Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 383 | 149 | 46 | 24 | 51 | 10 | 18 | 35 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0002 | 0/0 | 383 | 105 | 28 | 21 | 48 | 2 | 6 | 37 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0003 | 0/1 | 383 | 71 | 1 | 9 | 47 | 2 | 11 | 38 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0004 | 1/0 | 383 | 59 | 8 | 12 | 30 | 2 | 6 | 25 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0005 | 0/0 | 383 | 5 | 1 | 3 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0006 | 0/0 | 383 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0007 | 0/0 | 383 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0008 | 0/0 | 383 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0009 | 0/0 | 383 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0010 | 0/0 | 383 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0011 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0012 | 0/0 | 383 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0013 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0014 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| a0015 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | MEPRA others(378): Show |
chr16 | 86525186 | 86560235 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1149 | 149 | 46 | 24 | 51 | 10 | 18 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0002c0002 | 0/0 | 1149 | 105 | 28 | 21 | 48 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0003c0003 | 0/1 | 1149 | 66 | 1 | 8 | 44 | 2 | 10 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0003c0006 | 0/0 | 1149 | 5 | 0 | 1 | 3 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0004c0004 | 1/0 | 1149 | 58 | 8 | 12 | 29 | 2 | 6 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0004c0016 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0005c0007 | 0/0 | 1149 | 5 | 1 | 3 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0006c0005 | 0/0 | 1149 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0007c0008 | 0/0 | 1149 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0008c0011 | 0/0 | 1149 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0009c0010 | 0/0 | 1149 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0010c0009 | 0/0 | 1149 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0011c0015 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0012c0017 | 0/0 | 1149 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0013c0012 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0014c0014 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 | ||
| a0015c0013 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ATGGA others(1144): Show |
chr16 | 86525186 | 86560235 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3028 | 108 | 15 | 19 | 47 | 10 | 17 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0002 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0003 | 0/0 | 3028 | 5 | 4 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0004 | 0/0 | 3027 | 8 | 8 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0007 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0008 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0009 | 0/0 | 3029 | 5 | 4 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0011 | 0/0 | 3021 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3016): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0012 | 0/0 | 3028 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0013 | 0/0 | 3028 | 3 | 1 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0017 | 0/0 | 3028 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0018 | 0/0 | 3028 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0023 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0026 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0027 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0028 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0030 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0001c0001t0031 | 0/0 | 3028 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0002 | 0/0 | 3028 | 92 | 26 | 20 | 40 | 2 | 4 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0006 | 0/0 | 3028 | 7 | 0 | 1 | 6 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0024 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0025 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0032 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0033 | 0/0 | 3028 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0035 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0002c0002t0036 | 0/0 | 3028 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0003c0003t0003 | 0/1 | 3028 | 63 | 1 | 8 | 42 | 1 | 10 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0003c0003t0019 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0003c0003t0021 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0003c0003t0022 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0003c0006t0003 | 0/0 | 3028 | 4 | 0 | 1 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0003c0006t0020 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0001 | 1/0 | 3028 | 38 | 4 | 5 | 28 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0002 | 0/0 | 3028 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0005 | 0/0 | 3028 | 8 | 0 | 5 | 0 | 2 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0008 | 0/0 | 3027 | 4 | 0 | 0 | 1 | 0 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0014 | 0/0 | 3028 | 3 | 0 | 2 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0015 | 0/0 | 3028 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0004t0029 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0004c0016t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0005c0007t0007 | 0/0 | 3027 | 5 | 1 | 3 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0006c0005t0010 | 0/0 | 3029 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| a0007c0008t0016 | 0/0 | 3027 | 3 | 2 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0008c0011t0001 | 0/0 | 3028 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0009c0010t0003 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0009c0010t0034 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0010c0009t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0010c0009t0008 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3022): Show |
chr16 | 86525186 | 86560235 |
| a0011c0015t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0012c0017t0001 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0013c0012t0003 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0014c0014t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3023): Show |
chr16 | 86525186 | 86560235 |
| a0015c0013t0009 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | ACTAC others(3024): Show |
chr16 | 86525186 | 86560235 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 22 | 1 | 0 | 13 | 3 | 5 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0006 | 0/0 | 9 | 2 | 4 | 0 | 2 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0028 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0011g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0012g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0013g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0013g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0017g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0017g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0023g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0026g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0027g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0028g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0030g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0001c0001t0031g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0001 | 0/0 | 30 | 3 | 8 | 15 | 1 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0007 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0006g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0024g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0025g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0032g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0033g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0035g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0002c0002t0036g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0003 | 0/0 | 21 | 1 | 0 | 18 | 0 | 2 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0005 | 0/0 | 13 | 0 | 2 | 11 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0011 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0019g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0021g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0003t0022g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0006t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0006t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0006t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0003c0006t0020g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0004 | 1/0 | 20 | 1 | 2 | 16 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0005g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0005g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0005g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0008g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0008g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0014g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0015g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0015g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0004t0029g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0004c0016t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0005c0007t0007g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0005c0007t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0005c0007t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0005c0007t0007g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0006c0005t0010g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0006c0005t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0006c0005t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0007c0008t0016g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0007c0008t0016g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0008c0011t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0009c0010t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0009c0010t0034g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0010c0009t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0010c0009t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0011c0015t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0012c0017t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0013c0012t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0014c0014t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| a0015c0013t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0107 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00140 | hp1 | a0003 | c0003 | t0021 | g0132 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00323 | hp1 | a0003 | c0003 | t0003 | g0011 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00408 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00423 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00558 | hp2 | a0011 | c0015 | t0001 | g0163 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00597 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0060 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00738 | hp2 | a0002 | c0002 | t0006 | g0156 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01069 | hp2 | a0004 | c0004 | t0005 | g0009 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01070 | hp2 | a0005 | c0007 | t0007 | g0096 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01074 | hp1 | a0003 | c0003 | t0003 | g0023 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01074 | hp2 | a0004 | c0004 | t0005 | g0009 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01081 | hp1 | a0004 | c0004 | t0001 | g0077 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01081 | hp2 | a0004 | c0004 | t0001 | g0058 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0172 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01168 | hp1 | a0004 | c0004 | t0014 | g0032 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0173 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01169 | hp2 | a0004 | c0004 | t0014 | g0032 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01175 | hp1 | a0001 | c0001 | t0031 | g0087 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01175 | hp2 | a0003 | c0003 | t0003 | g0011 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0149 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01192 | hp2 | a0005 | c0007 | t0007 | g0034 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01243 | hp2 | a0007 | c0008 | t0016 | g0139 | AMR | PUR | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01255 | hp1 | a0003 | c0003 | t0003 | g0023 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01255 | hp2 | a0004 | c0004 | t0005 | g0009 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01256 | hp1 | a0005 | c0007 | t0007 | g0097 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01346 | hp2 | a0004 | c0004 | t0001 | g0004 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01361 | hp1 | a0003 | c0003 | t0003 | g0005 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0131 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01515 | hp1 | a0004 | c0004 | t0005 | g0030 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01517 | hp1 | a0004 | c0004 | t0005 | g0030 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0056 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01891 | hp1 | a0004 | c0004 | t0001 | g0045 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01934 | hp1 | a0003 | c0003 | t0003 | g0135 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01934 | hp2 | a0001 | c0001 | t0007 | g0121 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01943 | hp1 | a0003 | c0006 | t0003 | g0168 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01978 | hp2 | a0004 | c0004 | t0005 | g0009 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0004 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01993 | hp1 | a0004 | c0004 | t0005 | g0009 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02040 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02055 | hp1 | a0004 | c0004 | t0015 | g0212 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02055 | hp2 | a0006 | c0005 | t0010 | g0022 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02056 | hp2 | a0004 | c0004 | t0001 | g0062 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02071 | hp2 | a0003 | c0003 | t0019 | g0122 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02074 | hp1 | a0001 | c0001 | t0030 | g0180 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02074 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02083 | hp1 | a0004 | c0004 | t0001 | g0061 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02129 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02135 | hp2 | a0003 | c0003 | t0003 | g0130 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02165 | hp1 | a0002 | c0002 | t0006 | g0150 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0119 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0117 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0195 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02293 | hp1 | a0003 | c0003 | t0003 | g0124 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02300 | hp2 | a0003 | c0003 | t0003 | g0005 | AMR | PEL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02451 | hp2 | a0004 | c0004 | t0001 | g0004 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02523 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02602 | hp1 | a0004 | c0004 | t0014 | g0065 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0019 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02630 | hp1 | a0006 | c0005 | t0010 | g0102 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0106 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02735 | hp2 | a0004 | c0004 | t0008 | g0199 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02809 | hp1 | a0005 | c0007 | t0007 | g0095 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02809 | hp2 | a0002 | c0002 | t0033 | g0108 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0027 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02895 | hp1 | a0001 | c0001 | t0017 | g0057 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02976 | hp2 | a0002 | c0002 | t0036 | g0116 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03017 | hp2 | a0003 | c0003 | t0003 | g0123 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03041 | hp1 | a0006 | c0005 | t0010 | g0022 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03041 | hp2 | a0001 | c0001 | t0023 | g0051 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03098 | hp2 | a0008 | c0011 | t0001 | g0040 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03139 | hp2 | a0008 | c0011 | t0001 | g0040 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0078 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03239 | hp1 | a0012 | c0017 | t0001 | g0075 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03453 | hp2 | a0004 | c0004 | t0015 | g0047 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0027 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03490 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03492 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0171 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03540 | hp2 | a0004 | c0004 | t0015 | g0047 | AFR | GWD | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0027 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03579 | hp2 | a0006 | c0005 | t0010 | g0206 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03669 | hp1 | a0004 | c0004 | t0008 | g0205 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03688 | hp2 | a0004 | c0004 | t0008 | g0198 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03704 | hp1 | a0003 | c0003 | t0003 | g0011 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03704 | hp2 | a0003 | c0003 | t0003 | g0023 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03710 | hp1 | a0004 | c0004 | t0029 | g0066 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03710 | hp2 | a0003 | c0003 | t0003 | g0003 | SAS | PJL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0109 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03831 | hp2 | a0004 | c0004 | t0005 | g0074 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03834 | hp2 | a0005 | c0007 | t0007 | g0034 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03927 | hp2 | a0003 | c0003 | t0003 | g0100 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03942 | hp1 | a0003 | c0003 | t0003 | g0048 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03942 | hp2 | a0003 | c0006 | t0020 | g0103 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04184 | hp1 | a0009 | c0010 | t0003 | g0147 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04184 | hp2 | a0002 | c0002 | t0032 | g0154 | SAS | BEB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0166 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04204 | hp1 | a0003 | c0003 | t0003 | g0003 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18612 | hp1 | a0004 | c0004 | t0001 | g0072 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18612 | hp2 | a0004 | c0004 | t0001 | g0181 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18747 | hp1 | a0003 | c0003 | t0003 | g0126 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0194 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18939 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18940 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18941 | hp1 | a0002 | c0002 | t0006 | g0015 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18941 | hp2 | a0010 | c0009 | t0001 | g0064 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18942 | hp1 | a0004 | c0004 | t0001 | g0071 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18943 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18947 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18949 | hp1 | a0003 | c0003 | t0022 | g0133 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18949 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18950 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18950 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18951 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18952 | hp1 | a0003 | c0006 | t0003 | g0158 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18952 | hp2 | a0004 | c0004 | t0001 | g0073 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18953 | hp1 | a0002 | c0002 | t0024 | g0160 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18953 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0136 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18960 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18963 | hp1 | a0003 | c0006 | t0003 | g0036 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18963 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18964 | hp2 | a0002 | c0002 | t0006 | g0200 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18965 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18966 | hp2 | a0002 | c0002 | t0006 | g0015 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18967 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0187 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18968 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18971 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18973 | hp1 | a0003 | c0003 | t0003 | g0207 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18973 | hp2 | a0001 | c0001 | t0028 | g0177 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18974 | hp1 | a0001 | c0001 | t0027 | g0179 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18974 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18975 | hp2 | a0003 | c0006 | t0003 | g0036 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18977 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18977 | hp2 | a0002 | c0002 | t0006 | g0015 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18979 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18979 | hp2 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18981 | hp2 | a0003 | c0003 | t0003 | g0127 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18983 | hp2 | a0002 | c0002 | t0006 | g0015 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18984 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18987 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18989 | hp2 | a0004 | c0004 | t0001 | g0059 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18990 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18991 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18995 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18995 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18997 | hp2 | a0004 | c0004 | t0001 | g0079 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19000 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19001 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19001 | hp2 | a0013 | c0012 | t0003 | g0129 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19002 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19005 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19007 | hp1 | a0003 | c0003 | t0003 | g0137 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19007 | hp2 | a0004 | c0004 | t0001 | g0182 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19009 | hp1 | a0002 | c0002 | t0025 | g0161 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19009 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0115 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0197 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19054 | hp1 | a0004 | c0004 | t0001 | g0070 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0138 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19066 | hp2 | a0014 | c0014 | t0001 | g0178 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19067 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19068 | hp1 | a0003 | c0003 | t0003 | g0010 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19068 | hp2 | a0004 | c0016 | t0001 | g0068 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19072 | hp1 | a0010 | c0009 | t0008 | g0063 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19072 | hp2 | a0003 | c0003 | t0003 | g0134 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19074 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19074 | hp2 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19075 | hp1 | a0004 | c0004 | t0001 | g0004 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19075 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19078 | hp2 | a0004 | c0004 | t0008 | g0067 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19080 | hp1 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19081 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19083 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19084 | hp1 | a0009 | c0010 | t0034 | g0128 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19087 | hp1 | a0004 | c0004 | t0001 | g0076 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19087 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19088 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19089 | hp2 | a0003 | c0003 | t0003 | g0005 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19090 | hp2 | a0004 | c0004 | t0001 | g0069 | EAS | JPT | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0196 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ASW | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20129 | hp2 | a0007 | c0008 | t0016 | g0035 | AFR | ASW | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20905 | hp2 | a0002 | c0002 | t0035 | g0155 | SAS | GIH | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02109 | hp1 | a0004 | c0004 | t0001 | g0045 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0019 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG02559 | hp2 | a0004 | c0004 | t0002 | g0211 | AFR | ACB | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03471 | hp1 | a0001 | c0001 | t0026 | g0192 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG03471 | hp2 | a0006 | c0005 | t0010 | g0022 | AFR | MSL | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0003 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20300 | hp1 | a0015 | c0013 | t0009 | g0118 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | USA | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA21309 | hp1 | a0007 | c0008 | t0016 | g0035 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0113 | AFR | LWK | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0003 | g0125 | REF | REF | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0001 | g0004 | REF | REF | MTHFSD_chr16_86525186_86560235 | MTHFSD | chr16 | 86525186 | 86560235 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86532220 | C | G | 12 | a0001 a0002 a0003 others(9): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0002 a0007 |
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 | a0006 | 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 | a0011 | 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 | a0014 | 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 | a0003 a0009 a0013 |
73 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(70): 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 | a0003 a0013 |
71 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(68): 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 | a0013 | 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 | a0007 a0015 |
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 | a0010 | 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 | a0012 | 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 | a0005 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86532323 | C | T | 1 | a0006c0005 | 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 | a0003c0003 a0009c0010 a0013c0012 |
68 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(65): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86530236 | C | G | 1 | a0004c0004t0015 | 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 | a0001c0001t0003 a0003c0003t0003 a0003c0003t0019 others(7): Show |
78 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(75): 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 | a0006c0005t0010 | 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 | a0001c0001t0030 | 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 | a0004c0004t0005 | 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 | 8 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0030 others(5): 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 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 others(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 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0023 others(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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(13): Show |
96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): 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 | a0001c0001t0018 | 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 | a0001c0001t0011 | 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 | a0004c0004t0029 | 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 | a0001c0001t0028 | 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 | a0004c0004t0014 | 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 | a0001c0001t0017 | 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 | a0001c0001t0027 | 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 | a0001c0001t0026 | 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 | a0001c0001t0004 a0001c0001t0023 a0007c0008t0016 |
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 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0002 others(16): Show |
180 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(177): 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 | a0003c0003t0021 | 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 | a0002c0002t0025 | 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 | a0006c0005t0010 | 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 | a0001c0001t0013 | 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 | a0003c0003t0022 | 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 | a0001c0001t0031 | 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 | a0002c0002t0036 | 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 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0023 others(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 | a0002c0002t0033 | 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 | a0001c0001t0023 | 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 | a0002c0002t0032 | 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 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0013 others(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 | 27 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(24): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): 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 | a0002c0002t0025 | 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 | a0007c0008t0016 | 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 | a0002c0002t0024 a0002c0002t0025 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(12): Show |
98 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*80G>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 8/8 | 80 | chr16 | 86531931 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:86532509 | T | C | 12 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0004c0004t0001g0045 a0004c0004t0002g0211 a0004c0004t0015g0047 others(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 | a0004c0004t0001g0060 | 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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(173): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0001t0001g0021 a0001c0001t0007g0121 a0001c0001t0009g0052 others(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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0004c0004t0008g0198 a0004c0004t0008g0199 a0004c0004t0008g0205 others(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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(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 | 171 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(168): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): 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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0007c0008t0016g0035 a0007c0008t0016g0139 |
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 | 85 | a0001c0001t0002g0153 a0001c0001t0003g0080 a0001c0001t0003g0081 others(82): Show |
188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): 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 | a0001c0001t0009g0052 a0001c0001t0017g0056 a0001c0001t0017g0057 |
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 | a0002c0002t0002g0157 | 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 | a0014c0014t0001g0178 | 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 | a0001c0001t0001g0021 | 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 | a0003c0003t0003g0003 a0003c0003t0003g0005 a0003c0003t0003g0010 others(26): Show |
71 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(68): 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 | a0003c0003t0003g0010 a0003c0003t0003g0130 |
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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0001c0001t0018g0196 a0001c0001t0018g0197 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(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 | a0004c0004t0001g0069 | 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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | 99 | a0001c0001t0001g0021 a0001c0001t0002g0153 a0001c0001t0003g0080 others(96): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): 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 | a0003c0003t0003g0134 | 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 | a0007c0008t0016g0035 a0007c0008t0016g0139 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(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 | a0004c0004t0001g0070 | 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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | 47 | a0001c0001t0002g0153 a0002c0002t0002g0001 a0002c0002t0002g0007 others(44): 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 | a0002c0002t0002g0152 | 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 | a0004c0004t0001g0071 | 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 | a0001c0001t0001g0021 a0001c0001t0009g0052 a0001c0001t0009g0193 others(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 | a0001c0001t0001g0021 a0001c0001t0009g0052 a0001c0001t0009g0193 others(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 | 45 | a0001c0001t0002g0153 a0002c0002t0002g0001 a0002c0002t0002g0007 others(42): 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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(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 | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(169): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.682-2718T>C | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535199 | |||||||
| chr16:86535205 | A | AGG | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(169): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): 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 | 172 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(169): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): 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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0003c0003t0003g0126 | 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 |
182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(179): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): 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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
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 | a0002c0002t0002g0151 | 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 | a0001c0001t0001g0021 | 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 | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(167): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): 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 | a0001c0001t0023g0051 | 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 | a0001c0001t0018g0196 a0001c0001t0018g0197 |
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 | a0001c0001t0018g0196 a0001c0001t0018g0197 |
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 | 101 | a0001c0001t0001g0021 a0001c0001t0001g0188 a0001c0001t0001g0208 others(98): Show |
209 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.682-3115delT | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86535595 | |||||||
| chr16:86535595 | TAA | T | 7 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0001c0001t0001g0021 a0001c0001t0003g0080 a0001c0001t0003g0081 others(50): Show |
103 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(100): 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 | a0004c0004t0008g0198 a0004c0004t0008g0199 a0004c0004t0008g0205 others(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 | 179 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(176): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0002c0002t0002g0001 | 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 | a0001c0001t0028g0177 | 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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0003c0003t0003g0123 | 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 | a0003c0003t0003g0131 | 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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0003c0003t0003g0130 | 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 | a0003c0003t0003g0136 | 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 | a0004c0004t0001g0060 | 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 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(46): Show |
94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.682-4302G>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86536783 | |||||||
| chr16:86536791 | C | T | 46 | a0001c0001t0002g0153 a0001c0001t0008g0113 a0002c0002t0002g0001 others(43): 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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0001c0001t0001g0021 | 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 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(39): Show |
87 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.681+4590T>A | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537107 | |||||||
| chr16:86537189 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(174): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.681+4508C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 7/7 | chr16 | 86537189 | |||||||
| chr16:86537301 | A | T | 50 | a0001c0001t0002g0153 a0001c0001t0008g0113 a0002c0002t0002g0001 others(47): 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 | a0001c0001t0008g0113 | 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 | a0004c0004t0001g0045 | 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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(185): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): 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 | 184 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(181): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): 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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0003c0003t0003g0023 | 3 | HG01074.hp1 HG01255.hp1 HG03704.hp2 |
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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0004c0004t0001g0078 | 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 | a0002c0002t0002g0008 a0002c0002t0002g0013 |
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 | a0001c0001t0017g0056 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0001c0001t0004g0053 a0001c0001t0004g0104 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(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 | a0004c0004t0001g0060 | 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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0001c0001t0001g0083 a0001c0001t0001g0176 a0001c0001t0001g0186 |
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 | a0015c0013t0009g0118 | 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 | a0002c0002t0002g0148 | 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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | 53 | a0001c0001t0002g0153 a0002c0002t0002g0001 a0002c0002t0002g0007 others(50): 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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0001g0089 a0003c0003t0003g0135 |
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 | a0002c0002t0002g0162 a0002c0002t0024g0160 a0002c0002t0025g0161 |
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 | a0008c0011t0001g0040 | 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 | a0001c0001t0001g0017 | 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 | a0004c0004t0014g0032 | 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 | a0004c0004t0008g0198 a0004c0004t0008g0199 a0004c0004t0008g0205 others(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 | a0001c0001t0007g0121 a0001c0001t0009g0193 a0001c0001t0009g0194 others(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 | a0004c0004t0001g0045 a0004c0004t0002g0211 a0004c0004t0015g0047 others(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 | a0002c0002t0002g0111 a0002c0002t0002g0117 |
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 | a0004c0004t0008g0198 a0004c0004t0008g0199 a0004c0004t0008g0205 others(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 | a0001c0001t0011g0054 | 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 | a0001c0001t0026g0192 a0008c0011t0001g0040 |
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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0021 a0001c0001t0003g0080 a0001c0001t0003g0081 others(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 | a0008c0011t0001g0040 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0009g0193 others(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 | a0004c0004t0008g0198 a0004c0004t0008g0199 a0004c0004t0008g0205 others(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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | 60 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(57): 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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | 163 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(160): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): 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 | a0008c0011t0001g0040 | 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 | a0002c0002t0002g0105 a0002c0002t0002g0106 |
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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0004c0004t0015g0212 | 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 | a0001c0001t0018g0196 a0001c0001t0018g0197 a0003c0003t0003g0003 others(25): Show |
70 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(67): 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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0002c0002t0002g0149 | 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 | 59 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(56): 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 | a0001c0001t0003g0202 a0001c0001t0004g0018 a0001c0001t0004g0049 others(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 | 55 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(52): 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 | 55 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(52): 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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | a0004c0004t0001g0060 | 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 | a0004c0004t0001g0073 | 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 | a0001c0001t0001g0021 a0001c0001t0003g0080 a0001c0001t0003g0081 others(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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | 119 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0021 others(116): Show |
240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): 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 | a0001c0001t0018g0196 a0001c0001t0018g0197 a0003c0003t0003g0003 others(27): Show |
72 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(69): 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 | a0006c0005t0010g0022 a0006c0005t0010g0102 a0006c0005t0010g0206 |
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 | a0001c0001t0007g0121 a0003c0003t0003g0005 a0003c0003t0003g0010 others(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 | a0001c0001t0018g0196 | 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 | a0005c0007t0007g0095 | 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 | a0012c0017t0001g0075 | 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 | a0001c0001t0003g0202 a0001c0001t0004g0018 a0001c0001t0004g0049 others(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 | a0001c0001t0003g0080 a0001c0001t0003g0201 |
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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
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 | a0001c0001t0001g0021 a0001c0001t0003g0080 a0001c0001t0003g0081 others(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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0008c0011t0001g0040 | 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 | a0004c0004t0005g0074 | 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 | a0001c0001t0013g0172 a0001c0001t0013g0173 |
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 | a0007c0008t0016g0035 a0007c0008t0016g0139 a0015c0013t0009g0118 |
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 | a0004c0004t0002g0211 a0004c0004t0015g0047 a0004c0004t0015g0212 |
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 | 111 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0021 others(108): Show |
229 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(226): 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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(106): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): 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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(113): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): 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 | a0003c0003t0003g0123 | 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 | a0005c0007t0007g0095 | 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 | a0001c0001t0007g0121 a0001c0001t0018g0196 a0001c0001t0018g0197 others(26): Show |
71 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(68): 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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0002c0002t0002g0007 a0002c0002t0002g0141 a0002c0002t0002g0165 |
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 | a0004c0004t0001g0061 a0015c0013t0009g0118 |
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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0001c0001t0004g0104 a0002c0002t0002g0013 |
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 | a0007c0008t0016g0035 a0007c0008t0016g0139 a0015c0013t0009g0118 |
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 | a0001c0001t0004g0050 | 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 | a0003c0003t0003g0136 | 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0004c0004t0001g0076 | 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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0003c0003t0019g0122 | 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 | a0004c0004t0001g0045 | 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 | a0004c0004t0001g0045 | 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 | a0004c0004t0002g0211 a0004c0004t0015g0047 a0004c0004t0015g0212 |
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 | a0007c0008t0016g0035 a0007c0008t0016g0139 a0015c0013t0009g0118 |
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 | a0002c0002t0002g0110 a0002c0002t0002g0111 |
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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | 59 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(56): 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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | a0002c0002t0002g0148 | 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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | 56 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(53): 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 | a0001c0001t0007g0121 a0005c0007t0007g0034 a0005c0007t0007g0095 others(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 | a0015c0013t0009g0118 | 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 | 127 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0021 others(124): Show |
248 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.351+704C>T | MTHFSD | ENSG00000103248.19 | transcript | ENST00000360900.11 | protein_coding | 4/7 | chr16 | 86547760 | |||||||
| chr16:86547792 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(56): 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 | a0015c0013t0009g0118 | 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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0004c0004t0001g0061 | 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 | a0001c0001t0001g0021 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | a0008c0011t0001g0040 | 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 | a0006c0005t0010g0022 a0006c0005t0010g0102 |
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 | a0004c0004t0001g0058 | 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 | a0001c0001t0009g0187 | 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 | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(174): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): 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 | a0001c0001t0011g0054 | 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 | a0001c0001t0004g0053 | 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 | a0002c0002t0002g0119 | 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 | a0006c0005t0010g0206 | 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 | a0001c0001t0011g0019 a0001c0001t0011g0054 |
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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 | a0001c0001t0001g0143 | 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 | 64 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0039 others(61): 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 | a0006c0005t0010g0022 a0006c0005t0010g0102 |
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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0001c0001t0009g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(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 | a0006c0005t0010g0022 a0006c0005t0010g0102 |
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 | a0002c0002t0002g0146 | 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 | a0001c0001t0001g0021 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0094 |
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 | a0002c0002t0002g0120 a0003c0006t0003g0036 |
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 | a0006c0005t0010g0022 a0006c0005t0010g0102 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0188 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(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 | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(179): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): 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 | a0002c0002t0002g0119 | 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 | a0004c0004t0001g0079 | 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 | a0002c0002t0033g0108 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
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 | a0001c0001t0001g0145 a0002c0002t0002g0144 |
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 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0017 others(114): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): 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 | a0001c0001t0012g0027 a0001c0001t0013g0171 a0001c0001t0013g0172 others(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 | a0002c0002t0002g0142 | 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 | a0004c0004t0014g0032 | 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 | a0002c0002t0002g0105 a0002c0002t0002g0106 |
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 | a0001c0001t0018g0196 a0001c0001t0018g0197 |
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 | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(178): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): 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 | a0001c0001t0001g0021 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0001c0001t0004g0049 | 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 | 126 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(123): 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 | a0003c0006t0020g0103 | 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 | a0003c0003t0003g0138 | 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 | a0002c0002t0006g0200 | 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 | a0001c0001t0017g0056 a0001c0001t0017g0057 |
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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0002c0002t0002g0120 a0003c0006t0003g0036 |
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 | a0002c0002t0002g0141 | 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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0001c0001t0001g0021 a0001c0001t0003g0081 a0001c0001t0003g0082 others(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 | a0004c0004t0001g0058 | 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 | 65 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0024 others(62): 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 | a0001c0001t0004g0055 | 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 | a0008c0011t0001g0040 | 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 | a0001c0001t0004g0104 a0002c0002t0002g0008 a0002c0002t0002g0013 |
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 | 67 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0024 others(64): 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 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
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 | a0002c0002t0002g0140 | 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 | a0001c0001t0007g0121 a0002c0002t0002g0120 a0003c0003t0003g0003 others(21): Show |
63 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(60): 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 | a0007c0008t0016g0139 | 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 | a0007c0008t0016g0035 a0007c0008t0016g0139 a0015c0013t0009g0118 |
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 | a0001c0001t0017g0056 a0001c0001t0017g0057 |
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 | 41 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0024 others(38): 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 | a0001c0001t0004g0055 | 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 | 106 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0024 others(103): Show |
224 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(221): 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 | a0006c0005t0010g0206 | 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 | a0001c0001t0003g0080 a0003c0003t0003g0207 |
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 | a0005c0007t0007g0034 a0005c0007t0007g0095 a0005c0007t0007g0096 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0084 others(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 | a0004c0004t0002g0211 a0004c0004t0015g0047 a0004c0004t0015g0212 |
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 | a0001c0001t0001g0021 a0001c0001t0003g0081 a0001c0001t0003g0082 |
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 | 180 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(177): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(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 |