| geneid | 57409 |
|---|---|
| ensemblid | ENSG00000125457.15 |
| hgncid | 24030 |
| symbol | MIF4GD |
| name | MIF4G domain containing |
| refseq_nuc | NM_001370592.1 |
| refseq_prot | NP_001357521.1 |
| ensembl_nuc | ENST00000325102.13 |
| ensembl_prot | ENSP00000321625.8 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 75266228 |
| end | 75271231 |
| strand | - |
| ver | v1.2 |
| region | chr17:75266228-75271231 |
| region5000 | chr17:75261228-75276231 |
| regionname0 | MIF4GD_chr17_75266228_75271231 |
| regionname5000 | MIF4GD_chr17_75261228_75276231 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 222 | 288 | 76 | 53 | 105 | 14 | 38 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0002 | 0/0 | 222 | 47 | 18 | 9 | 12 | 0 | 8 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0003 | 0/0 | 222 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 669 | 287 | 76 | 53 | 104 | 14 | 38 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| c0002 | 0/0 | 669 | 47 | 18 | 9 | 12 | 0 | 8 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| c0003 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| c0004 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 651 | 266 | 55 | 50 | 106 | 14 | 39 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0002 | 0/0 | 651 | 29 | 16 | 3 | 3 | 0 | 7 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0003 | 0/0 | 650 | 16 | 1 | 6 | 9 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0004 | 0/0 | 651 | 15 | 14 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0005 | 0/0 | 651 | 4 | 2 | 2 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0006 | 0/0 | 650 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0007 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0008 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| t0009 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 59 | 2 | 13 | 27 | 4 | 13 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0002 | 0/0 | 48 | 3 | 8 | 31 | 2 | 4 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0003 | 0/1 | 19 | 1 | 6 | 0 | 2 | 9 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0004 | 0/0 | 18 | 0 | 4 | 9 | 4 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0005 | 0/0 | 12 | 6 | 1 | 0 | 0 | 5 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0006 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0007 | 1/0 | 10 | 9 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0008 | 0/0 | 9 | 2 | 2 | 5 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0009 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0010 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0011 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0012 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0013 | 0/0 | 7 | 0 | 2 | 2 | 0 | 3 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0014 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0017 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0026 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0027 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 287 | 76 | 53 | 104 | 14 | 38 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 47 | 18 | 9 | 12 | 0 | 8 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 263 | 55 | 50 | 104 | 14 | 38 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 15 | 14 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 29 | 16 | 3 | 3 | 0 | 7 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0002c0002t0003 | a0002 | c0002 | t0003 | 0/0 | 16 | 1 | 6 | 9 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0002c0002t0009 | a0002 | c0002 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 59 | 2 | 13 | 27 | 4 | 13 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 48 | 3 | 8 | 31 | 2 | 4 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/1 | 19 | 1 | 6 | 0 | 2 | 9 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 18 | 0 | 4 | 9 | 4 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 1/0 | 10 | 9 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 9 | 2 | 2 | 5 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 7 | 0 | 2 | 2 | 0 | 3 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0004g0015 | a0001 | c0001 | t0004 | g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0004g0016 | a0001 | c0001 | t0004 | g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0004g0020 | a0001 | c0001 | t0004 | g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0004g0057 | a0001 | c0001 | t0004 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0005g0032 | a0001 | c0001 | t0005 | g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0005g0059 | a0001 | c0001 | t0005 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0005g0063 | a0001 | c0001 | t0005 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0006g0022 | a0001 | c0001 | t0006 | g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0007g0058 | a0001 | c0001 | t0007 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0001t0008g0062 | a0001 | c0001 | t0008 | g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0001c0003t0001g0047 | a0001 | c0003 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0001g0068 | a0002 | c0002 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0005 | a0002 | c0002 | t0002 | g0005 | 0/0 | 12 | 6 | 1 | 0 | 0 | 5 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0011 | a0002 | c0002 | t0002 | g0011 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0027 | a0002 | c0002 | t0002 | g0027 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0056 | a0002 | c0002 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0066 | a0002 | c0002 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0067 | a0002 | c0002 | t0002 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0070 | a0002 | c0002 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0071 | a0002 | c0002 | t0002 | g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0002g0074 | a0002 | c0002 | t0002 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0003g0006 | a0002 | c0002 | t0003 | g0006 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0003g0026 | a0002 | c0002 | t0003 | g0026 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0003g0072 | a0002 | c0002 | t0003 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0003g0073 | a0002 | c0002 | t0003 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0002c0002t0009g0069 | a0002 | c0002 | t0009 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| a0003c0004t0001g0041 | a0003 | c0004 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00544 | hp1 | a0003 | c0004 | t0001 | g0041 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00733 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01071 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0071 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0059 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0006 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0006 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0072 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02071 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02080 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02145 | hp2 | a0002 | c0002 | t0009 | g0069 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | CDX | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | CDX | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0062 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | YRI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | YRI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18947 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18967 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | LWK | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | YRI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ASW | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0067 | AFR | MSL | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | USA | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | MIF4GD_chr17_75261228_75276231 | MIF4GD |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75266745
|
C | T | 1 | a0003 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.664G>A | p.Asp222Asn | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 802/1319 | 664/669 | 222/222 | chr17 | 75266745 | ||
| chr17:75266931
|
C | T | 1 | a0002 | 47 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
missense_variant | MODERATE | c.478G>A | p.Glu160Lys | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 616/1319 | 478/669 | 160/222 | chr17 | 75266931 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75266908
|
C | T | 1 | a0001c0003 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.501G>A | p.Gly167Gly | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 639/1319 | 501/669 | 167/222 | chr17 | 75266908 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75266314
|
G | A | 1 | a0001c0001t0008 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 426 | chr17 | 75266314 | |||||
| chr17:75266360
|
A | G | 1 | a0001c0001t0007 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380T>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 380 | chr17 | 75266360 | |||||
| chr17:75266526
|
G | T | 1 | a0002c0002t0009 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 214 | chr17 | 75266526 | |||||
| chr17:75266534
|
G | A | 3 | a0002c0002t0002a0002c0002t0003a0002c0002t0009 | 46 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 206 | chr17 | 75266534 | |||||
| chr17:75266631
|
TC | T | 1 | a0002c0002t0003 | 16 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*108delG | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 108 | chr17 | 75266631 | |||||
| chr17:75266671
|
C | T | 2 | a0001c0001t0004a0001c0001t0007 | 16 | HG00738.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 69 | chr17 | 75266671 | |||||
| chr17:75266717
|
T | C | 1 | a0001c0001t0005 | 4 | HG00639.hp1 HG01109.hp1 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*23A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 6/6 | 23 | chr17 | 75266717 | |||||
| chr17:75271215
|
GC | G | 1 | a0001c0001t0006 | 3 | HG01884.hp2 HG02717.hp1 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123delG | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 1/6 | 1021 | chr17 | 75271215 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:75267069
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0025 | 8 | HG00140.hp2 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-102A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267069 | ||||||
| chr17:75267135
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054 | 6 | HG00438.hp1 HG02040.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-168C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267135 | ||||||
| chr17:75267181
|
G | GTTTCCAA others(6): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0044 | 2 | HG03654.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.442-215_442-214ins others(13): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267181 | ||||||
| chr17:75267185
|
C | CCAAACCA others(6): Show |
37 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(34): Show | 208 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.442-231_442-219dup others(13): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267185 | ||||||
| chr17:75267185
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0044 | 2 | HG03654.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.442-218G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267185 | ||||||
| chr17:75267254
|
G | A | 1 | a0001c0001t0001g0030 | 2 | NA19002.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.441+284C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267254 | ||||||
| chr17:75267477
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.441+61C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 5/5 | chr17 | 75267477 | ||||||
| chr17:75267981
|
T | C | 5 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0020others(2): Show | 16 | HG00738.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.193-80A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 3/5 | chr17 | 75267981 | ||||||
| chr17:75268001
|
C | T | 20 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0020others(17): Show | 63 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.192+82G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 3/5 | chr17 | 75268001 | ||||||
| chr17:75268244
|
T | C | 3 | a0001c0001t0005g0032a0001c0001t0005g0059a0001c0001t0005g0063 | 4 | HG00639.hp1 HG01109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-52A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268244 | ||||||
| chr17:75268430
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(9): Show | 67 | HG00544.hp2 HG00597.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-238C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268430 | ||||||
| chr17:75268451
|
G | C | 1 | a0002c0002t0002g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.83-259C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268451 | ||||||
| chr17:75268563
|
T | G | 1 | a0001c0001t0001g0034 | 2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.83-371A>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268563 | ||||||
| chr17:75268620
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0028a0001c0001t0001g0046 | 7 | HG02056.hp2 NA18951.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-428G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268620 | ||||||
| chr17:75268666
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0024a0001c0001t0001g0061others(1): Show | 16 | HG01069.hp1 HG01884.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-474G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268666 | ||||||
| chr17:75268671
|
C | CA | 6 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 9 | HG00438.hp1 HG02818.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.83-480dupT | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268671 | ||||||
| chr17:75268689
|
G | T | 2 | a0001c0001t0005g0032a0001c0001t0005g0063 | 3 | HG00639.hp1 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.83-497C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268689 | ||||||
| chr17:75268717
|
G | A | 5 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0020others(2): Show | 16 | HG00738.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.83-525C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268717 | ||||||
| chr17:75268809
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.83-617C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268809 | ||||||
| chr17:75268873
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.83-681C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75268873 | ||||||
| chr17:75269028
|
G | A | 1 | a0002c0002t0002g0071 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.83-836C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269028 | ||||||
| chr17:75269161
|
C | A | 1 | a0002c0002t0003g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.82+953G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269161 | ||||||
| chr17:75269526
|
T | C | 15 | a0002c0002t0001g0068a0002c0002t0002g0005a0002c0002t0002g0011others(12): Show | 47 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.82+588A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269526 | ||||||
| chr17:75269548
|
C | CTTTT | 2 | a0001c0001t0001g0017a0001c0001t0005g0059 | 6 | HG00735.hp2 HG01069.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+562_82+565dupAA others(2): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTT | C | 2 | a0001c0001t0004g0057a0002c0002t0002g0011 | 9 | HG01243.hp1 HG02258.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+564_82+565delAA | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTT | C | 7 | a0001c0001t0004g0015a0001c0001t0005g0063a0002c0002t0002g0027others(4): Show | 15 | HG02055.hp2 HG02071.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.82+563_82+565delAA others(1): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTT | C | 11 | a0001c0001t0001g0042a0001c0001t0004g0020a0001c0001t0005g0032others(8): Show | 36 | HG00639.hp1 HG00733.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.82+562_82+565delAA others(2): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTTT | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0043 | 11 | HG00140.hp1 HG00621.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.82+561_82+565delAA others(3): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTTTT | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(8): Show | 79 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.82+560_82+565delAA others(4): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTTTTT | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0019others(13): Show | 74 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.82+559_82+565delAA others(5): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTTTTT others(2): Show |
C | 1 | a0001c0001t0001g0010 | 9 | HG02055.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+557_82+565delAA others(7): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTTTTT others(6): Show |
C | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(10): Show | 72 | HG00544.hp2 HG00597.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.82+553_82+565delAA others(11): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269548
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0065 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.82+552_82+565delAA others(12): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269548 | ||||||
| chr17:75269737
|
C | CT | 17 | a0001c0001t0004g0015a0001c0001t0004g0016a0001c0001t0004g0020others(14): Show | 60 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.82+376dupA | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269737 | ||||||
| chr17:75269737
|
C | CTTT | 2 | a0001c0001t0001g0031a0001c0001t0001g0050 | 3 | HG01074.hp1 HG01099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.82+374_82+376dupAA others(1): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269737 | ||||||
| chr17:75269737
|
C | CTTTT | 18 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(15): Show | 139 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.82+376_82+377insAA others(2): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269737 | ||||||
| chr17:75269737
|
C | CTTTTT | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0028others(5): Show | 21 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.82+376_82+377insAA others(3): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269737 | ||||||
| chr17:75269737
|
C | T | 1 | a0001c0001t0001g0037 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.82+377G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269737 | ||||||
| chr17:75269737
|
CTTTCTTT | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0034others(2): Show | 41 | HG00544.hp2 HG00597.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.82+370_82+376delAA others(5): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269737 | ||||||
| chr17:75269739
|
TTC | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0060others(1): Show | 18 | HG01069.hp1 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.82+373_82+374delGA | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269739 | ||||||
| chr17:75269740
|
TC | T | 2 | a0001c0001t0001g0024a0001c0001t0006g0022 | 6 | HG01884.hp2 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+373delG | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269740 | ||||||
| chr17:75269741
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(50): Show | 233 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.82+373G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269741 | ||||||
| chr17:75269741
|
CT | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0021 | 13 | HG02055.hp1 HG02109.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.82+372delA | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269741 | ||||||
| chr17:75269825
|
C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0054 | 6 | HG00438.hp1 HG02040.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+289G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269825 | ||||||
| chr17:75269869
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+245C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269869 | ||||||
| chr17:75269871
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+243C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269871 | ||||||
| chr17:75269872
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+242G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269872 | ||||||
| chr17:75269873
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+241G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269873 | ||||||
| chr17:75269874
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+240A>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269874 | ||||||
| chr17:75269884
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+230C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269884 | ||||||
| chr17:75269891
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+223A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269891 | ||||||
| chr17:75269900
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+214T>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269900 | ||||||
| chr17:75269901
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+213C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269901 | ||||||
| chr17:75269916
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+198C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269916 | ||||||
| chr17:75269917
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+197T>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269917 | ||||||
| chr17:75269921
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+193C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269921 | ||||||
| chr17:75269922
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+191_82+192insAA others(8): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269922 | ||||||
| chr17:75269925
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+189C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269925 | ||||||
| chr17:75269927
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+187C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269927 | ||||||
| chr17:75269929
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+185A>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269929 | ||||||
| chr17:75269930
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+184A>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269930 | ||||||
| chr17:75269935
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+179G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269935 | ||||||
| chr17:75269936
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+178A>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269936 | ||||||
| chr17:75269938
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+176G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269938 | ||||||
| chr17:75269943
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+171A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269943 | ||||||
| chr17:75269946
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+168A>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269946 | ||||||
| chr17:75269949
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+165G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269949 | ||||||
| chr17:75269954
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+160T>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269954 | ||||||
| chr17:75269956
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+158C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269956 | ||||||
| chr17:75269962
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+152A>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269962 | ||||||
| chr17:75269968
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+146G>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269968 | ||||||
| chr17:75269969
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+145G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269969 | ||||||
| chr17:75269971
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+143C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269971 | ||||||
| chr17:75269974
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+140G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269974 | ||||||
| chr17:75269975
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+139T>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269975 | ||||||
| chr17:75269977
|
G | A | 1 | a0001c0001t0001g0014 | 7 | HG01891.hp2 HG02109.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+137C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269977 | ||||||
| chr17:75269979
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+135T>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269979 | ||||||
| chr17:75269981
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+133A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269981 | ||||||
| chr17:75269983
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+131G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269983 | ||||||
| chr17:75269986
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+128A>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269986 | ||||||
| chr17:75269987
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+127C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269987 | ||||||
| chr17:75269988
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+126G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269988 | ||||||
| chr17:75269989
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82+125G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269989 | ||||||
| chr17:75269996
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+118A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269996 | ||||||
| chr17:75269998
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+116A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75269998 | ||||||
| chr17:75270000
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+114C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270000 | ||||||
| chr17:75270008
|
A | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+106T>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270008 | ||||||
| chr17:75270009
|
T | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+105A>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270009 | ||||||
| chr17:75270010
|
G | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+104C>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270010 | ||||||
| chr17:75270011
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+103T>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270011 | ||||||
| chr17:75270014
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+100C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270014 | ||||||
| chr17:75270015
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+99C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270015 | ||||||
| chr17:75270023
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+91C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270023 | ||||||
| chr17:75270024
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+90T>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270024 | ||||||
| chr17:75270027
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+87G>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270027 | ||||||
| chr17:75270033
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+81G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270033 | ||||||
| chr17:75270038
|
CTCAGCCT others(3): Show |
C | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+66_82+75delCAGA others(6): Show |
MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270038 | ||||||
| chr17:75270053
|
T | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+61A>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270053 | ||||||
| chr17:75270054
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+60C>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270054 | ||||||
| chr17:75270057
|
C | A | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+57G>T | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270057 | ||||||
| chr17:75270058
|
A | T | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+56T>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270058 | ||||||
| chr17:75270060
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.82+54T>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270060 | ||||||
| chr17:75270099
|
G | C | 15 | a0002c0002t0001g0068a0002c0002t0002g0005a0002c0002t0002g0011others(12): Show | 47 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.82+15C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 2/5 | chr17 | 75270099 | ||||||
| chr17:75270496
|
A | G | 1 | a0001c0001t0001g0023 | 3 | HG02622.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-50-251T>C | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 1/5 | chr17 | 75270496 | ||||||
| chr17:75270667
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-50-422G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 1/5 | chr17 | 75270667 | ||||||
| chr17:75270669
|
C | T | 1 | a0002c0002t0002g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-50-424G>A | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 1/5 | chr17 | 75270669 | ||||||
| chr17:75270944
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-51+200C>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 1/5 | chr17 | 75270944 | ||||||
| chr17:75271088
|
A | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(29): Show | 167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-51+56T>G | MIF4GD | ENSG00000125457.15 | transcript | ENST00000325102.13 | protein_coding | 1/5 | chr17 | 75271088 |