Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 130951 |
|---|---|
| ensemblid | ENSG00000159374.18 |
| hgncid | 25183 |
| symbol | M1AP |
| name | meiosis 1 associated protein |
| refseq_nuc | NM_001321739.2 |
| refseq_prot | NP_001308668.1 |
| ensembl_nuc | ENST00000421985.2 |
| ensembl_prot | ENSP00000414882.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 74557883 |
| end | 74648330 |
| strand | - |
| ver | v1.2 |
| region | chr2:74557883-74648330 |
| region5000 | chr2:74552883-74653330 |
| regionname0 | M1AP_chr2_74557883_74648330 |
| regionname5000 | M1AP_chr2_74552883_74653330 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001 | 1/1 | 530 | 233 | 84 | 43 | 86 | 2 | 16 | 68 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0002 | 0/0 | 530 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0003 | 0/0 | 530 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0004 | 0/0 | 530 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1593 | 221 | 76 | 41 | 84 | 2 | 16 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0002 | 0/0 | 1593 | 8 | 7 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0003 | 0/0 | 1593 | 5 | 0 | 0 | 5 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0004 | 0/0 | 1593 | 3 | 2 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0005 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0006 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0007 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0008 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0009 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0010 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| c0011 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 952 | 79 | 24 | 20 | 25 | 1 | 7 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0002 | 0/0 | 954 | 51 | 10 | 7 | 28 | 1 | 5 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0003 | 0/0 | 952 | 25 | 21 | 0 | 3 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0004 | 0/0 | 955 | 25 | 4 | 5 | 13 | 0 | 3 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0005 | 0/0 | 953 | 22 | 5 | 4 | 13 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0006 | 0/0 | 951 | 20 | 18 | 2 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0007 | 0/0 | 956 | 7 | 1 | 4 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0008 | 0/0 | 952 | 5 | 5 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0009 | 0/0 | 952 | 4 | 0 | 0 | 4 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0010 | 0/0 | 953 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0011 | 0/0 | 953 | 2 | 0 | 0 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0012 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0013 | 0/0 | 953 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0014 | 0/0 | 952 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0015 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| t0016 | 0/0 | 952 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0008 | 0/0 | 1624 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001 | 1/1 | 1593 | 221 | 76 | 41 | 84 | 2 | 16 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0002 | 0/0 | 1593 | 8 | 7 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0007 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0009 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0010 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0011 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0002c0005 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0002c0006 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0003c0003 | 0/0 | 1593 | 5 | 0 | 0 | 5 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0004c0004 | 0/0 | 1593 | 3 | 2 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0008t0002 | 0/0 | 2577 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0001 | 1/1 | 2544 | 76 | 23 | 19 | 24 | 1 | 7 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0002 | 0/0 | 2546 | 47 | 10 | 7 | 24 | 1 | 5 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0003 | 0/0 | 2544 | 16 | 12 | 0 | 3 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0004 | 0/0 | 2547 | 24 | 3 | 5 | 13 | 0 | 3 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0005 | 0/0 | 2545 | 16 | 3 | 3 | 10 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0006 | 0/0 | 2543 | 20 | 18 | 2 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0007 | 0/0 | 2548 | 7 | 1 | 4 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0008 | 0/0 | 2544 | 5 | 5 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0009 | 0/0 | 2544 | 4 | 0 | 0 | 4 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0011 | 0/0 | 2545 | 2 | 0 | 0 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0012 | 0/0 | 2546 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0014 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0015 | 0/0 | 2543 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0001t0016 | 0/0 | 2544 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0002t0001 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0002t0003 | 0/0 | 2544 | 5 | 5 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0002t0004 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0002t0013 | 0/0 | 2545 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0007t0005 | 0/0 | 2545 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0009t0003 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0010t0001 | 0/0 | 2544 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0001c0011t0001 | 0/0 | 2544 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0002c0005t0010 | 0/0 | 2545 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0002c0006t0003 | 0/0 | 2544 | 3 | 3 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0003c0003t0002 | 0/0 | 2546 | 3 | 0 | 0 | 3 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0003c0003t0005 | 0/0 | 2545 | 2 | 0 | 0 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| a0004c0004t0005 | 0/0 | 2545 | 3 | 2 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | copy fasta | chr2 | 74552883 | 74653330 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0008t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0014g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0001t0016g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0002t0013g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0007t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0009t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0010t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0001c0011t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0002c0005t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0002c0005t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0002c0005t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0002c0006t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0002c0006t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0002c0006t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0003c0003t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0003c0003t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0004c0004t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0004c0004t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| a0004c0004t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0125 | EUR | FIN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | CHS | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | CHS | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | CHS | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | CHS | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0211 | EAS | CHS | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00733 | hp1 | a0001 | c0011 | t0001 | g0160 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00735 | hp2 | a0001 | c0001 | t0016 | g0246 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0050 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0120 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01192 | hp2 | a0001 | c0002 | t0013 | g0147 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01243 | hp1 | a0004 | c0004 | t0005 | g0243 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0155 | AMR | PUR | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0028 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0109 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01891 | hp2 | a0002 | c0005 | t0010 | g0032 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0118 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01952 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01952 | hp2 | a0001 | c0001 | t0007 | g0123 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0119 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | CDX | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02257 | hp2 | a0002 | c0006 | t0003 | g0006 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | KHV | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02615 | hp1 | a0001 | c0009 | t0003 | g0039 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0034 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0149 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0150 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0023 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0244 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0146 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0059 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03225 | hp1 | a0002 | c0006 | t0003 | g0005 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03486 | hp1 | a0004 | c0004 | t0005 | g0242 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03516 | hp2 | a0002 | c0005 | t0010 | g0030 | AFR | ESN | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03540 | hp1 | a0004 | c0004 | t0005 | g0029 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | BEB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | BEB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18522 | hp1 | a0001 | c0002 | t0003 | g0145 | AFR | YRI | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | YRI | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | YRI | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | YRI | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18948 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18951 | hp2 | a0001 | c0001 | t0009 | g0206 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18970 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18971 | hp1 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18979 | hp1 | a0001 | c0001 | t0009 | g0158 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18979 | hp2 | a0000 | c0008 | t0002 | g0077 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18981 | hp2 | a0003 | c0003 | t0005 | g0063 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18983 | hp2 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18986 | hp1 | a0001 | c0001 | t0009 | g0164 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18998 | hp1 | a0003 | c0003 | t0005 | g0061 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19070 | hp1 | a0001 | c0007 | t0005 | g0070 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19074 | hp2 | a0001 | c0001 | t0012 | g0131 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19078 | hp2 | a0001 | c0001 | t0014 | g0159 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0239 | AFR | YRI | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ASW | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ASW | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | GIH | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0114 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03471 | hp1 | a0002 | c0005 | t0010 | g0031 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG06807 | hp1 | a0002 | c0006 | t0003 | g0004 | AFR | USA | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | USA | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18955 | hp1 | a0001 | c0010 | t0001 | g0168 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | USA | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0210 | REF | REF | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0231 | REF | REF | M1AP_chr2_74552883_74653330 | M1AP | chr2 | 74552883 | 74653330 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74558799
|
A | AGGCTCTG others(24): Show |
1 | a0000 | 1 | NA18979.hp2 | frameshift_variant | HIGH | c.1479_1509dupCCTGCC others(25): Show |
p.Ser504fs | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 1627/2544 | 1509/1593 | 503/530 | chr2 | 74558799 | ||
| chr2:74607174
|
T | A | 1 | a0003 | 5 | NA18970.hp2 NA18981.hp2 NA18983.hp2 others(2): Show |
missense_variant | MODERATE | c.476A>T | p.Glu159Val | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/11 | 594/2544 | 476/1593 | 159/530 | chr2 | 74607174 | ||
| chr2:74640067
|
T | C | 1 | a0002 | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
missense_variant | MODERATE | c.209A>G | p.Gln70Arg | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/11 | 327/2544 | 209/1593 | 70/530 | chr2 | 74640067 | ||
| chr2:74640262
|
C | T | 1 | a0004 | 3 | HG01243.hp1 HG03486.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.14G>A | p.Arg5Gln | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/11 | 132/2544 | 14/1593 | 5/530 | chr2 | 74640262 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74575531
|
C | T | 1 | a0001c0007 | 1 | NA19070.hp1 | synonymous_variant | LOW | c.981G>A | p.Pro327Pro | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/11 | 1099/2544 | 981/1593 | 327/530 | chr2 | 74575531 | ||
| chr2:74575549
|
T | G | 1 | a0001c0009 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.963A>C | p.Ser321Ser | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/11 | 1081/2544 | 963/1593 | 321/530 | chr2 | 74575549 | ||
| chr2:74576569
|
G | A | 1 | a0001c0010 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.819C>T | p.Leu273Leu | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 6/11 | 937/2544 | 819/1593 | 273/530 | chr2 | 74576569 | ||
| chr2:74615024
|
T | C | 1 | a0001c0011 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.366A>G | p.Gln122Gln | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/11 | 484/2544 | 366/1593 | 122/530 | chr2 | 74615024 | ||
| chr2:74615045
|
T | A | 1 | a0002c0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.345A>T | p.Ala115Ala | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/11 | 463/2544 | 345/1593 | 115/530 | chr2 | 74615045 | ||
| chr2:74640189
|
A | G | 1 | a0001c0002 | 8 | HG01192.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
synonymous_variant | LOW | c.87T>C | p.Ile29Ile | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/11 | 205/2544 | 87/1593 | 29/530 | chr2 | 74640189 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74557918
|
T | TG | 6 | a0001c0001t0005a0001c0001t0011a0001c0002t0013others(3): Show | 25 | HG00741.hp2 HG01106.hp2 HG01192.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*797dupC | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 797 | chr2 | 74557918 | |||||
| chr2:74557918
|
T | TGG | 4 | a0000c0008t0002a0001c0001t0002a0001c0001t0012others(1): Show | 52 | HG00323.hp2 HG00609.hp1 HG00733.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*796_*797dupCC | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 797 | chr2 | 74557918 | |||||
| chr2:74557918
|
T | TGGG | 2 | a0001c0001t0004a0001c0002t0004 | 25 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*797_*798insCCC | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 797 | chr2 | 74557918 | |||||
| chr2:74557918
|
T | TGGGG | 1 | a0001c0001t0007 | 7 | HG01109.hp2 HG01175.hp1 HG01346.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*797_*798insCCCC | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 797 | chr2 | 74557918 | |||||
| chr2:74557920
|
GC | G | 2 | a0001c0001t0006a0001c0001t0015 | 21 | HG01243.hp2 HG01256.hp2 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*795delG | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 795 | chr2 | 74557920 | |||||
| chr2:74557921
|
C | G | 21 | a0000c0008t0002a0001c0001t0002a0001c0001t0003others(18): Show | 144 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*795G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 795 | chr2 | 74557921 | |||||
| chr2:74557926
|
G | GC | 1 | a0002c0005t0010 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*789_*790insG | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 789 | chr2 | 74557926 | |||||
| chr2:74557927
|
G | C | 1 | a0001c0001t0008 | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*789C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 789 | chr2 | 74557927 | |||||
| chr2:74557956
|
G | A | 1 | a0001c0002t0013 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 760 | chr2 | 74557956 | |||||
| chr2:74558096
|
G | A | 1 | a0001c0001t0011 | 2 | NA18971.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*620C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 620 | chr2 | 74558096 | |||||
| chr2:74558231
|
G | A | 1 | a0001c0001t0014 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*485C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 485 | chr2 | 74558231 | |||||
| chr2:74558533
|
G | T | 1 | a0001c0001t0009 | 4 | HG00609.hp2 NA18951.hp2 NA18979.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*183C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 183 | chr2 | 74558533 | |||||
| chr2:74558623
|
C | T | 1 | a0001c0001t0012 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 11/11 | 93 | chr2 | 74558623 | |||||
| chr2:74640301
|
T | C | 1 | a0001c0001t0015 | 1 | HG02965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/11 | chr2 | 74640301 | ||||||
| chr2:74648318
|
C | A | 1 | a0001c0001t0016 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/11 | 8043 | chr2 | 74648318 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74559164
|
A | AT | 6 | a0001c0001t0004g0044a0001c0001t0004g0073a0001c0001t0008g0035others(3): Show | 6 | HG02451.hp2 HG02970.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1435-291dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559164 | ||||||
| chr2:74559164
|
AT | A | 65 | a0001c0001t0002g0049a0001c0001t0002g0052a0001c0001t0002g0054others(62): Show | 65 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1435-291delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559164 | ||||||
| chr2:74559190
|
GCT | G | 6 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(3): Show | 6 | HG01175.hp2 HG01928.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1435-318_1435-317d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559190 | ||||||
| chr2:74559247
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1435-373G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559247 | ||||||
| chr2:74559363
|
T | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1434+335A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559363 | ||||||
| chr2:74559450
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA19055.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1434+248C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559450 | ||||||
| chr2:74559510
|
TTAA | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0245 | 2 | HG01175.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1434+185_1434+187d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559510 | ||||||
| chr2:74559687
|
C | G | 17 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 18 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1434+11G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 10/10 | chr2 | 74559687 | ||||||
| chr2:74559889
|
G | T | 1 | a0001c0001t0002g0098 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1423-180C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 9/10 | chr2 | 74559889 | ||||||
| chr2:74560374
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1282-83C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74560374 | ||||||
| chr2:74560872
|
C | A | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1282-581G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74560872 | ||||||
| chr2:74560930
|
C | T | 1 | a0001c0001t0004g0046 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1282-639G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74560930 | ||||||
| chr2:74561016
|
C | T | 8 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0057others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1282-725G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561016 | ||||||
| chr2:74561029
|
AAGG | A | 17 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 18 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1282-741_1282-739d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561029 | ||||||
| chr2:74561067
|
G | GAGGAGGA others(152): Show |
1 | a0004c0004t0005g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1282-777_1282-776i others(161): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561067 | ||||||
| chr2:74561067
|
G | GAGGAGGA others(167): Show |
1 | a0004c0004t0005g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1282-777_1282-776i others(176): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561067 | ||||||
| chr2:74561076
|
GAGGAGGA others(8): Show |
G | 14 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(11): Show | 15 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-800_1282-786d others(17): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561076 | ||||||
| chr2:74561079
|
GAGGAGGA others(26): Show |
G | 1 | a0001c0001t0004g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1282-821_1282-789d others(35): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561079 | ||||||
| chr2:74561082
|
G | A | 18 | a0001c0001t0006g0019a0001c0001t0006g0025a0001c0001t0006g0026others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1282-791C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561082 | ||||||
| chr2:74561085
|
GAGGAGAA others(5): Show |
G | 1 | a0001c0001t0006g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1282-806_1282-795d others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561085 | ||||||
| chr2:74561088
|
GAGAAGGA others(2): Show |
G | 7 | a0001c0001t0005g0128a0001c0002t0001g0148a0001c0002t0003g0037others(4): Show | 7 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-806_1282-798d others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561088 | ||||||
| chr2:74561088
|
GAGAAGGA others(32): Show |
G | 2 | a0001c0001t0006g0019a0001c0001t0006g0026 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1282-836_1282-798d others(41): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561088 | ||||||
| chr2:74561091
|
A | AAGGAGAA others(8): Show |
3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0002g0076 | 3 | NA18983.hp1 NA19055.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1282-815_1282-801d others(17): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561091 | ||||||
| chr2:74561091
|
A | G | 16 | a0001c0001t0006g0025a0001c0001t0008g0033a0001c0001t0008g0034others(13): Show | 16 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-800T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561091 | ||||||
| chr2:74561091
|
AAGGAGAA others(8): Show |
A | 12 | a0001c0001t0002g0091a0001c0001t0003g0139a0001c0001t0003g0140others(9): Show | 12 | HG01109.hp2 HG01346.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-815_1282-801d others(17): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561091 | ||||||
| chr2:74561091
|
AAGGAGAA others(140): Show |
A | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1282-947_1282-801d others(2): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561091 | ||||||
| chr2:74561097
|
A | AAGGAGGA others(2): Show |
13 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(10): Show | 13 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1282-815_1282-807d others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561097 | ||||||
| chr2:74561097
|
A | G | 2 | a0001c0001t0002g0088a0001c0002t0003g0239 | 2 | NA18971.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1282-806T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561097 | ||||||
| chr2:74561103
|
GAGGAGGA others(44): Show |
G | 1 | a0001c0001t0006g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1282-863_1282-813d others(53): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561103 | ||||||
| chr2:74561106
|
G | A | 10 | a0001c0001t0002g0088a0001c0001t0005g0128a0001c0001t0006g0151others(7): Show | 10 | HG01192.hp2 HG01884.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1282-815C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561106 | ||||||
| chr2:74561112
|
A | AAGG | 7 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1282-824_1282-822d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561112 | ||||||
| chr2:74561118
|
GAGGAGGA others(2): Show |
G | 14 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(11): Show | 15 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-836_1282-828d others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561118 | ||||||
| chr2:74561121
|
G | A | 1 | a0001c0001t0004g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1282-830C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561121 | ||||||
| chr2:74561122
|
A | T | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1282-831T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561122 | ||||||
| chr2:74561135
|
GGAGGAGA others(7): Show |
G | 1 | a0001c0001t0014g0159 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1282-858_1282-845d others(16): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561135 | ||||||
| chr2:74561139
|
G | A | 31 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(28): Show | 32 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1282-848C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561139 | ||||||
| chr2:74561142
|
A | AAGG | 15 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-854_1282-852d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561142 | ||||||
| chr2:74561142
|
A | AAGGAGGA others(8): Show |
1 | a0001c0001t0001g0190 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1282-866_1282-852d others(17): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561142 | ||||||
| chr2:74561142
|
A | AAGGAGGA others(65): Show |
1 | a0001c0001t0005g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1282-852_1282-851i others(74): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561142 | ||||||
| chr2:74561142
|
A | G | 31 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(28): Show | 32 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1282-851T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561142 | ||||||
| chr2:74561142
|
AAGGAGGA others(8): Show |
A | 1 | a0001c0001t0004g0082 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1282-866_1282-852d others(17): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561142 | ||||||
| chr2:74561145
|
GAGGAGGA others(2): Show |
G | 16 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(13): Show | 17 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-863_1282-855d others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561145 | ||||||
| chr2:74561154
|
A | G | 1 | a0001c0001t0005g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1282-863T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561154 | ||||||
| chr2:74561154
|
AAGG | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-866_1282-864d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561154 | ||||||
| chr2:74561157
|
G | A | 1 | a0001c0001t0005g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1282-866C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561157 | ||||||
| chr2:74561184
|
AAGGAGGA others(11): Show |
A | 4 | a0001c0001t0002g0110a0001c0001t0002g0125a0001c0001t0002g0130others(1): Show | 4 | HG00323.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-911_1282-894d others(20): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561184 | ||||||
| chr2:74561187
|
G | GAGGAGGA others(2): Show |
5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282-897_1282-896i others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561187 | ||||||
| chr2:74561199
|
A | G | 6 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1282-908T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561199 | ||||||
| chr2:74561199
|
AAGG | A | 117 | a0000c0008t0002g0077a0001c0001t0001g0153a0001c0001t0002g0002others(114): Show | 119 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1282-911_1282-909d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561199 | ||||||
| chr2:74561202
|
G | A | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282-911C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561202 | ||||||
| chr2:74561202
|
G | GAGGAGGA others(2): Show |
3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1282-912_1282-911i others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561202 | ||||||
| chr2:74561202
|
G | GAGGAGGA others(17): Show |
2 | a0004c0004t0005g0242a0004c0004t0005g0243 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1282-912_1282-911i others(26): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561202 | ||||||
| chr2:74561202
|
G | GAGGAGGA others(32): Show |
3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1282-912_1282-911i others(41): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561202 | ||||||
| chr2:74561202
|
G | GAGGAGGA others(5): Show |
5 | a0001c0001t0002g0075a0001c0001t0002g0108a0001c0001t0002g0116others(2): Show | 5 | HG02040.hp1 HG02071.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1282-912_1282-911i others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561202 | ||||||
| chr2:74561202
|
G | GAGGAGGA others(32): Show |
1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1282-912_1282-911i others(41): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561202 | ||||||
| chr2:74561205
|
GAGGAGGA others(5): Show |
G | 1 | a0001c0001t0012g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1282-926_1282-915d others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561205 | ||||||
| chr2:74561208
|
G | A | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1282-917C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561208 | ||||||
| chr2:74561211
|
G | GAGA | 4 | a0001c0001t0006g0151a0001c0002t0003g0037a0001c0002t0003g0146others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-921_1282-920i others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561211 | ||||||
| chr2:74561214
|
G | A | 10 | a0001c0001t0002g0088a0001c0001t0002g0091a0001c0001t0004g0072others(7): Show | 10 | HG01192.hp2 HG02602.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1282-923C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561214 | ||||||
| chr2:74561217
|
A | G | 16 | a0001c0001t0002g0088a0001c0001t0002g0091a0001c0001t0004g0072others(13): Show | 16 | HG01192.hp2 HG01884.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-926T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561217 | ||||||
| chr2:74561220
|
GAGGAGGA others(5): Show |
G | 28 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(25): Show | 29 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1282-941_1282-930d others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561220 | ||||||
| chr2:74561223
|
G | A | 2 | a0001c0001t0006g0025a0001c0009t0003g0039 | 2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1282-932C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561223 | ||||||
| chr2:74561223
|
GAGGAGGA others(2): Show |
G | 15 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(12): Show | 16 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1282-941_1282-933d others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561223 | ||||||
| chr2:74561226
|
G | A | 4 | a0001c0001t0006g0151a0001c0002t0003g0037a0001c0002t0003g0146others(1): Show | 4 | HG01884.hp1 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-935C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561226 | ||||||
| chr2:74561229
|
G | A | 10 | a0001c0001t0002g0088a0001c0001t0002g0091a0001c0001t0004g0072others(7): Show | 10 | HG01192.hp2 HG02602.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.1282-938C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561229 | ||||||
| chr2:74561232
|
A | AAGG | 12 | a0001c0001t0001g0154a0001c0001t0001g0173a0001c0001t0001g0175others(9): Show | 12 | HG01167.hp1 HG02257.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-944_1282-942d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561232 | ||||||
| chr2:74561232
|
A | AAGGAGGA others(2): Show |
5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1282-950_1282-942d others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561232 | ||||||
| chr2:74561232
|
A | G | 17 | a0001c0001t0002g0088a0001c0001t0002g0091a0001c0001t0004g0072others(14): Show | 17 | HG01192.hp2 HG01884.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1282-941T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561232 | ||||||
| chr2:74561232
|
AAGG | A | 15 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(12): Show | 15 | HG01884.hp2 HG01928.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1282-944_1282-942d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561232 | ||||||
| chr2:74561235
|
G | GAGGAGGA others(20): Show |
3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1282-945_1282-944i others(29): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561235 | ||||||
| chr2:74561411
|
G | T | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1281+806C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561411 | ||||||
| chr2:74561441
|
C | CAGTT | 29 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(26): Show | 30 | HG01243.hp1 HG01256.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1281+775_1281+776i others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561441 | ||||||
| chr2:74561684
|
C | T | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+533G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74561684 | ||||||
| chr2:74562067
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1281+150T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74562067 | ||||||
| chr2:74562103
|
C | T | 7 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+114G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74562103 | ||||||
| chr2:74562121
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1281+96C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74562121 | ||||||
| chr2:74562175
|
T | A | 6 | a0001c0001t0002g0051a0001c0001t0002g0081a0001c0001t0002g0088others(3): Show | 6 | HG02602.hp1 HG02683.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281+42A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 8/10 | chr2 | 74562175 | ||||||
| chr2:74562566
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG01070.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1075-143A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74562566 | ||||||
| chr2:74562573
|
A | T | 173 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(170): Show | 175 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.1075-150T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74562573 | ||||||
| chr2:74562648
|
C | G | 1 | a0001c0001t0001g0173 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1075-225G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74562648 | ||||||
| chr2:74562768
|
G | A | 11 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0057others(8): Show | 11 | HG00323.hp2 HG01261.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1075-345C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74562768 | ||||||
| chr2:74562869
|
T | G | 1 | a0001c0001t0005g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1075-446A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74562869 | ||||||
| chr2:74563033
|
A | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(12): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1075-610T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563033 | ||||||
| chr2:74563144
|
G | C | 1 | a0001c0001t0004g0046 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1075-721C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563144 | ||||||
| chr2:74563249
|
A | T | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1075-826T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563249 | ||||||
| chr2:74563606
|
T | TA | 35 | a0001c0001t0001g0027a0001c0001t0001g0201a0001c0001t0001g0202others(32): Show | 35 | HG00609.hp1 HG00733.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.1075-1184dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563606 | ||||||
| chr2:74563606
|
TA | T | 8 | a0001c0001t0001g0176a0001c0001t0001g0194a0001c0001t0002g0111others(5): Show | 8 | HG02040.hp1 HG02257.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-1184delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563606 | ||||||
| chr2:74563822
|
C | T | 2 | a0004c0004t0005g0242a0004c0004t0005g0243 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1075-1399G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563822 | ||||||
| chr2:74563869
|
C | T | 1 | a0002c0006t0003g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1075-1446G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563869 | ||||||
| chr2:74563956
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1075-1533G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74563956 | ||||||
| chr2:74564146
|
C | T | 1 | a0001c0001t0005g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1075-1723G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74564146 | ||||||
| chr2:74564234
|
G | T | 1 | a0001c0001t0002g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1075-1811C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74564234 | ||||||
| chr2:74564399
|
G | C | 30 | a0001c0001t0002g0049a0001c0001t0002g0108a0001c0001t0002g0110others(27): Show | 30 | HG00438.hp2 HG00558.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1075-1976C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74564399 | ||||||
| chr2:74564424
|
G | C | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1075-2001C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74564424 | ||||||
| chr2:74564612
|
T | A | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1075-2189A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74564612 | ||||||
| chr2:74564668
|
A | C | 2 | a0002c0006t0003g0004a0002c0006t0003g0005 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1075-2245T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74564668 | ||||||
| chr2:74565210
|
G | A | 8 | a0001c0001t0005g0128a0001c0002t0001g0148a0001c0002t0003g0037others(5): Show | 8 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075-2787C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565210 | ||||||
| chr2:74565222
|
C | CA | 16 | a0001c0001t0002g0052a0001c0001t0005g0128a0001c0002t0001g0148others(13): Show | 16 | HG01192.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1075-2800dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565222 | ||||||
| chr2:74565516
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1075-3093G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565516 | ||||||
| chr2:74565588
|
A | T | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1075-3165T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565588 | ||||||
| chr2:74565618
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0174 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1075-3195C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565618 | ||||||
| chr2:74565686
|
G | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1075-3263C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565686 | ||||||
| chr2:74565700
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0186others(1): Show | 4 | HG02040.hp2 HG02523.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-3277C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565700 | ||||||
| chr2:74565825
|
T | TCA | 9 | a0001c0001t0001g0153a0001c0001t0001g0210a0001c0001t0002g0104others(6): Show | 9 | HG01261.hp2 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-3404_1075-340 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
T | TCACA | 27 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0171others(24): Show | 27 | HG00735.hp2 HG01106.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1075-3406_1075-340 others(8): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
T | TCACACA | 35 | a0001c0001t0001g0027a0001c0001t0001g0188a0001c0001t0001g0189others(32): Show | 35 | HG00438.hp1 HG00609.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1075-3408_1075-340 others(10): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
T | TCACACAC others(1): Show |
28 | a0001c0001t0002g0002a0001c0001t0002g0052a0001c0001t0002g0088others(25): Show | 29 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1075-3410_1075-340 others(12): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0002g0121a0001c0001t0005g0068a0001c0001t0005g0079 | 3 | HG02040.hp1 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1075-3412_1075-340 others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
T | TCACACAC others(5): Show |
1 | a0001c0001t0002g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1075-3414_1075-340 others(16): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0002g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1075-3418_1075-340 others(20): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
TCA | T | 62 | a0001c0001t0001g0038a0001c0001t0001g0152a0001c0001t0001g0154others(59): Show | 62 | HG00323.hp1 HG00609.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1075-3404_1075-340 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
TCACA | T | 14 | a0001c0001t0001g0194a0001c0001t0001g0196a0001c0001t0003g0010others(11): Show | 14 | HG01243.hp2 HG01256.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1075-3406_1075-340 others(8): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
TCACACA | T | 23 | a0001c0001t0001g0205a0001c0001t0002g0125a0001c0001t0003g0011others(20): Show | 23 | HG00323.hp2 HG01192.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1075-3408_1075-340 others(10): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
TCACACAC others(1): Show |
T | 5 | a0001c0001t0007g0109a0001c0001t0008g0035a0001c0001t0008g0036others(2): Show | 5 | HG01243.hp1 HG01346.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075-3410_1075-340 others(12): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
TCACACAC others(3): Show |
T | 1 | a0004c0004t0005g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1075-3412_1075-340 others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565825
|
TCACACAC others(5): Show |
T | 2 | a0001c0001t0008g0033a0001c0001t0008g0034 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1075-3414_1075-340 others(16): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565825 | ||||||
| chr2:74565867
|
A | ACAC | 3 | a0001c0001t0001g0182a0003c0003t0002g0064a0003c0003t0005g0061 | 3 | HG06807.hp2 NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1075-3445_1075-344 others(7): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74565867 | ||||||
| chr2:74566310
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1075-3887C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566310 | ||||||
| chr2:74566539
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1075-4116C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566539 | ||||||
| chr2:74566611
|
C | T | 2 | a0004c0004t0005g0242a0004c0004t0005g0243 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1075-4188G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566611 | ||||||
| chr2:74566644
|
C | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1075-4221G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566644 | ||||||
| chr2:74566650
|
A | C | 13 | a0001c0001t0006g0001a0001c0001t0006g0013a0001c0001t0006g0014others(10): Show | 14 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1075-4227T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566650 | ||||||
| chr2:74566652
|
C | G | 1 | a0001c0001t0006g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1075-4229G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566652 | ||||||
| chr2:74566683
|
T | C | 1 | a0001c0001t0002g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1075-4260A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566683 | ||||||
| chr2:74566809
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1075-4386A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566809 | ||||||
| chr2:74566823
|
A | C | 1 | a0001c0001t0003g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1075-4400T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74566823 | ||||||
| chr2:74567010
|
G | A | 1 | a0004c0004t0005g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1075-4587C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74567010 | ||||||
| chr2:74567043
|
C | T | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1075-4620G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74567043 | ||||||
| chr2:74567390
|
A | G | 1 | a0001c0001t0006g0021 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1075-4967T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74567390 | ||||||
| chr2:74567636
|
T | C | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1075-5213A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74567636 | ||||||
| chr2:74568347
|
G | T | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1075-5924C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74568347 | ||||||
| chr2:74568773
|
T | C | 7 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-6350A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74568773 | ||||||
| chr2:74568790
|
G | A | 1 | a0001c0001t0009g0164 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1075-6367C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74568790 | ||||||
| chr2:74568864
|
A | T | 1 | a0001c0001t0001g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1075-6441T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74568864 | ||||||
| chr2:74568980
|
A | G | 17 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 18 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1074+6458T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74568980 | ||||||
| chr2:74569174
|
A | C | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074+6264T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569174 | ||||||
| chr2:74569312
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1074+6126T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569312 | ||||||
| chr2:74569355
|
A | G | 1 | a0001c0001t0007g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1074+6083T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569355 | ||||||
| chr2:74569377
|
C | CT | 17 | a0001c0001t0001g0152a0001c0001t0001g0203a0001c0001t0001g0205others(14): Show | 17 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.1074+6060dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569377 | ||||||
| chr2:74569377
|
CT | C | 5 | a0001c0001t0002g0130a0001c0001t0004g0115a0001c0001t0005g0079others(2): Show | 5 | HG02615.hp1 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074+6060delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569377 | ||||||
| chr2:74569572
|
G | T | 1 | a0001c0001t0006g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1074+5866C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569572 | ||||||
| chr2:74569840
|
T | C | 5 | a0000c0008t0002g0077a0001c0001t0005g0078a0001c0001t0005g0079others(2): Show | 5 | NA18951.hp1 NA18979.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074+5598A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569840 | ||||||
| chr2:74569876
|
T | TTG | 3 | a0001c0001t0004g0107a0001c0001t0004g0118a0001c0001t0007g0106 | 3 | HG01070.hp2 HG01175.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1074+5560_1074+556 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569876 | ||||||
| chr2:74569909
|
C | CGT | 49 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0235others(46): Show | 50 | HG00558.hp2 HG00741.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1074+5527_1074+552 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569909 | ||||||
| chr2:74569909
|
C | CGTGT | 10 | a0001c0001t0002g0135a0001c0001t0003g0011a0001c0001t0003g0126others(7): Show | 10 | HG00438.hp2 HG00558.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.1074+5525_1074+552 others(8): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569909 | ||||||
| chr2:74569909
|
CGTGTGT | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074+5523_1074+552 others(10): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74569909 | ||||||
| chr2:74570136
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1074+5302T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74570136 | ||||||
| chr2:74570245
|
G | A | 25 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(22): Show | 26 | HG01243.hp1 HG01256.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1074+5193C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74570245 | ||||||
| chr2:74570826
|
A | AT | 15 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(12): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1074+4611dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74570826 | ||||||
| chr2:74570905
|
G | T | 6 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+4533C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74570905 | ||||||
| chr2:74570962
|
A | G | 1 | a0001c0001t0003g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1074+4476T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74570962 | ||||||
| chr2:74571041
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1074+4397G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571041 | ||||||
| chr2:74571092
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1074+4346C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571092 | ||||||
| chr2:74571602
|
G | A | 105 | a0000c0008t0002g0077a0001c0001t0002g0002a0001c0001t0002g0047others(102): Show | 106 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1074+3836C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571602 | ||||||
| chr2:74571718
|
C | T | 25 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(22): Show | 26 | HG01243.hp1 HG01256.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1074+3720G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571718 | ||||||
| chr2:74571931
|
G | A | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1074+3507C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571931 | ||||||
| chr2:74571985
|
G | A | 1 | a0001c0001t0003g0142 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1074+3453C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571985 | ||||||
| chr2:74571997
|
C | CA | 13 | a0001c0001t0001g0192a0001c0001t0001g0205a0001c0001t0002g0108others(10): Show | 13 | HG02040.hp1 HG02071.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074+3440dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74571997 | ||||||
| chr2:74572011
|
A | G | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074+3427T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74572011 | ||||||
| chr2:74572338
|
C | G | 1 | a0001c0001t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1074+3100G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74572338 | ||||||
| chr2:74572342
|
C | A | 6 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(3): Show | 6 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+3096G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74572342 | ||||||
| chr2:74572378
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1074+3060A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74572378 | ||||||
| chr2:74572605
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1074+2833C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74572605 | ||||||
| chr2:74572633
|
C | T | 2 | a0001c0001t0006g0019a0001c0001t0006g0026 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1074+2805G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74572633 | ||||||
| chr2:74573142
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1074+2296C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573142 | ||||||
| chr2:74573256
|
A | G | 1 | a0001c0007t0005g0070 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1074+2182T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573256 | ||||||
| chr2:74573496
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1074+1942C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573496 | ||||||
| chr2:74573694
|
G | T | 1 | a0001c0001t0006g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1074+1744C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573694 | ||||||
| chr2:74573766
|
G | T | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1074+1672C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573766 | ||||||
| chr2:74573781
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1074+1657G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573781 | ||||||
| chr2:74573893
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(56): Show | 60 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1074+1545A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74573893 | ||||||
| chr2:74574000
|
C | T | 1 | a0004c0004t0005g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074+1438G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574000 | ||||||
| chr2:74574001
|
G | A | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1074+1437C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574001 | ||||||
| chr2:74574063
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1074+1375G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574063 | ||||||
| chr2:74574097
|
C | T | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074+1341G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574097 | ||||||
| chr2:74574335
|
C | G | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.1074+1103G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574335 | ||||||
| chr2:74574571
|
C | T | 1 | a0001c0001t0005g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1074+867G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574571 | ||||||
| chr2:74574615
|
G | T | 35 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(32): Show | 36 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.1074+823C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574615 | ||||||
| chr2:74574647
|
T | C | 1 | a0001c0001t0004g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1074+791A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74574647 | ||||||
| chr2:74575082
|
T | A | 2 | a0002c0006t0003g0004a0002c0006t0003g0005 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1074+356A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74575082 | ||||||
| chr2:74575090
|
A | G | 173 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(170): Show | 175 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.1074+348T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74575090 | ||||||
| chr2:74575207
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1074+231C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74575207 | ||||||
| chr2:74575401
|
C | T | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1074+37G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 7/10 | chr2 | 74575401 | ||||||
| chr2:74575601
|
C | G | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.933-22G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 6/10 | chr2 | 74575601 | ||||||
| chr2:74575844
|
GT | G | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-266delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 6/10 | chr2 | 74575844 | ||||||
| chr2:74575930
|
G | A | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-351C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 6/10 | chr2 | 74575930 | ||||||
| chr2:74576390
|
G | C | 35 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(32): Show | 36 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.932+66C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 6/10 | chr2 | 74576390 | ||||||
| chr2:74576636
|
T | C | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.770-18A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74576636 | ||||||
| chr2:74576837
|
C | T | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.770-219G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74576837 | ||||||
| chr2:74577348
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.770-730C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74577348 | ||||||
| chr2:74577606
|
C | G | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.770-988G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74577606 | ||||||
| chr2:74577652
|
A | G | 1 | a0001c0001t0006g0022 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.770-1034T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74577652 | ||||||
| chr2:74578036
|
A | G | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.770-1418T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578036 | ||||||
| chr2:74578076
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.770-1458C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578076 | ||||||
| chr2:74578417
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.770-1799G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578417 | ||||||
| chr2:74578476
|
G | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0175a0001c0001t0001g0178others(2): Show | 5 | HG01167.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-1858C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578476 | ||||||
| chr2:74578506
|
G | A | 1 | a0001c0001t0005g0060 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.770-1888C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578506 | ||||||
| chr2:74578612
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.770-1994G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578612 | ||||||
| chr2:74578718
|
A | G | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.770-2100T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578718 | ||||||
| chr2:74578724
|
G | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-2106C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578724 | ||||||
| chr2:74578862
|
A | AT | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.770-2245dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578862 | ||||||
| chr2:74578932
|
C | A | 35 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(32): Show | 36 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.770-2314G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578932 | ||||||
| chr2:74578949
|
G | GTGGT | 39 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(36): Show | 40 | HG00735.hp2 HG00741.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.770-2332_770-2331i others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578949 | ||||||
| chr2:74578999
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.770-2381G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74578999 | ||||||
| chr2:74579766
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.769+1908C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74579766 | ||||||
| chr2:74579769
|
C | T | 5 | a0001c0001t0005g0128a0001c0002t0003g0145a0001c0002t0003g0149others(2): Show | 5 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+1905G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74579769 | ||||||
| chr2:74579782
|
C | CT | 5 | a0001c0001t0002g0110a0001c0001t0002g0124a0001c0001t0004g0082others(2): Show | 5 | HG02155.hp2 NA18968.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+1891dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74579782 | ||||||
| chr2:74579790
|
T | A | 1 | a0001c0001t0002g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.769+1884A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74579790 | ||||||
| chr2:74579790
|
T | C | 1 | a0001c0001t0004g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.769+1884A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74579790 | ||||||
| chr2:74579791
|
A | T | 22 | a0001c0001t0001g0197a0001c0001t0002g0085a0001c0001t0002g0091others(19): Show | 22 | HG01243.hp1 HG01891.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.769+1883T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74579791 | ||||||
| chr2:74580006
|
C | T | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.769+1668G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74580006 | ||||||
| chr2:74580200
|
T | C | 3 | a0001c0001t0002g0108a0001c0001t0002g0116a0001c0001t0002g0121 | 3 | HG02040.hp1 HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.769+1474A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74580200 | ||||||
| chr2:74580297
|
A | T | 1 | a0001c0001t0002g0090 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.769+1377T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74580297 | ||||||
| chr2:74580366
|
A | T | 4 | a0001c0001t0002g0111a0001c0001t0002g0113a0001c0001t0004g0041others(1): Show | 4 | HG00558.hp2 NA18962.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+1308T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74580366 | ||||||
| chr2:74580523
|
C | A | 2 | a0001c0001t0008g0033a0001c0001t0008g0034 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.769+1151G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74580523 | ||||||
| chr2:74580995
|
C | T | 1 | a0002c0005t0010g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.769+679G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74580995 | ||||||
| chr2:74581064
|
C | T | 1 | a0001c0001t0003g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.769+610G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74581064 | ||||||
| chr2:74581424
|
G | A | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+250C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74581424 | ||||||
| chr2:74581606
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.769+68G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 5/10 | chr2 | 74581606 | ||||||
| chr2:74582316
|
C | T | 1 | a0002c0006t0003g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.596-469G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74582316 | ||||||
| chr2:74582690
|
G | C | 1 | a0001c0001t0002g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.596-843C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74582690 | ||||||
| chr2:74582906
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.596-1059T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74582906 | ||||||
| chr2:74583078
|
AAAAC | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-1235_596-1232d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74583078 | ||||||
| chr2:74583488
|
G | A | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-1641C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74583488 | ||||||
| chr2:74584324
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0004g0072 | 2 | HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.596-2477G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584324 | ||||||
| chr2:74584448
|
C | CA | 25 | a0001c0001t0001g0175a0001c0001t0001g0178a0001c0001t0001g0179others(22): Show | 25 | HG00323.hp1 HG00558.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.596-2602dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584448 | ||||||
| chr2:74584466
|
G | A | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.596-2619C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584466 | ||||||
| chr2:74584587
|
G | T | 8 | a0001c0001t0005g0128a0001c0002t0001g0148a0001c0002t0003g0037others(5): Show | 8 | HG01192.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.596-2740C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584587 | ||||||
| chr2:74584745
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.596-2898T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584745 | ||||||
| chr2:74584781
|
C | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-2934G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584781 | ||||||
| chr2:74584805
|
C | CAT | 14 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0193others(11): Show | 14 | HG01070.hp1 HG01106.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.596-2960_596-2959d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584805 | ||||||
| chr2:74584805
|
C | CATAT | 5 | a0001c0001t0001g0152a0001c0001t0006g0151a0002c0005t0010g0030others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-2962_596-2959d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584805 | ||||||
| chr2:74584805
|
C | CATATAT | 8 | a0001c0001t0001g0225a0001c0001t0005g0128a0001c0002t0003g0037others(5): Show | 8 | HG01192.hp2 HG01261.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.596-2964_596-2959d others(8): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584805 | ||||||
| chr2:74584805
|
CAT | C | 121 | a0000c0008t0002g0077a0001c0001t0001g0153a0001c0001t0001g0209others(118): Show | 122 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.596-2960_596-2959d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584805 | ||||||
| chr2:74584805
|
CATAT | C | 5 | a0001c0001t0004g0044a0001c0001t0004g0093a0004c0004t0005g0029others(2): Show | 5 | HG01243.hp1 HG03486.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-2962_596-2959d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584805 | ||||||
| chr2:74584813
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.596-2966A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584813 | ||||||
| chr2:74584828
|
A | T | 1 | a0001c0001t0007g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.596-2981T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584828 | ||||||
| chr2:74584830
|
T | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.596-2983A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584830 | ||||||
| chr2:74584936
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.596-3089C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74584936 | ||||||
| chr2:74585265
|
A | G | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-3418T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585265 | ||||||
| chr2:74585283
|
G | C | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-3436C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585283 | ||||||
| chr2:74585296
|
A | G | 3 | a0001c0001t0009g0158a0001c0001t0009g0206a0001c0001t0009g0211 | 3 | HG00609.hp2 NA18951.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.596-3449T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585296 | ||||||
| chr2:74585354
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.596-3507G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585354 | ||||||
| chr2:74585400
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0130a0001c0002t0004g0150 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.596-3553C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585400 | ||||||
| chr2:74585439
|
G | A | 35 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(32): Show | 36 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.596-3592C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585439 | ||||||
| chr2:74585508
|
G | A | 1 | a0002c0005t0010g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.596-3661C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585508 | ||||||
| chr2:74585738
|
T | C | 29 | a0001c0001t0002g0049a0001c0001t0002g0108a0001c0001t0002g0110others(26): Show | 29 | HG00438.hp2 HG00558.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.596-3891A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585738 | ||||||
| chr2:74585748
|
T | C | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0005g0007others(1): Show | 4 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.596-3901A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585748 | ||||||
| chr2:74585782
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.596-3935A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74585782 | ||||||
| chr2:74586079
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.596-4232A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586079 | ||||||
| chr2:74586489
|
C | T | 36 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(33): Show | 37 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.596-4642G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586489 | ||||||
| chr2:74586673
|
T | C | 1 | a0001c0001t0006g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.596-4826A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586673 | ||||||
| chr2:74586722
|
C | T | 1 | a0001c0001t0001g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.596-4875G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586722 | ||||||
| chr2:74586728
|
C | T | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.596-4881G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586728 | ||||||
| chr2:74586956
|
C | T | 3 | a0001c0001t0006g0013a0001c0001t0006g0014a0001c0001t0006g0015 | 3 | HG02145.hp1 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.596-5109G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586956 | ||||||
| chr2:74586971
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.596-5124A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74586971 | ||||||
| chr2:74587002
|
C | CA | 19 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(16): Show | 20 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.596-5156dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587002 | ||||||
| chr2:74587002
|
CA | C | 7 | a0001c0001t0001g0214a0001c0001t0001g0229a0001c0001t0004g0082others(4): Show | 7 | HG00735.hp2 HG01192.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.596-5156delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587002 | ||||||
| chr2:74587139
|
TTCCTTTT others(15): Show |
T | 1 | a0003c0003t0002g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.596-5314_596-5293d others(24): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587139 | ||||||
| chr2:74587162
|
T | C | 1 | a0003c0003t0002g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.596-5315A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587162 | ||||||
| chr2:74587166
|
C | T | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-5319G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587166 | ||||||
| chr2:74587192
|
C | CT | 12 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-5346dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587192 | ||||||
| chr2:74587466
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.596-5619C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587466 | ||||||
| chr2:74587483
|
C | T | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.596-5636G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587483 | ||||||
| chr2:74587709
|
C | T | 33 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(30): Show | 34 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.596-5862G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587709 | ||||||
| chr2:74587871
|
A | G | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-6024T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587871 | ||||||
| chr2:74587963
|
T | A | 139 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(136): Show | 140 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.596-6116A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587963 | ||||||
| chr2:74587964
|
TA | T | 139 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(136): Show | 140 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.596-6118delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74587964 | ||||||
| chr2:74588242
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.596-6395T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74588242 | ||||||
| chr2:74588362
|
CA | C | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-6516delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74588362 | ||||||
| chr2:74588366
|
A | G | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.596-6519T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74588366 | ||||||
| chr2:74588409
|
C | A | 3 | a0004c0004t0005g0029a0004c0004t0005g0242a0004c0004t0005g0243 | 3 | HG01243.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.596-6562G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74588409 | ||||||
| chr2:74588669
|
G | C | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.596-6822C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74588669 | ||||||
| chr2:74588920
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.596-7073A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74588920 | ||||||
| chr2:74589157
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.596-7310G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74589157 | ||||||
| chr2:74589337
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.596-7490G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74589337 | ||||||
| chr2:74589740
|
A | G | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-7893T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74589740 | ||||||
| chr2:74589762
|
T | C | 1 | a0001c0001t0004g0101 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.596-7915A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74589762 | ||||||
| chr2:74590049
|
G | A | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.596-8202C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74590049 | ||||||
| chr2:74590075
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.596-8228A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74590075 | ||||||
| chr2:74590136
|
C | T | 35 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(32): Show | 36 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.596-8289G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74590136 | ||||||
| chr2:74590185
|
G | A | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.596-8338C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74590185 | ||||||
| chr2:74590277
|
C | T | 11 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0071others(8): Show | 12 | HG00609.hp1 HG02071.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-8430G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74590277 | ||||||
| chr2:74590658
|
C | A | 1 | a0001c0001t0002g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.596-8811G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74590658 | ||||||
| chr2:74591480
|
T | C | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.596-9633A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591480 | ||||||
| chr2:74591668
|
C | G | 1 | a0001c0001t0005g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.596-9821G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591668 | ||||||
| chr2:74591676
|
A | C | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-9829T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591676 | ||||||
| chr2:74591698
|
A | C | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.596-9851T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591698 | ||||||
| chr2:74591746
|
A | C | 3 | a0001c0001t0006g0012a0001c0001t0006g0020a0001c0001t0006g0022 | 3 | HG02895.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.596-9899T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591746 | ||||||
| chr2:74591759
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.596-9912G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591759 | ||||||
| chr2:74591844
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.596-9997C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591844 | ||||||
| chr2:74591974
|
A | T | 1 | a0001c0001t0006g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.596-10127T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74591974 | ||||||
| chr2:74592024
|
G | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.596-10177C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74592024 | ||||||
| chr2:74592318
|
T | C | 5 | a0000c0008t0002g0077a0001c0001t0005g0078a0001c0001t0005g0079others(2): Show | 5 | NA18951.hp1 NA18979.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-10471A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74592318 | ||||||
| chr2:74592455
|
G | T | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.596-10608C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74592455 | ||||||
| chr2:74593313
|
G | T | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.596-11466C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74593313 | ||||||
| chr2:74593433
|
T | C | 5 | a0001c0001t0002g0047a0001c0001t0002g0075a0001c0001t0004g0044others(2): Show | 5 | HG00609.hp1 HG02071.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-11586A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74593433 | ||||||
| chr2:74593754
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.596-11907A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74593754 | ||||||
| chr2:74594098
|
C | A | 23 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(20): Show | 24 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.596-12251G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74594098 | ||||||
| chr2:74594185
|
T | G | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.596-12338A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74594185 | ||||||
| chr2:74594278
|
A | G | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.596-12431T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74594278 | ||||||
| chr2:74594581
|
G | C | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+12474C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74594581 | ||||||
| chr2:74594777
|
G | A | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.595+12278C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74594777 | ||||||
| chr2:74595220
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595+11835C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595220 | ||||||
| chr2:74595254
|
A | G | 106 | a0000c0008t0002g0077a0001c0001t0002g0002a0001c0001t0002g0047others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.595+11801T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595254 | ||||||
| chr2:74595363
|
T | A | 7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | NA18939.hp2 NA18948.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.595+11692A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595363 | ||||||
| chr2:74595509
|
G | C | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.595+11546C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595509 | ||||||
| chr2:74595617
|
G | T | 4 | a0001c0001t0003g0009a0001c0001t0003g0010a0001c0001t0005g0007others(1): Show | 4 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.595+11438C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595617 | ||||||
| chr2:74595765
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.595+11290T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595765 | ||||||
| chr2:74595772
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.595+11283C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595772 | ||||||
| chr2:74595941
|
A | G | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+11114T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74595941 | ||||||
| chr2:74596042
|
A | G | 1 | a0001c0001t0005g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.595+11013T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596042 | ||||||
| chr2:74596126
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(38): Show | 42 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.595+10929A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596126 | ||||||
| chr2:74596245
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.595+10810T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596245 | ||||||
| chr2:74596292
|
C | A | 1 | a0001c0001t0002g0047 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.595+10763G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596292 | ||||||
| chr2:74596332
|
C | T | 2 | a0001c0001t0006g0025a0001c0001t0006g0028 | 2 | HG01256.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.595+10723G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596332 | ||||||
| chr2:74596356
|
G | C | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.595+10699C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596356 | ||||||
| chr2:74596434
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.595+10621A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596434 | ||||||
| chr2:74596586
|
G | GAAC | 50 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(47): Show | 52 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.595+10466_595+1046 others(7): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596586 | ||||||
| chr2:74596586
|
G | GAACAAC | 2 | a0001c0001t0002g0233a0001c0001t0014g0159 | 2 | NA19078.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.595+10463_595+1046 others(10): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596586 | ||||||
| chr2:74596586
|
GAACAAC | G | 2 | a0001c0001t0002g0104a0004c0004t0005g0029 | 2 | HG01261.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.595+10463_595+1046 others(10): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596586 | ||||||
| chr2:74596623
|
T | C | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.595+10432A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596623 | ||||||
| chr2:74596803
|
C | T | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.595+10252G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596803 | ||||||
| chr2:74596806
|
A | G | 1 | a0001c0001t0007g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.595+10249T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596806 | ||||||
| chr2:74596897
|
C | T | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+10158G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596897 | ||||||
| chr2:74596937
|
G | A | 36 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0051others(33): Show | 37 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.595+10118C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74596937 | ||||||
| chr2:74597033
|
T | C | 23 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(20): Show | 24 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.595+10022A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597033 | ||||||
| chr2:74597064
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0225 | 2 | HG01167.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.595+9991G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597064 | ||||||
| chr2:74597272
|
C | T | 1 | a0001c0001t0001g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.595+9783G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597272 | ||||||
| chr2:74597471
|
A | C | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.595+9584T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597471 | ||||||
| chr2:74597737
|
A | G | 4 | a0001c0001t0002g0127a0001c0001t0002g0130a0001c0001t0004g0048others(1): Show | 4 | HG02630.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+9318T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597737 | ||||||
| chr2:74597760
|
C | T | 1 | a0001c0001t0008g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.595+9295G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597760 | ||||||
| chr2:74597843
|
A | G | 174 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(171): Show | 176 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.595+9212T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74597843 | ||||||
| chr2:74598024
|
T | C | 104 | a0000c0008t0002g0077a0001c0001t0002g0002a0001c0001t0002g0047others(101): Show | 105 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.595+9031A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598024 | ||||||
| chr2:74598052
|
C | T | 1 | a0001c0001t0007g0109 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.595+9003G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598052 | ||||||
| chr2:74598075
|
T | C | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.595+8980A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598075 | ||||||
| chr2:74598121
|
C | T | 3 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0241 | 3 | HG02622.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.595+8934G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598121 | ||||||
| chr2:74598222
|
A | G | 6 | a0001c0001t0006g0001a0001c0001t0006g0016a0001c0001t0006g0017others(3): Show | 7 | HG02109.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.595+8833T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598222 | ||||||
| chr2:74598292
|
G | A | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.595+8763C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598292 | ||||||
| chr2:74598339
|
G | A | 101 | a0000c0008t0002g0077a0001c0001t0002g0002a0001c0001t0002g0047others(98): Show | 102 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.595+8716C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598339 | ||||||
| chr2:74598381
|
C | CAATA | 47 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0057others(44): Show | 47 | HG00323.hp2 HG00558.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.595+8670_595+8673d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598381 | ||||||
| chr2:74598381
|
C | CAATAAAT others(1): Show |
14 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(11): Show | 14 | HG00741.hp2 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.595+8666_595+8673d others(10): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598381 | ||||||
| chr2:74598381
|
C | CAATAAAT others(5): Show |
5 | a0001c0001t0006g0013a0001c0001t0006g0014a0001c0001t0006g0016others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+8662_595+8673d others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598381 | ||||||
| chr2:74598381
|
C | CAATAAAT others(9): Show |
10 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0015others(7): Show | 11 | HG02258.hp1 HG02615.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.595+8658_595+8673d others(18): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598381 | ||||||
| chr2:74598621
|
CT | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0153a0001c0001t0001g0188others(9): Show | 12 | HG00735.hp2 HG01106.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.595+8433delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598621 | ||||||
| chr2:74598621
|
CTT | C | 132 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0154others(129): Show | 133 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.595+8432_595+8433d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598621 | ||||||
| chr2:74598621
|
CTTT | C | 27 | a0001c0001t0003g0011a0001c0001t0004g0044a0001c0001t0004g0053others(24): Show | 28 | HG01243.hp1 HG01256.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.595+8431_595+8433d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598621 | ||||||
| chr2:74598621
|
CTTTT | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+8430_595+8433d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74598621 | ||||||
| chr2:74599043
|
C | T | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.595+8012G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599043 | ||||||
| chr2:74599089
|
C | T | 17 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(14): Show | 18 | HG01256.hp2 HG02109.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.595+7966G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599089 | ||||||
| chr2:74599276
|
A | G | 3 | a0001c0001t0006g0012a0001c0001t0006g0020a0001c0001t0006g0022 | 3 | HG02895.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.595+7779T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599276 | ||||||
| chr2:74599578
|
G | A | 17 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(14): Show | 17 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.595+7477C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599578 | ||||||
| chr2:74599720
|
A | T | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.595+7335T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599720 | ||||||
| chr2:74599759
|
C | A | 40 | a0001c0001t0001g0188a0001c0001t0002g0047a0001c0001t0002g0075others(37): Show | 41 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.595+7296G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599759 | ||||||
| chr2:74599769
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0003g0009 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.595+7274_595+7285d others(14): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599769 | ||||||
| chr2:74599832
|
A | AT | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.595+7222dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599832 | ||||||
| chr2:74599863
|
T | C | 1 | a0003c0003t0002g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.595+7192A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599863 | ||||||
| chr2:74599953
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.595+7102C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74599953 | ||||||
| chr2:74600327
|
C | T | 39 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(36): Show | 40 | HG00735.hp2 HG00741.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.595+6728G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600327 | ||||||
| chr2:74600368
|
T | C | 1 | a0001c0007t0005g0070 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.595+6687A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600368 | ||||||
| chr2:74600543
|
G | T | 1 | a0001c0001t0005g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.595+6512C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600543 | ||||||
| chr2:74600572
|
A | G | 32 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(29): Show | 32 | HG01070.hp1 HG01433.hp1 HG01981.hp2 others(29): Show |
intron_variant | MODIFIER | c.595+6483T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600572 | ||||||
| chr2:74600590
|
G | A | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.595+6465C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600590 | ||||||
| chr2:74600643
|
G | C | 2 | a0001c0001t0006g0019a0001c0001t0006g0026 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.595+6412C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600643 | ||||||
| chr2:74600657
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.595+6398A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600657 | ||||||
| chr2:74600733
|
T | C | 2 | a0001c0001t0008g0035a0001c0001t0008g0036 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.595+6322A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600733 | ||||||
| chr2:74600905
|
G | C | 1 | a0001c0001t0011g0066 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.595+6150C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74600905 | ||||||
| chr2:74601106
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.595+5949T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74601106 | ||||||
| chr2:74601156
|
A | C | 5 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(2): Show | 5 | HG00558.hp2 NA18962.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+5899T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74601156 | ||||||
| chr2:74601473
|
T | C | 24 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(21): Show | 25 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.595+5582A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74601473 | ||||||
| chr2:74601610
|
C | T | 1 | a0001c0001t0004g0101 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.595+5445G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74601610 | ||||||
| chr2:74601899
|
A | T | 1 | a0001c0001t0003g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.595+5156T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74601899 | ||||||
| chr2:74602442
|
A | G | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.595+4613T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74602442 | ||||||
| chr2:74602596
|
C | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.595+4459G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74602596 | ||||||
| chr2:74602670
|
C | A | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.595+4385G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74602670 | ||||||
| chr2:74602816
|
T | C | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+4239A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74602816 | ||||||
| chr2:74602882
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595+4173T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74602882 | ||||||
| chr2:74602986
|
A | G | 1 | a0001c0001t0006g0012 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.595+4069T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74602986 | ||||||
| chr2:74603138
|
C | T | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+3917G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74603138 | ||||||
| chr2:74603326
|
C | A | 7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | NA18939.hp2 NA18948.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.595+3729G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74603326 | ||||||
| chr2:74603881
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.595+3174T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74603881 | ||||||
| chr2:74603910
|
G | A | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.595+3145C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74603910 | ||||||
| chr2:74604143
|
C | T | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+2912G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604143 | ||||||
| chr2:74604182
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.595+2873G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604182 | ||||||
| chr2:74604283
|
C | T | 1 | a0001c0001t0005g0079 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.595+2772G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604283 | ||||||
| chr2:74604305
|
A | C | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.595+2750T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604305 | ||||||
| chr2:74604400
|
T | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+2655A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604400 | ||||||
| chr2:74604721
|
T | C | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.595+2334A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604721 | ||||||
| chr2:74604916
|
G | T | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.595+2139C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604916 | ||||||
| chr2:74604934
|
G | A | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.595+2121C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74604934 | ||||||
| chr2:74605004
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.595+2051G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605004 | ||||||
| chr2:74605067
|
G | A | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.595+1988C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605067 | ||||||
| chr2:74605120
|
C | T | 1 | a0004c0004t0005g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.595+1935G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605120 | ||||||
| chr2:74605229
|
T | C | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01109.hp1 HG01167.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.595+1826A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605229 | ||||||
| chr2:74605452
|
A | G | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.595+1603T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605452 | ||||||
| chr2:74605533
|
A | G | 1 | a0001c0001t0004g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.595+1522T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605533 | ||||||
| chr2:74605557
|
G | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.595+1498C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605557 | ||||||
| chr2:74605716
|
C | T | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.595+1339G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605716 | ||||||
| chr2:74605848
|
C | G | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.595+1207G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605848 | ||||||
| chr2:74605858
|
G | A | 1 | a0001c0001t0005g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.595+1197C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605858 | ||||||
| chr2:74605900
|
C | CA | 16 | a0001c0001t0003g0011a0001c0001t0005g0236a0001c0001t0006g0001others(13): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.595+1154dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605900 | ||||||
| chr2:74605900
|
CA | C | 5 | a0001c0001t0002g0125a0001c0002t0003g0146a0002c0006t0003g0004others(2): Show | 5 | HG00323.hp2 HG02257.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.595+1154delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74605900 | ||||||
| chr2:74606061
|
A | G | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.595+994T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74606061 | ||||||
| chr2:74606382
|
T | C | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.595+673A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74606382 | ||||||
| chr2:74606601
|
C | CAT | 5 | a0001c0001t0006g0003a0001c0009t0003g0039a0002c0005t0010g0030others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+452_595+453dup others(2): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74606601 | ||||||
| chr2:74606601
|
C | CATAT | 4 | a0001c0001t0009g0158a0001c0001t0009g0164a0001c0001t0009g0206others(1): Show | 4 | HG00609.hp2 NA18951.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+450_595+453dup others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74606601 | ||||||
| chr2:74606630
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0130a0001c0002t0004g0150 | 3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.595+425C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74606630 | ||||||
| chr2:74607045
|
A | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.595+10T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 4/10 | chr2 | 74607045 | ||||||
| chr2:74607568
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.427-345C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607568 | ||||||
| chr2:74607577
|
G | A | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.427-354C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607577 | ||||||
| chr2:74607632
|
C | A | 2 | a0002c0006t0003g0004a0002c0006t0003g0005 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.427-409G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607632 | ||||||
| chr2:74607727
|
G | A | 23 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(20): Show | 24 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.427-504C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607727 | ||||||
| chr2:74607735
|
G | A | 1 | a0001c0001t0005g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.427-512C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607735 | ||||||
| chr2:74607735
|
G | C | 6 | a0001c0001t0006g0001a0001c0001t0006g0016a0001c0001t0006g0017others(3): Show | 7 | HG02109.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.427-512C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607735 | ||||||
| chr2:74607754
|
G | GT | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0193others(2): Show | 5 | NA19007.hp1 NA19011.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-532dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607754 | ||||||
| chr2:74607932
|
A | AT | 5 | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 5 | HG02083.hp1 HG02135.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-710dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74607932 | ||||||
| chr2:74608010
|
T | C | 1 | a0001c0001t0009g0164 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.427-787A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608010 | ||||||
| chr2:74608016
|
T | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-793A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608016 | ||||||
| chr2:74608085
|
AATCACCC others(4): Show |
A | 15 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(12): Show | 16 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.427-873_427-863del others(11): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608085 | ||||||
| chr2:74608286
|
A | G | 2 | a0001c0001t0003g0096a0004c0004t0005g0029 | 2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.427-1063T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608286 | ||||||
| chr2:74608322
|
T | C | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-1099A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608322 | ||||||
| chr2:74608406
|
A | G | 177 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(174): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.427-1183T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608406 | ||||||
| chr2:74608480
|
T | G | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.427-1257A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608480 | ||||||
| chr2:74608526
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.427-1303G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608526 | ||||||
| chr2:74608555
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.427-1332G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74608555 | ||||||
| chr2:74609143
|
G | A | 175 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(172): Show | 177 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.427-1920C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609143 | ||||||
| chr2:74609215
|
C | CTCAG | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.427-1993_427-1992i others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609215 | ||||||
| chr2:74609218
|
C | G | 1 | a0001c0001t0004g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.427-1995G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609218 | ||||||
| chr2:74609218
|
C | T | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.427-1995G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609218 | ||||||
| chr2:74609219
|
C | CTGA | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.427-1997_427-1996i others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609219 | ||||||
| chr2:74609222
|
T | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.427-1999A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609222 | ||||||
| chr2:74609312
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.427-2089G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609312 | ||||||
| chr2:74609397
|
T | C | 30 | a0001c0001t0002g0049a0001c0001t0002g0108a0001c0001t0002g0110others(27): Show | 30 | HG00438.hp2 HG00558.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.427-2174A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609397 | ||||||
| chr2:74609398
|
C | T | 1 | a0001c0001t0002g0137 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.427-2175G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609398 | ||||||
| chr2:74609466
|
A | C | 1 | a0001c0001t0004g0072 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.427-2243T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609466 | ||||||
| chr2:74609528
|
A | G | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.427-2305T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609528 | ||||||
| chr2:74609571
|
A | G | 2 | a0001c0001t0008g0035a0001c0001t0008g0036 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.427-2348T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609571 | ||||||
| chr2:74609788
|
G | T | 2 | a0001c0001t0005g0128a0001c0002t0003g0149 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.427-2565C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609788 | ||||||
| chr2:74609932
|
G | A | 1 | a0001c0001t0002g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.427-2709C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74609932 | ||||||
| chr2:74610004
|
A | AT | 22 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(19): Show | 22 | HG00609.hp1 HG01109.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.427-2782dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610004 | ||||||
| chr2:74610140
|
C | G | 53 | a0001c0001t0001g0161a0001c0001t0001g0237a0001c0001t0002g0002others(50): Show | 54 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.427-2917G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610140 | ||||||
| chr2:74610152
|
C | T | 1 | a0001c0001t0004g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.427-2929G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610152 | ||||||
| chr2:74610176
|
A | AT | 30 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(27): Show | 31 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.427-2954dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610176 | ||||||
| chr2:74610176
|
A | ATT | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.427-2955_427-2954d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610176 | ||||||
| chr2:74610324
|
A | T | 1 | a0001c0001t0002g0089 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.427-3101T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610324 | ||||||
| chr2:74610404
|
T | G | 1 | a0001c0001t0006g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.427-3181A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610404 | ||||||
| chr2:74610441
|
G | A | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.427-3218C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610441 | ||||||
| chr2:74610593
|
T | C | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.427-3370A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74610593 | ||||||
| chr2:74611015
|
A | C | 1 | a0001c0007t0005g0070 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.427-3792T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611015 | ||||||
| chr2:74611160
|
C | T | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.426+3804G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611160 | ||||||
| chr2:74611249
|
T | C | 2 | a0001c0001t0011g0065a0001c0001t0011g0066 | 2 | NA18971.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.426+3715A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611249 | ||||||
| chr2:74611297
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.426+3667T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611297 | ||||||
| chr2:74611321
|
C | T | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.426+3643G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611321 | ||||||
| chr2:74611658
|
C | T | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.426+3306G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611658 | ||||||
| chr2:74611691
|
G | C | 1 | a0001c0001t0006g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.426+3273C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611691 | ||||||
| chr2:74611792
|
A | G | 3 | a0004c0004t0005g0029a0004c0004t0005g0242a0004c0004t0005g0243 | 3 | HG01243.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.426+3172T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611792 | ||||||
| chr2:74611819
|
C | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | NA19007.hp1 NA19011.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.426+3145G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611819 | ||||||
| chr2:74611882
|
G | GT | 41 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(38): Show | 41 | HG00323.hp2 HG00558.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.426+3081dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611882 | ||||||
| chr2:74611882
|
G | GTT | 117 | a0000c0008t0002g0077a0001c0001t0001g0027a0001c0001t0001g0161others(114): Show | 119 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.426+3080_426+3081d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611882 | ||||||
| chr2:74611882
|
G | GTTT | 65 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0171others(62): Show | 65 | HG00438.hp1 HG00609.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.426+3079_426+3081d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611882 | ||||||
| chr2:74611882
|
G | GTTTT | 10 | a0001c0001t0001g0038a0001c0001t0001g0193a0001c0001t0001g0201others(7): Show | 10 | HG01884.hp1 HG01952.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.426+3078_426+3081d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74611882 | ||||||
| chr2:74612062
|
T | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+2902A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612062 | ||||||
| chr2:74612096
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.426+2868C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612096 | ||||||
| chr2:74612180
|
T | C | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.426+2784A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612180 | ||||||
| chr2:74612284
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0104 | 2 | HG01261.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.426+2680A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612284 | ||||||
| chr2:74612458
|
A | G | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.426+2506T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612458 | ||||||
| chr2:74612591
|
T | C | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.426+2373A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612591 | ||||||
| chr2:74612625
|
TTTC | T | 3 | a0004c0004t0005g0029a0004c0004t0005g0242a0004c0004t0005g0243 | 3 | HG01243.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.426+2336_426+2338d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612625 | ||||||
| chr2:74612705
|
A | G | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.426+2259T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612705 | ||||||
| chr2:74612920
|
G | T | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.426+2044C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612920 | ||||||
| chr2:74612966
|
T | A | 2 | a0002c0006t0003g0004a0002c0006t0003g0005 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.426+1998A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612966 | ||||||
| chr2:74612977
|
G | GT | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.426+1986dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74612977 | ||||||
| chr2:74613103
|
A | T | 3 | a0001c0001t0001g0196a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01070.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.426+1861T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613103 | ||||||
| chr2:74613233
|
C | G | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.426+1731G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613233 | ||||||
| chr2:74613267
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.426+1697G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613267 | ||||||
| chr2:74613392
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.426+1572A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613392 | ||||||
| chr2:74613420
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.426+1544C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613420 | ||||||
| chr2:74613459
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.426+1505A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613459 | ||||||
| chr2:74613545
|
A | AT | 164 | a0000c0008t0002g0077a0001c0001t0001g0161a0001c0001t0001g0237others(161): Show | 166 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.426+1418dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613545 | ||||||
| chr2:74613561
|
T | C | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.426+1403A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613561 | ||||||
| chr2:74613750
|
T | G | 1 | a0001c0001t0003g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.426+1214A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613750 | ||||||
| chr2:74613788
|
G | A | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.426+1176C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613788 | ||||||
| chr2:74613825
|
A | G | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+1139T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613825 | ||||||
| chr2:74613902
|
C | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.426+1062G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613902 | ||||||
| chr2:74613939
|
C | T | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+1025G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74613939 | ||||||
| chr2:74614072
|
G | A | 1 | a0001c0001t0004g0042 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.426+892C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74614072 | ||||||
| chr2:74614152
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.426+812A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74614152 | ||||||
| chr2:74614442
|
C | T | 63 | a0000c0008t0002g0077a0001c0001t0001g0234a0001c0001t0001g0237others(60): Show | 64 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.426+522G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 3/10 | chr2 | 74614442 | ||||||
| chr2:74615312
|
C | T | 1 | a0002c0005t0010g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.241-163G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615312 | ||||||
| chr2:74615336
|
A | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0221 | 2 | HG01928.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.241-187T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615336 | ||||||
| chr2:74615422
|
A | C | 33 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(30): Show | 34 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.241-273T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615422 | ||||||
| chr2:74615435
|
T | C | 3 | a0004c0004t0005g0029a0004c0004t0005g0242a0004c0004t0005g0243 | 3 | HG01243.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.241-286A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615435 | ||||||
| chr2:74615454
|
TA | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.241-306delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615454 | ||||||
| chr2:74615540
|
G | A | 1 | a0001c0001t0012g0131 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.241-391C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615540 | ||||||
| chr2:74615612
|
C | T | 1 | a0002c0006t0003g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.241-463G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615612 | ||||||
| chr2:74615668
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.241-519T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615668 | ||||||
| chr2:74615774
|
A | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-625T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615774 | ||||||
| chr2:74615802
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.241-653G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74615802 | ||||||
| chr2:74616029
|
C | T | 1 | a0001c0002t0003g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.241-880G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74616029 | ||||||
| chr2:74616082
|
G | A | 1 | a0001c0001t0001g0210 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.241-933C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74616082 | ||||||
| chr2:74616321
|
C | G | 38 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(35): Show | 39 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-1172G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74616321 | ||||||
| chr2:74616419
|
T | C | 1 | a0001c0011t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.241-1270A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74616419 | ||||||
| chr2:74616881
|
A | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-1732T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74616881 | ||||||
| chr2:74617115
|
C | A | 1 | a0001c0001t0006g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.241-1966G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74617115 | ||||||
| chr2:74617235
|
G | T | 1 | a0001c0001t0006g0016 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.241-2086C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74617235 | ||||||
| chr2:74617379
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.241-2230G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74617379 | ||||||
| chr2:74617532
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.241-2383C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74617532 | ||||||
| chr2:74617696
|
AT | A | 3 | a0001c0001t0008g0035a0001c0001t0008g0036a0001c0001t0008g0244 | 3 | HG02451.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.241-2548delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74617696 | ||||||
| chr2:74618360
|
C | T | 1 | a0001c0002t0003g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.241-3211G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74618360 | ||||||
| chr2:74618754
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.241-3605A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74618754 | ||||||
| chr2:74618813
|
T | C | 24 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(21): Show | 25 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.241-3664A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74618813 | ||||||
| chr2:74619014
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.241-3865G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74619014 | ||||||
| chr2:74619119
|
C | T | 4 | a0001c0001t0001g0234a0001c0001t0002g0002a0001c0001t0002g0233others(1): Show | 5 | NA18986.hp2 NA19078.hp1 NA19078.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-3970G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74619119 | ||||||
| chr2:74619403
|
T | A | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-4254A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74619403 | ||||||
| chr2:74619468
|
C | T | 1 | a0002c0005t0010g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.241-4319G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74619468 | ||||||
| chr2:74619579
|
T | C | 1 | a0004c0004t0005g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.241-4430A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74619579 | ||||||
| chr2:74620003
|
C | T | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-4854G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620003 | ||||||
| chr2:74620180
|
G | T | 1 | a0001c0002t0003g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.241-5031C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620180 | ||||||
| chr2:74620251
|
T | C | 1 | a0001c0001t0009g0211 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.241-5102A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620251 | ||||||
| chr2:74620328
|
A | G | 55 | a0000c0008t0002g0077a0001c0001t0002g0049a0001c0001t0002g0052others(52): Show | 55 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.241-5179T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620328 | ||||||
| chr2:74620532
|
T | C | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.241-5383A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620532 | ||||||
| chr2:74620618
|
T | C | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.241-5469A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620618 | ||||||
| chr2:74620670
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.241-5521C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620670 | ||||||
| chr2:74620688
|
A | G | 33 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(30): Show | 34 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.241-5539T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620688 | ||||||
| chr2:74620746
|
T | C | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-5597A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74620746 | ||||||
| chr2:74621060
|
A | G | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-5911T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621060 | ||||||
| chr2:74621209
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.241-6060C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621209 | ||||||
| chr2:74621374
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.241-6225C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621374 | ||||||
| chr2:74621576
|
G | C | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.241-6427C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621576 | ||||||
| chr2:74621674
|
T | A | 3 | a0001c0001t0002g0097a0001c0001t0002g0098a0001c0001t0003g0096 | 3 | HG01123.hp2 HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.241-6525A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621674 | ||||||
| chr2:74621855
|
C | T | 7 | a0000c0008t0002g0077a0001c0001t0005g0040a0001c0001t0005g0078others(4): Show | 7 | HG02135.hp1 NA18948.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-6706G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621855 | ||||||
| chr2:74621945
|
T | TA | 22 | a0001c0001t0001g0165a0001c0001t0001g0217a0001c0001t0001g0225others(19): Show | 22 | HG00323.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.241-6797dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74621945 | ||||||
| chr2:74622019
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0216 | 2 | HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.241-6870G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622019 | ||||||
| chr2:74622302
|
C | G | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.241-7153G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622302 | ||||||
| chr2:74622543
|
C | CT | 21 | a0001c0001t0001g0027a0001c0001t0001g0172a0001c0001t0001g0173others(18): Show | 21 | HG01167.hp1 HG01167.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.241-7395dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622543 | ||||||
| chr2:74622543
|
C | CTTT | 7 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0005g0007others(4): Show | 7 | HG00741.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-7397_241-7395d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622543 | ||||||
| chr2:74622543
|
C | CTTTT | 19 | a0001c0001t0003g0011a0001c0001t0006g0001a0001c0001t0006g0012others(16): Show | 20 | HG01243.hp1 HG01256.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.241-7398_241-7395d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622543 | ||||||
| chr2:74622543
|
CT | C | 98 | a0000c0008t0002g0077a0001c0001t0001g0170a0001c0001t0001g0195others(95): Show | 99 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.241-7395delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622543 | ||||||
| chr2:74622648
|
G | GATAT | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-7503_241-7500d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622648 | ||||||
| chr2:74622826
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.241-7677G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622826 | ||||||
| chr2:74622908
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.241-7759G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622908 | ||||||
| chr2:74622957
|
G | GA | 35 | a0001c0001t0001g0038a0001c0001t0001g0196a0001c0001t0001g0216others(32): Show | 36 | HG00741.hp2 HG01175.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.241-7809dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622957 | ||||||
| chr2:74622970
|
C | A | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.241-7821G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74622970 | ||||||
| chr2:74623329
|
C | G | 1 | a0001c0001t0005g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.241-8180G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623329 | ||||||
| chr2:74623427
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG01175.hp2 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-8278G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623427 | ||||||
| chr2:74623522
|
A | G | 2 | a0004c0004t0005g0242a0004c0004t0005g0243 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.241-8373T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623522 | ||||||
| chr2:74623604
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.241-8455T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623604 | ||||||
| chr2:74623698
|
G | T | 1 | a0001c0001t0006g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.241-8549C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623698 | ||||||
| chr2:74623703
|
G | C | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.241-8554C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623703 | ||||||
| chr2:74623930
|
C | T | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-8781G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74623930 | ||||||
| chr2:74624016
|
G | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0212a0001c0001t0001g0213 | 3 | HG01070.hp1 HG01433.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.241-8867C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74624016 | ||||||
| chr2:74624051
|
C | A | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-8902G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74624051 | ||||||
| chr2:74624241
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.241-9092C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74624241 | ||||||
| chr2:74624712
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.241-9563G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74624712 | ||||||
| chr2:74625035
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.241-9886C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74625035 | ||||||
| chr2:74625434
|
T | A | 5 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-10285A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74625434 | ||||||
| chr2:74625512
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.241-10363T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74625512 | ||||||
| chr2:74625517
|
T | C | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.241-10368A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74625517 | ||||||
| chr2:74625599
|
C | A | 1 | a0002c0006t0003g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.241-10450G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74625599 | ||||||
| chr2:74625908
|
T | C | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.241-10759A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74625908 | ||||||
| chr2:74626038
|
G | A | 1 | a0001c0001t0006g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.241-10889C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626038 | ||||||
| chr2:74626192
|
T | C | 1 | a0001c0001t0004g0101 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.241-11043A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626192 | ||||||
| chr2:74626252
|
T | A | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-11103A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626252 | ||||||
| chr2:74626256
|
A | AT | 5 | a0001c0001t0008g0035a0001c0001t0008g0036a0001c0001t0008g0244others(2): Show | 5 | HG02451.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-11108_241-1110 others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626256 | ||||||
| chr2:74626256
|
A | ATT | 9 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(6): Show | 9 | HG00741.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.241-11108_241-1110 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626256 | ||||||
| chr2:74626256
|
A | ATTT | 17 | a0001c0001t0003g0011a0001c0001t0006g0001a0001c0001t0006g0012others(14): Show | 18 | HG01243.hp2 HG01256.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-11108_241-1110 others(7): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626256 | ||||||
| chr2:74626257
|
G | GT | 18 | a0001c0001t0001g0153a0001c0001t0001g0177a0001c0001t0001g0196others(15): Show | 18 | HG01167.hp2 HG01175.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.241-11109dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626257 | ||||||
| chr2:74626257
|
G | GTT | 10 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0172others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.241-11110_241-1110 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626257 | ||||||
| chr2:74626257
|
G | T | 34 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(31): Show | 35 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.241-11108C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626257 | ||||||
| chr2:74626257
|
GT | G | 8 | a0001c0001t0001g0189a0001c0001t0002g0058a0001c0001t0005g0043others(5): Show | 8 | HG00735.hp2 HG01952.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-11109delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626257 | ||||||
| chr2:74626398
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.241-11249G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626398 | ||||||
| chr2:74626521
|
A | C | 1 | a0002c0006t0003g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.241-11372T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626521 | ||||||
| chr2:74626523
|
T | G | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-11374A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626523 | ||||||
| chr2:74626872
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.241-11723C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74626872 | ||||||
| chr2:74627167
|
A | C | 2 | a0001c0001t0004g0107a0001c0001t0007g0106 | 2 | HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.241-12018T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627167 | ||||||
| chr2:74627214
|
T | C | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.241-12065A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627214 | ||||||
| chr2:74627295
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.241-12146A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627295 | ||||||
| chr2:74627417
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.241-12268T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627417 | ||||||
| chr2:74627428
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.241-12279G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627428 | ||||||
| chr2:74627577
|
C | T | 32 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.241-12428G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627577 | ||||||
| chr2:74627771
|
A | G | 6 | a0001c0001t0001g0165a0001c0001t0001g0190a0001c0001t0001g0191others(3): Show | 6 | NA18968.hp1 NA19007.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+12265T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74627771 | ||||||
| chr2:74628062
|
C | T | 2 | a0001c0001t0001g0192a0001c0002t0003g0037 | 2 | HG03225.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.240+11974G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628062 | ||||||
| chr2:74628303
|
C | A | 1 | a0002c0005t0010g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.240+11733G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628303 | ||||||
| chr2:74628353
|
C | T | 31 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(28): Show | 32 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.240+11683G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628353 | ||||||
| chr2:74628424
|
C | A | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.240+11612G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628424 | ||||||
| chr2:74628530
|
C | CA | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+11505dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628530 | ||||||
| chr2:74628586
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.240+11450G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628586 | ||||||
| chr2:74628588
|
C | G | 1 | a0001c0001t0003g0140 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.240+11448G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628588 | ||||||
| chr2:74628725
|
GACA | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02922.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.240+11308_240+1131 others(7): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628725 | ||||||
| chr2:74628882
|
C | G | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+11154G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628882 | ||||||
| chr2:74628989
|
T | A | 2 | a0001c0011t0001g0160a0003c0003t0002g0067 | 2 | HG00733.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.240+11047A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628989 | ||||||
| chr2:74628996
|
C | T | 222 | a0000c0008t0002g0077a0001c0001t0001g0027a0001c0001t0001g0152others(219): Show | 224 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.240+11040G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74628996 | ||||||
| chr2:74629108
|
A | G | 7 | a0001c0001t0002g0052a0001c0001t0003g0126a0001c0001t0004g0042others(4): Show | 7 | HG00558.hp1 HG01952.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+10928T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629108 | ||||||
| chr2:74629251
|
A | G | 6 | a0001c0001t0006g0001a0001c0001t0006g0016a0001c0001t0006g0017others(3): Show | 7 | HG02109.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+10785T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629251 | ||||||
| chr2:74629479
|
G | A | 32 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.240+10557C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629479 | ||||||
| chr2:74629543
|
G | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+10493C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629543 | ||||||
| chr2:74629689
|
T | C | 5 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+10347A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629689 | ||||||
| chr2:74629751
|
C | CA | 12 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(9): Show | 12 | HG00741.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.240+10284dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629751 | ||||||
| chr2:74629751
|
C | CAA | 21 | a0001c0001t0001g0027a0001c0001t0006g0001a0001c0001t0006g0012others(18): Show | 22 | HG01243.hp1 HG01256.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.240+10283_240+1028 others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629751 | ||||||
| chr2:74629879
|
C | A | 7 | a0001c0002t0001g0148a0001c0002t0003g0145a0001c0002t0003g0146others(4): Show | 7 | HG01192.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+10157G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629879 | ||||||
| chr2:74629893
|
G | A | 2 | a0004c0004t0005g0242a0004c0004t0005g0243 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.240+10143C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629893 | ||||||
| chr2:74629915
|
A | T | 2 | a0001c0002t0003g0149a0001c0002t0004g0150 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.240+10121T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629915 | ||||||
| chr2:74629940
|
C | CT | 6 | a0001c0001t0001g0172a0001c0001t0003g0134a0001c0001t0008g0035others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+10095dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629940 | ||||||
| chr2:74629940
|
CT | C | 13 | a0001c0001t0001g0177a0001c0001t0001g0223a0001c0001t0002g0054others(10): Show | 13 | HG01167.hp2 HG01243.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.240+10095delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74629940 | ||||||
| chr2:74630019
|
C | CA | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+10016dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630019 | ||||||
| chr2:74630453
|
G | A | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.240+9583C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630453 | ||||||
| chr2:74630704
|
TACC | T | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+9329_240+9331d others(5): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630704 | ||||||
| chr2:74630796
|
T | G | 7 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+9240A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630796 | ||||||
| chr2:74630804
|
T | C | 16 | a0001c0001t0001g0027a0001c0001t0006g0001a0001c0001t0006g0012others(13): Show | 17 | HG02109.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.240+9232A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630804 | ||||||
| chr2:74630845
|
T | C | 5 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(2): Show | 5 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+9191A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630845 | ||||||
| chr2:74630941
|
C | A | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.240+9095G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630941 | ||||||
| chr2:74630965
|
T | C | 33 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(30): Show | 34 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.240+9071A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74630965 | ||||||
| chr2:74631014
|
CTCTT | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+9018_240+9021d others(6): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74631014 | ||||||
| chr2:74631081
|
C | G | 2 | a0002c0006t0003g0004a0002c0006t0003g0005 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.240+8955G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74631081 | ||||||
| chr2:74631082
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.240+8954T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74631082 | ||||||
| chr2:74631740
|
T | C | 3 | a0001c0001t0003g0143a0001c0001t0003g0144a0001c0001t0003g0241 | 3 | HG02622.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.240+8296A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74631740 | ||||||
| chr2:74631841
|
C | A | 1 | a0001c0001t0008g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.240+8195G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74631841 | ||||||
| chr2:74631936
|
C | T | 8 | a0001c0001t0005g0060a0001c0001t0011g0065a0001c0001t0011g0066others(5): Show | 8 | NA18970.hp2 NA18971.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+8100G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74631936 | ||||||
| chr2:74632038
|
T | C | 33 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(30): Show | 34 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.240+7998A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632038 | ||||||
| chr2:74632086
|
G | A | 2 | a0004c0004t0005g0242a0004c0004t0005g0243 | 2 | HG01243.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.240+7950C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632086 | ||||||
| chr2:74632089
|
C | T | 14 | a0001c0001t0006g0001a0001c0001t0006g0012a0001c0001t0006g0013others(11): Show | 15 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.240+7947G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632089 | ||||||
| chr2:74632105
|
T | C | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+7931A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632105 | ||||||
| chr2:74632245
|
CACACCAG others(19): Show |
C | 1 | a0001c0001t0005g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.240+7765_240+7790d others(28): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632245 | ||||||
| chr2:74632273
|
A | C | 1 | a0001c0001t0005g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.240+7763T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632273 | ||||||
| chr2:74632277
|
C | T | 1 | a0001c0001t0005g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.240+7759G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632277 | ||||||
| chr2:74632278
|
A | T | 1 | a0001c0001t0005g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.240+7758T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632278 | ||||||
| chr2:74632572
|
G | A | 27 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(24): Show | 28 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.240+7464C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632572 | ||||||
| chr2:74632595
|
T | G | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.240+7441A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632595 | ||||||
| chr2:74632609
|
C | T | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+7427G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632609 | ||||||
| chr2:74632701
|
G | A | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+7335C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74632701 | ||||||
| chr2:74633152
|
G | A | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.240+6884C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74633152 | ||||||
| chr2:74633277
|
A | T | 2 | a0001c0001t0002g0047a0001c0001t0004g0046 | 2 | HG00609.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.240+6759T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74633277 | ||||||
| chr2:74633319
|
A | G | 39 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 40 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.240+6717T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74633319 | ||||||
| chr2:74633644
|
T | C | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+6392A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74633644 | ||||||
| chr2:74634143
|
T | C | 2 | a0001c0001t0006g0025a0001c0001t0006g0026 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240+5893A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74634143 | ||||||
| chr2:74634165
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.240+5871T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74634165 | ||||||
| chr2:74634367
|
G | C | 7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | NA18939.hp2 NA18948.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.240+5669C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74634367 | ||||||
| chr2:74634453
|
G | A | 11 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG01109.hp1 HG01167.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.240+5583C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74634453 | ||||||
| chr2:74634831
|
T | A | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.240+5205A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74634831 | ||||||
| chr2:74635043
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.240+4993T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74635043 | ||||||
| chr2:74635130
|
A | G | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+4906T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74635130 | ||||||
| chr2:74635385
|
C | T | 1 | a0001c0001t0004g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.240+4651G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74635385 | ||||||
| chr2:74635532
|
T | C | 1 | a0004c0004t0005g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240+4504A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74635532 | ||||||
| chr2:74635634
|
G | A | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.240+4402C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74635634 | ||||||
| chr2:74635892
|
T | C | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+4144A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74635892 | ||||||
| chr2:74636025
|
A | G | 3 | a0001c0001t0006g0013a0001c0001t0006g0014a0001c0001t0006g0015 | 3 | HG02145.hp1 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.240+4011T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636025 | ||||||
| chr2:74636239
|
C | T | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+3797G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636239 | ||||||
| chr2:74636295
|
T | C | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+3741A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636295 | ||||||
| chr2:74636434
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.240+3602A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636434 | ||||||
| chr2:74636547
|
C | T | 1 | a0001c0001t0008g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.240+3489G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636547 | ||||||
| chr2:74636587
|
C | T | 37 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(34): Show | 38 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.240+3449G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636587 | ||||||
| chr2:74636715
|
T | C | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.240+3321A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636715 | ||||||
| chr2:74636872
|
C | A | 3 | a0001c0001t0008g0035a0001c0001t0008g0036a0001c0001t0008g0244 | 3 | HG02451.hp2 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.240+3164G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74636872 | ||||||
| chr2:74637192
|
G | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.240+2844C>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637192 | ||||||
| chr2:74637199
|
A | C | 1 | a0001c0001t0003g0011 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.240+2837T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637199 | ||||||
| chr2:74637434
|
C | G | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+2602G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637434 | ||||||
| chr2:74637525
|
C | T | 1 | a0002c0005t0010g0030 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.240+2511G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637525 | ||||||
| chr2:74637667
|
T | G | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.240+2369A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637667 | ||||||
| chr2:74637861
|
T | C | 1 | a0002c0006t0003g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.240+2175A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637861 | ||||||
| chr2:74637872
|
C | G | 178 | a0000c0008t0002g0077a0001c0001t0001g0027a0001c0001t0001g0152others(175): Show | 180 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.240+2164G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637872 | ||||||
| chr2:74637949
|
T | A | 1 | a0001c0001t0005g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.240+2087A>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74637949 | ||||||
| chr2:74638058
|
C | CT | 9 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0008g0033others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+1977dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638058 | ||||||
| chr2:74638158
|
G | T | 5 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(2): Show | 5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1878C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638158 | ||||||
| chr2:74638198
|
G | T | 107 | a0000c0008t0002g0077a0001c0001t0001g0182a0001c0001t0001g0183others(104): Show | 108 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.240+1838C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638198 | ||||||
| chr2:74638268
|
G | GACCAACT others(6): Show |
1 | a0001c0001t0003g0011 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.240+1767_240+1768i others(15): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638268 | ||||||
| chr2:74638366
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.240+1670G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638366 | ||||||
| chr2:74638528
|
T | C | 32 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(29): Show | 33 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.240+1508A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638528 | ||||||
| chr2:74638613
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.240+1423G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638613 | ||||||
| chr2:74638726
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01167.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.240+1310A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638726 | ||||||
| chr2:74638755
|
T | C | 24 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(21): Show | 25 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.240+1281A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638755 | ||||||
| chr2:74638906
|
C | T | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.240+1130G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74638906 | ||||||
| chr2:74639179
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.240+857T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74639179 | ||||||
| chr2:74639388
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.240+648A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74639388 | ||||||
| chr2:74639494
|
C | T | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.240+542G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74639494 | ||||||
| chr2:74640028
|
A | G | 1 | a0001c0001t0003g0143 | 1 | HG02809.hp1 | splice_region_variant&intron_variant | LOW | c.240+8T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 2/10 | chr2 | 74640028 | ||||||
| chr2:74640375
|
G | A | 1 | a0001c0001t0005g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-52-48C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640375 | ||||||
| chr2:74640403
|
C | T | 8 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(5): Show | 8 | HG01167.hp2 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-76G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640403 | ||||||
| chr2:74640463
|
A | AT | 11 | a0001c0001t0002g0002a0001c0001t0005g0040a0001c0001t0006g0003others(8): Show | 12 | HG02135.hp1 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-52-137dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640463 | ||||||
| chr2:74640463
|
AT | A | 27 | a0001c0001t0001g0171a0001c0001t0002g0049a0001c0001t0002g0108others(24): Show | 27 | HG00438.hp2 HG00558.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52-137delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640463 | ||||||
| chr2:74640487
|
A | G | 7 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(4): Show | 7 | NA18939.hp2 NA18948.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-160T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640487 | ||||||
| chr2:74640492
|
C | T | 23 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(20): Show | 24 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.-52-165G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640492 | ||||||
| chr2:74640563
|
C | T | 1 | a0001c0001t0009g0164 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-52-236G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640563 | ||||||
| chr2:74640675
|
C | T | 8 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0057others(5): Show | 8 | HG02109.hp2 HG02280.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-348G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640675 | ||||||
| chr2:74640676
|
T | C | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-52-349A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640676 | ||||||
| chr2:74640745
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG02572.hp2 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-52-418G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640745 | ||||||
| chr2:74640766
|
TATTTTAA others(11): Show |
T | 1 | a0001c0011t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-52-457_-52-440del others(18): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640766 | ||||||
| chr2:74640790
|
T | G | 1 | a0001c0001t0001g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-52-463A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74640790 | ||||||
| chr2:74641057
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-52-730G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641057 | ||||||
| chr2:74641204
|
C | G | 102 | a0000c0008t0002g0077a0001c0001t0001g0234a0001c0001t0002g0002others(99): Show | 103 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.-52-877G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641204 | ||||||
| chr2:74641257
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-52-930G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641257 | ||||||
| chr2:74641297
|
C | G | 1 | a0001c0001t0008g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-52-970G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641297 | ||||||
| chr2:74641431
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-52-1104A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641431 | ||||||
| chr2:74641619
|
T | C | 1 | a0001c0001t0003g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-52-1292A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641619 | ||||||
| chr2:74641633
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-52-1306T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641633 | ||||||
| chr2:74641641
|
C | CT | 39 | a0001c0001t0001g0027a0001c0001t0002g0051a0001c0001t0003g0008others(36): Show | 40 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.-52-1315dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641641 | ||||||
| chr2:74641835
|
A | C | 1 | a0001c0001t0005g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-52-1508T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641835 | ||||||
| chr2:74641835
|
A | G | 1 | a0001c0002t0003g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-52-1508T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641835 | ||||||
| chr2:74641847
|
A | AT | 95 | a0000c0008t0002g0077a0001c0001t0001g0234a0001c0001t0002g0002others(92): Show | 96 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-52-1521dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641847 | ||||||
| chr2:74641847
|
A | ATT | 6 | a0001c0001t0002g0049a0001c0001t0002g0135a0001c0001t0002g0137others(3): Show | 6 | HG00438.hp2 HG02523.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-1522_-52-1521d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641847 | ||||||
| chr2:74641847
|
AT | A | 15 | a0001c0001t0006g0001a0001c0001t0006g0013a0001c0001t0006g0014others(12): Show | 16 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-52-1521delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641847 | ||||||
| chr2:74641900
|
C | T | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-52-1573G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641900 | ||||||
| chr2:74641908
|
T | C | 2 | a0001c0002t0003g0149a0001c0002t0004g0150 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52-1581A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641908 | ||||||
| chr2:74641948
|
C | T | 1 | a0001c0001t0006g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-52-1621G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74641948 | ||||||
| chr2:74642249
|
A | G | 7 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52-1922T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74642249 | ||||||
| chr2:74642275
|
C | CA | 14 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(11): Show | 14 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-1949dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74642275 | ||||||
| chr2:74642275
|
C | CAA | 24 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(21): Show | 25 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-52-1950_-52-1949d others(4): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74642275 | ||||||
| chr2:74642746
|
T | C | 18 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(15): Show | 18 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-52-2419A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74642746 | ||||||
| chr2:74642964
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52-2637G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74642964 | ||||||
| chr2:74643226
|
G | A | 1 | a0001c0001t0006g0155 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-52-2899C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643226 | ||||||
| chr2:74643266
|
T | G | 1 | a0001c0001t0006g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-52-2939A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643266 | ||||||
| chr2:74643390
|
GT | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-3064delA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643390 | ||||||
| chr2:74643590
|
C | CT | 40 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(37): Show | 41 | HG00741.hp2 HG01192.hp2 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.-52-3264dupA | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643590 | ||||||
| chr2:74643592
|
T | TC | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-52-3266_-52-3265i others(3): Show |
M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643592 | ||||||
| chr2:74643645
|
C | T | 4 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-3318G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643645 | ||||||
| chr2:74643729
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0004g0046 | 2 | HG00609.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-52-3402G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643729 | ||||||
| chr2:74643935
|
A | G | 1 | a0001c0001t0004g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-52-3608T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74643935 | ||||||
| chr2:74644057
|
T | C | 3 | a0004c0004t0005g0029a0004c0004t0005g0242a0004c0004t0005g0243 | 3 | HG01243.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-3730A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74644057 | ||||||
| chr2:74644232
|
A | G | 7 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0141others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52-3905T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74644232 | ||||||
| chr2:74644537
|
C | CA | 11 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0235others(8): Show | 11 | HG01261.hp1 HG02083.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-53+3727dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74644537 | ||||||
| chr2:74644537
|
CA | C | 8 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(5): Show | 8 | HG00741.hp2 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+3727delT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74644537 | ||||||
| chr2:74644630
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-53+3635C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74644630 | ||||||
| chr2:74644999
|
T | C | 29 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(26): Show | 30 | HG00741.hp2 HG01256.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-53+3266A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74644999 | ||||||
| chr2:74645042
|
G | A | 1 | a0004c0004t0005g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-53+3223C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645042 | ||||||
| chr2:74645088
|
C | G | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-53+3177G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645088 | ||||||
| chr2:74645134
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-53+3131G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645134 | ||||||
| chr2:74645151
|
A | C | 241 | a0000c0008t0002g0077a0001c0001t0001g0027a0001c0001t0001g0038others(238): Show | 243 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.-53+3114T>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645151 | ||||||
| chr2:74645223
|
C | T | 1 | a0002c0006t0003g0006 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-53+3042G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645223 | ||||||
| chr2:74645439
|
G | A | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+2826C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645439 | ||||||
| chr2:74645445
|
C | A | 1 | a0001c0001t0016g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-53+2820G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645445 | ||||||
| chr2:74645467
|
A | G | 1 | a0001c0001t0004g0042 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-53+2798T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645467 | ||||||
| chr2:74645617
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-53+2648G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645617 | ||||||
| chr2:74645686
|
T | C | 106 | a0000c0008t0002g0077a0001c0001t0001g0234a0001c0001t0001g0237others(103): Show | 107 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-53+2579A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645686 | ||||||
| chr2:74645835
|
C | T | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-53+2430G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645835 | ||||||
| chr2:74645901
|
T | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0137a0001c0001t0003g0134others(3): Show | 6 | HG00438.hp2 HG02523.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+2364A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74645901 | ||||||
| chr2:74646022
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-53+2243G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646022 | ||||||
| chr2:74646029
|
C | T | 2 | a0001c0001t0005g0040a0001c0001t0005g0236 | 2 | HG02135.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-53+2236G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646029 | ||||||
| chr2:74646178
|
C | G | 103 | a0000c0008t0002g0077a0001c0001t0001g0234a0001c0001t0002g0002others(100): Show | 104 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-53+2087G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646178 | ||||||
| chr2:74646202
|
G | A | 6 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+2063C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646202 | ||||||
| chr2:74646254
|
C | T | 163 | a0000c0008t0002g0077a0001c0001t0001g0152a0001c0001t0001g0153others(160): Show | 165 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.-53+2011G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646254 | ||||||
| chr2:74646401
|
T | C | 3 | a0001c0001t0001g0234a0001c0001t0002g0002a0001c0001t0002g0233 | 4 | NA18986.hp2 NA19078.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+1864A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646401 | ||||||
| chr2:74646506
|
C | CA | 3 | a0002c0005t0010g0030a0002c0005t0010g0031a0002c0005t0010g0032 | 3 | HG01891.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-53+1758dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74646506 | ||||||
| chr2:74647049
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-53+1216C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647049 | ||||||
| chr2:74647061
|
C | A | 1 | a0001c0001t0005g0236 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-53+1204G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647061 | ||||||
| chr2:74647066
|
T | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA19055.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-53+1199A>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647066 | ||||||
| chr2:74647125
|
C | G | 1 | a0001c0009t0003g0039 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-53+1140G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647125 | ||||||
| chr2:74647229
|
C | T | 2 | a0002c0006t0003g0004a0002c0006t0003g0005 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-53+1036G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647229 | ||||||
| chr2:74647244
|
C | A | 1 | a0001c0002t0003g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53+1021G>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647244 | ||||||
| chr2:74647255
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-53+1010G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647255 | ||||||
| chr2:74647335
|
A | T | 39 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 40 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.-53+930T>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647335 | ||||||
| chr2:74647415
|
G | A | 4 | a0001c0001t0008g0033a0001c0001t0008g0034a0001c0001t0008g0035others(1): Show | 4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+850C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647415 | ||||||
| chr2:74647415
|
G | T | 1 | a0001c0002t0003g0037 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-53+850C>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647415 | ||||||
| chr2:74647466
|
C | T | 23 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(20): Show | 24 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53+799G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647466 | ||||||
| chr2:74647542
|
G | A | 1 | a0001c0002t0003g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53+723C>T | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647542 | ||||||
| chr2:74647620
|
A | G | 39 | a0001c0001t0001g0027a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 40 | HG00741.hp2 HG01243.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.-53+645T>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647620 | ||||||
| chr2:74647633
|
C | T | 3 | a0002c0006t0003g0004a0002c0006t0003g0005a0002c0006t0003g0006 | 3 | HG02257.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-53+632G>A | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647633 | ||||||
| chr2:74647641
|
C | G | 1 | a0001c0001t0006g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53+624G>C | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647641 | ||||||
| chr2:74647737
|
T | TA | 5 | a0001c0001t0003g0241a0001c0001t0005g0240a0001c0001t0008g0244others(2): Show | 5 | HG01243.hp1 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53+527dupT | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647737 | ||||||
| chr2:74647837
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-53+428A>G | M1AP | ENSG00000159374.18 | transcript | ENST00000421985.2 | protein_coding | 1/10 | chr2 | 74647837 |