | chr22 | 41799360 | ||||
| chr22:41799406
|
T | C | 2 | a0001c0001t0002a0001c0002t0002 | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*107T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 31/31 | 107 | chr22 | 41799406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41699721
|
G | A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+9G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699721 | ||||||
| chr22:41699900
|
A | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.174+188A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699900 | ||||||
| chr22:41699908
|
C | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+196C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699908 | ||||||
| chr22:41699945
|
G | C | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+233G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699945 | ||||||
| chr22:41700057
|
C | T | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+345C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700057 | ||||||
| chr22:41700079
|
GCTCCCGC others(9): Show |
G | 7 | a0001c0001t0001g0128a0001c0008t0003g0108a0001c0008t0003g0110others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+388_174+403del others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700079 | |||||
| chr22:41700098
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+386C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700098 | ||||||
| chr22:41700101
|
G | C | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+389G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700101 | ||||||
| chr22:41700111
|
C | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+399C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700111 | ||||||
| chr22:41700143
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.174+431G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700143 | ||||||
| chr22:41700226
|
G | T | 1 | a0001c0002t0002g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.174+514G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700226 | ||||||
| chr22:41700563
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.174+851T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700563 | ||||||
| chr22:41700579
|
CCTCGGCT others(10): Show |
C | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.174+870_174+886del others(17): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700579 | |||||
| chr22:41700619
|
C | T | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+907C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700619 | ||||||
| chr22:41700749
|
A | AT | 5 | a0001c0002t0002g0102a0001c0002t0002g0103a0001c0002t0002g0104others(2): Show | 5 | HG01175.hp1 HG01358.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+1063dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
A | ATT | 12 | a0001c0003t0004g0024a0001c0004t0003g0039a0001c0004t0003g0040others(9): Show | 12 | HG00639.hp1 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+1062_174+1063d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
A | ATTT | 7 | a0001c0004t0003g0043a0001c0004t0003g0118a0001c0004t0003g0120others(4): Show | 7 | HG02818.hp1 HG02976.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+1061_174+1063d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
A | ATTTT | 5 | a0001c0004t0003g0124a0001c0004t0003g0125a0001c0004t0003g0127others(2): Show | 5 | HG02895.hp2 HG02896.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+1060_174+1063d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
AT | A | 9 | a0001c0002t0002g0065a0001c0002t0002g0066a0001c0002t0002g0067others(6): Show | 9 | HG00639.hp2 HG01070.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+1063delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
ATTTT | A | 12 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+1060_174+1063d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
ATTTTTTT others(2): Show |
A | 130 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.174+1055_174+1063d others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
ATTTTTTT others(3): Show |
A | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.174+1054_174+1063d others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700749
|
ATTTTTTT others(5): Show |
A | 11 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(8): Show | 11 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+1052_174+1063d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | |||||
| chr22:41700751
|
T | TA | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.174+1039_174+1040i others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700751 | ||||||
| chr22:41700775
|
T | C | 3 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028 | 3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.174+1063T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700775 | ||||||
| chr22:41700789
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1077C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700789 | ||||||
| chr22:41700921
|
A | G | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+1209A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700921 | ||||||
| chr22:41700939
|
C | CT | 13 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(10): Show | 13 | HG00544.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1244dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700939 | |||||
| chr22:41700939
|
C | CTT | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1243_174+1244d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700939 | |||||
| chr22:41700939
|
CT | C | 15 | a0001c0002t0002g0068a0001c0002t0002g0069a0001c0002t0002g0070others(12): Show | 15 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.174+1244delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700939 | |||||
| chr22:41700999
|
G | A | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.174+1287G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700999 | ||||||
| chr22:41701065
|
G | C | 12 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+1353G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701065 | ||||||
| chr22:41701127
|
C | T | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.174+1415C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701127 | ||||||
| chr22:41701234
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.174+1522C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701234 | ||||||
| chr22:41701237
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.174+1525C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701237 | ||||||
| chr22:41701396
|
C | T | 1 | a0001c0004t0003g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.174+1684C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701396 | ||||||
| chr22:41701458
|
A | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.174+1746A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701458 | ||||||
| chr22:41701459
|
A | T | 1 | a0012c0013t0001g0053 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.174+1747A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701459 | ||||||
| chr22:41701839
|
C | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1492C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701839 | ||||||
| chr22:41702082
|
A | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02027.hp1 HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.175-1249A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702082 | ||||||
| chr22:41702150
|
C | T | 12 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(9): Show | 12 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.175-1181C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702150 | ||||||
| chr22:41702285
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-1046C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702285 | ||||||
| chr22:41702330
|
G | T | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.175-1001G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702330 | ||||||
| chr22:41702435
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG04204.hp1 NA18965.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-896G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702435 | ||||||
| chr22:41702455
|
C | CT | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-863dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41702455 | |||||
| chr22:41702488
|
C | A | 2 | a0001c0011t0003g0117a0001c0011t0003g0123 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.175-843C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702488 | ||||||
| chr22:41702683
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-648G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702683 | ||||||
| chr22:41702740
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-591C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702740 | ||||||
| chr22:41702741
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0254 | 2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.175-590G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702741 | ||||||
| chr22:41702759
|
T | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.175-572T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702759 | ||||||
| chr22:41702875
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.175-456A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702875 | ||||||
| chr22:41702880
|
C | T | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.175-451C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702880 | ||||||
| chr22:41702936
|
T | C | 1 | a0001c0004t0003g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.175-395T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702936 | ||||||
| chr22:41703013
|
C | T | 1 | a0002c0005t0001g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175-318C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703013 | ||||||
| chr22:41703053
|
A | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-278A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703053 | ||||||
| chr22:41703215
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-116C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703215 | ||||||
| chr22:41703296
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.175-35G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703296 | ||||||
| chr22:41703684
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.298+230A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41703684 | ||||||
| chr22:41703719
|
C | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+265C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41703719 | ||||||
| chr22:41703977
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.298+523G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41703977 | ||||||
| chr22:41704167
|
C | T | 2 | a0001c0001t0001g0249a0001c0003t0004g0025 | 2 | HG00621.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.298+713C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704167 | ||||||
| chr22:41704271
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.298+817A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704271 | ||||||
| chr22:41704362
|
C | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.298+908C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704362 | ||||||
| chr22:41704396
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+942G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704396 | ||||||
| chr22:41704407
|
T | A | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+953T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704407 | ||||||
| chr22:41704414
|
CT | C | 47 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(44): Show | 47 | HG00423.hp2 HG01109.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.298+977delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr22 | 41704414 | |||||
| chr22:41704414
|
CTT | C | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.298+976_298+977del others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr22 | 41704414 | |||||
| chr22:41704445
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.298+991G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704445 | ||||||
| chr22:41704461
|
C | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+1007C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704461 | ||||||
| chr22:41704677
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.299-827A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704677 | ||||||
| chr22:41704949
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.299-555C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704949 | ||||||
| chr22:41705003
|
C | T | 1 | a0005c0007t0004g0013 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-501C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705003 | ||||||
| chr22:41705005
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-499C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705005 | ||||||
| chr22:41705176
|
C | CT | 16 | a0001c0002t0002g0078a0001c0002t0002g0096a0001c0018t0001g0098others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-312dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr22 | 41705176 | |||||
| chr22:41705333
|
G | A | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-171G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705333 | ||||||
| chr22:41705369
|
G | A | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-135G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705369 | ||||||
| chr22:41705430
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-74C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705430 | ||||||
| chr22:41705461
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-43C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705461 | ||||||
| chr22:41705694
|
A | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+140A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41705694 | ||||||
| chr22:41705708
|
CT | C | 5 | a0001c0001t0001g0130a0001c0002t0002g0079a0004c0009t0001g0144others(2): Show | 5 | HG01257.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+171delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41705708 | |||||
| chr22:41705708
|
CTT | C | 74 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(71): Show | 74 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.349+170_349+171del others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41705708 | |||||
| chr22:41705771
|
A | G | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.349+217A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41705771 | ||||||
| chr22:41705811
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(127): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.349+257G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41705811 | ||||||
| chr22:41706060
|
C | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+506C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706060 | ||||||
| chr22:41706088
|
A | G | 5 | a0001c0004t0003g0114a0001c0004t0003g0124a0001c0004t0003g0125others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+534A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706088 | ||||||
| chr22:41706131
|
G | A | 5 | a0001c0004t0003g0114a0001c0004t0003g0124a0001c0004t0003g0125others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+577G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706131 | ||||||
| chr22:41706265
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.349+711T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706265 | ||||||
| chr22:41706269
|
T | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.349+715T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706269 | ||||||
| chr22:41706364
|
G | A | 4 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+810G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706364 | ||||||
| chr22:41706607
|
G | A | 1 | a0001c0004t0003g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.349+1053G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706607 | ||||||
| chr22:41706690
|
G | C | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349+1136G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706690 | ||||||
| chr22:41706707
|
C | G | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+1153C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706707 | ||||||
| chr22:41706726
|
A | C | 1 | a0001c0003t0004g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.349+1172A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706726 | ||||||
| chr22:41706857
|
G | A | 1 | a0002c0005t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.349+1303G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706857 | ||||||
| chr22:41706917
|
G | T | 1 | a0001c0022t0001g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.349+1363G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706917 | ||||||
| chr22:41707028
|
C | CA | 10 | a0001c0002t0002g0054a0001c0002t0002g0078a0001c0002t0002g0080others(7): Show | 10 | HG00735.hp2 HG00741.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+1499dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
C | CAA | 5 | a0001c0003t0001g0099a0002c0005t0001g0026a0002c0005t0001g0027others(2): Show | 5 | HG01934.hp2 HG01943.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1498_349+1499d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
C | CAAA | 7 | a0002c0005t0001g0030a0002c0005t0001g0031a0002c0005t0001g0032others(4): Show | 7 | HG00408.hp1 HG00673.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+1497_349+1499d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
CA | C | 6 | a0001c0003t0004g0004a0001c0003t0004g0005a0001c0003t0004g0006others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1499delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
CAAAAAA | C | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+1494_349+1499d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
CAAAAAAA | C | 8 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(5): Show | 8 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+1493_349+1499d others(9): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
CAAAAAAA others(1): Show |
C | 47 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.349+1492_349+1499d others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707028
|
CAAAAAAA others(2): Show |
C | 86 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(83): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.349+1491_349+1499d others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | |||||
| chr22:41707090
|
C | G | 1 | a0004c0009t0001g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.349+1536C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707090 | ||||||
| chr22:41707161
|
C | T | 3 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028 | 3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.349+1607C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707161 | ||||||
| chr22:41707452
|
A | G | 4 | a0004c0009t0001g0002a0004c0009t0001g0144a0004c0009t0001g0239others(1): Show | 5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+1898A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707452 | ||||||
| chr22:41707482
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.349+1928A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707482 | ||||||
| chr22:41707618
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.349+2064G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707618 | ||||||
| chr22:41707642
|
T | TA | 7 | a0001c0004t0003g0115a0001c0004t0003g0118a0001c0004t0003g0120others(4): Show | 7 | HG02886.hp2 HG02976.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+2097dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707642 | |||||
| chr22:41707665
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349+2111A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707665 | ||||||
| chr22:41707690
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.349+2136T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707690 | ||||||
| chr22:41708303
|
G | A | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+2749G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41708303 | ||||||
| chr22:41708741
|
G | C | 22 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(19): Show | 22 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.349+3187G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41708741 | ||||||
| chr22:41708925
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.349+3371A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41708925 | ||||||
| chr22:41709344
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.349+3790C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709344 | ||||||
| chr22:41709509
|
G | C | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+3955G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709509 | ||||||
| chr22:41709538
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349+3984C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709538 | ||||||
| chr22:41709554
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.349+4000G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709554 | ||||||
| chr22:41709556
|
C | T | 1 | a0001c0003t0001g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349+4002C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709556 | ||||||
| chr22:41709558
|
G | A | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.349+4004G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709558 | ||||||
| chr22:41709827
|
A | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-4175A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709827 | ||||||
| chr22:41709860
|
A | G | 16 | a0001c0002t0002g0068a0001c0002t0002g0069a0001c0002t0002g0070others(13): Show | 16 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.350-4142A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709860 | ||||||
| chr22:41709970
|
A | AC | 8 | a0001c0001t0001g0178a0001c0001t0001g0253a0001c0002t0002g0093others(5): Show | 8 | HG01243.hp2 HG02027.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-4026dupC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41709970 | |||||
| chr22:41709998
|
G | A | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-4004G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709998 | ||||||
| chr22:41710205
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-3797G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710205 | ||||||
| chr22:41710212
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.350-3790G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710212 | ||||||
| chr22:41710671
|
T | C | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.350-3331T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710671 | ||||||
| chr22:41710889
|
G | T | 1 | a0001c0002t0002g0064 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.350-3113G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710889 | ||||||
| chr22:41710992
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.350-3010T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710992 | ||||||
| chr22:41711222
|
G | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00099.hp2 NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.350-2780G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711222 | ||||||
| chr22:41711258
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.350-2744T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711258 | ||||||
| chr22:41711480
|
A | G | 3 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-2522A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711480 | ||||||
| chr22:41711482
|
C | T | 1 | a0006c0010t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-2520C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711482 | ||||||
| chr22:41711515
|
T | C | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.350-2487T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711515 | ||||||
| chr22:41711651
|
G | A | 1 | a0005c0007t0004g0013 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.350-2351G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711651 | ||||||
| chr22:41711740
|
C | T | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-2262C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711740 | ||||||
| chr22:41711741
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.350-2261A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711741 | ||||||
| chr22:41711854
|
CT | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-2139delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41711854 | |||||
| chr22:41711976
|
C | T | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.350-2026C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711976 | ||||||
| chr22:41712097
|
G | A | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.350-1905G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712097 | ||||||
| chr22:41712184
|
A | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1818A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712184 | ||||||
| chr22:41712204
|
C | CA | 46 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(43): Show | 46 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.350-1786dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712204
|
C | CAAA | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-1788_350-1786d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712204
|
C | CAAAAAAA others(5): Show |
8 | a0001c0001t0001g0130a0001c0001t0001g0175a0001c0001t0001g0176others(5): Show | 8 | HG00323.hp1 HG01167.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-1797_350-1786d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712204
|
C | CAAAAAAA others(6): Show |
140 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.350-1786_350-1785i others(15): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712204
|
C | CAAAAAAA others(7): Show |
44 | a0001c0001t0001g0128a0001c0001t0001g0145a0001c0001t0001g0146others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.350-1786_350-1785i others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712204
|
C | CAAAAAAA others(8): Show |
3 | a0001c0004t0003g0039a0001c0004t0003g0115a0001c0004t0003g0116 | 3 | HG01884.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.350-1786_350-1785i others(17): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712204
|
C | CAAAAAAA others(1081): Show |
1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.350-1786_350-1785i others(1090): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | |||||
| chr22:41712224
|
G | GT | 24 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(21): Show | 24 | HG02280.hp1 HG02559.hp1 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.350-1770dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712224 | |||||
| chr22:41712229
|
TTTTG | T | 8 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(5): Show | 8 | HG00673.hp2 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1757_350-1754d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712229 | |||||
| chr22:41712245
|
G | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-1757G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712245 | ||||||
| chr22:41712249
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.350-1753C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712249 | ||||||
| chr22:41712276
|
C | T | 1 | a0001c0003t0004g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.350-1726C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712276 | ||||||
| chr22:41712363
|
TA | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0233 | 3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.350-1638delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712363 | ||||||
| chr22:41712460
|
C | T | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG00140.hp1 HG01070.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1542C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712460 | ||||||
| chr22:41712470
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-1532C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712470 | ||||||
| chr22:41712494
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.350-1508C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712494 | ||||||
| chr22:41712594
|
A | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0177 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.350-1408A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712594 | ||||||
| chr22:41712671
|
G | GGT | 5 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | ||||||
| chr22:41712671
|
G | GGTGT | 9 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(6): Show | 9 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | ||||||
| chr22:41712671
|
G | GGTGTGT | 11 | a0001c0004t0003g0043a0001c0004t0003g0115a0001c0004t0003g0120others(8): Show | 11 | HG02559.hp1 HG02886.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | ||||||
| chr22:41712671
|
G | GGTGTGTG others(1): Show |
5 | a0001c0004t0003g0118a0001c0004t0003g0121a0001c0004t0003g0122others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | ||||||
| chr22:41712671
|
GATGTGTG others(9): Show |
G | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-1330_350-1315d others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | ||||||
| chr22:41712672
|
A | ATG | 14 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(11): Show | 14 | HG00735.hp2 HG01099.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1301_350-1300d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTG | 89 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.350-1303_350-1300d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTGTG | 43 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0140others(40): Show | 43 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.350-1305_350-1300d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0149a0001c0003t0004g0025a0005c0007t0004g0009others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1307_350-1300d others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTGTGT others(3): Show |
4 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0038others(1): Show | 4 | HG01934.hp2 HG01943.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-1309_350-1300d others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTGTGT others(5): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0233a0001c0003t0004g0003others(10): Show | 14 | HG00673.hp2 HG01243.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-1311_350-1300d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTGTGT others(7): Show |
12 | a0001c0003t0004g0008a0001c0003t0004g0015a0001c0003t0004g0016others(9): Show | 12 | HG00408.hp1 HG01109.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-1313_350-1300d others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | ATGTGTGT others(9): Show |
2 | a0001c0003t0004g0019a0002c0005t0001g0034 | 2 | HG00423.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.350-1315_350-1300d others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712672
|
A | G | 39 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(36): Show | 39 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.350-1330A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712672 | ||||||
| chr22:41712672
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0003t0004g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.350-1309_350-1300d others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | |||||
| chr22:41712703
|
G | T | 18 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(15): Show | 18 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.350-1299G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712703 | ||||||
| chr22:41712771
|
G | A | 3 | a0001c0001t0005g0183a0001c0001t0005g0190a0001c0001t0005g0191 | 3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.350-1231G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712771 | ||||||
| chr22:41712809
|
G | GT | 11 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0237others(8): Show | 11 | HG01109.hp2 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1177dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712809 | |||||
| chr22:41712826
|
A | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.350-1176A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712826 | ||||||
| chr22:41712878
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.350-1124G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712878 | ||||||
| chr22:41713483
|
G | GA | 208 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-507dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41713483 | |||||
| chr22:41713628
|
A | G | 1 | a0001c0003t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-374A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713628 | ||||||
| chr22:41713763
|
G | A | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-239G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713763 | ||||||
| chr22:41713793
|
C | A | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.350-209C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713793 | ||||||
| chr22:41713793
|
C | T | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-209C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713793 | ||||||
| chr22:41713840
|
G | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.350-162G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713840 | ||||||
| chr22:41713913
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.350-89A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713913 | ||||||
| chr22:41713939
|
C | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-63C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713939 | ||||||
| chr22:41714353
|
G | A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.423+278G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714353 | ||||||
| chr22:41714525
|
G | A | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+450G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714525 | ||||||
| chr22:41714568
|
G | A | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+493G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714568 | ||||||
| chr22:41714591
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.423+516C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714591 | ||||||
| chr22:41714600
|
A | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+525A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714600 | ||||||
| chr22:41714638
|
A | T | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.423+563A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714638 | ||||||
| chr22:41714716
|
CA | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.423+656delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr22 | 41714716 | |||||
| chr22:41714716
|
CAA | C | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+655_423+656del others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr22 | 41714716 | |||||
| chr22:41714835
|
C | T | 1 | a0001c0002t0002g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.423+760C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714835 | ||||||
| chr22:41714907
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.423+832A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714907 | ||||||
| chr22:41714999
|
C | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+924C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714999 | ||||||
| chr22:41715386
|
T | C | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-655T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715386 | ||||||
| chr22:41715397
|
AT | A | 8 | a0001c0001t0001g0143a0001c0002t0002g0083a0001c0004t0003g0127others(5): Show | 8 | HG00323.hp2 HG01109.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-628delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr22 | 41715397 | |||||
| chr22:41715597
|
G | T | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424-444G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715597 | ||||||
| chr22:41715689
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.424-352T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715689 | ||||||
| chr22:41715892
|
A | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.424-149A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715892 | ||||||
| chr22:41715909
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.424-132A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715909 | ||||||
| chr22:41715913
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.424-128A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715913 | ||||||
| chr22:41716037
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.424-4G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41716037 | ||||||
| chr22:41716355
|
C | CT | 17 | a0001c0002t0002g0060a0001c0002t0002g0061a0001c0002t0002g0062others(14): Show | 17 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.529+247dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTT | C | 5 | a0001c0003t0004g0004a0001c0003t0004g0005a0001c0003t0004g0007others(2): Show | 5 | HG01109.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+242_529+247del others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT | C | 11 | a0001c0003t0001g0101a0001c0003t0004g0003a0003c0006t0001g0045others(8): Show | 11 | HG02965.hp1 HG02970.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+241_529+247del others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0004g0016others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+240_529+247del others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(2): Show |
C | 16 | a0001c0002t0002g0081a0001c0002t0002g0083a0001c0002t0002g0093others(13): Show | 16 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+239_529+247del others(9): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0002t0002g0065a0001c0002t0002g0079a0001c0002t0002g0080others(2): Show | 5 | HG01070.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+238_529+247del others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0002t0002g0068 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.529+233_529+247del others(15): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(9): Show |
C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+232_529+247del others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(17): Show |
C | 156 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.529+224_529+247del others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716355
|
CTTTTTTT others(18): Show |
C | 2 | a0001c0001t0001g0193a0001c0001t0001g0213 | 2 | HG01943.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.529+223_529+247del others(25): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | |||||
| chr22:41716420
|
A | G | 1 | a0001c0002t0002g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.529+274A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716420 | ||||||
| chr22:41716433
|
A | G | 2 | a0001c0002t0002g0079a0001c0002t0002g0080 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.529+287A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716433 | ||||||
| chr22:41716564
|
C | T | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+418C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716564 | ||||||
| chr22:41716595
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.529+449T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716595 | ||||||
| chr22:41716686
|
CT | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.529+558delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716686 | |||||
| chr22:41716713
|
C | T | 15 | a0001c0002t0002g0062a0001c0002t0002g0063a0002c0005t0001g0026others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.529+567C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716713 | ||||||
| chr22:41716790
|
C | T | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+644C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716790 | ||||||
| chr22:41716814
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.529+668C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716814 | ||||||
| chr22:41717075
|
C | CT | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.529+935dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41717075 | |||||
| chr22:41717161
|
T | C | 6 | a0001c0002t0002g0065a0001c0002t0002g0079a0001c0002t0002g0080others(3): Show | 6 | HG00323.hp2 HG01070.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-910T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717161 | ||||||
| chr22:41717224
|
A | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.530-847A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717224 | ||||||
| chr22:41717272
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.530-799C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717272 | ||||||
| chr22:41717311
|
C | T | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.530-760C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717311 | ||||||
| chr22:41717359
|
C | T | 5 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-712C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717359 | ||||||
| chr22:41717456
|
C | G | 1 | a0008c0020t0001g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.530-615C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717456 | ||||||
| chr22:41717618
|
C | CT | 19 | a0001c0001t0001g0178a0001c0004t0003g0039a0001c0004t0003g0040others(16): Show | 19 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.530-438dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41717618 | |||||
| chr22:41717618
|
C | CTT | 7 | a0001c0004t0003g0115a0001c0004t0003g0118a0001c0004t0003g0120others(4): Show | 7 | HG02886.hp2 HG02976.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-439_530-438dup others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41717618 | |||||
| chr22:41717706
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-365C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717706 | ||||||
| chr22:41717771
|
A | C | 1 | a0001c0001t0001g0213 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.530-300A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717771 | ||||||
| chr22:41717942
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0233 | 3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.530-129A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717942 | ||||||
| chr22:41718023
|
G | A | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-48G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41718023 | ||||||
| chr22:41718300
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.733+26G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718300 | ||||||
| chr22:41718398
|
G | A | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733+124G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718398 | ||||||
| chr22:41718609
|
C | G | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.733+335C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718609 | ||||||
| chr22:41718805
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+531T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718805 | ||||||
| chr22:41718855
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.733+581T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718855 | ||||||
| chr22:41718856
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.733+582G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718856 | ||||||
| chr22:41718943
|
C | T | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.733+669C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718943 | ||||||
| chr22:41718977
|
T | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+703T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718977 | ||||||
| chr22:41718979
|
C | CT | 7 | a0001c0001t0001g0148a0001c0001t0001g0174a0001c0001t0001g0249others(4): Show | 7 | HG00621.hp2 HG01109.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+726dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41718979 | |||||
| chr22:41718979
|
CT | C | 61 | a0001c0001t0001g0151a0001c0001t0001g0182a0001c0001t0001g0248others(58): Show | 61 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.733+726delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41718979 | |||||
| chr22:41719026
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.733+752A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719026 | ||||||
| chr22:41719046
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.733+772A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719046 | ||||||
| chr22:41719046
|
A | T | 3 | a0001c0002t0002g0094a0001c0002t0002g0095a0001c0002t0002g0107 | 3 | HG02602.hp1 HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.733+772A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719046 | ||||||
| chr22:41719075
|
C | T | 1 | a0003c0006t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.733+801C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719075 | ||||||
| chr22:41719189
|
A | G | 1 | a0003c0006t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.733+915A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719189 | ||||||
| chr22:41719218
|
G | A | 3 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028 | 3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.733+944G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719218 | ||||||
| chr22:41719228
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.733+954C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719228 | ||||||
| chr22:41719246
|
G | T | 2 | a0001c0002t0002g0079a0001c0002t0002g0080 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.733+972G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719246 | ||||||
| chr22:41719281
|
G | A | 14 | a0001c0018t0001g0098a0002c0005t0001g0026a0002c0005t0001g0027others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.733+1007G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719281 | ||||||
| chr22:41719346
|
C | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+1072C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719346 | ||||||
| chr22:41719536
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.733+1262C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719536 | ||||||
| chr22:41720159
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.733+1885G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720159 | ||||||
| chr22:41720200
|
G | C | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.733+1926G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720200 | ||||||
| chr22:41720387
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0234 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.733+2113A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720387 | ||||||
| chr22:41720445
|
T | C | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733+2171T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720445 | ||||||
| chr22:41720556
|
G | T | 63 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(60): Show | 63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.733+2282G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720556 | ||||||
| chr22:41720580
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+2306C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720580 | ||||||
| chr22:41720597
|
A | AT | 144 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.733+2341dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41720597 | |||||
| chr22:41720597
|
A | ATT | 52 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(49): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.733+2340_733+2341d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41720597 | |||||
| chr22:41720706
|
C | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+2432C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720706 | ||||||
| chr22:41720858
|
G | A | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2584G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720858 | ||||||
| chr22:41720865
|
A | G | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2591A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720865 | ||||||
| chr22:41720873
|
G | A | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2599G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720873 | ||||||
| chr22:41721061
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.733+2787A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721061 | ||||||
| chr22:41721065
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.733+2791C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721065 | ||||||
| chr22:41721071
|
G | A | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.733+2797G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721071 | ||||||
| chr22:41721089
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.733+2815A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721089 | ||||||
| chr22:41721160
|
A | ATCTCGGC others(18): Show |
1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-2782_734-2758d others(27): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721160 | |||||
| chr22:41721224
|
C | T | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-2719C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721224 | ||||||
| chr22:41721229
|
C | T | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.734-2714C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721229 | ||||||
| chr22:41721237
|
C | CT | 25 | a0001c0001t0001g0138a0001c0001t0001g0148a0001c0001t0001g0169others(22): Show | 25 | HG00597.hp2 HG00621.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-2681dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | |||||
| chr22:41721237
|
C | CTTTTT | 9 | a0001c0003t0004g0019a0001c0003t0004g0022a0001c0003t0004g0023others(6): Show | 9 | HG00639.hp1 HG01496.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-2685_734-2681d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | |||||
| chr22:41721237
|
C | CTTTTTT | 7 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(4): Show | 7 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2686_734-2681d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | |||||
| chr22:41721237
|
CT | C | 44 | a0001c0001t0001g0151a0001c0001t0001g0195a0001c0001t0001g0196others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.734-2681delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | |||||
| chr22:41721237
|
CTT | C | 15 | a0001c0003t0004g0003a0001c0004t0003g0039a0001c0004t0003g0040others(12): Show | 15 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-2682_734-2681d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | |||||
| chr22:41721237
|
CTTT | C | 7 | a0001c0011t0003g0117a0003c0006t0001g0045a0003c0006t0001g0047others(4): Show | 7 | HG02965.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-2683_734-2681d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | |||||
| chr22:41721278
|
T | C | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-2665T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721278 | ||||||
| chr22:41721293
|
G | A | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.734-2650G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721293 | ||||||
| chr22:41721318
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(46): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.734-2625C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721318 | ||||||
| chr22:41721382
|
C | G | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.734-2561C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721382 | ||||||
| chr22:41721446
|
G | A | 1 | a0001c0002t0002g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.734-2497G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721446 | ||||||
| chr22:41721560
|
A | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-2383A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721560 | ||||||
| chr22:41721564
|
AT | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.734-2370delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721564 | |||||
| chr22:41721566
|
T | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-2377T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721566 | ||||||
| chr22:41721701
|
C | T | 3 | a0001c0002t0002g0088a0001c0002t0002g0089a0001c0002t0002g0096 | 3 | HG01346.hp1 HG02451.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.734-2242C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721701 | ||||||
| chr22:41721715
|
A | AC | 14 | a0001c0002t0002g0054a0001c0002t0002g0076a0001c0002t0002g0079others(11): Show | 14 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.734-2224dupC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721715 | |||||
| chr22:41721719
|
C | CCT | 4 | a0001c0001t0001g0141a0001c0001t0001g0185a0001c0001t0001g0188others(1): Show | 4 | HG00423.hp1 HG01934.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2224_734-2223i others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721719 | ||||||
| chr22:41721719
|
C | CT | 134 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0130others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.734-2204dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721719 | |||||
| chr22:41721719
|
C | CTT | 37 | a0001c0001t0001g0128a0001c0001t0001g0138a0001c0001t0001g0150others(34): Show | 37 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.734-2205_734-2204d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721719 | |||||
| chr22:41721719
|
C | CTTTTT | 7 | a0003c0006t0001g0046a0003c0006t0001g0047a0003c0006t0001g0048others(4): Show | 7 | HG01109.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2208_734-2204d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721719 | |||||
| chr22:41721720
|
T | C | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.734-2223T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721720 | ||||||
| chr22:41721952
|
C | G | 2 | a0001c0011t0003g0117a0001c0011t0003g0123 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.734-1991C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721952 | ||||||
| chr22:41722004
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.734-1939C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722004 | ||||||
| chr22:41722018
|
C | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-1925C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722018 | ||||||
| chr22:41722020
|
C | CT | 130 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(127): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.734-1908dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722020 | |||||
| chr22:41722225
|
G | C | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.734-1718G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722225 | ||||||
| chr22:41722245
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.734-1698G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722245 | ||||||
| chr22:41722467
|
A | AT | 17 | a0001c0001t0001g0170a0001c0001t0001g0225a0001c0001t0001g0227others(14): Show | 17 | HG00741.hp2 HG01109.hp1 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.734-1455dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722467 | |||||
| chr22:41722467
|
AT | A | 27 | a0001c0001t0001g0132a0001c0001t0001g0155a0001c0001t0001g0230others(24): Show | 27 | HG00639.hp1 HG01070.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.734-1455delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722467 | |||||
| chr22:41722467
|
ATT | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-1456_734-1455d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722467 | |||||
| chr22:41722623
|
C | T | 2 | a0001c0012t0001g0184a0001c0012t0001g0192 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.734-1320C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722623 | ||||||
| chr22:41722724
|
G | T | 1 | a0001c0002t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.734-1219G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722724 | ||||||
| chr22:41722743
|
G | C | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1200G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722743 | ||||||
| chr22:41722969
|
T | C | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.734-974T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722969 | ||||||
| chr22:41723062
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-881G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723062 | ||||||
| chr22:41723121
|
C | G | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-822C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723121 | ||||||
| chr22:41723218
|
GT | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.734-713delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41723218 | |||||
| chr22:41723473
|
C | G | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-470C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723473 | ||||||
| chr22:41723695
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-248C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723695 | ||||||
| chr22:41723824
|
A | G | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.734-119A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723824 | ||||||
| chr22:41723837
|
G | C | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-106G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723837 | ||||||
| chr22:41723874
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-69G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723874 | ||||||
| chr22:41724117
|
G | T | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+44G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724117 | ||||||
| chr22:41724124
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.864+51A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724124 | ||||||
| chr22:41724160
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.864+87A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724160 | ||||||
| chr22:41724201
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.864+128T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724201 | ||||||
| chr22:41724392
|
G | A | 1 | a0001c0002t0002g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.864+319G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724392 | ||||||
| chr22:41724571
|
C | A | 2 | a0001c0008t0003g0112a0001c0008t0003g0113 | 2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.864+498C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724571 | ||||||
| chr22:41724574
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0208 | 2 | HG00558.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.864+501C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724574 | ||||||
| chr22:41724616
|
C | CA | 19 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0150others(16): Show | 19 | HG00140.hp1 HG00741.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.864+562dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724616 | |||||
| chr22:41724616
|
CAAAA | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+559_864+562del others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724616 | |||||
| chr22:41724694
|
G | A | 1 | a0001c0002t0002g0086 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.864+621G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724694 | ||||||
| chr22:41724803
|
C | CT | 5 | a0001c0003t0004g0023a0004c0009t0001g0002a0004c0009t0001g0144others(2): Show | 6 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+745dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724803 | |||||
| chr22:41724803
|
CT | C | 16 | a0001c0001t0001g0154a0001c0001t0001g0198a0001c0001t0001g0211others(13): Show | 16 | HG01109.hp1 HG01169.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.864+745delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724803 | |||||
| chr22:41724826
|
G | A | 1 | a0001c0003t0004g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.864+753G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724826 | ||||||
| chr22:41724860
|
G | A | 55 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.864+787G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724860 | ||||||
| chr22:41724873
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.864+800G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724873 | ||||||
| chr22:41724903
|
A | G | 1 | a0001c0008t0003g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.864+830A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724903 | ||||||
| chr22:41724984
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.864+911G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724984 | ||||||
| chr22:41725074
|
T | A | 3 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.864+1001T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725074 | ||||||
| chr22:41725118
|
A | AT | 8 | a0001c0001t0001g0205a0001c0003t0004g0003a0001c0003t0004g0004others(5): Show | 8 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1047dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41725118 | |||||
| chr22:41725121
|
A | AT | 17 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(14): Show | 17 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.864+1058dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41725121 | |||||
| chr22:41725121
|
A | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.864+1048A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725121 | ||||||
| chr22:41725197
|
C | T | 7 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0137others(4): Show | 7 | NA18965.hp1 NA18977.hp2 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1124C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725197 | ||||||
| chr22:41725242
|
G | A | 1 | a0008c0020t0001g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.864+1169G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725242 | ||||||
| chr22:41725256
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.864+1183C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725256 | ||||||
| chr22:41725257
|
G | A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.864+1184G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725257 | ||||||
| chr22:41725274
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.864+1201G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725274 | ||||||
| chr22:41725476
|
G | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+1403G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725476 | ||||||
| chr22:41725606
|
C | A | 1 | a0001c0002t0002g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.864+1533C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725606 | ||||||
| chr22:41725717
|
A | C | 14 | a0001c0018t0001g0098a0002c0005t0001g0026a0002c0005t0001g0027others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+1644A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725717 | ||||||
| chr22:41725785
|
T | G | 55 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.864+1712T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725785 | ||||||
| chr22:41725862
|
C | T | 1 | a0002c0005t0001g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.864+1789C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725862 | ||||||
| chr22:41725905
|
C | T | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.864+1832C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725905 | ||||||
| chr22:41725985
|
A | C | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1912A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725985 | ||||||
| chr22:41726029
|
C | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1956C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726029 | ||||||
| chr22:41726138
|
C | T | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.864+2065C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726138 | ||||||
| chr22:41726242
|
AC | A | 40 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(37): Show | 40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.864+2170delC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726242 | ||||||
| chr22:41726363
|
T | C | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.864+2290T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726363 | ||||||
| chr22:41726750
|
TA | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.864+2681delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41726750 | |||||
| chr22:41726778
|
C | CT | 10 | a0001c0001t0001g0198a0001c0001t0001g0249a0001c0003t0004g0003others(7): Show | 10 | HG00621.hp2 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.864+2718dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41726778 | |||||
| chr22:41726865
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+2792C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726865 | ||||||
| chr22:41726922
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.865-2743C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726922 | ||||||
| chr22:41726974
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.865-2691C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726974 | ||||||
| chr22:41727049
|
T | G | 1 | a0005c0007t0004g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.865-2616T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727049 | ||||||
| chr22:41727095
|
A | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.865-2570A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727095 | ||||||
| chr22:41727395
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.865-2270C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727395 | ||||||
| chr22:41727559
|
A | G | 2 | a0002c0005t0001g0031a0002c0005t0001g0034 | 2 | HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.865-2106A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727559 | ||||||
| chr22:41727611
|
CA | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.865-2051delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41727611 | |||||
| chr22:41727733
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.865-1932A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727733 | ||||||
| chr22:41727866
|
G | A | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.865-1799G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727866 | ||||||
| chr22:41728007
|
G | T | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.865-1658G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728007 | ||||||
| chr22:41728092
|
C | T | 1 | a0001c0003t0004g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.865-1573C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728092 | ||||||
| chr22:41728103
|
T | C | 1 | a0002c0005t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.865-1562T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728103 | ||||||
| chr22:41728133
|
T | C | 1 | a0002c0005t0001g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.865-1532T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728133 | ||||||
| chr22:41728261
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.865-1404C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728261 | ||||||
| chr22:41728311
|
C | G | 40 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(37): Show | 40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.865-1354C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728311 | ||||||
| chr22:41728365
|
T | A | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.865-1300T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728365 | ||||||
| chr22:41728613
|
C | G | 2 | a0001c0008t0003g0108a0001c0008t0003g0110 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.865-1052C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728613 | ||||||
| chr22:41728816
|
A | G | 1 | a0001c0002t0002g0103 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.865-849A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728816 | ||||||
| chr22:41728860
|
C | CA | 32 | a0001c0001t0001g0231a0001c0001t0001g0250a0001c0003t0001g0099others(29): Show | 32 | HG00140.hp1 HG01109.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.865-796dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41728860 | |||||
| chr22:41728860
|
C | CAA | 17 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.865-797_865-796dup others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41728860 | |||||
| chr22:41728870
|
C | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.865-795C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728870 | ||||||
| chr22:41728891
|
C | T | 1 | a0002c0005t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.865-774C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728891 | ||||||
| chr22:41728921
|
T | A | 1 | a0001c0002t0002g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.865-744T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728921 | ||||||
| chr22:41728955
|
G | C | 1 | a0001c0003t0004g0016 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.865-710G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728955 | ||||||
| chr22:41728956
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.865-709G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728956 | ||||||
| chr22:41729078
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.865-587C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729078 | ||||||
| chr22:41729143
|
C | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.865-522C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729143 | ||||||
| chr22:41729164
|
C | CA | 30 | a0001c0002t0002g0078a0001c0003t0001g0099a0001c0003t0001g0100others(27): Show | 30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.865-482dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | |||||
| chr22:41729164
|
C | CAA | 23 | a0001c0001t0001g0130a0001c0001t0001g0177a0001c0003t0004g0003others(20): Show | 23 | HG00323.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.865-483_865-482dup others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | |||||
| chr22:41729164
|
C | CAAA | 146 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.865-484_865-482dup others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | |||||
| chr22:41729164
|
C | CAAAA | 11 | a0001c0001t0001g0132a0001c0001t0001g0142a0001c0001t0001g0145others(8): Show | 11 | HG00735.hp1 HG02027.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.865-485_865-482dup others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | |||||
| chr22:41729206
|
G | T | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-459G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729206 | ||||||
| chr22:41729313
|
C | G | 1 | a0002c0005t0001g0027 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.865-352C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729313 | ||||||
| chr22:41729933
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.979+154G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41729933 | ||||||
| chr22:41730003
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.979+224A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730003 | ||||||
| chr22:41730189
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.980-332T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730189 | ||||||
| chr22:41730275
|
C | T | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.980-246C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730275 | ||||||
| chr22:41730297
|
C | G | 59 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(56): Show | 60 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.980-224C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730297 | ||||||
| chr22:41730405
|
T | C | 2 | a0001c0003t0004g0006a0001c0003t0004g0007 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.980-116T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730405 | ||||||
| chr22:41730679
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1096+42C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41730679 | ||||||
| chr22:41730704
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1096+67C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41730704 | ||||||
| chr22:41730712
|
T | TG | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1096+81dupG | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41730712 | |||||
| chr22:41730815
|
C | G | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+178C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41730815 | ||||||
| chr22:41731023
|
T | G | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1096+386T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731023 | ||||||
| chr22:41731051
|
C | CT | 64 | a0001c0001t0001g0166a0001c0001t0001g0227a0001c0001t0001g0249others(61): Show | 64 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1096+434dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41731051 | |||||
| chr22:41731051
|
C | CTT | 15 | a0001c0003t0004g0022a0002c0005t0001g0026a0002c0005t0001g0027others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1096+433_1096+434d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41731051 | |||||
| chr22:41731090
|
G | A | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1096+453G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731090 | ||||||
| chr22:41731135
|
C | T | 63 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(60): Show | 63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1096+498C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731135 | ||||||
| chr22:41731207
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1096+570C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731207 | ||||||
| chr22:41731343
|
C | T | 1 | a0001c0003t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1096+706C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731343 | ||||||
| chr22:41731368
|
A | G | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1096+731A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731368 | ||||||
| chr22:41731440
|
T | C | 3 | a0002c0005t0001g0031a0002c0005t0001g0034a0002c0005t0001g0036 | 3 | HG00408.hp1 HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1096+803T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731440 | ||||||
| chr22:41731521
|
A | AT | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1097-717dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41731521 | |||||
| chr22:41731622
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1097-623T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731622 | ||||||
| chr22:41731661
|
T | C | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1097-584T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731661 | ||||||
| chr22:41731777
|
T | C | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1097-468T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731777 | ||||||
| chr22:41731953
|
C | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1097-292C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731953 | ||||||
| chr22:41731995
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1097-250T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731995 | ||||||
| chr22:41732093
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1097-152G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41732093 | ||||||
| chr22:41732457
|
T | A | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1197-12T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 10/30 | chr22 | 41732457 | ||||||
| chr22:41732774
|
A | C | 1 | a0001c0001t0001g0250 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1331+171A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41732774 | ||||||
| chr22:41732776
|
A | AT | 37 | a0001c0001t0001g0186a0001c0001t0001g0205a0001c0001t0001g0206others(34): Show | 37 | HG00735.hp1 HG01109.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1331+193dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41732776 | |||||
| chr22:41732776
|
A | ATT | 6 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0042others(3): Show | 6 | HG02280.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331+192_1331+193d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41732776 | |||||
| chr22:41732776
|
AT | A | 10 | a0001c0002t0002g0069a0001c0002t0002g0077a0001c0003t0004g0003others(7): Show | 10 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1331+193delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41732776 | |||||
| chr22:41732959
|
T | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1331+356T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41732959 | ||||||
| chr22:41732969
|
C | T | 6 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+366C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41732969 | ||||||
| chr22:41733005
|
G | A | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1331+402G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733005 | ||||||
| chr22:41733183
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1331+580C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733183 | ||||||
| chr22:41733353
|
G | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1331+750G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733353 | ||||||
| chr22:41733506
|
C | G | 40 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(37): Show | 40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.1331+903C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733506 | ||||||
| chr22:41733770
|
A | G | 1 | a0001c0002t0002g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1331+1167A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733770 | ||||||
| chr22:41733794
|
A | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18947.hp2 NA18970.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+1191A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733794 | ||||||
| chr22:41733960
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1331+1357T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733960 | ||||||
| chr22:41734060
|
G | A | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1331+1457G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734060 | ||||||
| chr22:41734129
|
A | AAAAAT | 38 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(35): Show | 38 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1331+1550_1331+155 others(9): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | |||||
| chr22:41734129
|
A | AAAAATAA others(3): Show |
8 | a0001c0003t0004g0016a0001c0003t0004g0017a0001c0003t0004g0018others(5): Show | 8 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1331+1545_1331+155 others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | |||||
| chr22:41734129
|
A | AAAAATAA others(8): Show |
4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+1540_1331+155 others(19): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | |||||
| chr22:41734129
|
A | AAAAATAA others(13): Show |
10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331+1535_1331+155 others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | |||||
| chr22:41734274
|
A | T | 6 | a0005c0007t0004g0009a0005c0007t0004g0010a0005c0007t0004g0011others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+1671A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734274 | ||||||
| chr22:41734320
|
C | T | 63 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(60): Show | 63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1331+1717C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734320 | ||||||
| chr22:41734379
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1331+1776A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734379 | ||||||
| chr22:41734405
|
C | T | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1331+1802C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734405 | ||||||
| chr22:41734533
|
C | G | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1331+1930C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734533 | ||||||
| chr22:41734553
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1331+1950A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734553 | ||||||
| chr22:41734626
|
A | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1331+2023A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734626 | ||||||
| chr22:41734627
|
G | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1331+2024G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734627 | ||||||
| chr22:41734674
|
G | C | 2 | a0001c0002t0002g0079a0001c0002t0002g0080 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1331+2071G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734674 | ||||||
| chr22:41734839
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(47): Show | 52 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1331+2236G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734839 | ||||||
| chr22:41734929
|
C | G | 3 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101 | 3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1331+2326C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734929 | ||||||
| chr22:41734957
|
T | A | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1331+2354T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734957 | ||||||
| chr22:41735075
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+2472C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735075 | ||||||
| chr22:41735107
|
G | A | 1 | a0001c0002t0002g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1331+2504G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735107 | ||||||
| chr22:41735153
|
G | A | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331+2550G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735153 | ||||||
| chr22:41735183
|
C | T | 1 | a0005c0007t0004g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1331+2580C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735183 | ||||||
| chr22:41735227
|
G | GT | 36 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0136others(33): Show | 36 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1331+2645dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41735227 | |||||
| chr22:41735227
|
GT | G | 45 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(42): Show | 45 | HG00408.hp1 HG00423.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1331+2645delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41735227 | |||||
| chr22:41735406
|
G | C | 2 | a0001c0002t0002g0055a0001c0002t0002g0056 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1331+2803G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735406 | ||||||
| chr22:41735426
|
G | A | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331+2823G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735426 | ||||||
| chr22:41735443
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(47): Show | 52 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1331+2840G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735443 | ||||||
| chr22:41735758
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1331+3155C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735758 | ||||||
| chr22:41735977
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1331+3374G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735977 | ||||||
| chr22:41736103
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1331+3500C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736103 | ||||||
| chr22:41736254
|
CT | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1331+3664delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41736254 | |||||
| chr22:41736477
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1331+3874T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736477 | ||||||
| chr22:41736506
|
G | A | 3 | a0001c0001t0001g0151a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG00099.hp1 HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1331+3903G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736506 | ||||||
| chr22:41736681
|
C | T | 17 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(14): Show | 17 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.1331+4078C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736681 | ||||||
| chr22:41736884
|
C | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1331+4281C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736884 | ||||||
| chr22:41737056
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1331+4453T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737056 | ||||||
| chr22:41737371
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1331+4768G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737371 | ||||||
| chr22:41737439
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1331+4836G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737439 | ||||||
| chr22:41737548
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1331+4945C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737548 | ||||||
| chr22:41737549
|
T | G | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1331+4946T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737549 | ||||||
| chr22:41737563
|
T | C | 6 | a0001c0002t0002g0065a0001c0002t0002g0079a0001c0002t0002g0080others(3): Show | 6 | HG00323.hp2 HG01070.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+4960T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737563 | ||||||
| chr22:41737704
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1331+5101G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737704 | ||||||
| chr22:41737771
|
T | A | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1331+5168T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737771 | ||||||
| chr22:41737824
|
A | G | 1 | a0001c0002t0002g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1331+5221A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737824 | ||||||
| chr22:41737910
|
T | TA | 40 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(37): Show | 40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.1332-5164dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41737910 | |||||
| chr22:41737917
|
T | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1332-5163T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737917 | ||||||
| chr22:41737920
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1332-5160T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737920 | ||||||
| chr22:41737979
|
C | A | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1332-5101C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737979 | ||||||
| chr22:41738107
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1332-4973G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738107 | ||||||
| chr22:41738385
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1332-4695G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738385 | ||||||
| chr22:41738392
|
G | A | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1332-4688G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738392 | ||||||
| chr22:41738490
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1332-4590G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738490 | ||||||
| chr22:41738535
|
C | T | 22 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(19): Show | 22 | HG00099.hp2 HG00621.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.1332-4545C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738535 | ||||||
| chr22:41738632
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1332-4448C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738632 | ||||||
| chr22:41738770
|
C | CA | 9 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(6): Show | 9 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-4299dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41738770 | |||||
| chr22:41738778
|
A | T | 6 | a0001c0002t0002g0068a0001c0002t0002g0070a0001c0002t0002g0071others(3): Show | 6 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-4302A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738778 | ||||||
| chr22:41738779
|
AAATAAAT | A | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-4298_1332-429 others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41738779 | |||||
| chr22:41738780
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1332-4300A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738780 | ||||||
| chr22:41738782
|
T | A | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1332-4298T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738782 | ||||||
| chr22:41738786
|
T | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1332-4294T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738786 | ||||||
| chr22:41738809
|
A | G | 3 | a0001c0001t0001g0172a0001c0001t0001g0212a0001c0001t0001g0223 | 3 | HG00597.hp1 HG02129.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1332-4271A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738809 | ||||||
| chr22:41738810
|
T | TAAAATA | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1332-4267_1332-426 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41738810 | |||||
| chr22:41738891
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1332-4189T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738891 | ||||||
| chr22:41738927
|
G | A | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1332-4153G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738927 | ||||||
| chr22:41738986
|
A | C | 2 | a0001c0002t0002g0082a0001c0002t0002g0105 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1332-4094A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738986 | ||||||
| chr22:41739033
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1332-4047G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739033 | ||||||
| chr22:41739140
|
CA | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1332-3926delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739140 | |||||
| chr22:41739155
|
T | C | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1332-3925T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739155 | ||||||
| chr22:41739357
|
C | G | 1 | a0002c0005t0001g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1332-3723C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739357 | ||||||
| chr22:41739381
|
C | G | 1 | a0001c0004t0006g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1332-3699C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739381 | ||||||
| chr22:41739481
|
T | A | 36 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1332-3599T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739481 | ||||||
| chr22:41739548
|
T | TAAAAATT others(315): Show |
1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1332-3519_1332-351 others(326): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | |||||
| chr22:41739548
|
T | TAAAAATT others(316): Show |
8 | a0001c0004t0003g0115a0001c0004t0003g0118a0001c0004t0003g0121others(5): Show | 8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332-3519_1332-351 others(327): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | |||||
| chr22:41739548
|
T | TAAAAATT others(317): Show |
12 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(9): Show | 12 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332-3519_1332-351 others(328): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | |||||
| chr22:41739548
|
T | TAAAAATT others(318): Show |
4 | a0001c0008t0003g0113a0001c0011t0003g0117a0001c0011t0003g0123others(1): Show | 4 | HG02559.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332-3519_1332-351 others(329): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | |||||
| chr22:41739747
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1332-3333T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739747 | ||||||
| chr22:41740036
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0233 | 3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1332-3044G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740036 | ||||||
| chr22:41740036
|
G | C | 1 | a0003c0006t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1332-3044G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740036 | ||||||
| chr22:41740036
|
G | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0226 | 2 | NA18968.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1332-3044G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740036 | ||||||
| chr22:41740038
|
G | A | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1332-3042G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740038 | ||||||
| chr22:41740062
|
C | T | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1332-3018C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740062 | ||||||
| chr22:41740089
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00621.hp2 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1332-2991G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740089 | ||||||
| chr22:41740144
|
C | A | 36 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1332-2936C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740144 | ||||||
| chr22:41740145
|
G | A | 2 | a0001c0001t0001g0169a0001c0004t0003g0116 | 2 | HG01884.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1332-2935G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740145 | ||||||
| chr22:41740314
|
G | A | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-2766G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740314 | ||||||
| chr22:41740596
|
G | C | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-2484G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740596 | ||||||
| chr22:41740614
|
C | T | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1332-2466C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740614 | ||||||
| chr22:41740645
|
G | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-2435G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740645 | ||||||
| chr22:41740715
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1332-2365G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740715 | ||||||
| chr22:41740728
|
T | TCAAAAA | 13 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(10): Show | 13 | HG02109.hp2 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1332-2329_1332-232 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41740728 | |||||
| chr22:41740728
|
TCAAAAAC others(5): Show |
T | 1 | a0001c0001t0001g0224 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1332-2335_1332-232 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41740728 | |||||
| chr22:41740764
|
A | C | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1332-2316A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740764 | ||||||
| chr22:41740926
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1332-2154T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740926 | ||||||
| chr22:41741178
|
C | T | 8 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(5): Show | 8 | HG00673.hp2 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332-1902C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741178 | ||||||
| chr22:41741179
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1332-1901G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741179 | ||||||
| chr22:41741456
|
T | C | 3 | a0001c0002t0002g0068a0001c0002t0002g0070a0001c0002t0002g0074 | 3 | HG00597.hp2 HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1332-1624T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741456 | ||||||
| chr22:41741688
|
G | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-1392G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741688 | ||||||
| chr22:41741747
|
G | A | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1332-1333G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741747 | ||||||
| chr22:41741869
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-1211G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741869 | ||||||
| chr22:41741942
|
C | CA | 51 | a0001c0002t0002g0087a0001c0003t0001g0099a0001c0003t0001g0100others(48): Show | 51 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(48): Show |
intron_variant | MODIFIER | c.1332-1120dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41741942 | |||||
| chr22:41741942
|
CA | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.1332-1120delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41741942 | |||||
| chr22:41741942
|
CAAAAAAA | C | 20 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(17): Show | 20 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1332-1126_1332-112 others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41741942 | |||||
| chr22:41741997
|
A | G | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-1083A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741997 | ||||||
| chr22:41742102
|
G | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1332-978G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742102 | ||||||
| chr22:41742102
|
G | T | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-978G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742102 | ||||||
| chr22:41742142
|
C | T | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1332-938C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742142 | ||||||
| chr22:41742175
|
G | A | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-905G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742175 | ||||||
| chr22:41742176
|
C | T | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-904C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742176 | ||||||
| chr22:41742196
|
G | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1332-884G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742196 | ||||||
| chr22:41742264
|
T | C | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1332-816T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742264 | ||||||
| chr22:41742489
|
A | T | 4 | a0004c0009t0001g0002a0004c0009t0001g0144a0004c0009t0001g0239others(1): Show | 5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332-591A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742489 | ||||||
| chr22:41742525
|
C | T | 6 | a0003c0006t0001g0044a0003c0006t0001g0047a0003c0006t0001g0048others(3): Show | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-555C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742525 | ||||||
| chr22:41742852
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1332-228C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742852 | ||||||
| chr22:41743039
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1332-41G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41743039 | ||||||
| chr22:41743050
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1332-30G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41743050 | ||||||
| chr22:41743074
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
splice_region_variant&intron_variant | LOW | c.1332-6A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41743074 | ||||||
| chr22:41743211
|
C | T | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+17C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743211 | ||||||
| chr22:41743264
|
A | G | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1446+70A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743264 | ||||||
| chr22:41743457
|
GA | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1446+265delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41743457 | |||||
| chr22:41743497
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1446+303A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743497 | ||||||
| chr22:41743651
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1446+457G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743651 | ||||||
| chr22:41743857
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1446+663G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743857 | ||||||
| chr22:41743879
|
A | AT | 7 | a0001c0003t0004g0019a0005c0007t0004g0009a0005c0007t0004g0010others(4): Show | 7 | HG01496.hp1 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1446+696dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41743879 | |||||
| chr22:41743940
|
G | A | 1 | a0001c0003t0004g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1446+746G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743940 | ||||||
| chr22:41744156
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1447-817C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41744156 | ||||||
| chr22:41744361
|
A | G | 5 | a0001c0004t0003g0114a0001c0004t0003g0124a0001c0004t0003g0125others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-612A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41744361 | ||||||
| chr22:41744474
|
GCTATGAT others(315): Show |
G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1447-485_1447-164d others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41744474 | |||||
| chr22:41744480
|
A | AT | 17 | a0001c0002t0002g0056a0001c0002t0002g0058a0001c0002t0002g0059others(14): Show | 17 | HG00597.hp2 HG00621.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1447-458dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41744480 | |||||
| chr22:41744480
|
A | ATTT | 5 | a0001c0002t0002g0066a0001c0002t0002g0082a0001c0002t0002g0085others(2): Show | 5 | HG00639.hp2 HG00741.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-460_1447-458d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41744480 | |||||
| chr22:41745129
|
T | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1538+65T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745129 | ||||||
| chr22:41745238
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1538+174C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745238 | ||||||
| chr22:41745322
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1538+258G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745322 | ||||||
| chr22:41745448
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1538+384A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745448 | ||||||
| chr22:41745636
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1539-249G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745636 | ||||||
| chr22:41745729
|
C | T | 1 | a0001c0004t0003g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1539-156C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745729 | ||||||
| chr22:41745867
|
C | CA | 23 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(20): Show | 23 | HG00099.hp2 HG00621.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1539-17dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr22 | 41745867 | |||||
| chr22:41746244
|
T | C | 5 | a0005c0007t0004g0009a0005c0007t0004g0010a0005c0007t0004g0011others(2): Show | 5 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1680+218T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746244 | ||||||
| chr22:41746302
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1680+276T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746302 | ||||||
| chr22:41746382
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1680+356G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746382 | ||||||
| chr22:41746389
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1680+363T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746389 | ||||||
| chr22:41746642
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18980.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1680+616T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746642 | ||||||
| chr22:41746713
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1680+687G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746713 | ||||||
| chr22:41746721
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1680+695G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746721 | ||||||
| chr22:41746817
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1680+791G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746817 | ||||||
| chr22:41746993
|
CTTCT | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1680+972_1680+975d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41746993 | |||||
| chr22:41747039
|
A | G | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1680+1013A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747039 | ||||||
| chr22:41747049
|
T | TATAATA | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1680+1037_1681-103 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747049 | |||||
| chr22:41747049
|
T | TATAATAA others(2): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0181a0001c0001t0001g0197 | 3 | NA18999.hp1 NA19060.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1680+1034_1681-103 others(13): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747049 | |||||
| chr22:41747237
|
C | CT | 8 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-855dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747237 | |||||
| chr22:41747237
|
C | CTT | 15 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(12): Show | 15 | HG00639.hp1 HG01243.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1681-856_1681-855d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747237 | |||||
| chr22:41747237
|
CT | C | 9 | a0001c0001t0001g0145a0001c0001t0001g0154a0001c0001t0001g0177others(6): Show | 9 | HG00323.hp1 HG00738.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1681-855delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747237 | |||||
| chr22:41747425
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1681-682C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747425 | ||||||
| chr22:41747524
|
C | T | 1 | a0001c0003t0004g0015 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1681-583C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747524 | ||||||
| chr22:41747533
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1681-574G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747533 | ||||||
| chr22:41747568
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1681-539A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747568 | ||||||
| chr22:41747595
|
C | G | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1681-512C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747595 | ||||||
| chr22:41747645
|
A | G | 3 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101 | 3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1681-462A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747645 | ||||||
| chr22:41747736
|
C | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1681-371C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747736 | ||||||
| chr22:41747770
|
A | G | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1681-337A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747770 | ||||||
| chr22:41747942
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1681-165C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747942 | ||||||
| chr22:41748368
|
G | A | 8 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0001t0001g0238others(5): Show | 8 | HG00099.hp2 HG01258.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792+150G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748368 | ||||||
| chr22:41748508
|
A | AC | 158 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(155): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.1792+294dupC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41748508 | |||||
| chr22:41748768
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1792+550C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748768 | ||||||
| chr22:41748812
|
T | G | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1792+594T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748812 | ||||||
| chr22:41748834
|
C | T | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1792+616C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748834 | ||||||
| chr22:41748835
|
G | A | 2 | a0001c0001t0001g0201a0001c0002t0002g0060 | 2 | HG02148.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1792+617G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748835 | ||||||
| chr22:41748922
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1792+704C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748922 | ||||||
| chr22:41748923
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1792+705G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748923 | ||||||
| chr22:41749040
|
G | A | 16 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.1792+822G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749040 | ||||||
| chr22:41749151
|
A | C | 2 | a0001c0012t0001g0184a0001c0012t0001g0192 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1792+933A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749151 | ||||||
| chr22:41749177
|
A | G | 12 | a0001c0004t0003g0114a0001c0004t0003g0115a0001c0004t0003g0118others(9): Show | 12 | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1792+959A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749177 | ||||||
| chr22:41749249
|
G | T | 1 | a0003c0006t0001g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1792+1031G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749249 | ||||||
| chr22:41749256
|
A | G | 12 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1792+1038A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749256 | ||||||
| chr22:41749279
|
CT | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1792+1074delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41749279 | |||||
| chr22:41749292
|
T | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792+1074T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749292 | ||||||
| chr22:41749361
|
C | T | 2 | a0001c0008t0003g0108a0001c0008t0003g0110 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1792+1143C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749361 | ||||||
| chr22:41749368
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1792+1150C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749368 | ||||||
| chr22:41749600
|
T | G | 2 | a0001c0003t0004g0006a0001c0003t0004g0007 | 2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1792+1382T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749600 | ||||||
| chr22:41749887
|
G | T | 1 | a0001c0002t0002g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1792+1669G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749887 | ||||||
| chr22:41749932
|
A | G | 3 | a0001c0001t0001g0151a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG00099.hp1 HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1792+1714A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749932 | ||||||
| chr22:41749979
|
CTG | C | 5 | a0001c0002t0002g0068a0001c0002t0002g0070a0001c0002t0002g0071others(2): Show | 5 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792+1765_1792+176 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41749979 | |||||
| chr22:41750156
|
A | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1792+1938A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750156 | ||||||
| chr22:41750297
|
C | T | 1 | a0001c0004t0003g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1792+2079C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750297 | ||||||
| chr22:41750375
|
A | G | 3 | a0005c0007t0004g0009a0005c0007t0004g0011a0011c0014t0004g0012 | 3 | HG02809.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1792+2157A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750375 | ||||||
| chr22:41750672
|
G | A | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1793-1919G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750672 | ||||||
| chr22:41750912
|
T | G | 4 | a0004c0009t0001g0002a0004c0009t0001g0144a0004c0009t0001g0239others(1): Show | 5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1793-1679T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750912 | ||||||
| chr22:41751071
|
A | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-1520A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751071 | ||||||
| chr22:41751073
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1793-1518C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751073 | ||||||
| chr22:41751175
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0135a0001c0001t0001g0141others(44): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1793-1416G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751175 | ||||||
| chr22:41751208
|
C | T | 1 | a0001c0002t0002g0105 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1793-1383C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751208 | ||||||
| chr22:41751467
|
GC | G | 63 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(60): Show | 63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1793-1122delC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41751467 | |||||
| chr22:41751623
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1793-968T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751623 | ||||||
| chr22:41751641
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1793-950G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751641 | ||||||
| chr22:41751721
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1793-870A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751721 | ||||||
| chr22:41751727
|
G | A | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1793-864G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751727 | ||||||
| chr22:41751772
|
T | TA | 136 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1793-802dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41751772 | |||||
| chr22:41751772
|
T | TAA | 27 | a0001c0001t0001g0143a0001c0001t0001g0155a0001c0001t0001g0166others(24): Show | 27 | HG00140.hp2 HG00639.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1793-803_1793-802d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41751772 | |||||
| chr22:41751776
|
A | AG | 7 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0230others(4): Show | 7 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1793-815_1793-814i others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751776 | ||||||
| chr22:41752071
|
G | GA | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1793-507dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41752071 | |||||
| chr22:41752072
|
A | G | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-519A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752072 | ||||||
| chr22:41752312
|
T | C | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1793-279T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752312 | ||||||
| chr22:41752314
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1793-277T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752314 | ||||||
| chr22:41752463
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1793-128G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752463 | ||||||
| chr22:41752674
|
T | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1853+23T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41752674 | ||||||
| chr22:41752771
|
G | A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1853+120G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41752771 | ||||||
| chr22:41753020
|
A | AT | 11 | a0001c0001t0001g0129a0001c0001t0001g0150a0001c0001t0001g0166others(8): Show | 11 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1853+385dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr22 | 41753020 | |||||
| chr22:41753364
|
C | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1854-585C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753364 | ||||||
| chr22:41753488
|
A | G | 1 | a0001c0002t0002g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1854-461A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753488 | ||||||
| chr22:41753566
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0211a0001c0018t0001g0098 | 3 | HG01169.hp1 HG01169.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1854-383G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753566 | ||||||
| chr22:41753636
|
C | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1854-313C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753636 | ||||||
| chr22:41754122
|
A | G | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1951+76A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754122 | ||||||
| chr22:41754142
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1951+96C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754142 | ||||||
| chr22:41754390
|
CTTCA | C | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951+353_1951+356d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr22 | 41754390 | |||||
| chr22:41754406
|
A | C | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951+360A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754406 | ||||||
| chr22:41754414
|
TTTTTTC | T | 63 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(60): Show | 63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1951+386_1951+391d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr22 | 41754414 | |||||
| chr22:41754624
|
G | T | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1951+578G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754624 | ||||||
| chr22:41755057
|
G | C | 1 | a0006c0010t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1951+1011G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755057 | ||||||
| chr22:41755068
|
C | G | 1 | a0001c0002t0002g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1951+1022C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755068 | ||||||
| chr22:41755138
|
A | T | 1 | a0001c0022t0001g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1951+1092A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755138 | ||||||
| chr22:41755225
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951+1179C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755225 | ||||||
| chr22:41755334
|
G | C | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951+1288G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755334 | ||||||
| chr22:41755347
|
A | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1951+1301A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755347 | ||||||
| chr22:41755551
|
C | T | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1951+1505C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755551 | ||||||
| chr22:41755647
|
G | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1951+1601G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755647 | ||||||
| chr22:41755676
|
T | C | 3 | a0006c0010t0001g0179a0006c0010t0001g0220a0006c0010t0001g0236 | 3 | HG01243.hp2 HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1951+1630T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755676 | ||||||
| chr22:41755943
|
C | T | 36 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1951+1897C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755943 | ||||||
| chr22:41756176
|
G | C | 1 | a0001c0002t0002g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1951+2130G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756176 | ||||||
| chr22:41756181
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951+2135C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756181 | ||||||
| chr22:41756262
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1952-2103A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756262 | ||||||
| chr22:41756425
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1952-1940C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756425 | ||||||
| chr22:41756485
|
T | C | 3 | a0001c0001t0005g0183a0001c0001t0005g0190a0001c0001t0005g0191 | 3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1952-1880T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756485 | ||||||
| chr22:41756765
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1952-1600C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756765 | ||||||
| chr22:41756984
|
A | C | 56 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.1952-1381A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756984 | ||||||
| chr22:41757093
|
C | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0214 | 2 | HG00423.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.1952-1272C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757093 | ||||||
| chr22:41757288
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1952-1077T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757288 | ||||||
| chr22:41757365
|
T | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00621.hp2 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1952-1000T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757365 | ||||||
| chr22:41757445
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1952-920C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757445 | ||||||
| chr22:41757485
|
G | A | 3 | a0001c0004t0003g0114a0001c0004t0003g0124a0001c0004t0003g0125 | 3 | HG02723.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1952-880G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757485 | ||||||
| chr22:41757506
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1952-859C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757506 | ||||||
| chr22:41757722
|
A | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1952-643A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757722 | ||||||
| chr22:41757783
|
T | C | 30 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0001g0171others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1952-582T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757783 | ||||||
| chr22:41757793
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1952-572G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757793 | ||||||
| chr22:41757969
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1952-396G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757969 | ||||||
| chr22:41758128
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1952-237G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41758128 | ||||||
| chr22:41758542
|
A | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120+9A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41758542 | ||||||
| chr22:41758999
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2120+466C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41758999 | ||||||
| chr22:41759040
|
G | A | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120+507G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759040 | ||||||
| chr22:41759357
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120+824C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759357 | ||||||
| chr22:41759572
|
G | A | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.2120+1039G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759572 | ||||||
| chr22:41759617
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0211a0010c0019t0001g0106 | 3 | HG01169.hp1 HG01169.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2120+1084G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759617 | ||||||
| chr22:41759629
|
C | CAATAAAT others(1): Show |
12 | a0001c0004t0003g0115a0001c0004t0003g0118a0001c0004t0003g0120others(9): Show | 12 | HG02559.hp1 HG02572.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | |||||
| chr22:41759629
|
C | CAATAAAT others(5): Show |
4 | a0001c0004t0003g0114a0001c0004t0003g0116a0001c0004t0003g0125others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | |||||
| chr22:41759629
|
C | CAATAAAT others(9): Show |
5 | a0001c0004t0003g0041a0001c0004t0003g0124a0001c0004t0006g0126others(2): Show | 5 | HG02723.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(20): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | |||||
| chr22:41759629
|
C | CAATAAAT others(13): Show |
4 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0042others(1): Show | 4 | HG02280.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | |||||
| chr22:41759629
|
CAAAA | C | 32 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(29): Show | 32 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2120+1099_2120+110 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | |||||
| chr22:41759632
|
A | T | 31 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(28): Show | 31 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.2120+1099A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759632 | ||||||
| chr22:41759632
|
AAAAT | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.2120+1127_2120+113 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759632 | |||||
| chr22:41759633
|
A | AAATAAAT others(665): Show |
6 | a0005c0007t0004g0009a0005c0007t0004g0010a0005c0007t0004g0011others(3): Show | 6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120+1126_2120+112 others(676): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759633 | |||||
| chr22:41759681
|
C | T | 1 | a0002c0005t0001g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2120+1148C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759681 | ||||||
| chr22:41759895
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2120+1362C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759895 | ||||||
| chr22:41759896
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2120+1363G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759896 | ||||||
| chr22:41759904
|
T | C | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2120+1371T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759904 | ||||||
| chr22:41759940
|
G | A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2120+1407G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759940 | ||||||
| chr22:41760152
|
A | G | 3 | a0002c0005t0001g0031a0002c0005t0001g0034a0002c0005t0001g0036 | 3 | HG00408.hp1 HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2120+1619A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760152 | ||||||
| chr22:41760205
|
G | T | 1 | a0003c0006t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2120+1672G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760205 | ||||||
| chr22:41760234
|
T | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00099.hp2 NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2120+1701T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760234 | ||||||
| chr22:41760265
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2120+1732G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760265 | ||||||
| chr22:41760339
|
A | G | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2120+1806A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760339 | ||||||
| chr22:41760381
|
C | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2120+1848C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760381 | ||||||
| chr22:41760386
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2120+1853G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760386 | ||||||
| chr22:41760441
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2120+1908G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760441 | ||||||
| chr22:41760449
|
C | G | 6 | a0003c0006t0001g0044a0003c0006t0001g0047a0003c0006t0001g0048others(3): Show | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2120+1916C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760449 | ||||||
| chr22:41760490
|
C | T | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120+1957C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760490 | ||||||
| chr22:41760513
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2120+1980A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760513 | ||||||
| chr22:41760544
|
T | C | 36 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(33): Show | 36 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(33): Show |
intron_variant | MODIFIER | c.2120+2011T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760544 | ||||||
| chr22:41760557
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2120+2024T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760557 | ||||||
| chr22:41760720
|
G | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2120+2187G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760720 | ||||||
| chr22:41760830
|
G | T | 1 | a0001c0002t0002g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2120+2297G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760830 | ||||||
| chr22:41760852
|
C | T | 1 | a0002c0005t0001g0034 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2120+2319C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760852 | ||||||
| chr22:41760960
|
GT | G | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2121-2206delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41760960 | |||||
| chr22:41761033
|
C | T | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2121-2141C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761033 | ||||||
| chr22:41761036
|
G | T | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2121-2138G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761036 | ||||||
| chr22:41761040
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2121-2134G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761040 | ||||||
| chr22:41761077
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2121-2097T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761077 | ||||||
| chr22:41761266
|
G | C | 1 | a0001c0001t0001g0134 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2121-1908G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761266 | ||||||
| chr22:41761306
|
GTGTTTTT others(4): Show |
G | 2 | a0001c0002t0002g0081a0001c0002t0002g0083 | 2 | HG00323.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2121-1855_2121-184 others(15): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41761306 | |||||
| chr22:41761308
|
G | GT | 5 | a0001c0001t0001g0235a0001c0002t0002g0068a0001c0002t0002g0078others(2): Show | 5 | HG00621.hp1 HG01175.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2121-1856dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41761308 | |||||
| chr22:41761319
|
G | T | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0018t0001g0098 | 3 | HG00621.hp2 NA18906.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2121-1855G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761319 | ||||||
| chr22:41761319
|
GT | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0133others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.2121-1842delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41761319 | |||||
| chr22:41761320
|
T | G | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2121-1854T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761320 | ||||||
| chr22:41761561
|
G | T | 2 | a0001c0012t0001g0184a0001c0012t0001g0192 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2121-1613G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761561 | ||||||
| chr22:41761727
|
A | T | 1 | a0001c0003t0004g0017 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2121-1447A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761727 | ||||||
| chr22:41761731
|
C | G | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.2121-1443C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761731 | ||||||
| chr22:41762150
|
A | G | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2121-1024A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762150 | ||||||
| chr22:41762198
|
A | G | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2121-976A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762198 | ||||||
| chr22:41762200
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2121-974T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762200 | ||||||
| chr22:41762327
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2121-847T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762327 | ||||||
| chr22:41762416
|
C | T | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2121-758C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762416 | ||||||
| chr22:41762549
|
G | GT | 33 | a0001c0001t0001g0134a0001c0001t0001g0140a0001c0001t0001g0145others(30): Show | 33 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.2121-625_2121-624i others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762549 | ||||||
| chr22:41762549
|
GA | G | 8 | a0001c0001t0001g0136a0001c0001t0001g0153a0001c0001t0001g0156others(5): Show | 8 | HG01106.hp1 HG01358.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2121-624delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762549 | ||||||
| chr22:41762550
|
A | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(198): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2121-624A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762550 | ||||||
| chr22:41762636
|
C | A | 4 | a0002c0005t0001g0032a0002c0005t0001g0033a0002c0005t0001g0035others(1): Show | 4 | HG00673.hp2 NA18994.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121-538C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762636 | ||||||
| chr22:41763068
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2121-106A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41763068 | ||||||
| chr22:41763069
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2121-105T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41763069 | ||||||
| chr22:41763405
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0254 | 2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2268+84T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763405 | ||||||
| chr22:41763438
|
G | A | 2 | a0001c0004t0003g0115a0001c0004t0006g0126 | 2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2268+117G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763438 | ||||||
| chr22:41763530
|
G | GATT | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2268+213_2268+215d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763530 | |||||
| chr22:41763577
|
C | T | 6 | a0003c0006t0001g0044a0003c0006t0001g0047a0003c0006t0001g0048others(3): Show | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+256C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763577 | ||||||
| chr22:41763785
|
C | A | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+464C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763785 | ||||||
| chr22:41763817
|
A | G | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2268+496A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763817 | ||||||
| chr22:41763943
|
CT | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(90): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.2268+643delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763943 | |||||
| chr22:41763943
|
CTT | C | 50 | a0001c0001t0001g0137a0001c0001t0001g0149a0001c0001t0001g0155others(47): Show | 50 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.2268+642_2268+643d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763943 | |||||
| chr22:41763943
|
CTTT | C | 57 | a0001c0001t0001g0189a0001c0003t0001g0099a0001c0003t0001g0100others(54): Show | 57 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(54): Show |
intron_variant | MODIFIER | c.2268+641_2268+643d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763943 | |||||
| chr22:41763970
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2268+649G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763970 | ||||||
| chr22:41763977
|
C | T | 3 | a0002c0005t0001g0031a0002c0005t0001g0034a0002c0005t0001g0036 | 3 | HG00408.hp1 HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2268+656C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763977 | ||||||
| chr22:41764002
|
AGTGGCAG others(7): Show |
A | 14 | a0001c0018t0001g0098a0002c0005t0001g0026a0002c0005t0001g0027others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.2268+697_2268+710d others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41764002 | |||||
| chr22:41764046
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2268+725C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764046 | ||||||
| chr22:41764150
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+829C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764150 | ||||||
| chr22:41764378
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2268+1057C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764378 | ||||||
| chr22:41764508
|
C | G | 1 | a0001c0004t0003g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2268+1187C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764508 | ||||||
| chr22:41764596
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2268+1275A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764596 | ||||||
| chr22:41764799
|
A | G | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+1478A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764799 | ||||||
| chr22:41765030
|
G | T | 1 | a0001c0002t0002g0085 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2268+1709G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765030 | ||||||
| chr22:41765109
|
A | G | 6 | a0001c0001t0001g0149a0001c0001t0001g0174a0001c0001t0001g0176others(3): Show | 6 | NA18947.hp1 NA18968.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+1788A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765109 | ||||||
| chr22:41765132
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2268+1811G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765132 | ||||||
| chr22:41765423
|
G | A | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2102G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765423 | ||||||
| chr22:41765684
|
C | T | 1 | a0001c0003t0004g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2268+2363C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765684 | ||||||
| chr22:41765794
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2473C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765794 | ||||||
| chr22:41765883
|
C | CT | 35 | a0001c0001t0001g0135a0001c0001t0001g0143a0001c0001t0001g0150others(32): Show | 35 | HG00558.hp2 HG00609.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2268+2587dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41765883 | |||||
| chr22:41765883
|
CT | C | 43 | a0001c0001t0001g0230a0001c0002t0002g0067a0001c0002t0002g0072others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.2268+2587delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41765883 | |||||
| chr22:41765911
|
A | G | 1 | a0005c0007t0004g0009 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2268+2590A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765911 | ||||||
| chr22:41765951
|
C | T | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2268+2630C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765951 | ||||||
| chr22:41765976
|
C | T | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2268+2655C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765976 | ||||||
| chr22:41766127
|
G | A | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2806G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766127 | ||||||
| chr22:41766169
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2268+2848C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766169 | ||||||
| chr22:41766185
|
G | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(205): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2268+2864G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766185 | ||||||
| chr22:41766185
|
G | T | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2864G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766185 | ||||||
| chr22:41766186
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2865T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766186 | ||||||
| chr22:41766297
|
A | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+2976A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766297 | ||||||
| chr22:41766307
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2986G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766307 | ||||||
| chr22:41766308
|
A | T | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2987A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766308 | ||||||
| chr22:41766310
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2989T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766310 | ||||||
| chr22:41766329
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2268+3008G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766329 | ||||||
| chr22:41766408
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2268+3087G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766408 | ||||||
| chr22:41766560
|
T | G | 12 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(9): Show | 12 | HG02280.hp1 HG02723.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.2268+3239T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766560 | ||||||
| chr22:41766665
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2268+3344G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766665 | ||||||
| chr22:41766804
|
T | A | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+3483T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766804 | ||||||
| chr22:41766856
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2268+3535C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766856 | ||||||
| chr22:41767071
|
G | A | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2269-3615G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767071 | ||||||
| chr22:41767097
|
A | G | 1 | a0005c0007t0004g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2269-3589A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767097 | ||||||
| chr22:41767255
|
T | C | 26 | a0001c0001t0001g0204a0001c0004t0003g0039a0001c0004t0003g0040others(23): Show | 26 | HG01099.hp2 HG01884.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2269-3431T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767255 | ||||||
| chr22:41767301
|
A | C | 1 | a0001c0002t0002g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2269-3385A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767301 | ||||||
| chr22:41767637
|
T | C | 8 | a0001c0001t0001g0204a0001c0004t0003g0115a0001c0004t0003g0118others(5): Show | 8 | HG01099.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-3049T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767637 | ||||||
| chr22:41768247
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-2439C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768247 | ||||||
| chr22:41768301
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2269-2385G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768301 | ||||||
| chr22:41768361
|
T | C | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-2325T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768361 | ||||||
| chr22:41768390
|
CA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2269-2280delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41768390 | |||||
| chr22:41768501
|
G | A | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2269-2185G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768501 | ||||||
| chr22:41768507
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269-2179G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768507 | ||||||
| chr22:41768512
|
C | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2269-2174C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768512 | ||||||
| chr22:41768656
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2269-2030T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768656 | ||||||
| chr22:41768720
|
C | G | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-1966C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768720 | ||||||
| chr22:41768858
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2269-1828A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768858 | ||||||
| chr22:41769040
|
C | G | 1 | a0005c0007t0004g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2269-1646C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769040 | ||||||
| chr22:41769380
|
A | T | 1 | a0001c0001t0001g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2269-1306A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769380 | ||||||
| chr22:41769476
|
A | AT | 136 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(133): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.2269-1197dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41769476 | |||||
| chr22:41769476
|
AT | A | 8 | a0001c0002t0002g0083a0001c0008t0003g0108a0001c0008t0003g0110others(5): Show | 8 | HG00323.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-1197delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41769476 | |||||
| chr22:41769566
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2269-1120G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769566 | ||||||
| chr22:41769582
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2269-1104C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769582 | ||||||
| chr22:41769720
|
C | A | 2 | a0001c0011t0003g0117a0001c0011t0003g0123 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2269-966C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769720 | ||||||
| chr22:41769849
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2269-837A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769849 | ||||||
| chr22:41769922
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2269-764G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769922 | ||||||
| chr22:41769929
|
G | A | 1 | a0001c0002t0002g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2269-757G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769929 | ||||||
| chr22:41769995
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2269-691A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769995 | ||||||
| chr22:41770070
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2269-616G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770070 | ||||||
| chr22:41770083
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269-603G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770083 | ||||||
| chr22:41770136
|
G | GA | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-539dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41770136 | |||||
| chr22:41770185
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269-501G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770185 | ||||||
| chr22:41770287
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2269-399A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770287 | ||||||
| chr22:41770412
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(45): Show | 50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2269-274A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770412 | ||||||
| chr22:41770482
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2269-204G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770482 | ||||||
| chr22:41770495
|
CT | C | 3 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101 | 3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2269-190delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770495 | ||||||
| chr22:41771083
|
T | C | 2 | a0001c0001t0001g0204a0001c0004t0003g0118 | 2 | HG01099.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2544+122T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771083 | ||||||
| chr22:41771140
|
T | G | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2544+179T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771140 | ||||||
| chr22:41771150
|
C | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG00099.hp2 NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2544+189C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771150 | ||||||
| chr22:41771256
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2544+295C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771256 | ||||||
| chr22:41771351
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2544+390G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771351 | ||||||
| chr22:41771358
|
C | T | 2 | a0002c0005t0001g0031a0002c0005t0001g0034 | 2 | HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2544+397C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771358 | ||||||
| chr22:41771437
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2544+476C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771437 | ||||||
| chr22:41771460
|
C | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2544+499C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771460 | ||||||
| chr22:41771537
|
G | T | 1 | a0001c0004t0003g0118 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2544+576G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771537 | ||||||
| chr22:41771610
|
C | CT | 207 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2544+659dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41771610 | |||||
| chr22:41771650
|
G | A | 1 | a0002c0005t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2544+689G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771650 | ||||||
| chr22:41771738
|
G | A | 1 | a0003c0006t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2544+777G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771738 | ||||||
| chr22:41771770
|
C | A | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2544+809C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771770 | ||||||
| chr22:41771977
|
T | C | 3 | a0001c0004t0003g0114a0001c0004t0003g0124a0001c0004t0003g0125 | 3 | HG02723.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2544+1016T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771977 | ||||||
| chr22:41772001
|
T | G | 4 | a0004c0009t0001g0002a0004c0009t0001g0144a0004c0009t0001g0239others(1): Show | 5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2544+1040T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772001 | ||||||
| chr22:41772177
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2544+1216A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772177 | ||||||
| chr22:41772409
|
G | A | 15 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(12): Show | 15 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.2544+1448G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772409 | ||||||
| chr22:41772482
|
T | C | 2 | a0001c0012t0001g0184a0001c0012t0001g0192 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2544+1521T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772482 | ||||||
| chr22:41772553
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2544+1592C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772553 | ||||||
| chr22:41772657
|
A | G | 3 | a0001c0002t0002g0085a0001c0002t0002g0094a0001c0002t0002g0107 | 3 | HG02602.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2544+1696A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772657 | ||||||
| chr22:41772763
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2544+1802G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772763 | ||||||
| chr22:41772877
|
A | C | 77 | a0001c0001t0001g0204a0001c0003t0001g0099a0001c0003t0001g0100others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.2544+1916A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772877 | ||||||
| chr22:41773050
|
C | T | 3 | a0001c0002t0002g0085a0001c0002t0002g0094a0001c0002t0002g0107 | 3 | HG02602.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2544+2089C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773050 | ||||||
| chr22:41773092
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2544+2131C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773092 | ||||||
| chr22:41773265
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(45): Show | 50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2544+2304T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773265 | ||||||
| chr22:41773472
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2544+2511G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773472 | ||||||
| chr22:41773560
|
TA | T | 55 | a0001c0001t0001g0155a0001c0001t0001g0165a0001c0002t0002g0054others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2545-2521delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41773560 | |||||
| chr22:41773560
|
TAA | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(87): Show | 92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.2545-2522_2545-252 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41773560 | |||||
| chr22:41773560
|
TAAA | T | 111 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(108): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.2545-2523_2545-252 others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41773560 | |||||
| chr22:41773614
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2545-2488G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773614 | ||||||
| chr22:41773628
|
C | T | 77 | a0001c0001t0001g0204a0001c0003t0001g0099a0001c0003t0001g0100others(74): Show | 77 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.2545-2474C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773628 | ||||||
| chr22:41773649
|
G | T | 5 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2545-2453G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773649 | ||||||
| chr22:41773699
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2545-2403C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773699 | ||||||
| chr22:41773732
|
G | A | 1 | a0001c0004t0006g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2545-2370G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773732 | ||||||
| chr22:41773746
|
G | A | 23 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(20): Show | 23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2545-2356G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773746 | ||||||
| chr22:41773870
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545-2232G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773870 | ||||||
| chr22:41773956
|
A | G | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2545-2146A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773956 | ||||||
| chr22:41774021
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2545-2081A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774021 | ||||||
| chr22:41774428
|
A | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2545-1674A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774428 | ||||||
| chr22:41774469
|
G | A | 1 | a0005c0007t0004g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2545-1633G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774469 | ||||||
| chr22:41774506
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2545-1596A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774506 | ||||||
| chr22:41774670
|
T | C | 3 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101 | 3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2545-1432T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774670 | ||||||
| chr22:41774901
|
C | A | 1 | a0001c0004t0003g0040 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2545-1201C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774901 | ||||||
| chr22:41774931
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2545-1171C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774931 | ||||||
| chr22:41775059
|
A | C | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2545-1043A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775059 | ||||||
| chr22:41775067
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545-1035C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775067 | ||||||
| chr22:41775296
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2545-806T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775296 | ||||||
| chr22:41775342
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2545-760C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775342 | ||||||
| chr22:41775594
|
C | CT | 16 | a0001c0001t0001g0167a0001c0001t0001g0238a0002c0005t0001g0026others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.2545-491dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41775594 | |||||
| chr22:41775594
|
CT | C | 16 | a0001c0001t0001g0189a0001c0003t0004g0015a0001c0003t0004g0016others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2545-491delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41775594 | |||||
| chr22:41775613
|
A | T | 36 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.2545-489A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775613 | ||||||
| chr22:41775742
|
T | TG | 6 | a0003c0006t0001g0044a0003c0006t0001g0047a0003c0006t0001g0048others(3): Show | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2545-359dupG | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41775742 | |||||
| chr22:41775795
|
C | T | 8 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(5): Show | 8 | HG00673.hp2 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2545-307C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775795 | ||||||
| chr22:41775813
|
C | T | 27 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0001g0171others(24): Show | 27 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2545-289C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775813 | ||||||
| chr22:41776046
|
C | T | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2545-56C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41776046 | ||||||
| chr22:41776076
|
C | T | 99 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(96): Show | 99 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.2545-26C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41776076 | ||||||
| chr22:41776322
|
G | A | 1 | a0001c0022t0001g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2710+55G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776322 | ||||||
| chr22:41776487
|
G | A | 1 | a0002c0005t0001g0028 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2710+220G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776487 | ||||||
| chr22:41776560
|
C | A | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2710+293C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776560 | ||||||
| chr22:41776620
|
C | T | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2710+353C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776620 | ||||||
| chr22:41776782
|
GTATT | G | 76 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2710+525_2710+528d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41776782 | |||||
| chr22:41777059
|
C | T | 12 | a0001c0003t0004g0003a0001c0004t0003g0039a0001c0004t0003g0040others(9): Show | 12 | HG02280.hp1 HG02723.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.2710+792C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777059 | ||||||
| chr22:41777108
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2710+841C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777108 | ||||||
| chr22:41777158
|
A | AT | 151 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(148): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.2710+906dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41777158 | |||||
| chr22:41777158
|
A | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2710+891A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777158 | ||||||
| chr22:41777158
|
AT | A | 10 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(7): Show | 10 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2710+906delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41777158 | |||||
| chr22:41777180
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2710+913G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777180 | ||||||
| chr22:41777217
|
G | A | 1 | a0001c0002t0002g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2710+950G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777217 | ||||||
| chr22:41777244
|
G | A | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2710+977G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777244 | ||||||
| chr22:41777289
|
G | A | 6 | a0003c0006t0001g0044a0003c0006t0001g0047a0003c0006t0001g0048others(3): Show | 6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2710+1022G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777289 | ||||||
| chr22:41777323
|
T | A | 1 | a0002c0005t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2710+1056T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777323 | ||||||
| chr22:41777371
|
G | A | 1 | a0001c0004t0003g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2710+1104G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777371 | ||||||
| chr22:41777479
|
C | T | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2710+1212C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777479 | ||||||
| chr22:41777829
|
C | T | 5 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2711-879C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777829 | ||||||
| chr22:41777852
|
GCTTC | G | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2711-839_2711-836d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41777852 | |||||
| chr22:41777875
|
T | C | 37 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(34): Show | 37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2711-833T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777875 | ||||||
| chr22:41778004
|
CCTTCCTT others(10): Show |
C | 1 | a0001c0002t0002g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2711-680_2711-664d others(19): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41778004 | |||||
| chr22:41778213
|
C | A | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2711-495C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778213 | ||||||
| chr22:41778223
|
G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0201a0001c0001t0001g0205 | 3 | HG02145.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2711-485G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778223 | ||||||
| chr22:41778227
|
C | T | 24 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(21): Show | 24 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.2711-481C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778227 | ||||||
| chr22:41778272
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2711-436C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778272 | ||||||
| chr22:41778301
|
A | AT | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2711-405dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41778301 | |||||
| chr22:41778555
|
G | A | 5 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2711-153G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778555 | ||||||
| chr22:41778887
|
T | G | 40 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(37): Show | 40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.2815+75T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41778887 | ||||||
| chr22:41779144
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2815+332G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779144 | ||||||
| chr22:41779227
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2815+415G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779227 | ||||||
| chr22:41779283
|
C | CA | 6 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2815+479dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr22 | 41779283 | |||||
| chr22:41779310
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2815+498T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779310 | ||||||
| chr22:41779314
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2815+502G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779314 | ||||||
| chr22:41779361
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2815+549G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779361 | ||||||
| chr22:41779606
|
A | G | 1 | a0001c0003t0004g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2815+794A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779606 | ||||||
| chr22:41779691
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(206): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2815+879A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779691 | ||||||
| chr22:41779828
|
C | T | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2815+1016C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779828 | ||||||
| chr22:41779947
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2815+1135C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779947 | ||||||
| chr22:41780054
|
C | T | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2816-1230C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780054 | ||||||
| chr22:41780055
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2816-1229G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780055 | ||||||
| chr22:41780219
|
C | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2816-1065C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780219 | ||||||
| chr22:41780279
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2816-1005G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780279 | ||||||
| chr22:41780335
|
G | A | 7 | a0001c0001t0001g0189a0001c0001t0001g0213a0001c0001t0001g0215others(4): Show | 7 | HG00609.hp1 HG04184.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2816-949G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780335 | ||||||
| chr22:41780411
|
G | T | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2816-873G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780411 | ||||||
| chr22:41780507
|
C | T | 1 | a0001c0003t0004g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2816-777C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780507 | ||||||
| chr22:41780553
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2816-731T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780553 | ||||||
| chr22:41780569
|
T | A | 1 | a0001c0002t0002g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2816-715T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780569 | ||||||
| chr22:41780576
|
C | CT | 31 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2816-704dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr22 | 41780576 | |||||
| chr22:41780576
|
C | CTT | 8 | a0001c0002t0002g0104a0001c0003t0004g0003a0001c0003t0004g0004others(5): Show | 8 | HG01175.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2816-705_2816-704d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr22 | 41780576 | |||||
| chr22:41780580
|
T | C | 19 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(16): Show | 19 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.2816-704T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780580 | ||||||
| chr22:41780580
|
TC | T | 13 | a0001c0002t0002g0102a0001c0004t0003g0120a0001c0004t0003g0125others(10): Show | 13 | HG01109.hp1 HG02258.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.2816-703delC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780580 | ||||||
| chr22:41780581
|
C | T | 95 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.2816-703C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780581 | ||||||
| chr22:41780583
|
T | C | 3 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101 | 3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2816-701T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780583 | ||||||
| chr22:41780681
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2816-603G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780681 | ||||||
| chr22:41780751
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2816-533T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780751 | ||||||
| chr22:41780865
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2816-419G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780865 | ||||||
| chr22:41780865
|
G | T | 1 | a0001c0002t0002g0071 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2816-419G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780865 | ||||||
| chr22:41780867
|
A | G | 9 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0150others(6): Show | 9 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2816-417A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780867 | ||||||
| chr22:41780904
|
G | T | 1 | a0001c0002t0002g0087 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2816-380G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780904 | ||||||
| chr22:41780906
|
C | T | 18 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(15): Show | 18 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.2816-378C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780906 | ||||||
| chr22:41780913
|
A | T | 124 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2816-371A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780913 | ||||||
| chr22:41781133
|
T | G | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2816-151T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41781133 | ||||||
| chr22:41781449
|
G | C | 124 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2926+55G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 23/30 | chr22 | 41781449 | ||||||
| chr22:41781582
|
CTGTT | C | 66 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2927-95_2927-92del others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr22 | 41781582 | |||||
| chr22:41781895
|
A | G | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3087+50A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41781895 | ||||||
| chr22:41782036
|
C | T | 108 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3087+191C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782036 | ||||||
| chr22:41782377
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3087+532G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782377 | ||||||
| chr22:41782437
|
G | A | 108 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3087+592G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782437 | ||||||
| chr22:41782546
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3087+701T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782546 | ||||||
| chr22:41782612
|
G | A | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3087+767G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782612 | ||||||
| chr22:41783107
|
C | A | 11 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(8): Show | 11 | HG02280.hp1 HG02723.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.3088-1232C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783107 | ||||||
| chr22:41783153
|
C | CT | 9 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(6): Show | 9 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3088-1178dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr22 | 41783153 | |||||
| chr22:41783327
|
T | C | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3088-1012T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783327 | ||||||
| chr22:41783384
|
C | T | 1 | a0001c0008t0003g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3088-955C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783384 | ||||||
| chr22:41783490
|
C | A | 4 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3088-849C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783490 | ||||||
| chr22:41783540
|
C | A | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3088-799C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783540 | ||||||
| chr22:41783572
|
G | A | 2 | a0001c0002t0002g0079a0001c0002t0002g0080 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3088-767G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783572 | ||||||
| chr22:41783658
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(45): Show | 50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.3088-681A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783658 | ||||||
| chr22:41784163
|
C | G | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3088-176C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41784163 | ||||||
| chr22:41784280
|
T | C | 1 | a0001c0003t0004g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3088-59T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41784280 | ||||||
| chr22:41784437
|
C | A | 5 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(2): Show | 5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3169+17C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 25/30 | chr22 | 41784437 | ||||||
| chr22:41784454
|
C | T | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3169+34C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 25/30 | chr22 | 41784454 | ||||||
| chr22:41784580
|
T | C | 60 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(57): Show | 60 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3170-28T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 25/30 | chr22 | 41784580 | ||||||
| chr22:41784850
|
G | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0233 | 3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3345+67G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784850 | ||||||
| chr22:41784887
|
T | TTGAG | 124 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.3345+105_3345+106i others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784887 | |||||
| chr22:41784899
|
T | A | 2 | a0001c0002t0002g0096a0003c0006t0001g0045 | 2 | HG01346.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3345+116T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784899 | ||||||
| chr22:41784905
|
A | T | 1 | a0001c0003t0004g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3345+122A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784905 | ||||||
| chr22:41784925
|
T | TTTTA | 44 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(41): Show | 44 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3345+167_3345+170d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | |||||
| chr22:41784925
|
T | TTTTATTT others(1): Show |
5 | a0001c0002t0002g0061a0001c0002t0002g0091a0001c0002t0002g0094others(2): Show | 5 | HG01175.hp1 HG01255.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.3345+163_3345+170d others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | |||||
| chr22:41784925
|
T | TTTTATTT others(5): Show |
40 | a0001c0002t0002g0084a0001c0003t0004g0003a0001c0003t0004g0004others(37): Show | 40 | HG00280.hp1 HG00639.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.3345+159_3345+170d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | |||||
| chr22:41784925
|
T | TTTTATTT others(9): Show |
2 | a0001c0003t0004g0006a0001c0004t0003g0115 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3345+155_3345+170d others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | |||||
| chr22:41784925
|
T | TTTTATTT others(10): Show |
1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+149_3345+150i others(19): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | |||||
| chr22:41784925
|
TTTTA | T | 16 | a0001c0002t0002g0068a0001c0002t0002g0070a0001c0002t0002g0074others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.3345+167_3345+170d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | |||||
| chr22:41784966
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0233 | 3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3345+183C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784966 | ||||||
| chr22:41785022
|
C | T | 37 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(34): Show | 37 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.3345+239C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785022 | ||||||
| chr22:41785125
|
C | T | 1 | a0001c0002t0002g0086 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3345+342C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785125 | ||||||
| chr22:41785178
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3345+395G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785178 | ||||||
| chr22:41785187
|
C | T | 17 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(14): Show | 17 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.3345+404C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785187 | ||||||
| chr22:41785227
|
G | A | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3345+444G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785227 | ||||||
| chr22:41785241
|
T | TTTTA | 5 | a0002c0005t0001g0038a0003c0006t0001g0045a0003c0006t0001g0046others(2): Show | 5 | HG01109.hp1 HG02970.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3345+482_3345+485d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785241 | |||||
| chr22:41785241
|
TTTTA | T | 71 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(68): Show | 71 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3345+482_3345+485d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785241 | |||||
| chr22:41785285
|
C | T | 1 | a0001c0002t0002g0103 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3345+502C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785285 | ||||||
| chr22:41785293
|
A | G | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3345+510A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785293 | ||||||
| chr22:41785494
|
T | C | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+711T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785494 | ||||||
| chr22:41785507
|
C | T | 29 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(26): Show | 29 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.3345+724C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785507 | ||||||
| chr22:41785698
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+915G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785698 | ||||||
| chr22:41785725
|
G | A | 3 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101 | 3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3345+942G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785725 | ||||||
| chr22:41785865
|
ATTTTTAT others(1): Show |
A | 34 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0001g0171others(31): Show | 34 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.3345+1119_3345+112 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785865 | |||||
| chr22:41785865
|
ATTTTTAT others(9): Show |
A | 2 | a0001c0001t0001g0166a0001c0018t0001g0098 | 2 | HG00140.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3345+1111_3345+112 others(20): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785865 | |||||
| chr22:41785895
|
A | AT | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+1119dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785895 | |||||
| chr22:41785906
|
T | TA | 44 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(41): Show | 44 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.3345+1123_3345+112 others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785906 | ||||||
| chr22:41785907
|
T | A | 4 | a0001c0002t0002g0060a0001c0002t0002g0085a0001c0002t0002g0094others(1): Show | 4 | HG02148.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+1124T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785907 | ||||||
| chr22:41785910
|
A | ATT | 6 | a0001c0002t0002g0068a0001c0002t0002g0070a0001c0002t0002g0074others(3): Show | 6 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.3345+1130_3345+113 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785910 | |||||
| chr22:41785910
|
A | T | 4 | a0001c0002t0002g0060a0001c0002t0002g0085a0001c0002t0002g0094others(1): Show | 4 | HG02148.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+1127A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785910 | ||||||
| chr22:41785911
|
T | A | 4 | a0001c0002t0002g0060a0001c0002t0002g0085a0001c0002t0002g0094others(1): Show | 4 | HG02148.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+1128T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785911 | ||||||
| chr22:41785912
|
T | TTA | 37 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(34): Show | 37 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.3345+1130_3345+113 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785912 | |||||
| chr22:41785915
|
A | AT | 22 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(19): Show | 22 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.3345+1145dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785915 | |||||
| chr22:41785915
|
A | T | 44 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(41): Show | 44 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.3345+1132A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785915 | ||||||
| chr22:41785920
|
T | A | 36 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.3345+1137T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785920 | ||||||
| chr22:41785931
|
G | A | 3 | a0001c0002t0002g0085a0001c0002t0002g0094a0001c0002t0002g0107 | 3 | HG02602.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3345+1148G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785931 | ||||||
| chr22:41785934
|
G | A | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+1151G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785934 | ||||||
| chr22:41785941
|
C | T | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.3345+1158C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785941 | ||||||
| chr22:41785972
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+1189G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785972 | ||||||
| chr22:41785996
|
C | T | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+1213C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785996 | ||||||
| chr22:41786003
|
C | T | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+1220C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786003 | ||||||
| chr22:41786011
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345+1228C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786011 | ||||||
| chr22:41786012
|
G | A | 1 | a0001c0002t0002g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3345+1229G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786012 | ||||||
| chr22:41786029
|
G | C | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+1246G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786029 | ||||||
| chr22:41786132
|
G | A | 15 | a0001c0001t0001g0140a0001c0001t0001g0172a0001c0001t0001g0212others(12): Show | 15 | HG00544.hp1 HG00597.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3345+1349G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786132 | ||||||
| chr22:41786135
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3345+1352C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786135 | ||||||
| chr22:41786228
|
A | G | 1 | a0001c0002t0002g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3345+1445A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786228 | ||||||
| chr22:41786295
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3345+1512C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786295 | ||||||
| chr22:41786512
|
T | C | 1 | a0002c0005t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3345+1729T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786512 | ||||||
| chr22:41786567
|
T | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0129others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3345+1784T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786567 | ||||||
| chr22:41787240
|
G | A | 1 | a0001c0002t0002g0067 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3345+2457G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787240 | ||||||
| chr22:41787286
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3345+2503G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787286 | ||||||
| chr22:41787405
|
T | C | 36 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.3345+2622T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787405 | ||||||
| chr22:41787436
|
C | A | 36 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.3345+2653C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787436 | ||||||
| chr22:41787464
|
C | T | 60 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(57): Show | 60 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.3345+2681C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787464 | ||||||
| chr22:41787473
|
C | A | 4 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+2690C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787473 | ||||||
| chr22:41787513
|
C | T | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+2730C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787513 | ||||||
| chr22:41787584
|
A | C | 1 | a0001c0002t0002g0071 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3345+2801A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787584 | ||||||
| chr22:41788135
|
T | A | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3345+3352T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788135 | ||||||
| chr22:41788139
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0202 | 3 | HG01258.hp2 HG01943.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3345+3356C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788139 | ||||||
| chr22:41788216
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3345+3433A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788216 | ||||||
| chr22:41788262
|
C | G | 1 | a0001c0002t0002g0071 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3345+3479C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788262 | ||||||
| chr22:41788525
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3345+3742C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788525 | ||||||
| chr22:41788572
|
TTGGGATT others(128): Show |
T | 1 | a0001c0001t0001g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3345+3806_3345+394 others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41788572 | |||||
| chr22:41788955
|
A | G | 2 | a0001c0004t0003g0042a0001c0004t0003g0043 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3345+4172A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788955 | ||||||
| chr22:41788977
|
C | T | 10 | a0003c0006t0001g0044a0003c0006t0001g0045a0003c0006t0001g0046others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3345+4194C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788977 | ||||||
| chr22:41789040
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+4257G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789040 | ||||||
| chr22:41789083
|
C | T | 66 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(63): Show | 66 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.3345+4300C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789083 | ||||||
| chr22:41789139
|
A | G | 1 | a0001c0003t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3345+4356A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789139 | ||||||
| chr22:41789181
|
G | A | 25 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(22): Show | 25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.3345+4398G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789181 | ||||||
| chr22:41789182
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0130others(106): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3345+4399C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789182 | ||||||
| chr22:41789236
|
C | T | 4 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(1): Show | 4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+4453C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789236 | ||||||
| chr22:41789591
|
C | G | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3346-4238C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789591 | ||||||
| chr22:41789679
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3346-4150C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789679 | ||||||
| chr22:41789965
|
C | G | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3346-3864C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789965 | ||||||
| chr22:41790076
|
T | C | 16 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(13): Show | 16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.3346-3753T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790076 | ||||||
| chr22:41790262
|
T | G | 37 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(34): Show | 37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3346-3567T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790262 | ||||||
| chr22:41790361
|
A | G | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3346-3468A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790361 | ||||||
| chr22:41790589
|
T | A | 24 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(21): Show | 24 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.3346-3240T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790589 | ||||||
| chr22:41790834
|
G | A | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3346-2995G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790834 | ||||||
| chr22:41790847
|
C | T | 1 | a0001c0022t0001g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3346-2982C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790847 | ||||||
| chr22:41791000
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3346-2829G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791000 | ||||||
| chr22:41791011
|
C | T | 48 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(45): Show | 48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3346-2818C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791011 | ||||||
| chr22:41791195
|
C | T | 114 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(111): Show | 114 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3346-2634C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791195 | ||||||
| chr22:41791323
|
T | TA | 24 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(21): Show | 24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3346-2500dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41791323 | |||||
| chr22:41791324
|
A | G | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3346-2505A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791324 | ||||||
| chr22:41791378
|
C | T | 28 | a0001c0001t0001g0140a0001c0001t0001g0149a0001c0001t0001g0171others(25): Show | 28 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.3346-2451C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791378 | ||||||
| chr22:41791480
|
C | A | 7 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(4): Show | 7 | HG02559.hp1 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3346-2349C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791480 | ||||||
| chr22:41791778
|
G | A | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3346-2051G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791778 | ||||||
| chr22:41791786
|
A | C | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3346-2043A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791786 | ||||||
| chr22:41792065
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3346-1764G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792065 | ||||||
| chr22:41792148
|
C | T | 13 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(10): Show | 13 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.3346-1681C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792148 | ||||||
| chr22:41792320
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3346-1509G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792320 | ||||||
| chr22:41792501
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3346-1328C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792501 | ||||||
| chr22:41792518
|
A | C | 1 | a0001c0003t0004g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3346-1311A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792518 | ||||||
| chr22:41792675
|
T | A | 1 | a0003c0006t0001g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3346-1154T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792675 | ||||||
| chr22:41792718
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0209a0001c0001t0001g0234 | 3 | HG01167.hp2 HG01169.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3346-1111A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792718 | ||||||
| chr22:41792865
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3346-964T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792865 | ||||||
| chr22:41792887
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(55): Show | 60 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.3346-942C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792887 | ||||||
| chr22:41792891
|
C | T | 1 | a0002c0005t0001g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3346-938C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792891 | ||||||
| chr22:41792918
|
T | TA | 7 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(4): Show | 7 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3346-896dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41792918 | |||||
| chr22:41792918
|
TA | T | 22 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0002t0002g0102others(19): Show | 22 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.3346-896delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41792918 | |||||
| chr22:41792918
|
TAA | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(139): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.3346-897_3346-896d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41792918 | |||||
| chr22:41792995
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3346-834G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792995 | ||||||
| chr22:41793019
|
G | C | 1 | a0001c0001t0001g0255 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3346-810G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793019 | ||||||
| chr22:41793032
|
C | CT | 25 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0149others(22): Show | 25 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.3346-766dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
C | CTTT | 8 | a0001c0001t0001g0129a0001c0001t0001g0176a0001c0001t0001g0198others(5): Show | 8 | HG01981.hp2 HG03704.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.3346-768_3346-766d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
C | CTTTT | 12 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0187others(9): Show | 12 | HG00621.hp2 HG00673.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.3346-769_3346-766d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
C | CTTTTT | 10 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0202others(7): Show | 10 | HG01109.hp2 HG01258.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.3346-770_3346-766d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
C | CTTTTTT | 7 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0182others(4): Show | 7 | HG01943.hp2 HG02004.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.3346-771_3346-766d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
CT | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0134others(22): Show | 26 | HG00099.hp1 HG00323.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3346-766delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
CTTT | C | 17 | a0001c0001t0002g0203a0001c0002t0002g0085a0001c0002t0002g0094others(14): Show | 17 | HG01175.hp1 HG02027.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3346-768_3346-766d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793032
|
CTTTT | C | 84 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.3346-769_3346-766d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | |||||
| chr22:41793048
|
T | C | 6 | a0001c0003t0004g0003a0001c0003t0004g0004a0001c0003t0004g0005others(3): Show | 6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3346-781T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793048 | ||||||
| chr22:41793049
|
T | C | 47 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(44): Show | 47 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.3346-780T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793049 | ||||||
| chr22:41793073
|
T | C | 1 | a0001c0002t0002g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3346-756T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793073 | ||||||
| chr22:41793086
|
C | G | 38 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(35): Show | 38 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3346-743C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793086 | ||||||
| chr22:41793131
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(51): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.3346-698G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793131 | ||||||
| chr22:41793142
|
A | G | 1 | a0001c0002t0002g0091 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3346-687A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793142 | ||||||
| chr22:41793226
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.3346-603T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793226 | ||||||
| chr22:41793372
|
G | A | 1 | a0001c0004t0006g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3346-457G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793372 | ||||||
| chr22:41793380
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(51): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.3346-449C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793380 | ||||||
| chr22:41793382
|
A | T | 6 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3346-447A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793382 | ||||||
| chr22:41793403
|
T | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.3346-426T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793403 | ||||||
| chr22:41793411
|
C | T | 5 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3346-418C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793411 | ||||||
| chr22:41793432
|
G | A | 1 | a0007c0021t0001g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3346-397G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793432 | ||||||
| chr22:41793547
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.3346-282A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793547 | ||||||
| chr22:41793758
|
T | C | 6 | a0001c0004t0003g0115a0001c0004t0003g0118a0001c0004t0003g0120others(3): Show | 6 | HG02886.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.3346-71T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793758 | ||||||
| chr22:41793806
|
ATT | A | 18 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(15): Show | 18 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.3346-8_3346-7delTT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793806 | |||||
| chr22:41794192
|
G | A | 1 | a0001c0018t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3428-179G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 27/30 | chr22 | 41794192 | ||||||
| chr22:41794305
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(55): Show | 60 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.3428-66A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 27/30 | chr22 | 41794305 | ||||||
| chr22:41794544
|
G | A | 1 | a0001c0003t0001g0099 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3534+67G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 28/30 | chr22 | 41794544 | ||||||
| chr22:41795021
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3535-390C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 28/30 | chr22 | 41795021 | ||||||
| chr22:41795238
|
C | A | 18 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0004t0003g0041others(15): Show | 18 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.3535-173C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 28/30 | chr22 | 41795238 | ||||||
| chr22:41795632
|
A | G | 115 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(112): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.3666+90A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 29/30 | chr22 | 41795632 | ||||||
| chr22:41796079
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0001g0224others(1): Show | 4 | HG00609.hp1 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.3779+232A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796079 | ||||||
| chr22:41796351
|
G | GT | 6 | a0001c0001t0001g0206a0001c0001t0001g0216a0001c0003t0001g0099others(3): Show | 6 | HG02109.hp2 HG02257.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.3779+520dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41796351 | |||||
| chr22:41796351
|
GT | G | 91 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0002g0203others(88): Show | 91 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.3779+520delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41796351 | |||||
| chr22:41796351
|
GTT | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0135others(58): Show | 63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.3779+519_3779+520d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41796351 | |||||
| chr22:41796430
|
G | A | 13 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3779+583G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796430 | ||||||
| chr22:41796478
|
G | A | 49 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3779+631G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796478 | ||||||
| chr22:41796546
|
G | A | 1 | a0002c0005t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3779+699G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796546 | ||||||
| chr22:41796590
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3779+743G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796590 | ||||||
| chr22:41796717
|
G | A | 1 | a0001c0004t0003g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3779+870G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796717 | ||||||
| chr22:41796718
|
G | A | 49 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3779+871G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796718 | ||||||
| chr22:41796932
|
A | G | 1 | a0001c0004t0003g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3779+1085A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796932 | ||||||
| chr22:41797341
|
G | A | 2 | a0001c0002t0002g0082a0001c0002t0002g0105 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3779+1494G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797341 | ||||||
| chr22:41797350
|
G | A | 1 | a0001c0003t0004g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3779+1503G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797350 | ||||||
| chr22:41797504
|
T | G | 6 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3779+1657T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797504 | ||||||
| chr22:41797650
|
G | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0249a0001c0001t0001g0250 | 3 | HG00621.hp2 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.3780-1604G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797650 | ||||||
| chr22:41797684
|
T | C | 1 | a0001c0004t0006g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3780-1570T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797684 | ||||||
| chr22:41797737
|
G | A | 62 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.3780-1517G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797737 | ||||||
| chr22:41797893
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3780-1361T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797893 | ||||||
| chr22:41797909
|
T | C | 49 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3780-1345T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797909 | ||||||
| chr22:41798116
|
A | AAC | 15 | a0001c0001t0001g0137a0001c0001t0001g0172a0001c0001t0001g0174others(12): Show | 15 | HG00140.hp1 HG00609.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.3780-1084_3780-108 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
A | AACAC | 3 | a0001c0001t0001g0128a0001c0001t0001g0215a0001c0001t0001g0228 | 3 | HG04199.hp2 NA18982.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.3780-1086_3780-108 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
A | AACACAC | 2 | a0001c0001t0001g0130a0001c0001t0001g0218 | 2 | NA18992.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.3780-1088_3780-108 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
A | AACACACA others(5): Show |
1 | a0001c0001t0001g0227 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3780-1094_3780-108 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AAC | A | 26 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0138others(23): Show | 26 | HG00280.hp2 HG00558.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3780-1084_3780-108 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACAC | A | 16 | a0001c0001t0001g0129a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 16 | HG00597.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.3780-1086_3780-108 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACAC | A | 8 | a0001c0001t0001g0139a0001c0001t0001g0250a0001c0003t0004g0006others(5): Show | 8 | HG01496.hp1 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.3780-1088_3780-108 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(1): Show |
A | 6 | a0001c0003t0004g0015a0001c0003t0004g0016a0001c0003t0004g0017others(3): Show | 6 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3780-1090_3780-108 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(3): Show |
A | 8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0182others(5): Show | 8 | HG00323.hp1 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3780-1092_3780-108 others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(5): Show |
A | 6 | a0001c0001t0001g0257a0001c0003t0004g0020a0001c0003t0004g0023others(3): Show | 6 | HG01981.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3780-1094_3780-108 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(7): Show |
A | 13 | a0001c0001t0001g0001a0001c0001t0001g0145a0001c0001t0001g0158others(10): Show | 14 | HG01433.hp1 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.3780-1096_3780-108 others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(9): Show |
A | 43 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0141others(40): Show | 44 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.3780-1098_3780-108 others(20): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(11): Show |
A | 23 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(20): Show | 23 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.3780-1100_3780-108 others(22): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(13): Show |
A | 53 | a0001c0001t0001g0178a0001c0001t0001g0241a0001c0001t0001g0242others(50): Show | 53 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.3780-1102_3780-108 others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798116
|
AACACACA others(15): Show |
A | 1 | a0010c0019t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3780-1104_3780-108 others(26): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | |||||
| chr22:41798154
|
CACACACA others(11): Show |
C | 1 | a0002c0005t0001g0031 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3780-1098_3780-108 others(22): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798154 | |||||
| chr22:41798162
|
CACACACA others(3): Show |
C | 1 | a0009c0016t0003g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3780-1090_3780-108 others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798162 | |||||
| chr22:41798164
|
CACACACA others(1): Show |
C | 3 | a0002c0005t0001g0026a0002c0005t0001g0027a0002c0005t0001g0028 | 3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3780-1088_3780-108 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798164 | |||||
| chr22:41798168
|
CACAT | C | 3 | a0002c0005t0001g0029a0002c0005t0001g0034a0002c0005t0001g0036 | 3 | HG00408.hp1 HG00423.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.3780-1084_3780-108 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798168 | |||||
| chr22:41798170
|
CAT | C | 3 | a0002c0005t0001g0030a0002c0005t0001g0032a0002c0005t0001g0035 | 3 | HG03704.hp1 NA18994.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3780-1082_3780-108 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798170 | |||||
| chr22:41798172
|
T | C | 2 | a0001c0001t0001g0227a0002c0005t0001g0033 | 2 | NA18965.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3780-1082T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798172 | ||||||
| chr22:41798225
|
G | GCACA | 49 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3780-1010_3780-100 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798225 | |||||
| chr22:41798310
|
C | G | 4 | a0003c0006t0001g0045a0003c0006t0001g0046a0003c0006t0001g0052others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3780-944C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798310 | ||||||
| chr22:41798535
|
G | A | 15 | a0001c0001t0001g0146a0001c0001t0001g0152a0001c0001t0001g0154others(12): Show | 15 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.3780-719G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798535 | ||||||
| chr22:41798557
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.3780-697A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798557 | ||||||
| chr22:41798563
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.3780-691C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798563 | ||||||
| chr22:41798576
|
T | C | 35 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(32): Show | 35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3780-678T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798576 | ||||||
| chr22:41798623
|
AATCCC | A | 4 | a0001c0003t0001g0099a0001c0003t0001g0100a0001c0003t0001g0101others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3780-629_3780-625d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798623 | |||||
| chr22:41798720
|
T | C | 35 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(32): Show | 35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3780-534T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798720 | ||||||
| chr22:41798724
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0132others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.3780-530C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798724 | ||||||
| chr22:41798728
|
C | CA | 6 | a0001c0008t0003g0108a0001c0008t0003g0110a0001c0008t0003g0111others(3): Show | 6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3780-525dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798728 | |||||
| chr22:41798778
|
C | A | 1 | a0001c0017t0001g0200 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3780-476C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798778 | ||||||
| chr22:41798868
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3780-386C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798868 | ||||||
| chr22:41798876
|
C | CA | 11 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0161others(8): Show | 11 | HG00099.hp1 HG00544.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.3780-361dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798876 | |||||
| chr22:41798876
|
C | CAA | 27 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0133others(24): Show | 27 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3780-362_3780-361d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798876 | |||||
| chr22:41798876
|
C | CAAA | 9 | a0001c0001t0001g0136a0001c0001t0001g0199a0001c0001t0001g0250others(6): Show | 9 | HG00408.hp1 HG01943.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.3780-363_3780-361d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798876 | |||||
| chr22:41798958
|
A | G | 49 | a0001c0001t0002g0203a0001c0002t0002g0054a0001c0002t0002g0055others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3780-296A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798958 |