Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10588 |
| ensemblid | ENSG00000136371.11 |
| hgncid | 7437 |
| symbol | MTHFS |
| name | methenyltetrahydrofolate synthetase |
| refseq_nuc | NM_006441.4 |
| refseq_prot | NP_006432.1 |
| ensembl_nuc | ENST00000258874.4 |
| ensembl_prot | ENSP00000258874.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 79843547 |
| end | 79897014 |
| strand | - |
| ver | v1.2 |
| region | chr15:79843547-79897014 |
| region5000 | chr15:79838547-79902014 |
| regionname0 | MTHFS_chr15_79843547_79897014 |
| regionname5000 | MTHFS_chr15_79838547_79902014 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 203 | 374 | 87 | 59 | 167 | 13 | 46 | 134 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0002 | 0/0 | 203 | 17 | 6 | 4 | 4 | 3 | 0 | 3 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0003 | 0/0 | 203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0004 | 0/0 | 203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0005 | 0/0 | 203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 612 | 368 | 84 | 58 | 166 | 13 | 45 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0002 | 0/0 | 612 | 17 | 6 | 4 | 4 | 3 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0003 | 0/0 | 612 | 4 | 3 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0004 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0005 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0006 | 0/0 | 612 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0007 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| c0008 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1690 | 123 | 34 | 19 | 58 | 2 | 9 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0002 | 0/0 | 1690 | 98 | 4 | 16 | 65 | 2 | 11 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0003 | 0/0 | 1690 | 43 | 6 | 4 | 32 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0004 | 0/0 | 1690 | 42 | 4 | 11 | 10 | 3 | 14 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0005 | 0/1 | 1690 | 31 | 11 | 4 | 1 | 5 | 9 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0006 | 0/0 | 1690 | 19 | 8 | 4 | 4 | 3 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0007 | 0/0 | 1690 | 11 | 11 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0008 | 0/0 | 1690 | 8 | 1 | 4 | 0 | 1 | 2 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0009 | 0/0 | 1690 | 6 | 6 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0010 | 0/0 | 1690 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0011 | 0/0 | 1690 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0012 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0013 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0014 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0015 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0016 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| t0017 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0002 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0005 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0006 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 612 | 368 | 84 | 58 | 166 | 13 | 45 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0001c0003 | 0/0 | 612 | 4 | 3 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0001c0005 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0001c0007 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0002c0002 | 0/0 | 612 | 17 | 6 | 4 | 4 | 3 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0003c0006 | 0/0 | 612 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0004c0004 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 | |
| a0005c0008 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2301 | 119 | 31 | 18 | 58 | 2 | 9 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0002 | 0/0 | 2301 | 95 | 4 | 15 | 63 | 2 | 11 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0003 | 0/0 | 2301 | 43 | 6 | 4 | 32 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0004 | 0/0 | 2301 | 41 | 4 | 11 | 10 | 3 | 13 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0005 | 0/1 | 2301 | 31 | 11 | 4 | 1 | 5 | 9 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0006 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0007 | 0/0 | 2301 | 10 | 10 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0008 | 0/0 | 2301 | 8 | 1 | 4 | 0 | 1 | 2 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0009 | 0/0 | 2301 | 6 | 6 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0010 | 0/0 | 2301 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0011 | 0/0 | 2301 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0012 | 0/0 | 2301 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0013 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0014 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0015 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0016 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0001t0017 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0003t0001 | 0/0 | 2301 | 4 | 3 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0005t0002 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0001c0007t0004 | 0/0 | 2301 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0002c0002t0006 | 0/0 | 2301 | 17 | 6 | 4 | 4 | 3 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0003c0006t0002 | 0/0 | 2301 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0004c0004t0002 | 0/0 | 2301 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| a0005c0008t0007 | 0/0 | 2301 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | copy fasta | chr15 | 79838547 | 79902014 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0003 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0005 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0006g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0009g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0010g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0011g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0011g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0011g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0012g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0012g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0015g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0016g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0001t0017g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0003t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0005t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0001c0007t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0002c0002t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0003c0006t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0004c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| a0005c0008t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0121 | EUR | GBR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0111 | EUR | GBR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | GBR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0071 | EUR | GBR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | FIN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0264 | EUR | FIN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0186 | EUR | FIN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0103 | EUR | FIN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00642 | hp1 | a0002 | c0002 | t0006 | g0171 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0233 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01081 | hp2 | a0001 | c0001 | t0013 | g0235 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0107 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01168 | hp1 | a0002 | c0002 | t0006 | g0182 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0183 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01256 | hp1 | a0002 | c0002 | t0006 | g0166 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0257 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01258 | hp1 | a0002 | c0002 | t0006 | g0018 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0279 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0325 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01515 | hp1 | a0002 | c0002 | t0006 | g0170 | EUR | IBS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0115 | EUR | IBS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | IBS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0104 | EUR | IBS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01517 | hp2 | a0002 | c0002 | t0006 | g0167 | EUR | IBS | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0185 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01975 | hp1 | a0003 | c0006 | t0002 | g0335 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0106 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02135 | hp1 | a0002 | c0002 | t0006 | g0169 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0101 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02145 | hp2 | a0002 | c0002 | t0006 | g0027 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02155 | hp2 | a0001 | c0001 | t0015 | g0285 | EAS | CDX | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | CDX | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02258 | hp1 | a0002 | c0002 | t0006 | g0013 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0324 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0271 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0219 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0028 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0228 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0256 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0222 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0309 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0281 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0319 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02896 | hp2 | a0001 | c0001 | t0009 | g0320 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02922 | hp2 | a0002 | c0002 | t0006 | g0243 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0327 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0153 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0307 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03098 | hp1 | a0002 | c0002 | t0006 | g0026 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0239 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03139 | hp2 | a0005 | c0008 | t0007 | g0337 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0308 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0240 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0278 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0096 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0013 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03490 | hp1 | a0001 | c0007 | t0004 | g0336 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0184 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0118 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0187 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0330 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0333 | AFR | ESN | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | GWD | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0326 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0221 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0119 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0313 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0250 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0227 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0334 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0109 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0112 | SAS | PJL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0116 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0252 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0229 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0272 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0277 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0201 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | YRI | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0113 | AFR | YRI | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18965 | hp2 | a0002 | c0002 | t0006 | g0172 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18987 | hp2 | a0004 | c0004 | t0002 | g0057 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18995 | hp2 | a0001 | c0005 | t0002 | g0190 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18997 | hp1 | a0002 | c0002 | t0006 | g0164 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0332 | AFR | LWK | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0215 | AFR | LWK | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19072 | hp2 | a0002 | c0002 | t0006 | g0168 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19075 | hp1 | a0001 | c0001 | t0017 | g0265 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0312 | AFR | ASW | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | ASW | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0310 | EUR | TSI | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA20752 | hp2 | a0002 | c0002 | t0006 | g0018 | EUR | TSI | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0110 | AMR | CLM | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0220 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02559 | hp1 | a0001 | c0001 | t0009 | g0318 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | USA | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | USA | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | USA | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | LWK | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0122 | REF | REF | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0244 | REF | REF | MTHFS_chr15_79838547_79902014 | MTHFS | chr15 | 79838547 | 79902014 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:79845218 | T | C | 1 | a0002 | 17 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(14): Show |
missense_variant | MODERATE | c.604A>G | p.Thr202Ala | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 630/2301 | 604/612 | 202/203 | chr15 | 79845218 | ||
| chr15:79889298 | C | T | 1 | a0004 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.174G>A | p.Met58Ile | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/3 | 200/2301 | 174/612 | 58/203 | chr15 | 79889298 | ||
| chr15:79896888 | C | A | 1 | a0003 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.101G>T | p.Arg34Leu | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/3 | 127/2301 | 101/612 | 34/203 | chr15 | 79896888 | ||
| chr15:79896975 | G | A | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.14C>T | p.Ala5Val | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/3 | 40/2301 | 14/612 | 5/203 | chr15 | 79896975 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:79845305 | A | G | 1 | a0001c0005 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.517T>C | p.Leu173Leu | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 543/2301 | 517/612 | 173/203 | chr15 | 79845305 | ||
| chr15:79845402 | G | A | 1 | a0001c0003 | 4 | HG01169.hp1 HG03130.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.420C>T | p.Asp140Asp | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 446/2301 | 420/612 | 140/203 | chr15 | 79845402 | ||
| chr15:79896962 | G | A | 1 | a0001c0007 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.27C>T | p.Ala9Ala | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/3 | 53/2301 | 27/612 | 9/203 | chr15 | 79896962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:79843609 | T | C | 1 | a0001c0001t0013 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1601 | chr15 | 79843609 | |||||
| chr15:79843644 | G | A | 1 | a0001c0001t0014 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1566C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1566 | chr15 | 79843644 | |||||
| chr15:79843679 | A | T | 2 | a0001c0001t0009a0001c0001t0010 | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1531T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1531 | chr15 | 79843679 | |||||
| chr15:79843787 | A | G | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0015others(5): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1423T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1423 | chr15 | 79843787 | |||||
| chr15:79843946 | C | A | 4 | a0001c0001t0007a0001c0001t0009a0001c0001t0010others(1): Show | 20 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1264G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1264 | chr15 | 79843946 | |||||
| chr15:79844096 | T | C | 1 | a0001c0001t0015 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1114 | chr15 | 79844096 | |||||
| chr15:79844120 | T | A | 1 | a0001c0001t0005 | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1090A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1090 | chr15 | 79844120 | |||||
| chr15:79844130 | G | C | 1 | a0001c0001t0016 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1080C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1080 | chr15 | 79844130 | |||||
| chr15:79844133 | G | C | 1 | a0001c0001t0017 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 1077 | chr15 | 79844133 | |||||
| chr15:79844275 | C | A | 2 | a0001c0001t0011a0001c0001t0012 | 5 | HG01346.hp1 HG02572.hp1 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*935G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 935 | chr15 | 79844275 | |||||
| chr15:79844305 | G | A | 3 | a0001c0001t0004a0001c0001t0017a0001c0007t0004 | 43 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*905C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 905 | chr15 | 79844305 | |||||
| chr15:79844395 | G | A | 1 | a0001c0001t0008 | 8 | HG00323.hp1 HG00738.hp2 HG01081.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 815 | chr15 | 79844395 | |||||
| chr15:79844402 | A | G | 2 | a0001c0001t0009a0001c0001t0010 | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*808T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 808 | chr15 | 79844402 | |||||
| chr15:79844430 | C | T | 8 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(5): Show | 113 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*780G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 780 | chr15 | 79844430 | |||||
| chr15:79844472 | T | C | 1 | a0001c0001t0010 | 3 | HG02486.hp1 HG02615.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*738A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 738 | chr15 | 79844472 | |||||
| chr15:79844490 | G | A | 2 | a0001c0001t0006a0002c0002t0006 | 19 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 720 | chr15 | 79844490 | |||||
| chr15:79844826 | C | T | 1 | a0001c0001t0012 | 2 | HG02572.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*384G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 384 | chr15 | 79844826 | |||||
| chr15:79844841 | A | C | 2 | a0001c0001t0009a0001c0001t0010 | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*369T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 3/3 | 369 | chr15 | 79844841 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:79845446 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.380-4G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79845446 | ||||||
| chr15:79845491 | T | G | 1 | a0001c0001t0002g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.380-49A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79845491 | ||||||
| chr15:79845820 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.380-378C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79845820 | ||||||
| chr15:79845822 | G | A | 2 | a0002c0002t0006g0169a0002c0002t0006g0172 | 2 | HG02135.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.380-380C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79845822 | ||||||
| chr15:79845910 | C | A | 1 | a0001c0001t0003g0216 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-468G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79845910 | ||||||
| chr15:79846229 | C | T | 78 | a0001c0001t0001g0080a0001c0001t0002g0001a0001c0001t0002g0002others(75): Show | 98 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.380-787G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846229 | ||||||
| chr15:79846261 | G | A | 1 | a0001c0001t0003g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.380-819C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846261 | ||||||
| chr15:79846326 | T | G | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.380-884A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846326 | ||||||
| chr15:79846332 | C | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0036others(5): Show | 10 | NA18947.hp2 NA18949.hp1 NA18984.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-890G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846332 | ||||||
| chr15:79846396 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.380-954A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846396 | ||||||
| chr15:79846403 | A | C | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-961T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846403 | ||||||
| chr15:79846410 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.380-968A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846410 | ||||||
| chr15:79846470 | G | C | 1 | a0001c0001t0002g0303 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.380-1028C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846470 | ||||||
| chr15:79846711 | C | CCT | 3 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215 | 3 | HG02145.hp1 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.380-1271_380-1270d others(4): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846711 | ||||||
| chr15:79846848 | C | T | 3 | a0001c0001t0009g0318a0001c0001t0009g0319a0001c0001t0009g0320 | 3 | HG02559.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.380-1406G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846848 | ||||||
| chr15:79846853 | A | C | 113 | a0001c0001t0001g0080a0001c0001t0002g0001a0001c0001t0002g0002others(110): Show | 143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.380-1411T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846853 | ||||||
| chr15:79846909 | T | C | 37 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-1467A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846909 | ||||||
| chr15:79846994 | C | T | 3 | a0001c0001t0010g0219a0001c0001t0010g0220a0001c0001t0010g0221 | 3 | HG02486.hp1 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.380-1552G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79846994 | ||||||
| chr15:79847004 | T | A | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-1562A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847004 | ||||||
| chr15:79847019 | C | A | 1 | a0001c0001t0003g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.380-1577G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847019 | ||||||
| chr15:79847019 | C | T | 28 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(25): Show | 36 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.380-1577G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847019 | ||||||
| chr15:79847081 | G | C | 1 | a0001c0001t0002g0189 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.380-1639C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847081 | ||||||
| chr15:79847113 | A | G | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-1671T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847113 | ||||||
| chr15:79847193 | A | G | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-1751T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847193 | ||||||
| chr15:79847207 | G | C | 29 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(26): Show | 37 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-1765C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847207 | ||||||
| chr15:79847241 | C | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(311): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.380-1799G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847241 | ||||||
| chr15:79847260 | A | G | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.380-1818T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847260 | ||||||
| chr15:79847387 | G | T | 29 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(26): Show | 37 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-1945C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847387 | ||||||
| chr15:79847479 | C | T | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-2037G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847479 | ||||||
| chr15:79847508 | TC | T | 3 | a0001c0001t0009g0318a0001c0001t0009g0319a0001c0001t0009g0320 | 3 | HG02559.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.380-2067delG | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847508 | ||||||
| chr15:79847557 | G | A | 1 | a0001c0001t0004g0312 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.380-2115C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847557 | ||||||
| chr15:79847561 | G | A | 1 | a0001c0001t0014g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.380-2119C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847561 | ||||||
| chr15:79847609 | G | A | 29 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(26): Show | 37 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-2167C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847609 | ||||||
| chr15:79847669 | CA | C | 250 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(247): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.380-2228delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847669 | ||||||
| chr15:79847669 | CAA | C | 18 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0084others(15): Show | 18 | HG02280.hp2 HG02523.hp1 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.380-2229_380-2228d others(4): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79847669 | ||||||
| chr15:79848107 | C | T | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0055 | 3 | NA18945.hp1 NA18963.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.380-2665G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848107 | ||||||
| chr15:79848250 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.380-2808T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848250 | ||||||
| chr15:79848257 | T | A | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-2815A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848257 | ||||||
| chr15:79848336 | C | T | 17 | a0001c0001t0006g0332a0001c0001t0006g0333a0002c0002t0006g0013others(14): Show | 19 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.380-2894G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848336 | ||||||
| chr15:79848389 | T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | NA18963.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.380-2947A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848389 | ||||||
| chr15:79848393 | T | C | 37 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-2951A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848393 | ||||||
| chr15:79848606 | G | T | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-3164C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848606 | ||||||
| chr15:79848648 | A | C | 5 | a0001c0001t0011g0325a0001c0001t0011g0326a0001c0001t0011g0330others(2): Show | 5 | HG01346.hp1 HG02572.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-3206T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848648 | ||||||
| chr15:79848782 | G | C | 29 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(26): Show | 37 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-3340C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848782 | ||||||
| chr15:79848793 | T | C | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-3351A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79848793 | ||||||
| chr15:79849097 | A | G | 10 | a0001c0001t0004g0308a0001c0001t0009g0100a0001c0001t0009g0101others(7): Show | 10 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-3655T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849097 | ||||||
| chr15:79849146 | C | T | 1 | a0001c0001t0015g0285 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.380-3704G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849146 | ||||||
| chr15:79849464 | C | G | 15 | a0002c0002t0006g0013a0002c0002t0006g0018a0002c0002t0006g0026others(12): Show | 17 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.380-4022G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849464 | ||||||
| chr15:79849575 | T | A | 1 | a0001c0001t0002g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.380-4133A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849575 | ||||||
| chr15:79849609 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.380-4167C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849609 | ||||||
| chr15:79849634 | G | A | 1 | a0001c0001t0009g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.380-4192C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849634 | ||||||
| chr15:79849655 | G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(311): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.380-4213C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849655 | ||||||
| chr15:79849675 | G | A | 2 | a0001c0001t0012g0113a0001c0001t0012g0324 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.380-4233C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849675 | ||||||
| chr15:79849812 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.380-4370C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849812 | ||||||
| chr15:79849831 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.380-4389C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79849831 | ||||||
| chr15:79850158 | G | T | 1 | a0001c0001t0002g0314 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.380-4716C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850158 | ||||||
| chr15:79850232 | G | A | 1 | a0001c0001t0005g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.380-4790C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850232 | ||||||
| chr15:79850376 | C | T | 1 | a0001c0001t0003g0128 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.380-4934G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850376 | ||||||
| chr15:79850506 | A | G | 2 | a0001c0001t0012g0113a0001c0001t0012g0324 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.380-5064T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850506 | ||||||
| chr15:79850548 | T | C | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-5106A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850548 | ||||||
| chr15:79850640 | C | A | 1 | a0001c0001t0005g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.380-5198G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850640 | ||||||
| chr15:79850652 | T | C | 1 | a0001c0001t0005g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.380-5210A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850652 | ||||||
| chr15:79850693 | T | C | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-5251A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850693 | ||||||
| chr15:79850733 | A | G | 32 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.380-5291T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850733 | ||||||
| chr15:79850743 | A | T | 10 | a0002c0002t0006g0018a0002c0002t0006g0164a0002c0002t0006g0166others(7): Show | 11 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-5301T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850743 | ||||||
| chr15:79850776 | G | A | 15 | a0002c0002t0006g0013a0002c0002t0006g0018a0002c0002t0006g0026others(12): Show | 17 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.380-5334C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850776 | ||||||
| chr15:79850856 | A | G | 10 | a0002c0002t0006g0018a0002c0002t0006g0164a0002c0002t0006g0166others(7): Show | 11 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-5414T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79850856 | ||||||
| chr15:79851110 | C | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0001g0055others(4): Show | 7 | NA18945.hp1 NA18966.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-5668G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851110 | ||||||
| chr15:79851293 | C | T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 3 | HG03098.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.380-5851G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851293 | ||||||
| chr15:79851471 | G | A | 73 | a0001c0001t0001g0305a0001c0001t0003g0003a0001c0001t0003g0011others(70): Show | 83 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(80): Show |
intron_variant | MODIFIER | c.380-6029C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851471 | ||||||
| chr15:79851791 | T | C | 1 | a0002c0002t0006g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.380-6349A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851791 | ||||||
| chr15:79851850 | C | A | 1 | a0001c0001t0004g0274 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.380-6408G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851850 | ||||||
| chr15:79851855 | T | C | 35 | a0001c0001t0001g0248a0001c0001t0002g0268a0001c0001t0004g0005others(32): Show | 45 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.380-6413A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851855 | ||||||
| chr15:79851859 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.380-6417C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79851859 | ||||||
| chr15:79852207 | A | G | 3 | a0001c0001t0002g0188a0001c0001t0002g0192a0001c0001t0002g0196 | 3 | NA18950.hp1 NA18966.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.380-6765T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79852207 | ||||||
| chr15:79852464 | TA | T | 3 | a0001c0001t0002g0175a0001c0001t0002g0178a0001c0001t0002g0180 | 3 | NA18942.hp2 NA18972.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.380-7023delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79852464 | ||||||
| chr15:79852572 | T | A | 1 | a0001c0001t0009g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.380-7130A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79852572 | ||||||
| chr15:79852673 | C | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0136 | 2 | NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.380-7231G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79852673 | ||||||
| chr15:79852790 | G | A | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-7348C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79852790 | ||||||
| chr15:79853456 | T | TCTC | 106 | a0001c0001t0001g0305a0001c0001t0002g0163a0001c0001t0003g0003others(103): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.380-8015_380-8014i others(5): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853456 | ||||||
| chr15:79853645 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.380-8203T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853645 | ||||||
| chr15:79853826 | T | C | 4 | a0001c0001t0001g0234a0001c0003t0001g0024a0001c0003t0001g0239others(1): Show | 5 | HG01169.hp1 HG03130.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-8384A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853826 | ||||||
| chr15:79853870 | A | C | 3 | a0001c0001t0005g0110a0001c0001t0005g0111a0001c0001t0005g0112 | 3 | HG00099.hp2 HG01123.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.380-8428T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853870 | ||||||
| chr15:79853886 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.380-8444T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853886 | ||||||
| chr15:79853887 | G | A | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.380-8445C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853887 | ||||||
| chr15:79853895 | T | C | 2 | a0001c0001t0001g0305a0001c0001t0014g0222 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.380-8453A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79853895 | ||||||
| chr15:79854089 | G | A | 1 | a0001c0001t0005g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.380-8647C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854089 | ||||||
| chr15:79854194 | C | T | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-8752G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854194 | ||||||
| chr15:79854369 | C | T | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-8927G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854369 | ||||||
| chr15:79854412 | G | A | 3 | a0002c0002t0006g0018a0002c0002t0006g0166a0002c0002t0006g0171 | 4 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-8970C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854412 | ||||||
| chr15:79854413 | C | T | 10 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-8971G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854413 | ||||||
| chr15:79854434 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-8992G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854434 | ||||||
| chr15:79854449 | C | T | 1 | a0001c0001t0014g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.380-9007G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854449 | ||||||
| chr15:79854527 | G | A | 2 | a0001c0001t0001g0305a0001c0001t0014g0222 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.380-9085C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854527 | ||||||
| chr15:79854627 | G | A | 3 | a0001c0001t0010g0219a0001c0001t0010g0220a0001c0001t0010g0221 | 3 | HG02486.hp1 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.380-9185C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854627 | ||||||
| chr15:79854841 | A | G | 41 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.380-9399T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854841 | ||||||
| chr15:79854878 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.380-9436T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79854878 | ||||||
| chr15:79855037 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.380-9595A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855037 | ||||||
| chr15:79855238 | A | T | 74 | a0001c0001t0001g0305a0001c0001t0002g0163a0001c0001t0003g0003others(71): Show | 84 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(81): Show |
intron_variant | MODIFIER | c.380-9796T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855238 | ||||||
| chr15:79855296 | T | A | 2 | a0001c0001t0001g0305a0001c0001t0014g0222 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.380-9854A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855296 | ||||||
| chr15:79855549 | G | A | 1 | a0001c0001t0004g0313 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.380-10107C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855549 | ||||||
| chr15:79855568 | G | A | 1 | a0001c0001t0014g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.380-10126C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855568 | ||||||
| chr15:79855594 | G | A | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-10152C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855594 | ||||||
| chr15:79855617 | G | A | 1 | a0001c0001t0011g0325 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.380-10175C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855617 | ||||||
| chr15:79855621 | T | A | 98 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(95): Show | 113 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.380-10179A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855621 | ||||||
| chr15:79855878 | T | C | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-10436A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855878 | ||||||
| chr15:79855982 | G | C | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-10540C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79855982 | ||||||
| chr15:79856037 | C | G | 1 | a0001c0001t0002g0261 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.380-10595G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856037 | ||||||
| chr15:79856433 | G | C | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-10991C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856433 | ||||||
| chr15:79856512 | C | A | 66 | a0001c0001t0001g0305a0001c0001t0003g0003a0001c0001t0003g0011others(63): Show | 76 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(73): Show |
intron_variant | MODIFIER | c.380-11070G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856512 | ||||||
| chr15:79856590 | G | A | 2 | a0001c0001t0001g0305a0001c0001t0014g0222 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.380-11148C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856590 | ||||||
| chr15:79856761 | G | A | 3 | a0001c0001t0002g0195a0001c0001t0002g0198a0001c0001t0002g0202 | 3 | NA18941.hp2 NA18979.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.380-11319C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856761 | ||||||
| chr15:79856780 | AAAAG | A | 10 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-11342_380-1133 others(8): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856780 | ||||||
| chr15:79856938 | C | T | 1 | a0001c0001t0002g0253 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.380-11496G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856938 | ||||||
| chr15:79856949 | A | T | 1 | a0001c0001t0002g0289 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.380-11507T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856949 | ||||||
| chr15:79856987 | C | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0266a0001c0001t0002g0301others(1): Show | 7 | NA18944.hp2 NA18946.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-11545G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79856987 | ||||||
| chr15:79857089 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.380-11647C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857089 | ||||||
| chr15:79857156 | C | A | 1 | a0001c0001t0003g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.380-11714G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857156 | ||||||
| chr15:79857181 | A | G | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.380-11739T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857181 | ||||||
| chr15:79857211 | T | C | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-11769A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857211 | ||||||
| chr15:79857566 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.380-12124T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857566 | ||||||
| chr15:79857604 | T | C | 1 | a0001c0001t0002g0189 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.380-12162A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857604 | ||||||
| chr15:79857628 | T | C | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-12186A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857628 | ||||||
| chr15:79857738 | C | T | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-12296G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857738 | ||||||
| chr15:79857832 | C | T | 29 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(26): Show | 37 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-12390G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79857832 | ||||||
| chr15:79858006 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.380-12564T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858006 | ||||||
| chr15:79858015 | C | CA | 14 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0124others(11): Show | 14 | HG01175.hp2 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.380-12574dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858015 | ||||||
| chr15:79858015 | C | CAA | 27 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(24): Show | 35 | HG01934.hp2 HG02004.hp2 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.380-12575_380-1257 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858015 | ||||||
| chr15:79858015 | C | CAAA | 27 | a0001c0001t0001g0305a0001c0001t0002g0163a0001c0001t0003g0128others(24): Show | 29 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.380-12576_380-1257 others(7): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858015 | ||||||
| chr15:79858015 | C | CAAAA | 46 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.380-12577_380-1257 others(8): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858015 | ||||||
| chr15:79858015 | C | CAAAAA | 6 | a0001c0001t0005g0116a0001c0001t0005g0165a0001c0001t0009g0100others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.380-12578_380-1257 others(9): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858015 | ||||||
| chr15:79858095 | G | C | 314 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(311): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.380-12653C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858095 | ||||||
| chr15:79858275 | A | T | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.380-12833T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858275 | ||||||
| chr15:79858325 | G | A | 1 | a0001c0001t0014g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.380-12883C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858325 | ||||||
| chr15:79858427 | GAA | G | 6 | a0002c0002t0006g0018a0002c0002t0006g0166a0002c0002t0006g0167others(3): Show | 7 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-12987_380-1298 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858427 | ||||||
| chr15:79858557 | A | C | 1 | a0001c0001t0010g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.380-13115T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858557 | ||||||
| chr15:79858671 | A | G | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-13229T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79858671 | ||||||
| chr15:79859032 | C | A | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.380-13590G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859032 | ||||||
| chr15:79859082 | G | C | 2 | a0001c0001t0001g0305a0001c0001t0014g0222 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.380-13640C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859082 | ||||||
| chr15:79859194 | G | A | 15 | a0002c0002t0006g0013a0002c0002t0006g0018a0002c0002t0006g0026others(12): Show | 17 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.380-13752C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859194 | ||||||
| chr15:79859359 | T | A | 2 | a0001c0001t0009g0101a0001c0001t0009g0215 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.380-13917A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859359 | ||||||
| chr15:79859448 | T | A | 2 | a0001c0001t0006g0332a0001c0001t0006g0333 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.380-14006A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859448 | ||||||
| chr15:79859520 | T | C | 2 | a0001c0001t0008g0184a0001c0001t0008g0187 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.380-14078A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859520 | ||||||
| chr15:79859565 | C | T | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-14123G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859565 | ||||||
| chr15:79859584 | G | A | 11 | a0001c0001t0006g0332a0001c0001t0006g0333a0001c0001t0009g0100others(8): Show | 11 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-14142C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859584 | ||||||
| chr15:79859589 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380-14147C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859589 | ||||||
| chr15:79859633 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.380-14191G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859633 | ||||||
| chr15:79859647 | G | A | 1 | a0001c0001t0004g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.380-14205C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859647 | ||||||
| chr15:79859728 | G | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0077 | 2 | NA18975.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.380-14286C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859728 | ||||||
| chr15:79859738 | A | G | 2 | a0001c0001t0004g0306a0001c0001t0004g0313 | 2 | HG02257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.380-14296T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859738 | ||||||
| chr15:79859773 | G | C | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-14331C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859773 | ||||||
| chr15:79859817 | C | CA | 51 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0070others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.380-14376dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859817 | ||||||
| chr15:79859817 | CA | C | 9 | a0001c0001t0001g0236a0001c0001t0002g0200a0001c0001t0002g0202others(6): Show | 9 | HG02056.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-14376delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859817 | ||||||
| chr15:79859817 | CAA | C | 52 | a0001c0001t0001g0305a0001c0001t0003g0003a0001c0001t0003g0011others(49): Show | 60 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(57): Show |
intron_variant | MODIFIER | c.380-14377_380-1437 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859817 | ||||||
| chr15:79859864 | T | C | 1 | a0001c0001t0002g0287 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.380-14422A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79859864 | ||||||
| chr15:79860088 | T | C | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218 | 3 | HG02257.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.380-14646A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860088 | ||||||
| chr15:79860156 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.380-14714C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860156 | ||||||
| chr15:79860372 | G | T | 1 | a0001c0001t0007g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-14930C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860372 | ||||||
| chr15:79860376 | G | A | 1 | a0001c0001t0014g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.380-14934C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860376 | ||||||
| chr15:79860655 | A | G | 32 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(29): Show | 34 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.380-15213T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860655 | ||||||
| chr15:79860676 | AT | A | 332 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(329): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.380-15235delA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860676 | ||||||
| chr15:79860798 | T | C | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-15356A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79860798 | ||||||
| chr15:79861307 | C | T | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-15865G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861307 | ||||||
| chr15:79861402 | G | A | 3 | a0001c0001t0004g0252a0001c0001t0004g0269a0001c0001t0004g0271 | 3 | HG00733.hp1 HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.380-15960C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861402 | ||||||
| chr15:79861556 | A | C | 1 | a0001c0001t0001g0321 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.380-16114T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861556 | ||||||
| chr15:79861579 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.380-16137T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861579 | ||||||
| chr15:79861589 | G | T | 3 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215 | 3 | HG02145.hp1 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.380-16147C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861589 | ||||||
| chr15:79861614 | A | G | 1 | a0001c0001t0005g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.380-16172T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861614 | ||||||
| chr15:79861650 | T | C | 29 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(26): Show | 37 | HG01934.hp2 HG01975.hp2 HG02004.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-16208A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861650 | ||||||
| chr15:79861770 | T | C | 3 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215 | 3 | HG02145.hp1 HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.380-16328A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861770 | ||||||
| chr15:79861790 | G | C | 2 | a0001c0001t0001g0305a0001c0001t0014g0222 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.380-16348C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861790 | ||||||
| chr15:79861852 | C | T | 1 | a0001c0001t0007g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.380-16410G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861852 | ||||||
| chr15:79861939 | A | T | 1 | a0001c0001t0009g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.380-16497T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79861939 | ||||||
| chr15:79862175 | CCT | C | 10 | a0002c0002t0006g0018a0002c0002t0006g0164a0002c0002t0006g0166others(7): Show | 11 | HG00642.hp1 HG01168.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-16735_380-1673 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862175 | ||||||
| chr15:79862229 | A | G | 31 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.380-16787T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862229 | ||||||
| chr15:79862435 | C | A | 10 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-16993G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862435 | ||||||
| chr15:79862640 | C | T | 105 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(102): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.380-17198G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862640 | ||||||
| chr15:79862824 | T | C | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG01175.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.380-17382A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862824 | ||||||
| chr15:79862826 | G | C | 9 | a0001c0001t0009g0100a0001c0001t0009g0101a0001c0001t0009g0215others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-17384C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862826 | ||||||
| chr15:79862831 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.380-17389A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862831 | ||||||
| chr15:79862910 | C | G | 3 | a0001c0001t0007g0151a0001c0001t0007g0153a0001c0001t0007g0154 | 3 | HG02895.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.380-17468G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862910 | ||||||
| chr15:79862918 | G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0267 | 2 | NA18969.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.380-17476C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862918 | ||||||
| chr15:79862925 | C | T | 1 | a0001c0001t0004g0264 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.380-17483G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862925 | ||||||
| chr15:79862934 | A | G | 3 | a0001c0001t0002g0253a0001c0001t0002g0296a0001c0001t0002g0297 | 3 | HG00438.hp2 NA18941.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.380-17492T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862934 | ||||||
| chr15:79862950 | G | C | 5 | a0001c0001t0011g0325a0001c0001t0011g0326a0001c0001t0011g0330others(2): Show | 5 | HG01346.hp1 HG02572.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.380-17508C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862950 | ||||||
| chr15:79862952 | C | A | 1 | a0001c0001t0007g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.380-17510G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79862952 | ||||||
| chr15:79863297 | A | G | 2 | a0001c0001t0002g0163a0001c0001t0002g0300 | 2 | HG01884.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.380-17855T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863297 | ||||||
| chr15:79863697 | C | T | 10 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-18255G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863697 | ||||||
| chr15:79863722 | A | G | 2 | a0002c0002t0006g0027a0002c0002t0006g0028 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.380-18280T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863722 | ||||||
| chr15:79863777 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.380-18335C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863777 | ||||||
| chr15:79863782 | G | A | 1 | a0001c0001t0002g0297 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.380-18340C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863782 | ||||||
| chr15:79863943 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.380-18501T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863943 | ||||||
| chr15:79863980 | C | T | 1 | a0001c0001t0005g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.380-18538G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79863980 | ||||||
| chr15:79864024 | C | T | 1 | a0001c0001t0005g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.380-18582G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864024 | ||||||
| chr15:79864028 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.380-18586G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864028 | ||||||
| chr15:79864546 | AC | A | 4 | a0001c0001t0007g0155a0001c0001t0007g0156a0001c0001t0007g0158others(1): Show | 4 | HG02280.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.380-19105delG | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864546 | ||||||
| chr15:79864547 | C | A | 2 | a0001c0001t0007g0152a0001c0001t0007g0157 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.380-19105G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | C | CA | 57 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0015others(54): Show | 64 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.380-19106dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | C | CAA | 21 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0030others(18): Show | 26 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.380-19107_380-1910 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | C | CAAA | 9 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0093others(6): Show | 10 | HG00323.hp1 HG00621.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.380-19108_380-1910 others(7): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0007g0153 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.380-19126_380-1910 others(25): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | C | CAAAAAAA others(15): Show |
1 | a0001c0001t0007g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380-19127_380-1910 others(26): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0007g0151 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.380-19133_380-1910 others(32): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CA | C | 18 | a0001c0001t0001g0037a0001c0001t0003g0160a0001c0001t0004g0270others(15): Show | 19 | HG01081.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.380-19106delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAA | C | 34 | a0001c0001t0002g0268a0001c0001t0003g0127a0001c0001t0003g0131others(31): Show | 44 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.380-19107_380-1910 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAA | C | 30 | a0001c0001t0003g0003a0001c0001t0003g0011a0001c0001t0003g0017others(27): Show | 38 | HG00140.hp2 HG01934.hp2 HG01975.hp2 others(35): Show |
intron_variant | MODIFIER | c.380-19108_380-1910 others(7): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0004g0224a0001c0001t0005g0106a0001c0001t0005g0114 | 3 | HG01243.hp1 HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.380-19115_380-1910 others(14): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0104others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.380-19116_380-1910 others(15): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0005g0327 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.380-19117_380-1910 others(16): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0002g0179others(2): Show | 7 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.380-19119_380-1910 others(18): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAAAAAA others(8): Show |
C | 74 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0002g0001others(71): Show | 94 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.380-19120_380-1910 others(19): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864547 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0097a0001c0001t0002g0188 | 2 | NA19043.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.380-19121_380-1910 others(20): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864547 | ||||||
| chr15:79864550 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.380-19108T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864550 | ||||||
| chr15:79864551 | A | C | 1 | a0001c0001t0001g0037 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.380-19109T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864551 | ||||||
| chr15:79864705 | A | AC | 9 | a0001c0001t0001g0078a0001c0001t0001g0223a0001c0001t0001g0242others(6): Show | 9 | HG00621.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.380-19264dupG | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864705 | ||||||
| chr15:79864923 | GT | G | 10 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-19482delA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864923 | ||||||
| chr15:79864976 | A | C | 10 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(7): Show | 10 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.380-19534T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79864976 | ||||||
| chr15:79865021 | G | T | 1 | a0001c0001t0007g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.380-19579C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865021 | ||||||
| chr15:79865164 | G | A | 1 | a0001c0001t0003g0216 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380-19722C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865164 | ||||||
| chr15:79865241 | T | C | 78 | a0001c0001t0001g0124a0001c0001t0002g0002a0001c0001t0002g0008others(75): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.380-19799A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865241 | ||||||
| chr15:79865250 | T | G | 2 | a0001c0001t0006g0332a0001c0001t0006g0333 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.380-19808A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865250 | ||||||
| chr15:79865354 | C | G | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.380-19912G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865354 | ||||||
| chr15:79865375 | A | G | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218 | 3 | HG02257.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.380-19933T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865375 | ||||||
| chr15:79865380 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.380-19938C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865380 | ||||||
| chr15:79865392 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.380-19950C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865392 | ||||||
| chr15:79865475 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.380-20033C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865475 | ||||||
| chr15:79865487 | G | A | 4 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218others(1): Show | 4 | HG01081.hp2 HG02257.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.380-20045C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865487 | ||||||
| chr15:79865537 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.380-20095C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865537 | ||||||
| chr15:79865592 | G | A | 8 | a0001c0001t0002g0253a0001c0001t0002g0258a0001c0001t0002g0282others(5): Show | 8 | HG00438.hp2 HG00621.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.380-20150C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865592 | ||||||
| chr15:79865649 | T | G | 15 | a0001c0001t0001g0232a0001c0001t0001g0234a0001c0001t0001g0273others(12): Show | 15 | HG00738.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.380-20207A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865649 | ||||||
| chr15:79865700 | A | C | 152 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(149): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.380-20258T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865700 | ||||||
| chr15:79865812 | C | T | 1 | a0001c0001t0004g0310 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.380-20370G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865812 | ||||||
| chr15:79865817 | G | A | 57 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0232others(54): Show | 65 | HG00738.hp2 HG01109.hp2 HG01255.hp2 others(62): Show |
intron_variant | MODIFIER | c.380-20375C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865817 | ||||||
| chr15:79865991 | C | T | 9 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(6): Show | 9 | HG01346.hp1 HG01891.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.380-20549G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79865991 | ||||||
| chr15:79866046 | G | GT | 12 | a0001c0001t0002g0300a0001c0001t0003g0128a0001c0001t0005g0103others(9): Show | 12 | HG00323.hp2 HG00741.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.380-20605dupA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866046 | ||||||
| chr15:79866046 | GT | G | 166 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(163): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.380-20605delA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866046 | ||||||
| chr15:79866090 | T | G | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.380-20648A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866090 | ||||||
| chr15:79866117 | G | T | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0009g0318others(2): Show | 5 | HG02559.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.380-20675C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866117 | ||||||
| chr15:79866179 | A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.380-20737T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866179 | ||||||
| chr15:79866715 | C | A | 1 | a0001c0001t0002g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.380-21273G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866715 | ||||||
| chr15:79866775 | A | G | 28 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(25): Show | 37 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.380-21333T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866775 | ||||||
| chr15:79866820 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.380-21378C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866820 | ||||||
| chr15:79866833 | G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0005c0008t0007g0337 | 3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.380-21391C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866833 | ||||||
| chr15:79866881 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.380-21439C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866881 | ||||||
| chr15:79866990 | G | GA | 126 | a0001c0001t0001g0124a0001c0001t0001g0136a0001c0001t0001g0148others(123): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.380-21549dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79866990 | ||||||
| chr15:79867018 | A | C | 1 | a0001c0001t0009g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.380-21576T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867018 | ||||||
| chr15:79867019 | A | C | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.380-21577T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867019 | ||||||
| chr15:79867318 | A | T | 2 | a0001c0001t0003g0134a0001c0001t0003g0135 | 2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.379+21775T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867318 | ||||||
| chr15:79867322 | T | C | 2 | a0001c0001t0006g0332a0001c0001t0006g0333 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.379+21771A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867322 | ||||||
| chr15:79867372 | C | CA | 13 | a0001c0001t0001g0082a0001c0001t0001g0305a0001c0001t0003g0160others(10): Show | 13 | HG01361.hp2 HG02280.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.379+21720dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867372 | ||||||
| chr15:79867386 | A | G | 54 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0036others(51): Show | 66 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.379+21707T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867386 | ||||||
| chr15:79867444 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.379+21649T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867444 | ||||||
| chr15:79867485 | T | C | 13 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(10): Show | 13 | HG01255.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.379+21608A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867485 | ||||||
| chr15:79867490 | C | CT | 308 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(305): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.379+21602dupA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867490 | ||||||
| chr15:79867569 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.379+21524G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867569 | ||||||
| chr15:79867585 | A | C | 1 | a0001c0001t0004g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379+21508T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867585 | ||||||
| chr15:79867669 | C | A | 21 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(18): Show | 22 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.379+21424G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867669 | ||||||
| chr15:79867900 | C | G | 1 | a0001c0001t0004g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.379+21193G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867900 | ||||||
| chr15:79867905 | G | A | 1 | a0001c0001t0004g0278 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379+21188C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867905 | ||||||
| chr15:79867970 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.379+21123G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867970 | ||||||
| chr15:79867984 | C | A | 1 | a0001c0001t0002g0176 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.379+21109G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867984 | ||||||
| chr15:79867985 | A | C | 1 | a0001c0001t0002g0176 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.379+21108T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79867985 | ||||||
| chr15:79868210 | T | C | 6 | a0001c0001t0007g0152a0001c0001t0007g0155a0001c0001t0007g0156others(3): Show | 6 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.379+20883A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868210 | ||||||
| chr15:79868432 | G | A | 1 | a0002c0002t0006g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.379+20661C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868432 | ||||||
| chr15:79868726 | A | G | 3 | a0001c0001t0005g0104a0001c0001t0005g0115a0001c0001t0005g0117 | 3 | HG01516.hp1 HG01517.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.379+20367T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868726 | ||||||
| chr15:79868826 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.379+20267G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868826 | ||||||
| chr15:79868899 | C | T | 7 | a0001c0001t0004g0012a0001c0001t0004g0252a0001c0001t0004g0269others(4): Show | 9 | HG00733.hp1 HG01261.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.379+20194G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868899 | ||||||
| chr15:79868932 | G | A | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218 | 3 | HG02257.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.379+20161C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868932 | ||||||
| chr15:79868953 | G | A | 10 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(7): Show | 10 | HG00738.hp2 HG01346.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.379+20140C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868953 | ||||||
| chr15:79868967 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.379+20126A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79868967 | ||||||
| chr15:79869306 | T | C | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+19787A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869306 | ||||||
| chr15:79869372 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.379+19721A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869372 | ||||||
| chr15:79869379 | TATAAA | T | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+19709_379+1971 others(9): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869379 | ||||||
| chr15:79869923 | A | C | 21 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(18): Show | 22 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.379+19170T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869923 | ||||||
| chr15:79869928 | A | C | 1 | a0001c0001t0003g0142 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.379+19165T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869928 | ||||||
| chr15:79869984 | T | C | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+19109A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869984 | ||||||
| chr15:79869985 | A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0046others(5): Show | 8 | HG02080.hp1 HG02523.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.379+19108T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79869985 | ||||||
| chr15:79870015 | G | A | 2 | a0001c0001t0002g0207a0001c0005t0002g0190 | 2 | NA18995.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.379+19078C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870015 | ||||||
| chr15:79870157 | C | A | 180 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(177): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.379+18936G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870157 | ||||||
| chr15:79870174 | C | A | 13 | a0001c0001t0001g0311a0001c0001t0002g0163a0001c0001t0003g0162others(10): Show | 13 | HG00280.hp1 HG02280.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+18919G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870174 | ||||||
| chr15:79870215 | G | T | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+18878C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870215 | ||||||
| chr15:79870302 | T | A | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+18791A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870302 | ||||||
| chr15:79870622 | C | A | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+18471G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870622 | ||||||
| chr15:79870664 | C | T | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+18429G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870664 | ||||||
| chr15:79870680 | T | C | 138 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(135): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.379+18413A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870680 | ||||||
| chr15:79870964 | G | A | 2 | a0001c0001t0009g0100a0001c0001t0009g0101 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.379+18129C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79870964 | ||||||
| chr15:79871034 | T | C | 7 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(4): Show | 7 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.379+18059A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871034 | ||||||
| chr15:79871308 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.379+17785C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871308 | ||||||
| chr15:79871330 | A | G | 21 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(18): Show | 22 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.379+17763T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871330 | ||||||
| chr15:79871401 | A | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0005c0008t0007g0337 | 3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.379+17692T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871401 | ||||||
| chr15:79871711 | C | T | 181 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(178): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.379+17382G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871711 | ||||||
| chr15:79871746 | T | C | 91 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(88): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.379+17347A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871746 | ||||||
| chr15:79871825 | G | T | 1 | a0001c0001t0005g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.379+17268C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871825 | ||||||
| chr15:79871829 | G | A | 28 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(25): Show | 37 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+17264C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871829 | ||||||
| chr15:79871848 | T | C | 62 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.379+17245A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871848 | ||||||
| chr15:79871912 | G | A | 13 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(10): Show | 13 | HG01255.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.379+17181C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871912 | ||||||
| chr15:79871918 | C | T | 1 | a0001c0001t0004g0007 | 4 | HG02132.hp1 NA18985.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+17175G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871918 | ||||||
| chr15:79871919 | A | G | 29 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(26): Show | 38 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.379+17174T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871919 | ||||||
| chr15:79871959 | G | C | 10 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG01346.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.379+17134C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871959 | ||||||
| chr15:79871971 | G | A | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+17122C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79871971 | ||||||
| chr15:79872099 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.379+16994C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872099 | ||||||
| chr15:79872103 | C | CA | 40 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0048others(37): Show | 50 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.379+16989dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872103 | ||||||
| chr15:79872103 | C | CAA | 22 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(19): Show | 23 | HG00738.hp2 HG01256.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.379+16988_379+1698 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872103 | ||||||
| chr15:79872103 | C | CAAA | 12 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(9): Show | 12 | HG00642.hp1 HG01346.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.379+16987_379+1698 others(7): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872103 | ||||||
| chr15:79872103 | CA | C | 40 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0051others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.379+16989delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872103 | ||||||
| chr15:79872103 | CAA | C | 30 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(27): Show | 38 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(35): Show |
intron_variant | MODIFIER | c.379+16988_379+1698 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872103 | ||||||
| chr15:79872103 | CAAAAAA | C | 46 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(43): Show | 56 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.379+16984_379+1698 others(10): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872103 | ||||||
| chr15:79872163 | A | C | 1 | a0001c0001t0005g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.379+16930T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872163 | ||||||
| chr15:79872165 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.379+16928T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872165 | ||||||
| chr15:79872411 | G | T | 1 | a0001c0001t0005g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.379+16682C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872411 | ||||||
| chr15:79872413 | G | A | 9 | a0001c0001t0007g0151a0001c0001t0007g0152a0001c0001t0007g0153others(6): Show | 9 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.379+16680C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872413 | ||||||
| chr15:79872459 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.379+16634C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872459 | ||||||
| chr15:79872487 | C | T | 27 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(24): Show | 36 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+16606G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872487 | ||||||
| chr15:79872532 | T | TAGCCCAG others(4): Show |
3 | a0001c0001t0011g0325a0001c0001t0011g0326a0001c0001t0012g0324 | 3 | HG01346.hp1 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.379+16550_379+1656 others(15): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872532 | ||||||
| chr15:79872584 | G | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0036others(10): Show | 15 | HG02165.hp2 NA18947.hp2 NA18949.hp1 others(12): Show |
intron_variant | MODIFIER | c.379+16509C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872584 | ||||||
| chr15:79872734 | C | T | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.379+16359G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872734 | ||||||
| chr15:79872796 | T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0056a0001c0001t0001g0059 | 3 | HG00438.hp1 HG00558.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.379+16297A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872796 | ||||||
| chr15:79872801 | A | G | 117 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(114): Show | 135 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.379+16292T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872801 | ||||||
| chr15:79872820 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.379+16273G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872820 | ||||||
| chr15:79872988 | G | C | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+16105C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79872988 | ||||||
| chr15:79873026 | A | G | 308 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(305): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.379+16067T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79873026 | ||||||
| chr15:79873158 | T | C | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.379+15935A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79873158 | ||||||
| chr15:79873193 | T | C | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0216others(2): Show | 5 | HG02257.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.379+15900A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79873193 | ||||||
| chr15:79873555 | G | GAA | 10 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG01346.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.379+15536_379+1553 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79873555 | ||||||
| chr15:79873620 | T | C | 35 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(32): Show | 45 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.379+15473A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79873620 | ||||||
| chr15:79874084 | T | C | 5 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+15009A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874084 | ||||||
| chr15:79874255 | C | A | 171 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(168): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.379+14838G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874255 | ||||||
| chr15:79874390 | C | T | 1 | a0001c0001t0006g0332 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.379+14703G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874390 | ||||||
| chr15:79874397 | C | T | 1 | a0001c0001t0002g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.379+14696G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874397 | ||||||
| chr15:79874514 | C | A | 36 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(33): Show | 46 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.379+14579G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874514 | ||||||
| chr15:79874657 | CA | C | 28 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(25): Show | 37 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+14435delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874657 | ||||||
| chr15:79874835 | C | T | 18 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(15): Show | 18 | HG01255.hp2 HG02145.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.379+14258G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874835 | ||||||
| chr15:79874948 | T | C | 21 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(18): Show | 22 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.379+14145A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874948 | ||||||
| chr15:79874994 | C | T | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+14099G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79874994 | ||||||
| chr15:79875182 | A | G | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+13911T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875182 | ||||||
| chr15:79875230 | C | T | 1 | a0001c0001t0011g0326 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379+13863G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875230 | ||||||
| chr15:79875240 | G | A | 48 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(45): Show | 58 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.379+13853C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875240 | ||||||
| chr15:79875262 | C | A | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+13831G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875262 | ||||||
| chr15:79875272 | G | A | 4 | a0001c0001t0001g0223a0001c0001t0010g0219a0001c0001t0010g0220others(1): Show | 4 | HG02486.hp1 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+13821C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875272 | ||||||
| chr15:79875274 | CA | C | 20 | a0001c0001t0001g0093a0001c0001t0001g0148a0001c0001t0001g0149others(17): Show | 22 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.379+13818delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875274 | ||||||
| chr15:79875458 | T | C | 5 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+13635A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875458 | ||||||
| chr15:79875617 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.379+13476T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875617 | ||||||
| chr15:79875635 | G | A | 21 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(18): Show | 22 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.379+13458C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875635 | ||||||
| chr15:79875665 | G | C | 2 | a0001c0001t0009g0100a0001c0001t0009g0101 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.379+13428C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875665 | ||||||
| chr15:79875670 | T | C | 5 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+13423A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875670 | ||||||
| chr15:79875756 | T | G | 1 | a0001c0001t0009g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.379+13337A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875756 | ||||||
| chr15:79875759 | A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0063 | 4 | HG01257.hp1 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+13334T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875759 | ||||||
| chr15:79875805 | C | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0005c0008t0007g0337 | 3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.379+13288G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875805 | ||||||
| chr15:79875809 | T | G | 2 | a0001c0001t0008g0184a0001c0001t0008g0187 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.379+13284A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875809 | ||||||
| chr15:79875876 | T | C | 180 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(177): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.379+13217A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875876 | ||||||
| chr15:79875940 | T | G | 20 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(17): Show | 21 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.379+13153A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875940 | ||||||
| chr15:79875979 | AAAAT | A | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+13110_379+1311 others(8): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79875979 | ||||||
| chr15:79876257 | G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0216others(2): Show | 5 | HG02257.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.379+12836C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876257 | ||||||
| chr15:79876260 | A | G | 11 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(8): Show | 11 | HG01255.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+12833T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876260 | ||||||
| chr15:79876338 | C | T | 2 | a0001c0001t0001g0267a0001c0001t0004g0299 | 2 | NA18969.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.379+12755G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876338 | ||||||
| chr15:79876403 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379+12690C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876403 | ||||||
| chr15:79876467 | T | C | 1 | a0001c0001t0010g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.379+12626A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876467 | ||||||
| chr15:79876472 | G | A | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+12621C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876472 | ||||||
| chr15:79876475 | C | T | 1 | a0001c0001t0017g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.379+12618G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876475 | ||||||
| chr15:79876543 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.379+12550T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876543 | ||||||
| chr15:79876551 | C | G | 1 | a0001c0001t0009g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.379+12542G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876551 | ||||||
| chr15:79876614 | C | CA | 82 | a0001c0001t0001g0060a0001c0001t0001g0079a0001c0001t0001g0148others(79): Show | 101 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.379+12478dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876614 | ||||||
| chr15:79876614 | C | CAA | 12 | a0001c0001t0002g0163a0001c0001t0004g0281a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.379+12477_379+1247 others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876614 | ||||||
| chr15:79876614 | CA | C | 19 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(16): Show | 20 | HG00738.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.379+12478delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876614 | ||||||
| chr15:79876653 | T | A | 1 | a0001c0001t0011g0326 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.379+12440A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876653 | ||||||
| chr15:79876653 | T | G | 2 | a0001c0001t0011g0325a0001c0001t0012g0324 | 2 | HG01346.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.379+12440A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876653 | ||||||
| chr15:79876714 | T | C | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218 | 3 | HG02257.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.379+12379A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876714 | ||||||
| chr15:79876723 | C | A | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.379+12370G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876723 | ||||||
| chr15:79876860 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.379+12233A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876860 | ||||||
| chr15:79876917 | C | T | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+12176G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79876917 | ||||||
| chr15:79877044 | T | A | 26 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(23): Show | 27 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.379+12049A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877044 | ||||||
| chr15:79877045 | A | T | 2 | a0001c0001t0001g0062a0005c0008t0007g0337 | 2 | HG03139.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.379+12048T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877045 | ||||||
| chr15:79877148 | G | T | 1 | a0001c0001t0005g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379+11945C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877148 | ||||||
| chr15:79877271 | A | G | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+11822T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877271 | ||||||
| chr15:79877305 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.379+11788T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877305 | ||||||
| chr15:79877391 | A | G | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+11702T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877391 | ||||||
| chr15:79877443 | G | A | 1 | a0001c0001t0002g0255 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.379+11650C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877443 | ||||||
| chr15:79877483 | G | A | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+11610C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877483 | ||||||
| chr15:79877585 | T | C | 138 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(135): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.379+11508A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877585 | ||||||
| chr15:79877642 | A | C | 1 | a0001c0001t0002g0301 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.379+11451T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877642 | ||||||
| chr15:79877671 | A | T | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.379+11422T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877671 | ||||||
| chr15:79877683 | G | C | 2 | a0001c0001t0006g0332a0001c0001t0006g0333 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.379+11410C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877683 | ||||||
| chr15:79877831 | C | G | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+11262G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877831 | ||||||
| chr15:79877868 | GA | G | 138 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(135): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.379+11224delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79877868 | ||||||
| chr15:79878221 | C | T | 180 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(177): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.379+10872G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878221 | ||||||
| chr15:79878260 | C | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0078others(2): Show | 6 | HG01123.hp1 HG01934.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.379+10833G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878260 | ||||||
| chr15:79878296 | G | A | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+10797C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878296 | ||||||
| chr15:79878343 | C | T | 1 | a0001c0001t0003g0133 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.379+10750G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878343 | ||||||
| chr15:79878433 | C | T | 1 | a0001c0001t0009g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.379+10660G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878433 | ||||||
| chr15:79878445 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.379+10648A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878445 | ||||||
| chr15:79878510 | T | A | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.379+10583A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878510 | ||||||
| chr15:79878661 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379+10432C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878661 | ||||||
| chr15:79878861 | C | CT | 132 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(129): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.379+10231dupA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878861 | ||||||
| chr15:79878865 | T | C | 1 | a0001c0001t0004g0313 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.379+10228A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79878865 | ||||||
| chr15:79879102 | T | A | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+9991A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879102 | ||||||
| chr15:79879120 | ATTTTCAT others(11): Show |
A | 1 | a0001c0001t0001g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.379+9955_379+9972d others(20): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879120 | ||||||
| chr15:79879121 | T | A | 21 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(18): Show | 22 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.379+9972A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879121 | ||||||
| chr15:79879226 | G | A | 2 | a0001c0001t0006g0332a0001c0001t0006g0333 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.379+9867C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879226 | ||||||
| chr15:79879288 | T | G | 2 | a0001c0001t0001g0080a0001c0001t0002g0049 | 2 | NA18952.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.379+9805A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879288 | ||||||
| chr15:79879315 | A | G | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+9778T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879315 | ||||||
| chr15:79879321 | C | CT | 44 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0050others(41): Show | 46 | HG00280.hp1 HG00642.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.379+9771dupA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879321 | ||||||
| chr15:79879321 | C | CTT | 35 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0251others(32): Show | 45 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.379+9770_379+9771d others(4): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879321 | ||||||
| chr15:79879321 | CT | C | 57 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(54): Show | 65 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.379+9771delA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879321 | ||||||
| chr15:79879321 | CTT | C | 26 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(23): Show | 27 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.379+9770_379+9771d others(4): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879321 | ||||||
| chr15:79879491 | CTAA | C | 27 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(24): Show | 36 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+9599_379+9601d others(5): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879491 | ||||||
| chr15:79879495 | T | A | 27 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(24): Show | 36 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+9598A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879495 | ||||||
| chr15:79879552 | G | T | 1 | a0001c0001t0004g0309 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.379+9541C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879552 | ||||||
| chr15:79879629 | A | G | 47 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(44): Show | 57 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.379+9464T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879629 | ||||||
| chr15:79879679 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+9414C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879679 | ||||||
| chr15:79879683 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.379+9410C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879683 | ||||||
| chr15:79879791 | C | T | 39 | a0001c0001t0001g0174a0001c0001t0002g0001a0001c0001t0002g0020others(36): Show | 49 | HG00140.hp1 HG00558.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.379+9302G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879791 | ||||||
| chr15:79879809 | C | A | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.379+9284G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879809 | ||||||
| chr15:79879856 | T | G | 35 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(32): Show | 45 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.379+9237A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79879856 | ||||||
| chr15:79880014 | C | T | 13 | a0001c0001t0001g0124a0001c0001t0005g0103a0001c0001t0005g0104others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+9079G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880014 | ||||||
| chr15:79880043 | A | C | 62 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.379+9050T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880043 | ||||||
| chr15:79880156 | GC | G | 26 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(23): Show | 27 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.379+8936delG | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880156 | ||||||
| chr15:79880257 | T | C | 4 | a0001c0001t0005g0109a0001c0001t0005g0110a0001c0001t0005g0111others(1): Show | 4 | HG00099.hp2 HG01123.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.379+8836A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880257 | ||||||
| chr15:79880374 | C | T | 1 | a0001c0001t0003g0127 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.379+8719G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880374 | ||||||
| chr15:79880432 | C | T | 62 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.379+8661G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880432 | ||||||
| chr15:79880483 | T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0033 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.379+8610A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880483 | ||||||
| chr15:79880534 | C | T | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+8559G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880534 | ||||||
| chr15:79880712 | C | T | 10 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG01346.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.379+8381G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880712 | ||||||
| chr15:79880791 | C | CA | 38 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0001g0149others(35): Show | 46 | HG01934.hp2 HG02055.hp2 HG02056.hp1 others(43): Show |
intron_variant | MODIFIER | c.379+8301dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880791 | ||||||
| chr15:79880791 | C | CAA | 20 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(17): Show | 21 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.379+8300_379+8301d others(4): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880791 | ||||||
| chr15:79880800 | A | AAAAC | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+8289_379+8292d others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880800 | ||||||
| chr15:79880803 | AC | A | 75 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(72): Show | 94 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.379+8289delG | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880803 | ||||||
| chr15:79880804 | C | A | 1 | a0001c0001t0002g0294 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.379+8289G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79880804 | ||||||
| chr15:79881041 | A | G | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.379+8052T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881041 | ||||||
| chr15:79881366 | T | A | 35 | a0001c0001t0001g0291a0001c0001t0002g0002a0001c0001t0002g0008others(32): Show | 45 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.379+7727A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881366 | ||||||
| chr15:79881441 | A | G | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+7652T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881441 | ||||||
| chr15:79881562 | G | A | 1 | a0001c0001t0003g0141 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.379+7531C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881562 | ||||||
| chr15:79881577 | G | GA | 25 | a0001c0001t0001g0124a0001c0001t0002g0295a0001c0001t0003g0099others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.379+7515dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881577 | ||||||
| chr15:79881674 | T | C | 7 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(4): Show | 7 | HG00558.hp1 NA18942.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.379+7419A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881674 | ||||||
| chr15:79881990 | G | A | 1 | a0001c0001t0012g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.379+7103C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79881990 | ||||||
| chr15:79882024 | T | C | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+7069A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882024 | ||||||
| chr15:79882037 | G | A | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0245others(3): Show | 6 | HG02258.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.379+7056C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882037 | ||||||
| chr15:79882046 | C | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(134): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.379+7047G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882046 | ||||||
| chr15:79882074 | TTAC | T | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG01255.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+7016_379+7018d others(5): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882074 | ||||||
| chr15:79882079 | T | G | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG01255.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.379+7014A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882079 | ||||||
| chr15:79882094 | T | C | 13 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(10): Show | 13 | HG01255.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.379+6999A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882094 | ||||||
| chr15:79882150 | G | A | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+6943C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882150 | ||||||
| chr15:79882195 | C | T | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.379+6898G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882195 | ||||||
| chr15:79882283 | C | CA | 29 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0002g0125others(26): Show | 37 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(34): Show |
intron_variant | MODIFIER | c.379+6809dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882283 | ||||||
| chr15:79882944 | G | A | 2 | a0001c0001t0009g0100a0001c0001t0009g0101 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.379+6149C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882944 | ||||||
| chr15:79882954 | C | T | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+6139G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882954 | ||||||
| chr15:79882975 | C | A | 1 | a0001c0001t0005g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.379+6118G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79882975 | ||||||
| chr15:79883166 | T | C | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.379+5927A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883166 | ||||||
| chr15:79883374 | T | A | 2 | a0001c0001t0001g0331a0001c0001t0011g0330 | 2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.379+5719A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883374 | ||||||
| chr15:79883418 | A | T | 27 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(24): Show | 36 | HG00280.hp2 HG00733.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+5675T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883418 | ||||||
| chr15:79883471 | G | GAGTCTA | 11 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(8): Show | 11 | HG00738.hp2 HG01346.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+5616_379+5621d others(8): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883471 | ||||||
| chr15:79883533 | C | A | 3 | a0001c0001t0002g0253a0001c0001t0002g0296a0001c0001t0002g0297 | 3 | HG00438.hp2 NA18941.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.379+5560G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883533 | ||||||
| chr15:79883533 | C | T | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.379+5560G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883533 | ||||||
| chr15:79883664 | C | T | 1 | a0001c0001t0002g0266 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.379+5429G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883664 | ||||||
| chr15:79883674 | T | C | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+5419A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883674 | ||||||
| chr15:79883692 | CACCTTAC others(1): Show |
C | 169 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(166): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.379+5393_379+5400d others(10): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883692 | ||||||
| chr15:79883953 | C | T | 41 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0321others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.379+5140G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79883953 | ||||||
| chr15:79884007 | C | T | 137 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(134): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.379+5086G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79884007 | ||||||
| chr15:79884519 | T | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0005c0008t0007g0337 | 3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.379+4574A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79884519 | ||||||
| chr15:79884531 | G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0005c0008t0007g0337 | 3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.379+4562C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79884531 | ||||||
| chr15:79884871 | G | C | 1 | a0002c0002t0006g0172 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.379+4222C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79884871 | ||||||
| chr15:79885052 | G | T | 1 | a0001c0001t0002g0049 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.379+4041C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885052 | ||||||
| chr15:79885187 | C | T | 1 | a0001c0001t0004g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.379+3906G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885187 | ||||||
| chr15:79885254 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.379+3839A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885254 | ||||||
| chr15:79885345 | A | G | 44 | a0001c0001t0001g0174a0001c0001t0002g0001a0001c0001t0002g0020others(41): Show | 54 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.379+3748T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885345 | ||||||
| chr15:79885597 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.379+3496C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885597 | ||||||
| chr15:79885916 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.379+3177T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885916 | ||||||
| chr15:79885941 | C | A | 170 | a0001c0001t0001g0083a0001c0001t0001g0124a0001c0001t0001g0136others(167): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.379+3152G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79885941 | ||||||
| chr15:79886027 | G | A | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218 | 3 | HG02257.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.379+3066C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886027 | ||||||
| chr15:79886039 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.379+3054C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886039 | ||||||
| chr15:79886243 | T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0033 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.379+2850A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886243 | ||||||
| chr15:79886270 | T | A | 44 | a0001c0001t0001g0174a0001c0001t0002g0001a0001c0001t0002g0020others(41): Show | 54 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.379+2823A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886270 | ||||||
| chr15:79886310 | T | C | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.379+2783A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886310 | ||||||
| chr15:79886401 | C | T | 1 | a0001c0001t0005g0327 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.379+2692G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886401 | ||||||
| chr15:79886410 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.379+2683T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886410 | ||||||
| chr15:79886453 | T | A | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.379+2640A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886453 | ||||||
| chr15:79886479 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.379+2614A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886479 | ||||||
| chr15:79886628 | C | G | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.379+2465G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886628 | ||||||
| chr15:79886722 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.379+2371T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886722 | ||||||
| chr15:79886968 | C | T | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.379+2125G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886968 | ||||||
| chr15:79886997 | G | C | 5 | a0001c0001t0003g0098a0001c0001t0003g0142a0001c0001t0003g0143others(2): Show | 5 | NA18968.hp1 NA18975.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.379+2096C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79886997 | ||||||
| chr15:79887066 | C | T | 1 | a0001c0001t0017g0265 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.379+2027G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887066 | ||||||
| chr15:79887080 | C | A | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+2013G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887080 | ||||||
| chr15:79887154 | G | A | 116 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(113): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.379+1939C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887154 | ||||||
| chr15:79887293 | A | G | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+1800T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887293 | ||||||
| chr15:79887353 | G | C | 3 | a0001c0001t0005g0104a0001c0001t0005g0115a0001c0001t0005g0117 | 3 | HG01516.hp1 HG01517.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.379+1740C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887353 | ||||||
| chr15:79887362 | T | C | 10 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG01346.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.379+1731A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887362 | ||||||
| chr15:79887395 | A | G | 116 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(113): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.379+1698T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887395 | ||||||
| chr15:79887419 | AAGATGTT others(13): Show |
A | 1 | a0001c0001t0005g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.379+1654_379+1673d others(22): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887419 | ||||||
| chr15:79887505 | C | T | 169 | a0001c0001t0001g0124a0001c0001t0001g0136a0001c0001t0001g0148others(166): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.379+1588G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887505 | ||||||
| chr15:79887764 | A | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(135): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.379+1329T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887764 | ||||||
| chr15:79887853 | T | C | 3 | a0001c0001t0003g0011a0001c0001t0003g0130a0001c0001t0003g0131 | 5 | NA18939.hp1 NA18946.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.379+1240A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79887853 | ||||||
| chr15:79888038 | T | G | 1 | a0001c0001t0004g0312 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.379+1055A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888038 | ||||||
| chr15:79888185 | G | C | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.379+908C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888185 | ||||||
| chr15:79888315 | C | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.379+778G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888315 | ||||||
| chr15:79888476 | C | T | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+617G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888476 | ||||||
| chr15:79888489 | GAAAGAAC others(5): Show |
G | 98 | a0001c0001t0001g0124a0001c0001t0001g0230a0001c0001t0001g0232others(95): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.379+592_379+603del others(12): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888489 | ||||||
| chr15:79888532 | A | G | 1 | a0001c0001t0005g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.379+561T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888532 | ||||||
| chr15:79888571 | G | C | 13 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(10): Show | 13 | HG01255.hp2 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.379+522C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888571 | ||||||
| chr15:79888579 | G | C | 5 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(2): Show | 5 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.379+514C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888579 | ||||||
| chr15:79888652 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.379+441T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888652 | ||||||
| chr15:79888968 | C | T | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.379+125G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888968 | ||||||
| chr15:79888970 | T | C | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.379+123A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79888970 | ||||||
| chr15:79889072 | T | C | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | HG01175.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.379+21A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 2/2 | chr15 | 79889072 | ||||||
| chr15:79889393 | A | G | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-39T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889393 | ||||||
| chr15:79889474 | A | G | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-120T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889474 | ||||||
| chr15:79889628 | G | A | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-274C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889628 | ||||||
| chr15:79889636 | G | A | 1 | a0001c0001t0009g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.118-282C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889636 | ||||||
| chr15:79889656 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.118-302C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889656 | ||||||
| chr15:79889689 | C | G | 10 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG01346.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.118-335G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889689 | ||||||
| chr15:79889704 | C | T | 9 | a0001c0001t0007g0151a0001c0001t0007g0152a0001c0001t0007g0153others(6): Show | 9 | HG02280.hp2 HG02717.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-350G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889704 | ||||||
| chr15:79889708 | T | C | 126 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(123): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.118-354A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889708 | ||||||
| chr15:79889876 | A | G | 26 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(23): Show | 27 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.118-522T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79889876 | ||||||
| chr15:79890071 | C | G | 1 | a0001c0001t0004g0264 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.118-717G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890071 | ||||||
| chr15:79890194 | GCT | G | 64 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(61): Show | 83 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.118-842_118-841del others(2): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890194 | ||||||
| chr15:79890207 | C | CT | 43 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0047others(40): Show | 51 | HG00621.hp2 HG01934.hp2 HG01978.hp2 others(48): Show |
intron_variant | MODIFIER | c.118-854dupA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890207 | C | CTT | 11 | a0001c0001t0001g0305a0001c0001t0002g0125a0001c0001t0002g0178others(8): Show | 12 | HG02071.hp2 NA18939.hp1 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.118-855_118-854dup others(2): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890207 | CT | C | 125 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(122): Show | 160 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.118-854delA | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890207 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(5): Show | 8 | HG01255.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-861_118-854del others(8): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890207 | CTTTTTTT others(3): Show |
C | 21 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.118-863_118-854del others(10): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890207 | CTTTTTTT others(7): Show |
C | 26 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(23): Show | 27 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.118-867_118-854del others(14): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890207 | CTTTTTTT others(10): Show |
C | 1 | a0005c0008t0007g0337 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118-870_118-854del others(17): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890207 | ||||||
| chr15:79890225 | T | C | 1 | a0001c0001t0005g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.118-871A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890225 | ||||||
| chr15:79890279 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.118-925C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890279 | ||||||
| chr15:79890489 | A | G | 2 | a0001c0001t0009g0100a0001c0001t0009g0101 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.118-1135T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890489 | ||||||
| chr15:79890593 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.118-1239G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890593 | ||||||
| chr15:79890667 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.118-1313A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890667 | ||||||
| chr15:79890743 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.118-1389A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890743 | ||||||
| chr15:79890809 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.118-1455A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890809 | ||||||
| chr15:79890929 | C | T | 1 | a0001c0001t0002g0258 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.118-1575G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890929 | ||||||
| chr15:79890988 | A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.118-1634T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79890988 | ||||||
| chr15:79891000 | G | A | 63 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(60): Show | 82 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.118-1646C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891000 | ||||||
| chr15:79891121 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.118-1767C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891121 | ||||||
| chr15:79891304 | T | C | 5 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(2): Show | 5 | HG00738.hp2 HG01346.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-1950A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891304 | ||||||
| chr15:79891363 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.118-2009C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891363 | ||||||
| chr15:79891364 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.118-2010T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891364 | ||||||
| chr15:79891365 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.118-2011C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891365 | ||||||
| chr15:79891365 | G | GA | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-2012dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891365 | ||||||
| chr15:79891424 | C | A | 296 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(293): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.118-2070G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891424 | ||||||
| chr15:79891495 | G | A | 1 | a0001c0001t0013g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.118-2141C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891495 | ||||||
| chr15:79891556 | G | T | 125 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(122): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.118-2202C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891556 | ||||||
| chr15:79891654 | CCAAAAAG others(26): Show |
C | 1 | a0001c0001t0005g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118-2333_118-2301d others(35): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891654 | ||||||
| chr15:79891725 | A | T | 308 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(305): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.118-2371T>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891725 | ||||||
| chr15:79891766 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.118-2412C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891766 | ||||||
| chr15:79891829 | G | A | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-2475C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891829 | ||||||
| chr15:79891900 | A | C | 1 | a0001c0001t0005g0256 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118-2546T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891900 | ||||||
| chr15:79891919 | T | C | 2 | a0001c0001t0009g0100a0001c0001t0009g0101 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.118-2565A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891919 | ||||||
| chr15:79891938 | G | A | 1 | a0001c0001t0004g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-2584C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891938 | ||||||
| chr15:79891963 | C | CA | 122 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(119): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.118-2610dupT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891963 | ||||||
| chr15:79891963 | CA | C | 28 | a0001c0001t0001g0136a0001c0001t0001g0316a0001c0001t0002g0125others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-2610delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891963 | ||||||
| chr15:79891963 | CAA | C | 27 | a0001c0001t0001g0124a0001c0001t0001g0236a0001c0001t0003g0160others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.118-2611_118-2610d others(4): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891963 | ||||||
| chr15:79891963 | CAAA | C | 90 | a0001c0001t0001g0223a0001c0001t0001g0230a0001c0001t0001g0232others(87): Show | 110 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.118-2612_118-2610d others(5): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891963 | ||||||
| chr15:79891963 | CAAAA | C | 8 | a0001c0001t0001g0321a0001c0001t0002g0253a0001c0001t0002g0300others(5): Show | 8 | HG01255.hp2 HG01256.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-2613_118-2610d others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891963 | ||||||
| chr15:79891987 | A | G | 84 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(81): Show | 104 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.118-2633T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79891987 | ||||||
| chr15:79892018 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.118-2664A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892018 | ||||||
| chr15:79892041 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118-2687T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892041 | ||||||
| chr15:79892163 | T | C | 45 | a0001c0001t0001g0174a0001c0001t0002g0001a0001c0001t0002g0020others(42): Show | 55 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.118-2809A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892163 | ||||||
| chr15:79892275 | G | A | 8 | a0001c0001t0001g0124a0001c0001t0005g0103a0001c0001t0005g0118others(5): Show | 8 | HG00099.hp1 HG00323.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-2921C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892275 | ||||||
| chr15:79892314 | A | G | 10 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(7): Show | 10 | HG00738.hp2 HG01346.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.118-2960T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892314 | ||||||
| chr15:79892315 | G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(126): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.118-2961C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892315 | ||||||
| chr15:79892333 | G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0216others(2): Show | 5 | HG02257.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-2979C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892333 | ||||||
| chr15:79892374 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.118-3020T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892374 | ||||||
| chr15:79892398 | A | G | 296 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(293): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.118-3044T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892398 | ||||||
| chr15:79892641 | C | T | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-3287G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892641 | ||||||
| chr15:79892670 | C | T | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-3316G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892670 | ||||||
| chr15:79892743 | G | C | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-3389C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892743 | ||||||
| chr15:79892806 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118-3452G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892806 | ||||||
| chr15:79892816 | T | C | 26 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0234others(23): Show | 27 | HG00642.hp1 HG00738.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.118-3462A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892816 | ||||||
| chr15:79892820 | G | A | 11 | a0001c0001t0002g0163a0001c0001t0007g0150a0001c0001t0007g0151others(8): Show | 11 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.118-3466C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892820 | ||||||
| chr15:79892875 | C | T | 1 | a0001c0001t0004g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-3521G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892875 | ||||||
| chr15:79892889 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118-3535A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892889 | ||||||
| chr15:79892923 | C | A | 1 | a0001c0001t0002g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.118-3569G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892923 | ||||||
| chr15:79892937 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118-3583C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892937 | ||||||
| chr15:79892963 | A | G | 115 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(112): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.118-3609T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79892963 | ||||||
| chr15:79893008 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.118-3654T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893008 | ||||||
| chr15:79893100 | A | G | 1 | a0001c0001t0002g0255 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.118-3746T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893100 | ||||||
| chr15:79893181 | G | T | 7 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0177others(4): Show | 7 | HG00558.hp1 NA18942.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+3691C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893181 | ||||||
| chr15:79893193 | A | G | 1 | a0001c0001t0007g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.117+3679T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893193 | ||||||
| chr15:79893306 | G | A | 11 | a0001c0001t0001g0223a0001c0001t0001g0321a0001c0001t0001g0322others(8): Show | 11 | HG01255.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+3566C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893306 | ||||||
| chr15:79893339 | T | C | 62 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.117+3533A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893339 | ||||||
| chr15:79893345 | T | A | 23 | a0001c0001t0001g0124a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.117+3527A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893345 | ||||||
| chr15:79893389 | G | A | 1 | a0001c0001t0005g0212 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+3483C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893389 | ||||||
| chr15:79893397 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.117+3475C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893397 | ||||||
| chr15:79893494 | C | T | 1 | a0001c0001t0009g0318 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.117+3378G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893494 | ||||||
| chr15:79893524 | C | T | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.117+3348G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893524 | ||||||
| chr15:79893555 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.117+3317C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893555 | ||||||
| chr15:79893606 | G | A | 10 | a0001c0001t0005g0165a0002c0002t0006g0018a0002c0002t0006g0164others(7): Show | 11 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+3266C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893606 | ||||||
| chr15:79893646 | C | T | 1 | a0001c0001t0004g0306 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.117+3226G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893646 | ||||||
| chr15:79893656 | C | A | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.117+3216G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893656 | ||||||
| chr15:79893697 | CA | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG00323.hp2 HG02896.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+3174delT | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893697 | ||||||
| chr15:79893754 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.117+3118T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893754 | ||||||
| chr15:79893782 | CAGAG | C | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+3086_117+3089d others(6): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893782 | ||||||
| chr15:79893800 | C | T | 310 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(307): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.117+3072G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893800 | ||||||
| chr15:79893938 | G | A | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0218 | 3 | HG02257.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.117+2934C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893938 | ||||||
| chr15:79893998 | C | T | 63 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(60): Show | 82 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.117+2874G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79893998 | ||||||
| chr15:79894012 | G | A | 4 | a0001c0001t0002g0022a0001c0001t0002g0213a0001c0001t0003g0214others(1): Show | 5 | HG01071.hp2 HG01358.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+2860C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894012 | ||||||
| chr15:79894014 | T | A | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117+2858A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894014 | ||||||
| chr15:79894015 | G | A | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117+2857C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894015 | ||||||
| chr15:79894016 | T | C | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117+2856A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894016 | ||||||
| chr15:79894017 | T | A | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.117+2855A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894017 | ||||||
| chr15:79894113 | A | G | 309 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(306): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.117+2759T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894113 | ||||||
| chr15:79894134 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.117+2738G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894134 | ||||||
| chr15:79894241 | C | T | 1 | a0001c0001t0004g0252 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.117+2631G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894241 | ||||||
| chr15:79894247 | G | A | 2 | a0001c0001t0006g0332a0001c0001t0006g0333 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.117+2625C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894247 | ||||||
| chr15:79894295 | C | T | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.117+2577G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894295 | ||||||
| chr15:79894399 | T | G | 3 | a0001c0001t0009g0318a0001c0001t0009g0319a0001c0001t0009g0320 | 3 | HG02559.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.117+2473A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894399 | ||||||
| chr15:79894545 | G | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(125): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.117+2327C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894545 | ||||||
| chr15:79894582 | A | C | 308 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(305): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.117+2290T>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894582 | ||||||
| chr15:79894601 | T | G | 28 | a0001c0001t0001g0136a0001c0001t0002g0125a0001c0001t0003g0003others(25): Show | 36 | HG01934.hp2 HG02056.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.117+2271A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894601 | ||||||
| chr15:79894635 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+2237C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894635 | ||||||
| chr15:79894732 | T | C | 1 | a0001c0001t0009g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.117+2140A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894732 | ||||||
| chr15:79894736 | C | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+2136G>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894736 | ||||||
| chr15:79894760 | T | C | 63 | a0001c0001t0001g0259a0001c0001t0001g0267a0001c0001t0001g0273others(60): Show | 82 | HG00280.hp2 HG00438.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.117+2112A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894760 | ||||||
| chr15:79894802 | A | G | 1 | a0001c0001t0005g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+2070T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894802 | ||||||
| chr15:79894847 | T | G | 2 | a0001c0001t0002g0301a0001c0001t0002g0302 | 2 | NA18965.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.117+2025A>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894847 | ||||||
| chr15:79894850 | C | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0005c0008t0007g0337 | 3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.117+2022G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894850 | ||||||
| chr15:79894877 | T | C | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+1995A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894877 | ||||||
| chr15:79894883 | G | A | 112 | a0001c0001t0001g0124a0001c0001t0001g0230a0001c0001t0001g0232others(109): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.117+1989C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894883 | ||||||
| chr15:79894941 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.117+1931T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79894941 | ||||||
| chr15:79895339 | C | G | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0216others(2): Show | 5 | HG02257.hp2 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1533G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895339 | ||||||
| chr15:79895362 | G | A | 13 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0328others(10): Show | 13 | HG01346.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+1510C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895362 | ||||||
| chr15:79895390 | C | T | 62 | a0001c0001t0001g0124a0001c0001t0001g0223a0001c0001t0001g0230others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.117+1482G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895390 | ||||||
| chr15:79895505 | T | C | 2 | a0001c0001t0002g0303a0001c0001t0002g0304 | 2 | HG02080.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.117+1367A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895505 | ||||||
| chr15:79895664 | G | T | 138 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(135): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.117+1208C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895664 | ||||||
| chr15:79895815 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.117+1057G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895815 | ||||||
| chr15:79895819 | T | C | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117+1053A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895819 | ||||||
| chr15:79895858 | T | C | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+1014A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895858 | ||||||
| chr15:79895960 | C | T | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+912G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79895960 | ||||||
| chr15:79896060 | T | C | 12 | a0001c0001t0002g0163a0001c0001t0003g0162a0001c0001t0007g0150others(9): Show | 12 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+812A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896060 | ||||||
| chr15:79896111 | C | T | 4 | a0002c0002t0006g0013a0002c0002t0006g0026a0002c0002t0006g0027others(1): Show | 5 | HG02145.hp2 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+761G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896111 | ||||||
| chr15:79896197 | G | A | 8 | a0001c0001t0001g0311a0001c0001t0004g0306a0001c0001t0004g0307others(5): Show | 8 | HG00280.hp1 HG02257.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+675C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896197 | ||||||
| chr15:79896205 | T | C | 2 | a0001c0001t0003g0160a0001c0001t0003g0161 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.117+667A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896205 | ||||||
| chr15:79896275 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.117+597C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896275 | ||||||
| chr15:79896413 | C | T | 1 | a0001c0001t0009g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.117+459G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896413 | ||||||
| chr15:79896445 | T | A | 2 | a0001c0001t0002g0314a0001c0001t0002g0315 | 2 | HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.117+427A>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896445 | ||||||
| chr15:79896473 | G | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.117+399C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896473 | ||||||
| chr15:79896531 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.117+341T>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896531 | ||||||
| chr15:79896542 | G | A | 3 | a0001c0001t0011g0325a0001c0001t0011g0326a0001c0001t0012g0324 | 3 | HG01346.hp1 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.117+330C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896542 | ||||||
| chr15:79896659 | C | G | 1 | a0001c0001t0003g0098 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.117+213G>C | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896659 | ||||||
| chr15:79896668 | G | A | 3 | a0001c0001t0009g0318a0001c0001t0009g0319a0001c0001t0009g0320 | 3 | HG02559.hp1 HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.117+204C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896668 | ||||||
| chr15:79896683 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.117+189A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896683 | ||||||
| chr15:79896716 | GCGTGCGC others(16): Show |
G | 80 | a0001c0001t0001g0124a0001c0001t0001g0136a0001c0001t0001g0148others(77): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.117+133_117+155del others(23): Show |
MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896716 | ||||||
| chr15:79896749 | G | A | 7 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(4): Show | 7 | HG01891.hp2 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+123C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896749 | ||||||
| chr15:79896750 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.117+122G>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896750 | ||||||
| chr15:79896760 | G | C | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01255.hp2 HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.117+112C>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896760 | ||||||
| chr15:79896761 | G | T | 79 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(76): Show | 94 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.117+111C>A | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896761 | ||||||
| chr15:79896826 | T | C | 10 | a0001c0001t0001g0328a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG01346.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+46A>G | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896826 | ||||||
| chr15:79896860 | G | A | 1 | a0001c0001t0004g0334 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117+12C>T | MTHFS | ENSG00000136371.11 | transcript | ENST00000258874.4 | protein_coding | 1/2 | chr15 | 79896860 |