Search by Gene
| geneid | 64779 |
|---|---|
| ensemblid | ENSG00000103248.19 |
| hgncid | 25778 |
| symbol | MTHFSD |
| name | methenyltetrahydrofolate synthetase domain containing |
| refseq_nuc | NM_001159377.2 |
| refseq_prot | NP_001152849.1 |
| ensembl_nuc | ENST00000360900.11 |
| ensembl_prot | ENSP00000354152.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 86530186 |
| end | 86555235 |
| strand | - |
| ver | v1.2 |
| region | chr16:86530186-86555235 |
| region5000 | chr16:86525186-86560235 |
| regionname0 | MTHFSD_chr16_86530186_86555235 |
| regionname5000 | MTHFSD_chr16_86525186_86560235 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 383 | 149 | 46 | 24 | 51 | 10 | 18 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002 | 0/0 | 383 | 105 | 28 | 21 | 48 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003 | 0/1 | 383 | 71 | 1 | 9 | 47 | 2 | 11 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004 | 1/0 | 383 | 59 | 8 | 12 | 30 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0005 | 0/0 | 383 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0006 | 0/0 | 383 | 5 | 1 | 3 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0007 | 0/0 | 383 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0008 | 0/0 | 383 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0009 | 0/0 | 383 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0010 | 0/0 | 383 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0011 | 0/0 | 383 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0012 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0013 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0014 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0015 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1152 | 149 | 46 | 24 | 51 | 10 | 18 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0002 | 0/0 | 1152 | 105 | 28 | 21 | 48 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0003 | 0/1 | 1152 | 66 | 1 | 8 | 44 | 2 | 10 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0004 | 1/0 | 1152 | 58 | 8 | 12 | 29 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0005 | 0/0 | 1152 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0006 | 0/0 | 1152 | 5 | 0 | 1 | 3 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0007 | 0/0 | 1152 | 5 | 1 | 3 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0008 | 0/0 | 1152 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0009 | 0/0 | 1152 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0010 | 0/0 | 1152 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0011 | 0/0 | 1152 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0012 | 0/0 | 1152 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0013 | 0/0 | 1152 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0014 | 0/0 | 1152 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0015 | 0/0 | 1152 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0016 | 0/0 | 1152 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| c0017 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1877 | 107 | 12 | 19 | 49 | 10 | 17 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0002 | 0/0 | 1877 | 94 | 27 | 20 | 40 | 2 | 5 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0003 | 0/1 | 1877 | 74 | 5 | 10 | 46 | 1 | 11 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0004 | 1/0 | 1877 | 46 | 9 | 5 | 30 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0005 | 0/0 | 1876 | 8 | 8 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0006 | 0/0 | 1877 | 8 | 0 | 5 | 0 | 2 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0007 | 0/0 | 1876 | 6 | 1 | 4 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0008 | 0/0 | 1876 | 5 | 0 | 0 | 2 | 0 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0009 | 0/0 | 1878 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0010 | 0/0 | 1878 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0011 | 0/0 | 1877 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0012 | 0/0 | 1870 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0013 | 0/0 | 1877 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0014 | 0/0 | 1877 | 3 | 1 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0015 | 0/0 | 1877 | 3 | 0 | 2 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0016 | 0/0 | 1877 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0017 | 0/0 | 1876 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0018 | 0/0 | 1877 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0019 | 0/0 | 1877 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0020 | 0/0 | 1877 | 2 | 0 | 1 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0021 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0022 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0023 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0024 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0025 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0026 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0027 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0028 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0029 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0030 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0031 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0032 | 0/0 | 1876 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0033 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0034 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0035 | 0/0 | 1877 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0036 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0037 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0038 | 0/0 | 1877 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0039 | 0/0 | 1877 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| t0040 | 0/0 | 1877 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 29 | 3 | 7 | 15 | 1 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0002 | 0/0 | 22 | 1 | 0 | 13 | 3 | 5 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0003 | 0/0 | 21 | 1 | 0 | 18 | 0 | 2 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0004 | 1/0 | 20 | 1 | 2 | 16 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0005 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0006 | 0/0 | 9 | 2 | 4 | 0 | 2 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0007 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0011 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0015 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0028 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 0/0 | 149 | 46 | 24 | 51 | 10 | 18 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 105 | 28 | 21 | 48 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/1 | 66 | 1 | 8 | 44 | 2 | 10 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0006 | a0003 | c0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004 | a0004 | c0004 | 1/0 | 58 | 8 | 12 | 29 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0016 | a0004 | c0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0005c0005 | a0005 | c0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0006c0007 | a0006 | c0007 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0007c0008 | a0007 | c0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0008c0011 | a0008 | c0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0009c0009 | a0009 | c0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0010c0010 | a0010 | c0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0011c0017 | a0011 | c0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0012c0014 | a0012 | c0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0013c0015 | a0013 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0014c0012 | a0014 | c0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0015c0013 | a0015 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 105 | 12 | 19 | 47 | 10 | 17 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 92 | 26 | 20 | 40 | 2 | 4 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0011 | a0002 | c0002 | t0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0020 | a0002 | c0002 | t0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0026 | a0002 | c0002 | t0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0027 | a0002 | c0002 | t0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0036 | a0002 | c0002 | t0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0037 | a0002 | c0002 | t0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0039 | a0002 | c0002 | t0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0002c0002t0040 | a0002 | c0002 | t0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0003t0003 | a0003 | c0003 | t0003 | 0/1 | 63 | 1 | 8 | 42 | 1 | 10 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0003t0021 | a0003 | c0003 | t0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0003t0023 | a0003 | c0003 | t0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0003t0024 | a0003 | c0003 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0006t0003 | a0003 | c0006 | t0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0003c0006t0022 | a0003 | c0006 | t0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0002 | a0004 | c0004 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0004 | a0004 | c0004 | t0004 | 1/0 | 38 | 4 | 5 | 28 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0006 | a0004 | c0004 | t0006 | 0/0 | 8 | 0 | 5 | 0 | 2 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0008 | a0004 | c0004 | t0008 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0015 | a0004 | c0004 | t0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0016 | a0004 | c0004 | t0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0004t0031 | a0004 | c0004 | t0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0004c0016t0004 | a0004 | c0016 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0005c0005t0010 | a0005 | c0005 | t0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0006c0007t0007 | a0006 | c0007 | t0007 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0007c0008t0017 | a0007 | c0008 | t0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0008c0011t0004 | a0008 | c0011 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0009c0009t0004 | a0009 | c0009 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0009c0009t0008 | a0009 | c0009 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0010c0010t0003 | a0010 | c0010 | t0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0010c0010t0038 | a0010 | c0010 | t0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0011c0017t0004 | a0011 | c0017 | t0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0012c0014t0001 | a0012 | c0014 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0013c0015t0001 | a0013 | c0015 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0014c0012t0003 | a0014 | c0012 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| a0015c0013t0009 | a0015 | c0013 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 22 | 1 | 0 | 13 | 3 | 5 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 9 | 2 | 4 | 0 | 2 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0002g0152 | a0001 | c0001 | t0002 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0003g0080 | a0001 | c0001 | t0003 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0003g0081 | a0001 | c0001 | t0003 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0003g0082 | a0001 | c0001 | t0003 | g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0003g0201 | a0001 | c0001 | t0003 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0003g0202 | a0001 | c0001 | t0003 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0004g0022 | a0001 | c0001 | t0004 | g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0005g0019 | a0001 | c0001 | t0005 | g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0005g0049 | a0001 | c0001 | t0005 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0005g0050 | a0001 | c0001 | t0005 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0005g0053 | a0001 | c0001 | t0005 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0005g0055 | a0001 | c0001 | t0005 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0005g0104 | a0001 | c0001 | t0005 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0007g0120 | a0001 | c0001 | t0007 | g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0009g0052 | a0001 | c0001 | t0009 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0009g0193 | a0001 | c0001 | t0009 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0009g0194 | a0001 | c0001 | t0009 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0009g0195 | a0001 | c0001 | t0009 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0012g0020 | a0001 | c0001 | t0012 | g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0012g0054 | a0001 | c0001 | t0012 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0013g0027 | a0001 | c0001 | t0013 | g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0014g0171 | a0001 | c0001 | t0014 | g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0014g0172 | a0001 | c0001 | t0014 | g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0014g0173 | a0001 | c0001 | t0014 | g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0018g0056 | a0001 | c0001 | t0018 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0018g0057 | a0001 | c0001 | t0018 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0019g0196 | a0001 | c0001 | t0019 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0019g0197 | a0001 | c0001 | t0019 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0025g0051 | a0001 | c0001 | t0025 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0028g0192 | a0001 | c0001 | t0028 | g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0029g0179 | a0001 | c0001 | t0029 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0030g0177 | a0001 | c0001 | t0030 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0032g0113 | a0001 | c0001 | t0032 | g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0033g0187 | a0001 | c0001 | t0033 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0034g0180 | a0001 | c0001 | t0034 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0001c0001t0035g0087 | a0001 | c0001 | t0035 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0001 | a0002 | c0002 | t0002 | g0001 | 0/0 | 29 | 3 | 7 | 15 | 1 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0007 | a0002 | c0002 | t0002 | g0007 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0008 | a0002 | c0002 | t0002 | g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0013 | a0002 | c0002 | t0002 | g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0014 | a0002 | c0002 | t0002 | g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0021 | a0002 | c0002 | t0002 | g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0025 | a0002 | c0002 | t0002 | g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0037 | a0002 | c0002 | t0002 | g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0038 | a0002 | c0002 | t0002 | g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0046 | a0002 | c0002 | t0002 | g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0105 | a0002 | c0002 | t0002 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0106 | a0002 | c0002 | t0002 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0107 | a0002 | c0002 | t0002 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0110 | a0002 | c0002 | t0002 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0111 | a0002 | c0002 | t0002 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0112 | a0002 | c0002 | t0002 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0114 | a0002 | c0002 | t0002 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0115 | a0002 | c0002 | t0002 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0117 | a0002 | c0002 | t0002 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0118 | a0002 | c0002 | t0002 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0119 | a0002 | c0002 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0139 | a0002 | c0002 | t0002 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0140 | a0002 | c0002 | t0002 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0141 | a0002 | c0002 | t0002 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0143 | a0002 | c0002 | t0002 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0145 | a0002 | c0002 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0147 | a0002 | c0002 | t0002 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0148 | a0002 | c0002 | t0002 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0150 | a0002 | c0002 | t0002 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0151 | a0002 | c0002 | t0002 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0156 | a0002 | c0002 | t0002 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0157 | a0002 | c0002 | t0002 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0162 | a0002 | c0002 | t0002 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0164 | a0002 | c0002 | t0002 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0165 | a0002 | c0002 | t0002 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0166 | a0002 | c0002 | t0002 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0002g0167 | a0002 | c0002 | t0002 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0011g0016 | a0002 | c0002 | t0011 | g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0011g0200 | a0002 | c0002 | t0011 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0020g0149 | a0002 | c0002 | t0020 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0020g0155 | a0002 | c0002 | t0020 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0026g0160 | a0002 | c0002 | t0026 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0027g0161 | a0002 | c0002 | t0027 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0036g0153 | a0002 | c0002 | t0036 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0037g0108 | a0002 | c0002 | t0037 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0039g0154 | a0002 | c0002 | t0039 | g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0002c0002t0040g0116 | a0002 | c0002 | t0040 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0003 | a0003 | c0003 | t0003 | g0003 | 0/0 | 21 | 1 | 0 | 18 | 0 | 2 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0005 | a0003 | c0003 | t0003 | g0005 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0010 | a0003 | c0003 | t0003 | g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0011 | a0003 | c0003 | t0003 | g0011 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0015 | a0003 | c0003 | t0003 | g0015 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0048 | a0003 | c0003 | t0003 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0100 | a0003 | c0003 | t0003 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0109 | a0003 | c0003 | t0003 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0122 | a0003 | c0003 | t0003 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0123 | a0003 | c0003 | t0003 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0124 | a0003 | c0003 | t0003 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0125 | a0003 | c0003 | t0003 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0128 | a0003 | c0003 | t0003 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0129 | a0003 | c0003 | t0003 | g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0132 | a0003 | c0003 | t0003 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0133 | a0003 | c0003 | t0003 | g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0134 | a0003 | c0003 | t0003 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0135 | a0003 | c0003 | t0003 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0136 | a0003 | c0003 | t0003 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0003g0207 | a0003 | c0003 | t0003 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0021g0121 | a0003 | c0003 | t0021 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0023g0130 | a0003 | c0003 | t0023 | g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0003t0024g0131 | a0003 | c0003 | t0024 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0006t0003g0035 | a0003 | c0006 | t0003 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0006t0003g0158 | a0003 | c0006 | t0003 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0006t0003g0168 | a0003 | c0006 | t0003 | g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0003c0006t0022g0103 | a0003 | c0006 | t0022 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0002g0211 | a0004 | c0004 | t0002 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0004 | a0004 | c0004 | t0004 | g0004 | 1/0 | 20 | 1 | 2 | 16 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0045 | a0004 | c0004 | t0004 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0058 | a0004 | c0004 | t0004 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0059 | a0004 | c0004 | t0004 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0060 | a0004 | c0004 | t0004 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0061 | a0004 | c0004 | t0004 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0062 | a0004 | c0004 | t0004 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0069 | a0004 | c0004 | t0004 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0070 | a0004 | c0004 | t0004 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0071 | a0004 | c0004 | t0004 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0072 | a0004 | c0004 | t0004 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0073 | a0004 | c0004 | t0004 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0076 | a0004 | c0004 | t0004 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0077 | a0004 | c0004 | t0004 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0078 | a0004 | c0004 | t0004 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0079 | a0004 | c0004 | t0004 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0181 | a0004 | c0004 | t0004 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0004g0182 | a0004 | c0004 | t0004 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0006g0009 | a0004 | c0004 | t0006 | g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0006g0030 | a0004 | c0004 | t0006 | g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0006g0074 | a0004 | c0004 | t0006 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0008g0067 | a0004 | c0004 | t0008 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0008g0198 | a0004 | c0004 | t0008 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0008g0199 | a0004 | c0004 | t0008 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0008g0205 | a0004 | c0004 | t0008 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0015g0032 | a0004 | c0004 | t0015 | g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0015g0065 | a0004 | c0004 | t0015 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0016g0047 | a0004 | c0004 | t0016 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0016g0212 | a0004 | c0004 | t0016 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0004t0031g0066 | a0004 | c0004 | t0031 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0004c0016t0004g0068 | a0004 | c0016 | t0004 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0005c0005t0010g0023 | a0005 | c0005 | t0010 | g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0005c0005t0010g0102 | a0005 | c0005 | t0010 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0005c0005t0010g0206 | a0005 | c0005 | t0010 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0006c0007t0007g0034 | a0006 | c0007 | t0007 | g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0006c0007t0007g0095 | a0006 | c0007 | t0007 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0006c0007t0007g0096 | a0006 | c0007 | t0007 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0006c0007t0007g0097 | a0006 | c0007 | t0007 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0007c0008t0017g0036 | a0007 | c0008 | t0017 | g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0007c0008t0017g0138 | a0007 | c0008 | t0017 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0008c0011t0004g0040 | a0008 | c0011 | t0004 | g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0009c0009t0004g0064 | a0009 | c0009 | t0004 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0009c0009t0008g0063 | a0009 | c0009 | t0008 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0010c0010t0003g0146 | a0010 | c0010 | t0003 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0010c0010t0038g0126 | a0010 | c0010 | t0038 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0011c0017t0004g0075 | a0011 | c0017 | t0004 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0012c0014t0001g0178 | a0012 | c0014 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0013c0015t0001g0163 | a0013 | c0015 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0014c0012t0003g0127 | a0014 | c0012 | t0003 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| a0015c0013t0009g0137 | a0015 | c0013 | t0009 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0107 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00140 | hp1 | a0003 | c0003 | t0023 | g0130 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00323 | hp1 | a0003 | c0003 | t0003 | g0011 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00408 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00423 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00558 | hp2 | a0013 | c0015 | t0001 | g0163 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00597 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00639 | hp2 | a0004 | c0004 | t0004 | g0060 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00738 | hp2 | a0002 | c0002 | t0020 | g0155 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01069 | hp2 | a0004 | c0004 | t0006 | g0009 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01070 | hp2 | a0006 | c0007 | t0007 | g0096 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01074 | hp1 | a0003 | c0003 | t0003 | g0015 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01074 | hp2 | a0004 | c0004 | t0006 | g0009 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01081 | hp1 | a0004 | c0004 | t0004 | g0077 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01081 | hp2 | a0004 | c0004 | t0004 | g0058 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0172 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01168 | hp1 | a0004 | c0004 | t0015 | g0032 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01169 | hp1 | a0001 | c0001 | t0014 | g0173 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01169 | hp2 | a0004 | c0004 | t0015 | g0032 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01175 | hp1 | a0001 | c0001 | t0035 | g0087 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01175 | hp2 | a0003 | c0003 | t0003 | g0011 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01192 | hp2 | a0006 | c0007 | t0007 | g0034 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01243 | hp2 | a0007 | c0008 | t0017 | g0138 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01255 | hp1 | a0003 | c0003 | t0003 | g0015 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01255 | hp2 | a0004 | c0004 | t0006 | g0009 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01256 | hp1 | a0006 | c0007 | t0007 | g0097 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01346 | hp2 | a0004 | c0004 | t0004 | g0004 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0005 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0129 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01515 | hp1 | a0004 | c0004 | t0006 | g0030 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01517 | hp1 | a0004 | c0004 | t0006 | g0030 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0056 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01891 | hp1 | a0004 | c0004 | t0004 | g0045 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01934 | hp1 | a0003 | c0003 | t0003 | g0133 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0120 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01943 | hp1 | a0003 | c0006 | t0003 | g0168 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0157 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01978 | hp2 | a0004 | c0004 | t0006 | g0009 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01981 | hp1 | a0004 | c0004 | t0004 | g0004 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01993 | hp1 | a0004 | c0004 | t0006 | g0009 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0140 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02040 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02055 | hp1 | a0004 | c0004 | t0016 | g0212 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02055 | hp2 | a0005 | c0005 | t0010 | g0023 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02056 | hp2 | a0004 | c0004 | t0004 | g0062 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02071 | hp2 | a0003 | c0003 | t0021 | g0121 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02074 | hp1 | a0001 | c0001 | t0034 | g0180 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02074 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02083 | hp1 | a0004 | c0004 | t0004 | g0061 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02129 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02135 | hp2 | a0003 | c0003 | t0003 | g0128 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02165 | hp1 | a0002 | c0002 | t0020 | g0149 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0118 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0117 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0195 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02293 | hp1 | a0003 | c0003 | t0003 | g0123 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02300 | hp2 | a0003 | c0003 | t0003 | g0005 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02451 | hp2 | a0004 | c0004 | t0004 | g0004 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0020 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02602 | hp1 | a0004 | c0004 | t0015 | g0065 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0020 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02630 | hp1 | a0005 | c0005 | t0010 | g0102 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0106 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02735 | hp2 | a0004 | c0004 | t0008 | g0199 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02809 | hp1 | a0006 | c0007 | t0007 | g0095 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02809 | hp2 | a0002 | c0002 | t0037 | g0108 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0027 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0057 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02976 | hp2 | a0002 | c0002 | t0040 | g0116 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03017 | hp2 | a0003 | c0003 | t0003 | g0122 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03041 | hp1 | a0005 | c0005 | t0010 | g0023 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03041 | hp2 | a0001 | c0001 | t0025 | g0051 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0054 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03098 | hp2 | a0008 | c0011 | t0004 | g0040 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03139 | hp2 | a0008 | c0011 | t0004 | g0040 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03225 | hp2 | a0004 | c0004 | t0004 | g0078 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03239 | hp1 | a0011 | c0017 | t0004 | g0075 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03453 | hp2 | a0004 | c0004 | t0016 | g0047 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0027 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03492 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03540 | hp1 | a0001 | c0001 | t0014 | g0171 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03540 | hp2 | a0004 | c0004 | t0016 | g0047 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03579 | hp2 | a0005 | c0005 | t0010 | g0206 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03669 | hp1 | a0004 | c0004 | t0008 | g0205 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03688 | hp2 | a0004 | c0004 | t0008 | g0198 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03704 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03704 | hp2 | a0003 | c0003 | t0003 | g0015 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03710 | hp1 | a0004 | c0004 | t0031 | g0066 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03710 | hp2 | a0003 | c0003 | t0003 | g0003 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0109 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03831 | hp2 | a0004 | c0004 | t0006 | g0074 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03834 | hp2 | a0006 | c0007 | t0007 | g0034 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03927 | hp2 | a0003 | c0003 | t0003 | g0100 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03942 | hp1 | a0003 | c0003 | t0003 | g0048 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03942 | hp2 | a0003 | c0006 | t0022 | g0103 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04184 | hp1 | a0010 | c0010 | t0003 | g0146 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04184 | hp2 | a0002 | c0002 | t0036 | g0153 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0166 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04204 | hp1 | a0003 | c0003 | t0003 | g0003 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18612 | hp1 | a0004 | c0004 | t0004 | g0072 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18612 | hp2 | a0004 | c0004 | t0004 | g0181 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18747 | hp1 | a0003 | c0003 | t0003 | g0124 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0194 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18940 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18941 | hp1 | a0002 | c0002 | t0011 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18941 | hp2 | a0009 | c0009 | t0004 | g0064 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18942 | hp1 | a0004 | c0004 | t0004 | g0071 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18943 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18946 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18947 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18949 | hp1 | a0003 | c0003 | t0024 | g0131 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18949 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18950 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18951 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18952 | hp1 | a0003 | c0006 | t0003 | g0158 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18952 | hp2 | a0004 | c0004 | t0004 | g0073 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18953 | hp1 | a0002 | c0002 | t0026 | g0160 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18953 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0134 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18960 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18963 | hp1 | a0003 | c0006 | t0003 | g0035 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18963 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18964 | hp2 | a0002 | c0002 | t0011 | g0200 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18965 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18966 | hp2 | a0002 | c0002 | t0011 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18967 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18968 | hp1 | a0001 | c0001 | t0033 | g0187 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18968 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18971 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0207 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18973 | hp2 | a0001 | c0001 | t0030 | g0177 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18974 | hp1 | a0001 | c0001 | t0029 | g0179 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18974 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18975 | hp2 | a0003 | c0006 | t0003 | g0035 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18977 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18977 | hp2 | a0002 | c0002 | t0011 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18979 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18979 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18981 | hp2 | a0003 | c0003 | t0003 | g0125 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18983 | hp2 | a0002 | c0002 | t0011 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18984 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18987 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18989 | hp2 | a0004 | c0004 | t0004 | g0059 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18990 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18991 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18995 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18995 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18997 | hp2 | a0004 | c0004 | t0004 | g0079 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19000 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19001 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19001 | hp2 | a0014 | c0012 | t0003 | g0127 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19002 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19005 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19007 | hp1 | a0003 | c0003 | t0003 | g0135 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19007 | hp2 | a0004 | c0004 | t0004 | g0182 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19009 | hp1 | a0002 | c0002 | t0027 | g0161 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19009 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0115 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0197 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19054 | hp1 | a0004 | c0004 | t0004 | g0070 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0136 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19066 | hp2 | a0012 | c0014 | t0001 | g0178 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19067 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19068 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19068 | hp2 | a0004 | c0016 | t0004 | g0068 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19072 | hp1 | a0009 | c0009 | t0008 | g0063 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19072 | hp2 | a0003 | c0003 | t0003 | g0132 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19074 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19074 | hp2 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19075 | hp1 | a0004 | c0004 | t0004 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19075 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19078 | hp2 | a0004 | c0004 | t0008 | g0067 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19080 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19081 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19083 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19084 | hp1 | a0010 | c0010 | t0038 | g0126 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19087 | hp1 | a0004 | c0004 | t0004 | g0076 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19087 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19088 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19089 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19090 | hp2 | a0004 | c0004 | t0004 | g0069 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0196 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | ASW | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20129 | hp2 | a0007 | c0008 | t0017 | g0036 | AFR | ASW | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20905 | hp2 | a0002 | c0002 | t0039 | g0154 | SAS | GIH | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02109 | hp1 | a0004 | c0004 | t0004 | g0045 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0020 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG02559 | hp2 | a0004 | c0004 | t0002 | g0211 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03471 | hp1 | a0001 | c0001 | t0028 | g0192 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG03471 | hp2 | a0005 | c0005 | t0010 | g0023 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20300 | hp1 | a0015 | c0013 | t0009 | g0137 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA21309 | hp1 | a0007 | c0008 | t0017 | g0036 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| NA21309 | hp2 | a0001 | c0001 | t0032 | g0113 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0003 | g0015 | REF | REF | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| homoSapiens_grch38 | hp1 | a0004 | c0004 | t0004 | g0004 | REF | REF | MTHFSD_chr16_86525186_86560235 | MTHFSD |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86532220
|
C | G | 12 | a0001a0002a0003others(9): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
missense_variant | MODERATE | c.943G>C | p.Gly315Arg | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 994/3028 | 943/1152 | 315/383 | chr16 | 86532220 | ||
| chr16:86532276
|
G | C | 2 | a0002a0007 | 108 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(105): Show |
missense_variant | MODERATE | c.887C>G | p.Ser296Cys | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 938/3028 | 887/1152 | 296/383 | chr16 | 86532276 | ||
| chr16:86532358
|
G | C | 1 | a0005 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.805C>G | p.Gln269Glu | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 856/3028 | 805/1152 | 269/383 | chr16 | 86532358 | ||
| chr16:86532391
|
C | T | 1 | a0013 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.772G>A | p.Glu258Lys | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 823/3028 | 772/1152 | 258/383 | chr16 | 86532391 | ||
| chr16:86532419
|
C | G | 1 | a0012 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.744G>C | p.Gln248His | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 795/3028 | 744/1152 | 248/383 | chr16 | 86532419 | ||
| chr16:86532433
|
C | T | 3 | a0003a0010a0014 | 74 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(71): Show |
missense_variant | MODERATE | c.730G>A | p.Ala244Thr | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 781/3028 | 730/1152 | 244/383 | chr16 | 86532433 | ||
| chr16:86532436
|
G | A | 2 | a0003a0014 | 72 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
missense_variant | MODERATE | c.727C>T | p.Arg243Cys | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 778/3028 | 727/1152 | 243/383 | chr16 | 86532436 | ||
| chr16:86541786
|
C | T | 1 | a0014 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.592G>A | p.Asp198Asn | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/8 | 643/3028 | 592/1152 | 198/383 | chr16 | 86541786 | ||
| chr16:86542109
|
C | T | 2 | a0007a0015 | 4 | HG01243.hp2 NA20129.hp2 NA20300.hp1 others(1): Show |
missense_variant | MODERATE | c.547G>A | p.Asp183Asn | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/8 | 598/3028 | 547/1152 | 183/383 | chr16 | 86542109 | ||
| chr16:86542161
|
C | T | 1 | a0009 | 2 | NA18941.hp2 NA19072.hp1 |
missense_variant | MODERATE | c.495G>A | p.Met165Ile | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/8 | 546/3028 | 495/1152 | 165/383 | chr16 | 86542161 | ||
| chr16:86542171
|
T | C | 1 | a0008 | 2 | HG03098.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.485A>G | p.Tyr162Cys | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/8 | 536/3028 | 485/1152 | 162/383 | chr16 | 86542171 | ||
| chr16:86546579
|
G | A | 1 | a0011 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.422C>T | p.Ser141Phe | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/8 | 473/3028 | 422/1152 | 141/383 | chr16 | 86546579 | ||
| chr16:86552137
|
G | C | 1 | a0006 | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
missense_variant | MODERATE | c.133C>G | p.Leu45Val | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/8 | 184/3028 | 133/1152 | 45/383 | chr16 | 86552137 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86532323
|
C | T | 1 | a0005c0005 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
synonymous_variant | LOW | c.840G>A | p.Pro280Pro | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 891/3028 | 840/1152 | 280/383 | chr16 | 86532323 | ||
| chr16:86532448
|
G | A | 1 | a0004c0016 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.715C>T | p.Leu239Leu | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 766/3028 | 715/1152 | 239/383 | chr16 | 86532448 | ||
| chr16:86542131
|
C | T | 3 | a0003c0003a0010c0010a0014c0012 | 69 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(66): Show |
synonymous_variant | LOW | c.525G>A | p.Thr175Thr | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/8 | 576/3028 | 525/1152 | 175/383 | chr16 | 86542131 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86530236
|
C | G | 1 | a0004c0004t0016 | 3 | HG02055.hp1 HG03453.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1775G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1775 | chr16 | 86530236 | |||||
| chr16:86530288
|
C | T | 10 | a0001c0001t0003a0003c0003t0003a0003c0003t0021others(7): Show | 79 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1723G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1723 | chr16 | 86530288 | |||||
| chr16:86530421
|
G | T | 1 | a0005c0005t0010 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1590C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1590 | chr16 | 86530421 | |||||
| chr16:86530522
|
G | A | 1 | a0001c0001t0034 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1489 | chr16 | 86530522 | |||||
| chr16:86530569
|
C | T | 1 | a0004c0004t0006 | 8 | HG01069.hp2 HG01074.hp2 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1442G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1442 | chr16 | 86530569 | |||||
| chr16:86530616
|
C | CA | 9 | a0001c0001t0009a0001c0001t0028a0001c0001t0033others(6): Show | 16 | HG02055.hp2 HG02071.hp2 HG02074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1394dupT | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1394 | chr16 | 86530616 | |||||
| chr16:86530616
|
CA | C | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0025others(5): Show | 24 | HG01070.hp2 HG01192.hp2 HG01243.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1394delT | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1394 | chr16 | 86530616 | |||||
| chr16:86530620
|
A | C | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0025others(1): Show | 15 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1391T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1391 | chr16 | 86530620 | |||||
| chr16:86530661
|
A | T | 12 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(9): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1350T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1350 | chr16 | 86530661 | |||||
| chr16:86530758
|
A | G | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(13): Show | 97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1253T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1253 | chr16 | 86530758 | |||||
| chr16:86530785
|
G | A | 1 | a0001c0001t0019 | 2 | NA19043.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1226C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1226 | chr16 | 86530785 | |||||
| chr16:86530805
|
AGAGGGCC | A | 1 | a0001c0001t0012 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1199_*1205delGGCC others(3): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1199 | chr16 | 86530805 | |||||
| chr16:86530821
|
A | G | 1 | a0004c0004t0031 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1190 | chr16 | 86530821 | |||||
| chr16:86530835
|
C | T | 1 | a0001c0001t0030 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1176G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1176 | chr16 | 86530835 | |||||
| chr16:86530929
|
C | T | 1 | a0004c0004t0015 | 3 | HG01168.hp1 HG01169.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1082G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1082 | chr16 | 86530929 | |||||
| chr16:86530954
|
C | G | 1 | a0001c0001t0018 | 2 | HG01884.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1057G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1057 | chr16 | 86530954 | |||||
| chr16:86530970
|
A | G | 1 | a0001c0001t0029 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1041T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 1041 | chr16 | 86530970 | |||||
| chr16:86531033
|
C | T | 1 | a0001c0001t0028 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*978G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 978 | chr16 | 86531033 | |||||
| chr16:86531050
|
G | A | 3 | a0001c0001t0005a0001c0001t0025a0007c0008t0017 | 12 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*961C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 961 | chr16 | 86531050 | |||||
| chr16:86531065
|
G | T | 19 | a0001c0001t0002a0001c0001t0003a0002c0002t0002others(16): Show | 181 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*946C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 946 | chr16 | 86531065 | |||||
| chr16:86531080
|
C | A | 1 | a0003c0003t0023 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 931 | chr16 | 86531080 | |||||
| chr16:86531128
|
A | T | 1 | a0002c0002t0027 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 883 | chr16 | 86531128 | |||||
| chr16:86531169
|
G | C | 1 | a0005c0005t0010 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*842C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 842 | chr16 | 86531169 | |||||
| chr16:86531290
|
G | A | 1 | a0001c0001t0014 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*721C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 721 | chr16 | 86531290 | |||||
| chr16:86531511
|
G | A | 1 | a0003c0003t0024 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 500 | chr16 | 86531511 | |||||
| chr16:86531552
|
G | C | 1 | a0001c0001t0035 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 459 | chr16 | 86531552 | |||||
| chr16:86531579
|
G | A | 1 | a0002c0002t0040 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 432 | chr16 | 86531579 | |||||
| chr16:86531581
|
A | T | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0025others(1): Show | 15 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*430T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 430 | chr16 | 86531581 | |||||
| chr16:86531587
|
C | T | 1 | a0002c0002t0037 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*424G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 424 | chr16 | 86531587 | |||||
| chr16:86531618
|
C | T | 1 | a0001c0001t0025 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 393 | chr16 | 86531618 | |||||
| chr16:86531624
|
C | T | 1 | a0002c0002t0036 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 387 | chr16 | 86531624 | |||||
| chr16:86531793
|
T | C | 4 | a0001c0001t0005a0001c0001t0013a0001c0001t0014others(1): Show | 15 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*218A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 218 | chr16 | 86531793 | |||||
| chr16:86531880
|
T | C | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(25): Show | 210 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*131A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 131 | chr16 | 86531880 | |||||
| chr16:86531889
|
G | A | 1 | a0002c0002t0027 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 122 | chr16 | 86531889 | |||||
| chr16:86531902
|
G | A | 1 | a0007c0008t0017 | 3 | HG01243.hp2 NA20129.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*109C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 109 | chr16 | 86531902 | |||||
| chr16:86531915
|
C | G | 2 | a0002c0002t0026a0002c0002t0027 | 2 | NA18953.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*96G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 96 | chr16 | 86531915 | |||||
| chr16:86531931
|
C | G | 15 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(12): Show | 99 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*80G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 80 | chr16 | 86531931 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86532509
|
T | C | 12 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(9): Show | 15 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.682-28A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532509 | ||||||
| chr16:86532547
|
T | A | 4 | a0004c0004t0002g0211a0004c0004t0004g0045a0004c0004t0016g0047others(1): Show | 6 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-66A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532547 | ||||||
| chr16:86532574
|
G | T | 1 | a0004c0004t0004g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.682-93C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532574 | ||||||
| chr16:86532728
|
G | A | 5 | a0001c0001t0007g0120a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-247C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532728 | ||||||
| chr16:86532736
|
C | T | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-255G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532736 | ||||||
| chr16:86532803
|
G | C | 1 | a0003c0003t0003g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.682-322C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532803 | ||||||
| chr16:86532816
|
C | T | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-335G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532816 | ||||||
| chr16:86532943
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(174): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.682-462T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532943 | ||||||
| chr16:86532990
|
T | C | 22 | a0001c0001t0004g0022a0001c0001t0007g0120a0001c0001t0009g0052others(19): Show | 30 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.682-509A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86532990 | ||||||
| chr16:86533125
|
A | T | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-644T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533125 | ||||||
| chr16:86533211
|
G | A | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-730C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533211 | ||||||
| chr16:86533246
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.682-765A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533246 | ||||||
| chr16:86533520
|
G | A | 4 | a0004c0004t0008g0198a0004c0004t0008g0199a0004c0004t0008g0205others(1): Show | 4 | HG02735.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-1039C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533520 | ||||||
| chr16:86533570
|
T | C | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-1089A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533570 | ||||||
| chr16:86533651
|
G | A | 1 | a0002c0002t0002g0114 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.682-1170C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533651 | ||||||
| chr16:86533658
|
A | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(85): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.682-1177T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533658 | ||||||
| chr16:86533664
|
G | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(169): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.682-1183C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533664 | ||||||
| chr16:86533688
|
C | G | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-1207G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533688 | ||||||
| chr16:86533773
|
T | C | 2 | a0007c0008t0017g0036a0007c0008t0017g0138 | 3 | HG01243.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.682-1292A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533773 | ||||||
| chr16:86533886
|
A | T | 86 | a0001c0001t0002g0152a0001c0001t0003g0080a0001c0001t0003g0081others(83): Show | 189 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.682-1405T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86533886 | ||||||
| chr16:86534057
|
T | A | 3 | a0001c0001t0009g0052a0001c0001t0018g0056a0001c0001t0018g0057 | 3 | HG01884.hp1 HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.682-1576A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534057 | ||||||
| chr16:86534178
|
G | A | 1 | a0002c0002t0002g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.682-1697C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534178 | ||||||
| chr16:86534220
|
C | T | 1 | a0012c0014t0001g0178 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.682-1739G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534220 | ||||||
| chr16:86534238
|
C | A | 1 | a0001c0001t0004g0022 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.682-1757G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534238 | ||||||
| chr16:86534323
|
G | A | 29 | a0003c0003t0003g0003a0003c0003t0003g0005a0003c0003t0003g0010others(26): Show | 72 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.682-1842C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534323 | ||||||
| chr16:86534384
|
C | T | 2 | a0003c0003t0003g0010a0003c0003t0003g0128 | 6 | HG02135.hp2 HG02523.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-1903G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534384 | ||||||
| chr16:86534425
|
G | A | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-1944C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534425 | ||||||
| chr16:86534428
|
A | T | 2 | a0001c0001t0019g0196a0001c0001t0019g0197 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.682-1947T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534428 | ||||||
| chr16:86534448
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(69): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.682-1967A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534448 | ||||||
| chr16:86534468
|
T | G | 1 | a0004c0004t0004g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.682-1987A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534468 | ||||||
| chr16:86534491
|
G | A | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-2010C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534491 | ||||||
| chr16:86534574
|
G | A | 5 | a0001c0001t0007g0120a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-2093C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534574 | ||||||
| chr16:86534724
|
A | G | 100 | a0001c0001t0002g0152a0001c0001t0003g0080a0001c0001t0003g0081others(97): Show | 210 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.682-2243T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534724 | ||||||
| chr16:86534725
|
T | G | 1 | a0003c0003t0003g0132 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.682-2244A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534725 | ||||||
| chr16:86534788
|
G | A | 2 | a0007c0008t0017g0036a0007c0008t0017g0138 | 3 | HG01243.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.682-2307C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534788 | ||||||
| chr16:86534795
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(62): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.682-2314C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534795 | ||||||
| chr16:86534797
|
G | C | 1 | a0004c0004t0004g0070 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.682-2316C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534797 | ||||||
| chr16:86534819
|
A | T | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-2338T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534819 | ||||||
| chr16:86534864
|
C | T | 48 | a0001c0001t0002g0152a0002c0002t0002g0001a0002c0002t0002g0007others(45): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.682-2383G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534864 | ||||||
| chr16:86534905
|
C | T | 1 | a0002c0002t0002g0151 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.682-2424G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534905 | ||||||
| chr16:86534906
|
G | A | 1 | a0004c0004t0004g0071 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.682-2425C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86534906 | ||||||
| chr16:86535022
|
C | T | 13 | a0001c0001t0004g0022a0001c0001t0009g0052a0001c0001t0009g0193others(10): Show | 18 | HG00639.hp2 HG01884.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.682-2541G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535022 | ||||||
| chr16:86535026
|
G | A | 15 | a0001c0001t0004g0022a0001c0001t0009g0052a0001c0001t0009g0193others(12): Show | 20 | HG00639.hp2 HG01884.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.682-2545C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535026 | ||||||
| chr16:86535035
|
C | G | 46 | a0001c0001t0002g0152a0002c0002t0002g0001a0002c0002t0002g0007others(43): Show | 104 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.682-2554G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535035 | ||||||
| chr16:86535087
|
C | T | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-2606G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535087 | ||||||
| chr16:86535095
|
T | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(62): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.682-2614A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535095 | ||||||
| chr16:86535199
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(170): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.682-2718T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535199 | ||||||
| chr16:86535205
|
A | AGG | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(170): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.682-2726_682-2725d others(4): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535205 | ||||||
| chr16:86535218
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(170): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.682-2737T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535218 | ||||||
| chr16:86535254
|
C | G | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-2773G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535254 | ||||||
| chr16:86535303
|
A | G | 1 | a0003c0003t0003g0124 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.682-2822T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535303 | ||||||
| chr16:86535329
|
A | ATGGAAAC others(7): Show |
183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(180): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.682-2849_682-2848i others(16): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535329 | ||||||
| chr16:86535329
|
A | ATGGAAAC others(7): Show |
3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG00741.hp1 HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.682-2849_682-2848i others(16): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535329 | ||||||
| chr16:86535375
|
C | T | 1 | a0002c0002t0002g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.682-2894G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535375 | ||||||
| chr16:86535388
|
C | T | 1 | a0001c0001t0004g0022 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.682-2907G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535388 | ||||||
| chr16:86535445
|
T | C | 171 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(168): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.682-2964A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535445 | ||||||
| chr16:86535485
|
C | T | 1 | a0001c0001t0025g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.682-3004G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535485 | ||||||
| chr16:86535487
|
A | G | 2 | a0001c0001t0019g0196a0001c0001t0019g0197 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.682-3006T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535487 | ||||||
| chr16:86535525
|
G | A | 2 | a0001c0001t0019g0196a0001c0001t0019g0197 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.682-3044C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535525 | ||||||
| chr16:86535595
|
TA | T | 102 | a0001c0001t0001g0188a0001c0001t0001g0208a0001c0001t0002g0152others(99): Show | 210 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.682-3115delT | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535595 | ||||||
| chr16:86535595
|
TAA | T | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-3116_682-3115d others(4): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535595 | ||||||
| chr16:86535652
|
A | C | 53 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(50): Show | 104 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.682-3171T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535652 | ||||||
| chr16:86535662
|
G | A | 4 | a0004c0004t0008g0198a0004c0004t0008g0199a0004c0004t0008g0205others(1): Show | 4 | HG02735.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-3181C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535662 | ||||||
| chr16:86535793
|
C | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(177): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.682-3312G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535793 | ||||||
| chr16:86535848
|
C | A | 1 | a0002c0002t0002g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.682-3367G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535848 | ||||||
| chr16:86535892
|
C | T | 1 | a0001c0001t0030g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.682-3411G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535892 | ||||||
| chr16:86535896
|
C | T | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682-3415G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535896 | ||||||
| chr16:86535915
|
C | A | 1 | a0003c0003t0003g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.682-3434G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535915 | ||||||
| chr16:86535974
|
C | T | 1 | a0003c0003t0003g0129 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.682-3493G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535974 | ||||||
| chr16:86535997
|
G | A | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-3516C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535997 | ||||||
| chr16:86535999
|
C | A | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-3518G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535999 | ||||||
| chr16:86536108
|
G | A | 10 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.682-3627C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536108 | ||||||
| chr16:86536314
|
G | A | 10 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 14 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.682-3833C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536314 | ||||||
| chr16:86536339
|
C | T | 1 | a0003c0003t0003g0128 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.682-3858G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536339 | ||||||
| chr16:86536377
|
C | T | 1 | a0003c0003t0003g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.682-3896G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536377 | ||||||
| chr16:86536385
|
C | G | 1 | a0004c0004t0004g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.682-3904G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536385 | ||||||
| chr16:86536591
|
G | A | 1 | a0002c0002t0002g0008 | 7 | HG02451.hp1 HG02486.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-4110C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536591 | ||||||
| chr16:86536777
|
G | T | 1 | a0001c0001t0009g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.682-4296C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536777 | ||||||
| chr16:86536783
|
C | T | 49 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(46): Show | 95 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.682-4302G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536783 | ||||||
| chr16:86536791
|
C | T | 47 | a0001c0001t0002g0152a0001c0001t0032g0113a0002c0002t0002g0001others(44): Show | 103 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.682-4310G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536791 | ||||||
| chr16:86536823
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.682-4342T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536823 | ||||||
| chr16:86536824
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.682-4343G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536824 | ||||||
| chr16:86536881
|
C | T | 5 | a0001c0001t0007g0120a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-4400G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536881 | ||||||
| chr16:86536932
|
C | T | 1 | a0001c0001t0004g0022 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.682-4451G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536932 | ||||||
| chr16:86537107
|
A | T | 42 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(39): Show | 88 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.681+4590T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537107 | ||||||
| chr16:86537189
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(175): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.681+4508C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537189 | ||||||
| chr16:86537301
|
A | T | 51 | a0001c0001t0002g0152a0001c0001t0032g0113a0002c0002t0002g0001others(48): Show | 108 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.681+4396T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537301 | ||||||
| chr16:86537445
|
T | C | 1 | a0001c0001t0032g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.681+4252A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537445 | ||||||
| chr16:86537594
|
G | C | 1 | a0002c0002t0002g0046 | 2 | NA18942.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.681+4103C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537594 | ||||||
| chr16:86537699
|
T | C | 1 | a0004c0004t0004g0045 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.681+3998A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537699 | ||||||
| chr16:86537774
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.681+3923T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537774 | ||||||
| chr16:86538000
|
G | T | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+3697C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538000 | ||||||
| chr16:86538046
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.681+3651G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538046 | ||||||
| chr16:86538230
|
C | CT | 189 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(186): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.681+3466_681+3467i others(3): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538230 | ||||||
| chr16:86538274
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(182): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.681+3423A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538274 | ||||||
| chr16:86538284
|
C | T | 5 | a0001c0001t0007g0120a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+3413G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538284 | ||||||
| chr16:86538313
|
G | C | 5 | a0001c0001t0007g0120a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+3384C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538313 | ||||||
| chr16:86538326
|
C | T | 1 | a0003c0003t0003g0015 | 4 | HG01074.hp1 HG01255.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+3371G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538326 | ||||||
| chr16:86538330
|
G | A | 1 | a0001c0001t0009g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.681+3367C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538330 | ||||||
| chr16:86538391
|
A | G | 5 | a0001c0001t0007g0120a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+3306T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538391 | ||||||
| chr16:86538515
|
G | A | 1 | a0004c0004t0004g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.681+3182C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538515 | ||||||
| chr16:86538645
|
G | A | 2 | a0002c0002t0002g0008a0002c0002t0002g0013 | 11 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+3052C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538645 | ||||||
| chr16:86538949
|
C | T | 5 | a0001c0001t0018g0056a0006c0007t0007g0034a0006c0007t0007g0095others(2): Show | 6 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+2748G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538949 | ||||||
| chr16:86538976
|
T | C | 2 | a0001c0001t0005g0053a0001c0001t0005g0104 | 2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.681+2721A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86538976 | ||||||
| chr16:86539042
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(66): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.681+2655T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539042 | ||||||
| chr16:86539115
|
G | C | 1 | a0004c0004t0004g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.681+2582C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539115 | ||||||
| chr16:86539156
|
G | T | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+2541C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539156 | ||||||
| chr16:86539230
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0176a0001c0001t0001g0186 | 3 | HG02056.hp1 HG02080.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.681+2467A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539230 | ||||||
| chr16:86539277
|
A | T | 1 | a0015c0013t0009g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.681+2420T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539277 | ||||||
| chr16:86539379
|
G | A | 1 | a0001c0001t0001g0043 | 2 | HG01358.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.681+2318C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539379 | ||||||
| chr16:86539507
|
G | A | 1 | a0002c0002t0002g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.681+2190C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539507 | ||||||
| chr16:86539680
|
T | A | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+2017A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539680 | ||||||
| chr16:86539708
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.681+1989G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539708 | ||||||
| chr16:86539774
|
G | C | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.681+1923C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539774 | ||||||
| chr16:86539875
|
C | T | 54 | a0001c0001t0002g0152a0002c0002t0002g0001a0002c0002t0002g0007others(51): Show | 112 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.681+1822G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539875 | ||||||
| chr16:86539963
|
G | A | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+1734C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86539963 | ||||||
| chr16:86540026
|
G | A | 2 | a0001c0001t0001g0089a0003c0003t0003g0133 | 2 | HG00280.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.681+1671C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540026 | ||||||
| chr16:86540106
|
T | C | 3 | a0002c0002t0002g0162a0002c0002t0026g0160a0002c0002t0027g0161 | 3 | NA18951.hp1 NA18953.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.681+1591A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540106 | ||||||
| chr16:86540156
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.681+1541G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540156 | ||||||
| chr16:86540242
|
C | A | 1 | a0008c0011t0004g0040 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.681+1455G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540242 | ||||||
| chr16:86540255
|
T | G | 1 | a0001c0001t0001g0090 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.681+1442A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540255 | ||||||
| chr16:86540259
|
G | C | 1 | a0001c0001t0001g0018 | 4 | NA18972.hp2 NA19054.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+1438C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540259 | ||||||
| chr16:86540309
|
C | A | 1 | a0001c0001t0001g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.681+1388G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540309 | ||||||
| chr16:86540310
|
C | T | 1 | a0004c0004t0015g0032 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.681+1387G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540310 | ||||||
| chr16:86540330
|
C | G | 4 | a0004c0004t0008g0198a0004c0004t0008g0199a0004c0004t0008g0205others(1): Show | 4 | HG02735.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+1367G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540330 | ||||||
| chr16:86540381
|
G | A | 16 | a0001c0001t0007g0120a0001c0001t0009g0193a0001c0001t0009g0194others(13): Show | 21 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.681+1316C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540381 | ||||||
| chr16:86540495
|
G | C | 4 | a0004c0004t0002g0211a0004c0004t0004g0045a0004c0004t0016g0047others(1): Show | 6 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+1202C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540495 | ||||||
| chr16:86540528
|
C | G | 1 | a0002c0002t0002g0037 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.681+1169G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540528 | ||||||
| chr16:86540616
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.681+1081G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540616 | ||||||
| chr16:86540738
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.681+959A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540738 | ||||||
| chr16:86540780
|
G | A | 2 | a0002c0002t0002g0111a0002c0002t0002g0117 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.681+917C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540780 | ||||||
| chr16:86540792
|
G | A | 4 | a0004c0004t0008g0198a0004c0004t0008g0199a0004c0004t0008g0205others(1): Show | 4 | HG02735.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+905C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540792 | ||||||
| chr16:86540807
|
G | A | 1 | a0001c0001t0012g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.681+890C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540807 | ||||||
| chr16:86540829
|
C | G | 1 | a0001c0001t0001g0024 | 3 | HG01070.hp1 HG01071.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.681+868G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540829 | ||||||
| chr16:86540839
|
C | T | 2 | a0001c0001t0028g0192a0008c0011t0004g0040 | 3 | HG03098.hp2 HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.681+858G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540839 | ||||||
| chr16:86540905
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.681+792C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86540905 | ||||||
| chr16:86541012
|
G | C | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+685C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541012 | ||||||
| chr16:86541120
|
C | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(58): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.681+577G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541120 | ||||||
| chr16:86541124
|
A | G | 9 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(6): Show | 11 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.681+573T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541124 | ||||||
| chr16:86541163
|
C | T | 1 | a0008c0011t0004g0040 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.681+534G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541163 | ||||||
| chr16:86541212
|
C | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(59): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.681+485G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541212 | ||||||
| chr16:86541256
|
T | C | 1 | a0002c0002t0002g0025 | 3 | HG00544.hp1 HG02083.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.681+441A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541256 | ||||||
| chr16:86541291
|
T | TA | 59 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(56): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.681+405dupT | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541291 | ||||||
| chr16:86541291
|
T | TAA | 9 | a0001c0001t0001g0044a0001c0001t0001g0175a0001c0001t0009g0193others(6): Show | 11 | HG01243.hp2 HG02280.hp1 HG03471.hp1 others(8): Show |
intron_variant | MODIFIER | c.681+404_681+405dup others(2): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541291 | ||||||
| chr16:86541331
|
A | G | 4 | a0004c0004t0008g0198a0004c0004t0008g0199a0004c0004t0008g0205others(1): Show | 4 | HG02735.hp2 HG03239.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+366T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541331 | ||||||
| chr16:86541360
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.681+337G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541360 | ||||||
| chr16:86541413
|
A | T | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+284T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541413 | ||||||
| chr16:86541428
|
A | G | 7 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(4): Show | 8 | HG01243.hp2 HG02280.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.681+269T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541428 | ||||||
| chr16:86541494
|
C | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(58): Show | 129 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.681+203G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541494 | ||||||
| chr16:86541675
|
G | A | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+22C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541675 | ||||||
| chr16:86541687
|
C | T | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+10G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86541687 | ||||||
| chr16:86541854
|
C | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(161): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.556-32G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/7 | chr16 | 86541854 | ||||||
| chr16:86541901
|
G | A | 1 | a0003c0003t0003g0109 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-79C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/7 | chr16 | 86541901 | ||||||
| chr16:86541908
|
T | G | 1 | a0008c0011t0004g0040 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.556-86A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/7 | chr16 | 86541908 | ||||||
| chr16:86542092
|
A | G | 2 | a0002c0002t0002g0105a0002c0002t0002g0106 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.555+9T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/7 | chr16 | 86542092 | ||||||
| chr16:86542097
|
G | C | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.555+4C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 6/7 | chr16 | 86542097 | ||||||
| chr16:86542252
|
G | A | 5 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(2): Show | 5 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-39C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542252 | ||||||
| chr16:86542260
|
G | A | 1 | a0004c0004t0016g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.443-47C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542260 | ||||||
| chr16:86542386
|
G | T | 28 | a0001c0001t0019g0196a0001c0001t0019g0197a0003c0003t0003g0003others(25): Show | 71 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.443-173C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542386 | ||||||
| chr16:86542420
|
G | A | 1 | a0004c0004t0008g0199 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.443-207C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542420 | ||||||
| chr16:86542655
|
C | T | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-442G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542655 | ||||||
| chr16:86542716
|
G | A | 1 | a0001c0001t0009g0195 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.443-503C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542716 | ||||||
| chr16:86542724
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.443-511G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542724 | ||||||
| chr16:86542725
|
A | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(57): Show | 128 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.443-512T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542725 | ||||||
| chr16:86542808
|
G | A | 8 | a0001c0001t0003g0202a0001c0001t0005g0019a0001c0001t0005g0049others(5): Show | 10 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-595C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542808 | ||||||
| chr16:86542867
|
G | A | 56 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(53): Show | 123 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.443-654C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542867 | ||||||
| chr16:86542953
|
C | T | 56 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(53): Show | 123 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.443-740G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86542953 | ||||||
| chr16:86543065
|
G | A | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-852C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543065 | ||||||
| chr16:86543101
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.443-888G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543101 | ||||||
| chr16:86543106
|
G | C | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-893C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543106 | ||||||
| chr16:86543315
|
G | C | 1 | a0004c0004t0004g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.443-1102C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543315 | ||||||
| chr16:86543519
|
G | A | 1 | a0004c0004t0004g0073 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.443-1306C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543519 | ||||||
| chr16:86543576
|
G | A | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 7 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.443-1363C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543576 | ||||||
| chr16:86543600
|
G | A | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-1387C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543600 | ||||||
| chr16:86543611
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.443-1398C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543611 | ||||||
| chr16:86543619
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.443-1406T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543619 | ||||||
| chr16:86543651
|
G | A | 120 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(117): Show | 241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.443-1438C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543651 | ||||||
| chr16:86543768
|
C | G | 30 | a0001c0001t0019g0196a0001c0001t0019g0197a0003c0003t0003g0003others(27): Show | 73 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.443-1555G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543768 | ||||||
| chr16:86543788
|
C | A | 1 | a0001c0001t0001g0041 | 2 | NA19057.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.443-1575G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543788 | ||||||
| chr16:86543841
|
C | A | 3 | a0005c0005t0010g0023a0005c0005t0010g0102a0005c0005t0010g0206 | 5 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-1628G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543841 | ||||||
| chr16:86543957
|
G | A | 17 | a0001c0001t0007g0120a0003c0003t0003g0005a0003c0003t0003g0010others(14): Show | 33 | HG00140.hp1 HG01361.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.443-1744C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86543957 | ||||||
| chr16:86544022
|
C | T | 1 | a0001c0001t0019g0196 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.443-1809G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544022 | ||||||
| chr16:86544023
|
G | A | 1 | a0006c0007t0007g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.443-1810C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544023 | ||||||
| chr16:86544028
|
G | C | 1 | a0011c0017t0004g0075 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.443-1815C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544028 | ||||||
| chr16:86544180
|
C | T | 13 | a0001c0001t0003g0202a0001c0001t0005g0019a0001c0001t0005g0049others(10): Show | 18 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.443-1967G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544180 | ||||||
| chr16:86544236
|
C | T | 1 | a0001c0001t0003g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.443-2023G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544236 | ||||||
| chr16:86544288
|
G | C | 2 | a0001c0001t0003g0080a0001c0001t0003g0201 | 2 | HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.443-2075C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544288 | ||||||
| chr16:86544333
|
C | G | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-2120G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544333 | ||||||
| chr16:86544766
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.442+1793G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544766 | ||||||
| chr16:86544797
|
G | C | 5 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082others(2): Show | 7 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.442+1762C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544797 | ||||||
| chr16:86544987
|
G | A | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1572C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544987 | ||||||
| chr16:86544988
|
T | A | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1571A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86544988 | ||||||
| chr16:86545017
|
G | C | 1 | a0001c0001t0001g0094 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.442+1542C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545017 | ||||||
| chr16:86545170
|
T | C | 1 | a0008c0011t0004g0040 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.442+1389A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545170 | ||||||
| chr16:86545203
|
C | T | 1 | a0002c0002t0002g0112 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.442+1356G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545203 | ||||||
| chr16:86545204
|
G | A | 1 | a0004c0004t0006g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.442+1355C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545204 | ||||||
| chr16:86545259
|
T | G | 2 | a0001c0001t0014g0172a0001c0001t0014g0173 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.442+1300A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545259 | ||||||
| chr16:86545281
|
G | C | 3 | a0007c0008t0017g0036a0007c0008t0017g0138a0015c0013t0009g0137 | 4 | HG01243.hp2 NA20129.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1278C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545281 | ||||||
| chr16:86545466
|
G | C | 3 | a0004c0004t0002g0211a0004c0004t0016g0047a0004c0004t0016g0212 | 4 | HG02055.hp1 HG02559.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+1093C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545466 | ||||||
| chr16:86545617
|
C | A | 112 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(109): Show | 230 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.442+942G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545617 | ||||||
| chr16:86545681
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(106): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.442+878G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545681 | ||||||
| chr16:86545830
|
C | T | 1 | a0002c0002t0002g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.442+729G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545830 | ||||||
| chr16:86545851
|
G | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(113): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.442+708C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545851 | ||||||
| chr16:86545880
|
G | A | 1 | a0002c0002t0002g0106 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442+679C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545880 | ||||||
| chr16:86545898
|
G | T | 1 | a0003c0003t0003g0122 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.442+661C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545898 | ||||||
| chr16:86545995
|
C | G | 1 | a0006c0007t0007g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.442+564G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86545995 | ||||||
| chr16:86546021
|
G | A | 29 | a0001c0001t0007g0120a0001c0001t0019g0196a0001c0001t0019g0197others(26): Show | 72 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.442+538C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546021 | ||||||
| chr16:86546051
|
G | T | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+508C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546051 | ||||||
| chr16:86546053
|
G | A | 3 | a0002c0002t0002g0007a0002c0002t0002g0140a0002c0002t0002g0165 | 11 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.442+506C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546053 | ||||||
| chr16:86546078
|
AAGTCTCG others(20): Show |
A | 2 | a0004c0004t0004g0061a0015c0013t0009g0137 | 2 | HG02083.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.442+454_442+480del others(27): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546078 | ||||||
| chr16:86546113
|
G | A | 4 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+446C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546113 | ||||||
| chr16:86546190
|
T | G | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+369A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546190 | ||||||
| chr16:86546199
|
C | T | 2 | a0001c0001t0005g0104a0002c0002t0002g0013 | 5 | HG01109.hp2 HG02280.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.442+360G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546199 | ||||||
| chr16:86546284
|
CAG | C | 3 | a0007c0008t0017g0036a0007c0008t0017g0138a0015c0013t0009g0137 | 4 | HG01243.hp2 NA20129.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+273_442+274del others(2): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546284 | ||||||
| chr16:86546297
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.442+262A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546297 | ||||||
| chr16:86546345
|
A | T | 1 | a0001c0001t0005g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.442+214T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546345 | ||||||
| chr16:86546422
|
T | C | 1 | a0003c0003t0003g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.442+137A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546422 | ||||||
| chr16:86546448
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.442+111G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 5/7 | chr16 | 86546448 | ||||||
| chr16:86546663
|
T | C | 1 | a0001c0001t0003g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.352-14A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546663 | ||||||
| chr16:86546699
|
A | C | 1 | a0001c0001t0001g0041 | 2 | NA19057.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.352-50T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546699 | ||||||
| chr16:86546789
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.352-140G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546789 | ||||||
| chr16:86546790
|
G | A | 1 | a0004c0004t0004g0076 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.352-141C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546790 | ||||||
| chr16:86546847
|
T | C | 1 | a0002c0002t0002g0038 | 2 | NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.352-198A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546847 | ||||||
| chr16:86546860
|
G | A | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-211C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546860 | ||||||
| chr16:86546981
|
A | G | 1 | a0003c0003t0021g0121 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.352-332T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86546981 | ||||||
| chr16:86547080
|
G | A | 1 | a0004c0004t0004g0045 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.352-431C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547080 | ||||||
| chr16:86547082
|
C | A | 1 | a0004c0004t0004g0045 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.352-433G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547082 | ||||||
| chr16:86547095
|
G | T | 3 | a0004c0004t0002g0211a0004c0004t0016g0047a0004c0004t0016g0212 | 4 | HG02055.hp1 HG02559.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.352-446C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547095 | ||||||
| chr16:86547112
|
G | A | 3 | a0007c0008t0017g0036a0007c0008t0017g0138a0015c0013t0009g0137 | 4 | HG01243.hp2 NA20129.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-463C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547112 | ||||||
| chr16:86547125
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.352-476T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547125 | ||||||
| chr16:86547181
|
A | G | 2 | a0002c0002t0002g0110a0002c0002t0002g0111 | 2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.352-532T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547181 | ||||||
| chr16:86547199
|
T | C | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-550A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547199 | ||||||
| chr16:86547251
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.352-602C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547251 | ||||||
| chr16:86547285
|
A | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(57): Show | 125 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.352-636T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547285 | ||||||
| chr16:86547391
|
A | T | 6 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(3): Show | 6 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.352-742T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547391 | ||||||
| chr16:86547470
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.352-821C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547470 | ||||||
| chr16:86547563
|
G | T | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+901C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547563 | ||||||
| chr16:86547579
|
A | G | 1 | a0002c0002t0002g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.351+885T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547579 | ||||||
| chr16:86547585
|
G | A | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+879C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547585 | ||||||
| chr16:86547588
|
T | C | 57 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(54): Show | 121 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.351+876A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547588 | ||||||
| chr16:86547669
|
A | C | 6 | a0001c0001t0007g0120a0005c0005t0010g0023a0005c0005t0010g0206others(3): Show | 9 | HG01070.hp2 HG01192.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.351+795T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547669 | ||||||
| chr16:86547756
|
C | T | 1 | a0015c0013t0009g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+708G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547756 | ||||||
| chr16:86547760
|
G | A | 128 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(125): Show | 249 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.351+704C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547760 | ||||||
| chr16:86547792
|
T | C | 60 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(57): Show | 125 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.351+672A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547792 | ||||||
| chr16:86547828
|
T | C | 1 | a0015c0013t0009g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.351+636A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547828 | ||||||
| chr16:86547888
|
A | T | 5 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(2): Show | 7 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+576T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547888 | ||||||
| chr16:86548084
|
C | T | 1 | a0004c0004t0004g0061 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.351+380G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86548084 | ||||||
| chr16:86548111
|
C | A | 1 | a0002c0002t0002g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.351+353G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86548111 | ||||||
| chr16:86548135
|
A | G | 14 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0201others(11): Show | 19 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.351+329T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86548135 | ||||||
| chr16:86548184
|
G | C | 1 | a0002c0002t0002g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.351+280C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86548184 | ||||||
| chr16:86548236
|
G | C | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+228C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86548236 | ||||||
| chr16:86548347
|
C | A | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+117G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86548347 | ||||||
| chr16:86548754
|
G | A | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-177C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86548754 | ||||||
| chr16:86548763
|
T | C | 1 | a0008c0011t0004g0040 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238-186A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86548763 | ||||||
| chr16:86548777
|
G | A | 2 | a0005c0005t0010g0023a0005c0005t0010g0102 | 4 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-200C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86548777 | ||||||
| chr16:86548805
|
G | C | 1 | a0004c0004t0004g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.238-228C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86548805 | ||||||
| chr16:86548893
|
T | C | 1 | a0001c0001t0033g0187 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.238-316A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86548893 | ||||||
| chr16:86549090
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.238-513G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549090 | ||||||
| chr16:86549183
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(175): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.238-606G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549183 | ||||||
| chr16:86549214
|
G | A | 1 | a0002c0002t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.238-637C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549214 | ||||||
| chr16:86549247
|
G | A | 1 | a0001c0001t0012g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.238-670C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549247 | ||||||
| chr16:86549273
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.238-696G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549273 | ||||||
| chr16:86549427
|
T | A | 1 | a0001c0001t0005g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.238-850A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549427 | ||||||
| chr16:86549515
|
C | G | 1 | a0002c0002t0002g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.238-938G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549515 | ||||||
| chr16:86549575
|
C | T | 1 | a0005c0005t0010g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.238-998G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549575 | ||||||
| chr16:86549630
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.238-1053A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549630 | ||||||
| chr16:86549651
|
A | G | 2 | a0001c0001t0012g0020a0001c0001t0012g0054 | 4 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-1074T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549651 | ||||||
| chr16:86549657
|
A | G | 7 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 9 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-1080T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549657 | ||||||
| chr16:86549679
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.238-1102G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549679 | ||||||
| chr16:86549830
|
T | C | 65 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0039others(62): Show | 134 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.238-1253A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549830 | ||||||
| chr16:86549905
|
G | A | 2 | a0005c0005t0010g0023a0005c0005t0010g0102 | 4 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-1328C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549905 | ||||||
| chr16:86549922
|
G | A | 8 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(5): Show | 10 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.238-1345C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549922 | ||||||
| chr16:86549929
|
C | T | 6 | a0001c0001t0009g0193a0001c0001t0009g0194a0001c0001t0009g0195others(3): Show | 6 | HG02280.hp1 HG03471.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-1352G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86549929 | ||||||
| chr16:86550017
|
T | C | 2 | a0005c0005t0010g0023a0005c0005t0010g0102 | 4 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-1440A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550017 | ||||||
| chr16:86550040
|
C | T | 1 | a0002c0002t0002g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.238-1463G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550040 | ||||||
| chr16:86550060
|
C | T | 5 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0201others(2): Show | 7 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-1483G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550060 | ||||||
| chr16:86550168
|
T | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0094 | 6 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-1591A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550168 | ||||||
| chr16:86550209
|
A | T | 2 | a0002c0002t0002g0119a0003c0006t0003g0035 | 3 | NA18940.hp2 NA18963.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.238-1632T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550209 | ||||||
| chr16:86550223
|
T | G | 2 | a0005c0005t0010g0023a0005c0005t0010g0102 | 4 | HG02055.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.238-1646A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550223 | ||||||
| chr16:86550317
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0188 | 4 | HG01496.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+1716A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550317 | ||||||
| chr16:86550337
|
G | T | 1 | a0001c0001t0003g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.237+1696C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550337 | ||||||
| chr16:86550399
|
C | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(52): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.237+1634G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550399 | ||||||
| chr16:86550496
|
T | A | 1 | a0002c0002t0002g0008 | 7 | HG02451.hp1 HG02486.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.237+1537A>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550496 | ||||||
| chr16:86550592
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(180): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.237+1441G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550592 | ||||||
| chr16:86550599
|
G | A | 1 | a0002c0002t0002g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.237+1434C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550599 | ||||||
| chr16:86550685
|
C | A | 1 | a0004c0004t0004g0079 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.237+1348G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550685 | ||||||
| chr16:86550825
|
C | G | 1 | a0002c0002t0037g0108 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237+1208G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86550825 | ||||||
| chr16:86551283
|
G | C | 1 | a0002c0002t0002g0167 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.237+750C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551283 | ||||||
| chr16:86551296
|
T | C | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG00741.hp1 HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.237+737A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551296 | ||||||
| chr16:86551407
|
G | T | 2 | a0001c0001t0001g0144a0002c0002t0002g0143 | 2 | NA18989.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.237+626C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551407 | ||||||
| chr16:86551532
|
C | G | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(114): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.237+501G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551532 | ||||||
| chr16:86551584
|
C | T | 4 | a0001c0001t0013g0027a0001c0001t0014g0171a0001c0001t0014g0172others(1): Show | 6 | HG01167.hp2 HG01169.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+449G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551584 | ||||||
| chr16:86551692
|
G | T | 1 | a0002c0002t0002g0141 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.237+341C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551692 | ||||||
| chr16:86551880
|
G | A | 1 | a0004c0004t0015g0032 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.237+153C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551880 | ||||||
| chr16:86551916
|
G | T | 2 | a0002c0002t0002g0105a0002c0002t0002g0106 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.237+117C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 3/7 | chr16 | 86551916 | ||||||
| chr16:86552169
|
T | C | 2 | a0001c0001t0019g0196a0001c0001t0019g0197 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.124-23A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86552169 | ||||||
| chr16:86552171
|
G | C | 1 | a0001c0001t0003g0202 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-25C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86552171 | ||||||
| chr16:86552299
|
C | A | 182 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(179): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.124-153G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86552299 | ||||||
| chr16:86552778
|
T | G | 8 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0201others(5): Show | 10 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-632A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86552778 | ||||||
| chr16:86552857
|
A | G | 1 | a0001c0001t0005g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.124-711T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86552857 | ||||||
| chr16:86553056
|
A | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(124): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.124-910T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553056 | ||||||
| chr16:86553304
|
G | A | 1 | a0003c0006t0022g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.124-1158C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553304 | ||||||
| chr16:86553439
|
G | A | 1 | a0003c0003t0003g0136 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.123+1206C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553439 | ||||||
| chr16:86553450
|
G | A | 1 | a0002c0002t0011g0200 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.123+1195C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553450 | ||||||
| chr16:86553467
|
T | C | 1 | a0003c0006t0003g0168 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.123+1178A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553467 | ||||||
| chr16:86553496
|
G | A | 2 | a0001c0001t0018g0056a0001c0001t0018g0057 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.123+1149C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553496 | ||||||
| chr16:86553508
|
G | A | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1137C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553508 | ||||||
| chr16:86553570
|
C | G | 2 | a0002c0002t0002g0119a0003c0006t0003g0035 | 3 | NA18940.hp2 NA18963.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.123+1075G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553570 | ||||||
| chr16:86553635
|
C | G | 1 | a0002c0002t0002g0140 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.123+1010G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553635 | ||||||
| chr16:86553644
|
C | T | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1001G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553644 | ||||||
| chr16:86553645
|
G | A | 5 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0201others(2): Show | 7 | HG01167.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+1000C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553645 | ||||||
| chr16:86553669
|
C | G | 1 | a0004c0004t0004g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.123+976G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553669 | ||||||
| chr16:86553674
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.123+971G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553674 | ||||||
| chr16:86553682
|
G | A | 1 | a0001c0001t0001g0039 | 2 | HG02165.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.123+963C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553682 | ||||||
| chr16:86553750
|
C | A | 66 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0024others(63): Show | 139 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.123+895G>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553750 | ||||||
| chr16:86553755
|
C | T | 1 | a0001c0001t0005g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123+890G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553755 | ||||||
| chr16:86553786
|
C | G | 1 | a0008c0011t0004g0040 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.123+859G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553786 | ||||||
| chr16:86553786
|
C | T | 3 | a0001c0001t0005g0104a0002c0002t0002g0008a0002c0002t0002g0013 | 12 | HG01109.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+859G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553786 | ||||||
| chr16:86553813
|
G | A | 68 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0024others(65): Show | 141 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.123+832C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553813 | ||||||
| chr16:86553855
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.123+790G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553855 | ||||||
| chr16:86553885
|
C | T | 1 | a0002c0002t0002g0139 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.123+760G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553885 | ||||||
| chr16:86553908
|
G | A | 24 | a0001c0001t0007g0120a0002c0002t0002g0119a0003c0003t0003g0003others(21): Show | 64 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.123+737C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553908 | ||||||
| chr16:86553978
|
G | C | 1 | a0007c0008t0017g0138 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123+667C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86553978 | ||||||
| chr16:86554014
|
CGGACCAA others(17): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.123+607_123+630del others(24): Show |
MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554014 | ||||||
| chr16:86554031
|
T | C | 3 | a0007c0008t0017g0036a0007c0008t0017g0138a0015c0013t0009g0137 | 4 | HG01243.hp2 NA20129.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+614A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554031 | ||||||
| chr16:86554112
|
C | T | 1 | a0001c0001t0003g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.123+533G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554112 | ||||||
| chr16:86554129
|
C | T | 2 | a0001c0001t0018g0056a0001c0001t0018g0057 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.123+516G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554129 | ||||||
| chr16:86554171
|
G | A | 42 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0024others(39): Show | 99 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.123+474C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554171 | ||||||
| chr16:86554176
|
T | G | 1 | a0001c0001t0005g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123+469A>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554176 | ||||||
| chr16:86554216
|
C | T | 1 | a0001c0001t0001g0026 | 3 | HG02258.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.123+429G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554216 | ||||||
| chr16:86554241
|
T | C | 1 | a0004c0004t0008g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.123+404A>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554241 | ||||||
| chr16:86554251
|
A | G | 107 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0024others(104): Show | 225 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.123+394T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554251 | ||||||
| chr16:86554301
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.123+344G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554301 | ||||||
| chr16:86554354
|
G | C | 1 | a0005c0005t0010g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.123+291C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554354 | ||||||
| chr16:86554446
|
G | A | 2 | a0001c0001t0003g0080a0003c0003t0003g0207 | 2 | HG06807.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.123+199C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554446 | ||||||
| chr16:86554476
|
G | A | 1 | a0002c0002t0002g0046 | 2 | NA18942.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.123+169C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554476 | ||||||
| chr16:86554484
|
A | C | 4 | a0006c0007t0007g0034a0006c0007t0007g0095a0006c0007t0007g0096others(1): Show | 5 | HG01070.hp2 HG01192.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+161T>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554484 | ||||||
| chr16:86554491
|
G | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0208others(2): Show | 10 | HG00423.hp1 HG00609.hp1 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.123+154C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554491 | ||||||
| chr16:86554498
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0084others(10): Show | 22 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.123+147G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554498 | ||||||
| chr16:86554561
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.123+84G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 2/7 | chr16 | 86554561 | ||||||
| chr16:86554787
|
G | A | 3 | a0004c0004t0002g0211a0004c0004t0016g0047a0004c0004t0016g0212 | 4 | HG02055.hp1 HG02559.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-36C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 1/7 | chr16 | 86554787 | ||||||
| chr16:86555016
|
C | G | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0004g0022 | 5 | HG01167.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+153G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 1/7 | chr16 | 86555016 | ||||||
| chr16:86555049
|
G | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(178): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.16+120C>G | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 1/7 | chr16 | 86555049 | ||||||
| chr16:86555065
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 13 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.16+104G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 1/7 | chr16 | 86555065 | ||||||
| chr16:86555118
|
G | T | 1 | a0003c0003t0003g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16+51C>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 1/7 | chr16 | 86555118 |