| geneid | 51251 |
|---|---|
| ensemblid | ENSG00000122643.23 |
| hgncid | 17820 |
| symbol | NT5C3A |
| name | 5'-nucleotidase, cytosolic IIIA |
| refseq_nuc | NM_001002010.5 |
| refseq_prot | NP_001002010.2 |
| ensembl_nuc | ENST00000610140.7 |
| ensembl_prot | ENSP00000476480.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 33014130 |
| end | 33062776 |
| strand | - |
| ver | v1.2 |
| region | chr7:33014130-33062776 |
| region5000 | chr7:33009130-33067776 |
| regionname0 | NT5C3A_chr7_33014130_33062776 |
| regionname5000 | NT5C3A_chr7_33009130_33067776 |
| 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 331 | 398 | 94 | 69 | 181 | 14 | 38 | 145 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0002 | 0/0 | 331 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0003 | 0/0 | 331 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 996 | 224 | 61 | 46 | 84 | 10 | 22 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| c0002 | 1/0 | 996 | 164 | 23 | 23 | 97 | 4 | 16 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| c0003 | 0/0 | 996 | 9 | 9 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| c0004 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| c0005 | 0/0 | 996 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| c0006 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 676 | 260 | 71 | 47 | 109 | 10 | 22 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0002 | 1/0 | 672 | 63 | 0 | 13 | 42 | 3 | 4 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0003 | 0/0 | 670 | 50 | 8 | 7 | 22 | 1 | 12 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0004 | 0/0 | 671 | 10 | 10 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0005 | 0/0 | 671 | 5 | 3 | 2 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0006 | 0/0 | 676 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0007 | 0/0 | 676 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0008 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0009 | 0/0 | 676 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0010 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0011 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0012 | 0/0 | 670 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0013 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| t0014 | 0/0 | 672 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0356 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 996 | 224 | 61 | 46 | 84 | 10 | 22 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002 | 1/0 | 996 | 164 | 23 | 23 | 97 | 4 | 16 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0003 | 0/0 | 996 | 9 | 9 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0004 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0002c0006 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0003c0005 | 0/0 | 996 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1671 | 220 | 61 | 45 | 81 | 10 | 22 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0001t0007 | 0/0 | 1671 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0001t0013 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0001t0014 | 0/0 | 1667 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0001 | 0/0 | 1671 | 30 | 2 | 1 | 27 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0002 | 1/0 | 1667 | 63 | 0 | 13 | 42 | 3 | 4 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0003 | 0/0 | 1665 | 50 | 8 | 7 | 22 | 1 | 12 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0004 | 0/0 | 1666 | 10 | 10 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0005 | 0/0 | 1666 | 5 | 3 | 2 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0006 | 0/0 | 1671 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0008 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0010 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0002t0011 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0003t0001 | 0/0 | 1671 | 8 | 8 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0003t0009 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0001c0004t0012 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0002c0006t0001 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| a0003c0005t0001 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | copy fasta | chr7 | 33009130 | 33067776 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0356 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0013g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0001t0014g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0003g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0006g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0006g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0006g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0002t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0003t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0001c0004t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0002c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| a0003c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | GBR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0142 | EUR | FIN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00438 | hp2 | a0001 | c0002 | t0006 | g0384 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0309 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0368 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0181 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01069 | hp2 | a0003 | c0005 | t0001 | g0016 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0153 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0155 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0080 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0079 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0379 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0378 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0110 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01255 | hp1 | a0001 | c0002 | t0005 | g0114 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0053 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0158 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0117 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | IBS | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0111 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0124 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0138 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0109 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0290 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0131 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | CDX | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0377 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0319 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02523 | hp2 | a0001 | c0002 | t0010 | g0086 | EAS | KHV | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0381 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0130 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0112 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0120 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0366 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0338 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0118 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0068 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0380 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0113 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0147 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0067 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03209 | hp1 | a0001 | c0004 | t0012 | g0015 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0069 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0119 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0052 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0128 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0374 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0149 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0376 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0133 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0159 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0160 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0284 | AFR | GWD | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03579 | hp2 | a0001 | c0003 | t0009 | g0283 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0375 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0143 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0145 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0098 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0103 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0156 | SAS | BEB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0157 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0146 | SAS | STU | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | CHB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18939 | hp2 | a0001 | c0002 | t0008 | g0034 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0076 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0311 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18970 | hp2 | a0001 | c0002 | t0006 | g0382 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18987 | hp2 | a0002 | c0006 | t0001 | g0203 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18988 | hp1 | a0001 | c0001 | t0013 | g0292 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19058 | hp1 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19091 | hp2 | a0001 | c0002 | t0006 | g0383 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | YRI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ASW | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0337 | AFR | ASW | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0347 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | MSL | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0151 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0336 | AFR | USA | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | LWK | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0356 | REF | REF | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0072 | REF | REF | NT5C3A_chr7_33009130_33067776 | NT5C3A | chr7 | 33009130 | 33067776 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33017477
|
C | T | 1 | a0002 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.655G>A | p.Val219Ile | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/9 | 726/1667 | 655/996 | 219/331 | chr7 | 33017477 | ||
| chr7:33062615
|
A | G | 1 | a0003 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.91T>C | p.Phe31Leu | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/9 | 162/1667 | 91/996 | 31/331 | chr7 | 33062615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33021304
|
A | G | 1 | a0001c0003 | 9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
synonymous_variant | LOW | c.408T>C | p.Thr136Thr | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/9 | 479/1667 | 408/996 | 136/331 | chr7 | 33021304 | ||
| chr7:33021334
|
A | G | 4 | a0001c0001a0001c0003a0002c0006others(1): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
synonymous_variant | LOW | c.378T>C | p.Tyr126Tyr | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/9 | 449/1667 | 378/996 | 126/331 | chr7 | 33021334 | ||
| chr7:33062685
|
C | T | 1 | a0001c0004 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.21G>A | p.Ala7Ala | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/9 | 92/1667 | 21/996 | 7/331 | chr7 | 33062685 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33014138
|
G | T | 1 | a0001c0002t0011 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 592 | chr7 | 33014138 | |||||
| chr7:33014248
|
A | G | 1 | a0001c0002t0010 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 482 | chr7 | 33014248 | |||||
| chr7:33014302
|
T | C | 1 | a0001c0004t0012 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 428 | chr7 | 33014302 | |||||
| chr7:33014321
|
A | G | 1 | a0001c0002t0005 | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 409 | chr7 | 33014321 | |||||
| chr7:33014415
|
G | A | 2 | a0001c0001t0007a0001c0001t0013 | 3 | HG00621.hp1 NA18967.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*315C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 315 | chr7 | 33014415 | |||||
| chr7:33014429
|
T | G | 1 | a0001c0001t0013 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 301 | chr7 | 33014429 | |||||
| chr7:33014500
|
A | G | 11 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(8): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*230T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 230 | chr7 | 33014500 | |||||
| chr7:33014502
|
CT | C | 2 | a0001c0002t0004a0001c0002t0005 | 15 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*227delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 227 | chr7 | 33014502 | |||||
| chr7:33014502
|
CTT | C | 2 | a0001c0002t0003a0001c0004t0012 | 51 | HG00280.hp2 HG00673.hp1 HG01070.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*226_*227delAA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 226 | chr7 | 33014502 | |||||
| chr7:33014505
|
T | TAAGA | 10 | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(7): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*224_*225insTCTT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 224 | chr7 | 33014505 | |||||
| chr7:33014506
|
T | A | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*224A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 224 | chr7 | 33014506 | |||||
| chr7:33014630
|
C | T | 1 | a0001c0003t0009 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 100 | chr7 | 33014630 | |||||
| chr7:33014674
|
C | G | 1 | a0001c0002t0008 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 9/9 | 56 | chr7 | 33014674 | |||||
| chr7:33062734
|
G | C | 1 | a0001c0002t0006 | 3 | HG00438.hp2 NA18970.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-29C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/9 | 29 | chr7 | 33062734 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:33014869
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0036a0001c0002t0001g0037 | 3 | NA18951.hp1 NA18977.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.895-38C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33014869 | ||||||
| chr7:33014947
|
C | A | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.895-116G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33014947 | ||||||
| chr7:33014964
|
G | C | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.895-133C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33014964 | ||||||
| chr7:33015084
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.895-253C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015084 | ||||||
| chr7:33015098
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.895-267G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015098 | ||||||
| chr7:33015104
|
G | C | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.895-273C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015104 | ||||||
| chr7:33015182
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.895-351A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015182 | ||||||
| chr7:33015200
|
C | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0020others(76): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.895-369G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015200 | ||||||
| chr7:33015304
|
C | T | 6 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0067others(3): Show | 7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.894+366G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015304 | ||||||
| chr7:33015409
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.894+261T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015409 | ||||||
| chr7:33015507
|
G | A | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.894+163C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015507 | ||||||
| chr7:33015529
|
C | T | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.894+141G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015529 | ||||||
| chr7:33015537
|
T | C | 1 | a0001c0002t0002g0098 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.894+133A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015537 | ||||||
| chr7:33015552
|
T | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.894+118A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015552 | ||||||
| chr7:33015557
|
C | CA | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.894+112dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015557 | ||||||
| chr7:33015609
|
T | C | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.894+61A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 8/8 | chr7 | 33015609 | ||||||
| chr7:33016006
|
G | C | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.694-136C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016006 | ||||||
| chr7:33016046
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.694-176G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016046 | ||||||
| chr7:33016097
|
C | T | 1 | a0001c0002t0002g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694-227G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016097 | ||||||
| chr7:33016293
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.694-423C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016293 | ||||||
| chr7:33016438
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.694-568T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016438 | ||||||
| chr7:33016519
|
A | G | 1 | a0001c0002t0002g0080 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.694-649T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016519 | ||||||
| chr7:33016530
|
T | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.694-660A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016530 | ||||||
| chr7:33016540
|
G | A | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-670C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016540 | ||||||
| chr7:33016669
|
C | CA | 144 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(141): Show | 148 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.693+769dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016669 | ||||||
| chr7:33016669
|
C | CAA | 42 | a0001c0001t0001g0204a0001c0001t0001g0224a0001c0001t0001g0225others(39): Show | 44 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.693+768_693+769dup others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016669 | ||||||
| chr7:33016758
|
A | G | 2 | a0001c0002t0003g0159a0001c0002t0003g0160 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.693+681T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016758 | ||||||
| chr7:33016803
|
G | C | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.693+636C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33016803 | ||||||
| chr7:33017080
|
G | A | 13 | a0001c0001t0001g0182a0001c0001t0001g0287a0001c0001t0001g0288others(10): Show | 13 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.693+359C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017080 | ||||||
| chr7:33017182
|
CA | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(222): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.693+256delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017182 | ||||||
| chr7:33017182
|
CAA | C | 40 | a0001c0001t0001g0163a0001c0001t0001g0178a0001c0001t0001g0188others(37): Show | 41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.693+255_693+256del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017182 | ||||||
| chr7:33017284
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.693+155A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017284 | ||||||
| chr7:33017308
|
G | A | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+131C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 7/8 | chr7 | 33017308 | ||||||
| chr7:33017824
|
C | T | 1 | a0001c0001t0001g0354 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.531-223G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017824 | ||||||
| chr7:33017896
|
A | G | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.531-295T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017896 | ||||||
| chr7:33017982
|
C | A | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.531-381G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017982 | ||||||
| chr7:33017985
|
C | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.531-384G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33017985 | ||||||
| chr7:33018008
|
T | C | 1 | a0001c0002t0002g0081 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.531-407A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018008 | ||||||
| chr7:33018134
|
C | T | 262 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.531-533G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018134 | ||||||
| chr7:33018139
|
C | T | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.531-538G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018139 | ||||||
| chr7:33018438
|
C | T | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.531-837G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018438 | ||||||
| chr7:33018572
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.531-971G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018572 | ||||||
| chr7:33018588
|
C | T | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.531-987G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018588 | ||||||
| chr7:33018707
|
G | A | 14 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+928C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018707 | ||||||
| chr7:33018719
|
G | A | 101 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0161others(98): Show | 103 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.530+916C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018719 | ||||||
| chr7:33018722
|
C | T | 1 | a0001c0002t0002g0059 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.530+913G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018722 | ||||||
| chr7:33018828
|
C | T | 7 | a0001c0001t0001g0217a0001c0001t0001g0221a0001c0001t0001g0223others(4): Show | 7 | HG00738.hp1 HG01106.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.530+807G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018828 | ||||||
| chr7:33018829
|
A | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.530+806T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018829 | ||||||
| chr7:33018844
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.530+791C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018844 | ||||||
| chr7:33018844
|
G | GA | 16 | a0001c0001t0001g0358a0001c0002t0003g0009a0001c0002t0003g0053others(13): Show | 17 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.530+790dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018844 | ||||||
| chr7:33018857
|
T | C | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.530+778A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018857 | ||||||
| chr7:33018914
|
C | A | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.530+721G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33018914 | ||||||
| chr7:33019003
|
C | T | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.530+632G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019003 | ||||||
| chr7:33019034
|
G | A | 4 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(1): Show | 4 | HG01952.hp2 HG02273.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.530+601C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019034 | ||||||
| chr7:33019100
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.530+535G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019100 | ||||||
| chr7:33019179
|
C | T | 1 | a0001c0002t0004g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.530+456G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019179 | ||||||
| chr7:33019237
|
C | G | 1 | a0001c0002t0001g0041 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.530+398G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019237 | ||||||
| chr7:33019256
|
TA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0020others(79): Show | 84 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.530+378delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019256 | ||||||
| chr7:33019276
|
C | G | 2 | a0001c0001t0001g0298a0001c0001t0001g0301 | 2 | HG01070.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.530+359G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019276 | ||||||
| chr7:33019354
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.530+281C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 6/8 | chr7 | 33019354 | ||||||
| chr7:33019795
|
A | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(282): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.441-71T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33019795 | ||||||
| chr7:33019939
|
A | G | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.441-215T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33019939 | ||||||
| chr7:33020045
|
T | C | 1 | a0001c0002t0002g0094 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.441-321A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020045 | ||||||
| chr7:33020282
|
G | C | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.441-558C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020282 | ||||||
| chr7:33020314
|
ACT | A | 11 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0308others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.441-592_441-591del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020314 | ||||||
| chr7:33020362
|
C | T | 1 | a0001c0001t0001g0333 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.441-638G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020362 | ||||||
| chr7:33020495
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.441-771A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020495 | ||||||
| chr7:33020566
|
G | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(282): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.440+706C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020566 | ||||||
| chr7:33020655
|
T | C | 35 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(32): Show | 36 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(33): Show |
intron_variant | MODIFIER | c.440+617A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020655 | ||||||
| chr7:33020687
|
C | T | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.440+585G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020687 | ||||||
| chr7:33020694
|
A | C | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.440+578T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020694 | ||||||
| chr7:33020700
|
G | C | 1 | a0001c0002t0002g0059 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.440+572C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020700 | ||||||
| chr7:33020775
|
A | AT | 261 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.440+496dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020775 | ||||||
| chr7:33020793
|
C | T | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.440+479G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020793 | ||||||
| chr7:33020834
|
C | T | 6 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0067others(3): Show | 7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.440+438G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020834 | ||||||
| chr7:33020853
|
G | A | 5 | a0001c0002t0005g0110a0001c0002t0005g0111a0001c0002t0005g0112others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+419C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020853 | ||||||
| chr7:33020863
|
TG | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.440+408delC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020863 | ||||||
| chr7:33020887
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.440+385G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020887 | ||||||
| chr7:33020984
|
G | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.440+288C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020984 | ||||||
| chr7:33020991
|
TCA | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.440+279_440+280del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33020991 | ||||||
| chr7:33021143
|
A | C | 31 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(28): Show | 32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.440+129T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33021143 | ||||||
| chr7:33021263
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.440+9A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 5/8 | chr7 | 33021263 | ||||||
| chr7:33021505
|
T | A | 1 | a0001c0002t0003g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.355-148A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021505 | ||||||
| chr7:33021520
|
A | C | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.355-163T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021520 | ||||||
| chr7:33021623
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.355-266A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021623 | ||||||
| chr7:33021787
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.354+266A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021787 | ||||||
| chr7:33021851
|
C | T | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.354+202G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 4/8 | chr7 | 33021851 | ||||||
| chr7:33022213
|
C | T | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.308-114G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022213 | ||||||
| chr7:33022418
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.308-319A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022418 | ||||||
| chr7:33022433
|
AAC | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.308-336_308-335del others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022433 | ||||||
| chr7:33022641
|
C | T | 1 | a0001c0002t0002g0101 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.308-542G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022641 | ||||||
| chr7:33022851
|
C | T | 1 | a0001c0002t0002g0093 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.308-752G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022851 | ||||||
| chr7:33022866
|
T | C | 5 | a0001c0002t0003g0156a0001c0002t0003g0157a0001c0002t0003g0158others(2): Show | 5 | HG01361.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.308-767A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022866 | ||||||
| chr7:33022920
|
G | GT | 9 | a0001c0001t0001g0020a0001c0001t0001g0215a0001c0001t0001g0233others(6): Show | 9 | HG01099.hp2 HG01109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.308-822dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022920 | ||||||
| chr7:33022934
|
T | TC | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01952.hp2 HG02273.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.308-836dupG | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33022934 | ||||||
| chr7:33023023
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.308-924G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023023 | ||||||
| chr7:33023171
|
C | T | 1 | a0001c0001t0001g0356 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.307+868G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023171 | ||||||
| chr7:33023211
|
G | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.307+828C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023211 | ||||||
| chr7:33023268
|
CT | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.307+770delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023268 | ||||||
| chr7:33023341
|
C | T | 7 | a0001c0002t0002g0007a0001c0002t0002g0060a0001c0002t0002g0061others(4): Show | 8 | HG00621.hp2 NA18944.hp1 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.307+698G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023341 | ||||||
| chr7:33023422
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(2): Show | 5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+617G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023422 | ||||||
| chr7:33023451
|
G | T | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.307+588C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023451 | ||||||
| chr7:33023585
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.307+454C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023585 | ||||||
| chr7:33023586
|
T | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.307+453A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023586 | ||||||
| chr7:33023666
|
T | G | 14 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.307+373A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023666 | ||||||
| chr7:33023725
|
A | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(2): Show | 5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.307+314T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023725 | ||||||
| chr7:33023851
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.307+188G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023851 | ||||||
| chr7:33023880
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.307+159T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33023880 | ||||||
| chr7:33024004
|
G | A | 7 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+35C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 3/8 | chr7 | 33024004 | ||||||
| chr7:33024309
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.238-201A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024309 | ||||||
| chr7:33024347
|
A | G | 5 | a0001c0002t0005g0110a0001c0002t0005g0111a0001c0002t0005g0112others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.238-239T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024347 | ||||||
| chr7:33024439
|
AAATAAGA others(7): Show |
A | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.238-345_238-332del others(14): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024439 | ||||||
| chr7:33024807
|
G | A | 1 | a0001c0001t0001g0362 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.238-699C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024807 | ||||||
| chr7:33024912
|
G | A | 6 | a0001c0001t0001g0167a0001c0001t0001g0173a0001c0001t0001g0242others(3): Show | 6 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-804C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33024912 | ||||||
| chr7:33025084
|
A | C | 1 | a0001c0001t0001g0194 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.238-976T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025084 | ||||||
| chr7:33025097
|
C | T | 6 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0067others(3): Show | 7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.238-989G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025097 | ||||||
| chr7:33025162
|
A | G | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.238-1054T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025162 | ||||||
| chr7:33025236
|
A | G | 7 | a0001c0002t0002g0007a0001c0002t0002g0060a0001c0002t0002g0061others(4): Show | 8 | HG00621.hp2 NA18944.hp1 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-1128T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025236 | ||||||
| chr7:33025490
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(124): Show | 130 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.237+1327A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025490 | ||||||
| chr7:33025521
|
T | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(2): Show | 5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1296A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025521 | ||||||
| chr7:33025570
|
C | T | 285 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(282): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.237+1247G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025570 | ||||||
| chr7:33025596
|
T | A | 8 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+1221A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025596 | ||||||
| chr7:33025625
|
A | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.237+1192T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025625 | ||||||
| chr7:33025685
|
C | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.237+1132G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025685 | ||||||
| chr7:33025686
|
T | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.237+1131A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025686 | ||||||
| chr7:33025708
|
T | TA | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+1108dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025708 | ||||||
| chr7:33025960
|
T | C | 1 | a0001c0002t0003g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237+857A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33025960 | ||||||
| chr7:33026003
|
T | C | 3 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120 | 3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.237+814A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026003 | ||||||
| chr7:33026241
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.237+576C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026241 | ||||||
| chr7:33026306
|
G | A | 10 | a0001c0001t0001g0167a0001c0001t0001g0269a0001c0001t0001g0270others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.237+511C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026306 | ||||||
| chr7:33026353
|
G | GAA | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+462_237+463dup others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | ||||||
| chr7:33026353
|
G | GAAAA | 6 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0339others(3): Show | 6 | HG03041.hp2 NA18747.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.237+460_237+463dup others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | ||||||
| chr7:33026353
|
G | GAAAAA | 107 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0163others(104): Show | 110 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.237+459_237+463dup others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | ||||||
| chr7:33026353
|
G | GAAAAAA | 130 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(127): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.237+458_237+463dup others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | ||||||
| chr7:33026353
|
G | GAAAAAAA | 13 | a0001c0001t0001g0184a0001c0001t0001g0204a0001c0001t0001g0207others(10): Show | 13 | HG00741.hp1 HG01106.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.237+457_237+463dup others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | ||||||
| chr7:33026353
|
G | GGAAAAA | 4 | a0001c0001t0001g0173a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02630.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.237+463_237+464ins others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026353 | ||||||
| chr7:33026441
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0001g0313a0001c0001t0001g0316 | 3 | NA18999.hp1 NA19079.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.237+376C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026441 | ||||||
| chr7:33026498
|
GC | G | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.237+318delG | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026498 | ||||||
| chr7:33026516
|
G | A | 1 | a0001c0001t0001g0370 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237+301C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026516 | ||||||
| chr7:33026576
|
G | A | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.237+241C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026576 | ||||||
| chr7:33026608
|
C | T | 14 | a0001c0001t0001g0182a0001c0001t0001g0262a0001c0001t0001g0287others(11): Show | 14 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+209G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026608 | ||||||
| chr7:33026611
|
C | A | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.237+206G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026611 | ||||||
| chr7:33026653
|
G | A | 1 | a0001c0001t0001g0370 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.237+164C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026653 | ||||||
| chr7:33026657
|
A | AT | 8 | a0001c0001t0001g0161a0001c0001t0001g0168a0001c0001t0001g0180others(5): Show | 8 | HG02738.hp1 HG04199.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+159dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026657 | ||||||
| chr7:33026714
|
G | A | 2 | a0001c0002t0003g0010a0001c0002t0003g0123 | 3 | HG03471.hp2 NA18986.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.237+103C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 2/8 | chr7 | 33026714 | ||||||
| chr7:33026919
|
A | C | 3 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120 | 3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.139-4T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33026919 | ||||||
| chr7:33026946
|
T | G | 1 | a0001c0002t0002g0103 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.139-31A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33026946 | ||||||
| chr7:33027152
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 3 | HG01891.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139-237G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027152 | ||||||
| chr7:33027213
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.139-298G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027213 | ||||||
| chr7:33027353
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG01952.hp2 HG02273.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.139-438C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027353 | ||||||
| chr7:33027482
|
T | C | 5 | a0001c0001t0001g0210a0001c0001t0001g0254a0001c0001t0001g0257others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-567A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027482 | ||||||
| chr7:33027518
|
C | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.139-603G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027518 | ||||||
| chr7:33027667
|
C | CAG | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.139-754_139-753dup others(2): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027667 | ||||||
| chr7:33027777
|
T | A | 4 | a0001c0002t0003g0153a0001c0002t0003g0155a0001c0002t0003g0375others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-862A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027777 | ||||||
| chr7:33027788
|
C | G | 4 | a0001c0002t0003g0153a0001c0002t0003g0155a0001c0002t0003g0375others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-873G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027788 | ||||||
| chr7:33027796
|
C | T | 4 | a0001c0002t0003g0153a0001c0002t0003g0155a0001c0002t0003g0375others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-881G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027796 | ||||||
| chr7:33027798
|
A | T | 4 | a0001c0002t0003g0153a0001c0002t0003g0155a0001c0002t0003g0375others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-883T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027798 | ||||||
| chr7:33027882
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0301a0001c0001t0001g0322 | 3 | HG01070.hp2 HG02300.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.139-967A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027882 | ||||||
| chr7:33027918
|
A | ATTT | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-1006_139-1004d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33027918 | ||||||
| chr7:33028079
|
C | T | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1164G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028079 | ||||||
| chr7:33028253
|
C | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.139-1338G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028253 | ||||||
| chr7:33028268
|
T | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(282): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.139-1353A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028268 | ||||||
| chr7:33028291
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.139-1376G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028291 | ||||||
| chr7:33028493
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.139-1578A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028493 | ||||||
| chr7:33028741
|
C | T | 1 | a0001c0002t0002g0078 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.139-1826G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028741 | ||||||
| chr7:33028761
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-1846A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028761 | ||||||
| chr7:33028852
|
G | A | 1 | a0001c0002t0001g0026 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.139-1937C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028852 | ||||||
| chr7:33028879
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-1964A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028879 | ||||||
| chr7:33028887
|
C | G | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-1972G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028887 | ||||||
| chr7:33028892
|
G | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.139-1977C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028892 | ||||||
| chr7:33028915
|
C | T | 36 | a0001c0001t0001g0299a0001c0001t0001g0313a0001c0001t0001g0316others(33): Show | 37 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.139-2000G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028915 | ||||||
| chr7:33028980
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.139-2065C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33028980 | ||||||
| chr7:33029029
|
C | G | 1 | a0001c0001t0001g0333 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.139-2114G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029029 | ||||||
| chr7:33029244
|
A | AT | 261 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.139-2330dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029244 | ||||||
| chr7:33029341
|
G | A | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-2426C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029341 | ||||||
| chr7:33029401
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.139-2486T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029401 | ||||||
| chr7:33029461
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA18989.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.139-2546A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029461 | ||||||
| chr7:33029521
|
T | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-2606A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029521 | ||||||
| chr7:33029565
|
T | C | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-2650A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33029565 | ||||||
| chr7:33030017
|
T | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(2): Show | 5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-3102A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030017 | ||||||
| chr7:33030060
|
T | C | 1 | a0001c0002t0008g0034 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.139-3145A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030060 | ||||||
| chr7:33030430
|
C | T | 2 | a0001c0002t0001g0026a0001c0002t0001g0036 | 2 | NA18951.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.139-3515G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030430 | ||||||
| chr7:33030461
|
A | G | 6 | a0001c0002t0003g0128a0001c0002t0003g0130a0001c0002t0003g0131others(3): Show | 6 | HG00280.hp2 HG02083.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-3546T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030461 | ||||||
| chr7:33030471
|
T | C | 1 | a0001c0002t0003g0129 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.139-3556A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030471 | ||||||
| chr7:33030563
|
C | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.139-3648G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030563 | ||||||
| chr7:33030840
|
C | A | 1 | a0001c0002t0003g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.139-3925G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030840 | ||||||
| chr7:33030871
|
G | A | 1 | a0001c0001t0001g0347 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.139-3956C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030871 | ||||||
| chr7:33030885
|
G | A | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-3970C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030885 | ||||||
| chr7:33030925
|
C | T | 101 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0161others(98): Show | 103 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.139-4010G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030925 | ||||||
| chr7:33030971
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-4056G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030971 | ||||||
| chr7:33030993
|
G | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.139-4078C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33030993 | ||||||
| chr7:33031051
|
G | A | 1 | a0001c0002t0008g0034 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.139-4136C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031051 | ||||||
| chr7:33031107
|
C | CA | 243 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(240): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.139-4193dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031107 | ||||||
| chr7:33031107
|
CA | C | 32 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(29): Show | 33 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-4193delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031107 | ||||||
| chr7:33031184
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(1): Show | 4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-4269A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031184 | ||||||
| chr7:33031433
|
C | A | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.139-4518G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031433 | ||||||
| chr7:33031561
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-4646A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031561 | ||||||
| chr7:33031578
|
C | A | 1 | a0001c0002t0002g0059 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.139-4663G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031578 | ||||||
| chr7:33031593
|
A | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.139-4678T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031593 | ||||||
| chr7:33031605
|
T | A | 1 | a0001c0001t0001g0332 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.139-4690A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031605 | ||||||
| chr7:33031654
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(108): Show | 114 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-4739A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031654 | ||||||
| chr7:33031722
|
T | C | 1 | a0001c0002t0002g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.139-4807A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031722 | ||||||
| chr7:33031847
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-4932C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031847 | ||||||
| chr7:33031926
|
A | G | 1 | a0001c0001t0001g0377 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.139-5011T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031926 | ||||||
| chr7:33031945
|
T | C | 1 | a0001c0001t0001g0377 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.139-5030A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33031945 | ||||||
| chr7:33032002
|
G | GT | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-5088dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032002 | ||||||
| chr7:33032224
|
G | T | 1 | a0001c0002t0003g0141 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.139-5309C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032224 | ||||||
| chr7:33032280
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-5365C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032280 | ||||||
| chr7:33032297
|
C | G | 1 | a0001c0001t0001g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.139-5382G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032297 | ||||||
| chr7:33032423
|
C | CA | 8 | a0001c0002t0002g0074a0001c0002t0002g0088a0001c0002t0003g0132others(5): Show | 8 | HG02886.hp1 HG02897.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-5509dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | ||||||
| chr7:33032423
|
C | CAA | 189 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.139-5510_139-5509d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | ||||||
| chr7:33032423
|
C | CAAA | 33 | a0001c0001t0001g0022a0001c0001t0001g0161a0001c0001t0001g0166others(30): Show | 33 | HG00140.hp2 HG00423.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-5511_139-5509d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | ||||||
| chr7:33032423
|
C | CAAAAAA | 26 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0025others(23): Show | 27 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-5514_139-5509d others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | ||||||
| chr7:33032423
|
C | CAAAAAAA | 7 | a0001c0002t0001g0019a0001c0002t0001g0031a0001c0002t0001g0033others(4): Show | 7 | HG03516.hp2 NA18943.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-5515_139-5509d others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | ||||||
| chr7:33032423
|
CAAAA | C | 7 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-5512_139-5509d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032423 | ||||||
| chr7:33032518
|
G | A | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0308 | 3 | HG02258.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.139-5603C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032518 | ||||||
| chr7:33032524
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.139-5609A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032524 | ||||||
| chr7:33032564
|
C | T | 5 | a0001c0002t0001g0031a0001c0002t0001g0038a0001c0002t0001g0043others(2): Show | 5 | HG02293.hp1 NA18939.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-5649G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032564 | ||||||
| chr7:33032596
|
C | G | 132 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(129): Show | 135 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.139-5681G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032596 | ||||||
| chr7:33032897
|
C | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-5982G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032897 | ||||||
| chr7:33032920
|
T | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-6005A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33032920 | ||||||
| chr7:33033100
|
T | A | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-6185A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033100 | ||||||
| chr7:33033264
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.139-6349G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033264 | ||||||
| chr7:33033355
|
T | C | 2 | a0001c0002t0003g0159a0001c0002t0003g0160 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.139-6440A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033355 | ||||||
| chr7:33033387
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-6472A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033387 | ||||||
| chr7:33033483
|
G | A | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-6568C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033483 | ||||||
| chr7:33033498
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-6583A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033498 | ||||||
| chr7:33033717
|
A | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-6802T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033717 | ||||||
| chr7:33033763
|
T | C | 4 | a0001c0003t0001g0014a0001c0003t0001g0336a0001c0003t0001g0338others(1): Show | 5 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-6848A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033763 | ||||||
| chr7:33033788
|
T | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0183others(31): Show | 35 | HG00609.hp2 HG00738.hp2 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.139-6873A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033788 | ||||||
| chr7:33033877
|
C | CAT | 10 | a0001c0002t0002g0054a0001c0002t0002g0056a0001c0002t0002g0064others(7): Show | 10 | HG02074.hp1 HG02523.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-6964_139-6963d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | ||||||
| chr7:33033877
|
C | CATATATA others(5): Show |
5 | a0001c0001t0001g0262a0001c0001t0001g0288a0001c0001t0001g0289others(2): Show | 5 | HG01952.hp2 HG02273.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-6974_139-6963d others(14): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | ||||||
| chr7:33033877
|
C | CATATATA others(7): Show |
7 | a0001c0001t0001g0182a0001c0001t0001g0324a0001c0001t0001g0325others(4): Show | 7 | HG00733.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-6976_139-6963d others(16): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | ||||||
| chr7:33033877
|
C | CATATATA others(9): Show |
2 | a0001c0001t0001g0287a0001c0001t0001g0302 | 2 | HG03834.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.139-6978_139-6963d others(18): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033877 | ||||||
| chr7:33033894
|
A | ATAT | 176 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(173): Show | 180 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.139-6980_139-6979i others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033894 | ||||||
| chr7:33033894
|
A | ATATAT | 26 | a0001c0001t0001g0222a0001c0001t0001g0257a0001c0001t0001g0265others(23): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-6980_139-6979i others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033894 | ||||||
| chr7:33033894
|
A | ATATATAT | 7 | a0001c0001t0001g0339a0001c0001t0001g0351a0001c0001t0001g0352others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-6980_139-6979i others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033894 | ||||||
| chr7:33033895
|
A | AT | 31 | a0001c0002t0001g0003a0001c0002t0001g0019a0001c0002t0001g0025others(28): Show | 32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.139-6981dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033895 | ||||||
| chr7:33033895
|
A | T | 4 | a0001c0001t0001g0169a0001c0001t0001g0230a0001c0001t0001g0355others(1): Show | 4 | HG01943.hp1 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-6980T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033895 | ||||||
| chr7:33033896
|
T | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.139-6981A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033896 | ||||||
| chr7:33033922
|
C | T | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-7007G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033922 | ||||||
| chr7:33033926
|
T | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.139-7011A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33033926 | ||||||
| chr7:33034015
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.139-7100G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034015 | ||||||
| chr7:33034039
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.139-7124G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034039 | ||||||
| chr7:33034081
|
C | T | 3 | a0001c0001t0001g0299a0001c0001t0001g0313a0001c0001t0001g0316 | 3 | NA18999.hp1 NA19079.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.139-7166G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034081 | ||||||
| chr7:33034318
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0342 | 2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.139-7403G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034318 | ||||||
| chr7:33034394
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0237 | 2 | HG00735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.139-7479A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034394 | ||||||
| chr7:33034629
|
C | T | 18 | a0001c0001t0001g0182a0001c0001t0001g0262a0001c0001t0001g0287others(15): Show | 19 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(16): Show |
intron_variant | MODIFIER | c.139-7714G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034629 | ||||||
| chr7:33034642
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139-7727C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034642 | ||||||
| chr7:33034720
|
A | T | 1 | a0001c0002t0006g0382 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.139-7805T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034720 | ||||||
| chr7:33034744
|
C | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.139-7829G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034744 | ||||||
| chr7:33034768
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(2): Show | 5 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-7853G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034768 | ||||||
| chr7:33034792
|
TAGAG | T | 7 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-7881_139-7878d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034792 | ||||||
| chr7:33034863
|
A | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(1): Show | 4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-7948T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33034863 | ||||||
| chr7:33035028
|
T | TA | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-8114dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035028 | ||||||
| chr7:33035079
|
G | T | 278 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(275): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.139-8164C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035079 | ||||||
| chr7:33035164
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.139-8249C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035164 | ||||||
| chr7:33035173
|
A | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(107): Show | 113 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.139-8258T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035173 | ||||||
| chr7:33035189
|
G | GT | 228 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0017others(225): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.139-8275dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035189 | ||||||
| chr7:33035189
|
G | GTT | 48 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0021others(45): Show | 50 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-8276_139-8275d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035189 | ||||||
| chr7:33035189
|
GT | G | 16 | a0001c0002t0002g0070a0001c0002t0003g0009a0001c0002t0003g0010others(13): Show | 18 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.139-8275delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035189 | ||||||
| chr7:33035199
|
T | TG | 6 | a0001c0002t0003g0124a0001c0002t0003g0126a0001c0002t0003g0138others(3): Show | 6 | HG00673.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-8285_139-8284i others(3): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035199 | ||||||
| chr7:33035216
|
C | T | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.139-8301G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035216 | ||||||
| chr7:33035354
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-8439G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035354 | ||||||
| chr7:33035387
|
G | A | 1 | a0001c0001t0001g0362 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.139-8472C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035387 | ||||||
| chr7:33035443
|
T | G | 1 | a0001c0002t0003g0133 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.139-8528A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035443 | ||||||
| chr7:33035497
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-8582G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035497 | ||||||
| chr7:33035565
|
T | C | 1 | a0001c0001t0001g0356 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.139-8650A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035565 | ||||||
| chr7:33035636
|
A | G | 63 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0174others(60): Show | 64 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.139-8721T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035636 | ||||||
| chr7:33035728
|
C | T | 1 | a0001c0002t0002g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.139-8813G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035728 | ||||||
| chr7:33035795
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-8880A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035795 | ||||||
| chr7:33035961
|
A | G | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-9046T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33035961 | ||||||
| chr7:33036065
|
C | T | 4 | a0001c0001t0001g0293a0001c0001t0001g0312a0001c0001t0001g0323others(1): Show | 4 | NA18971.hp1 NA18987.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-9150G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036065 | ||||||
| chr7:33036066
|
C | G | 4 | a0001c0001t0001g0293a0001c0001t0001g0312a0001c0001t0001g0323others(1): Show | 4 | NA18971.hp1 NA18987.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-9151G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036066 | ||||||
| chr7:33036081
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-9166A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036081 | ||||||
| chr7:33036167
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.139-9252A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036167 | ||||||
| chr7:33036183
|
C | T | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-9268G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036183 | ||||||
| chr7:33036253
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.139-9338C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036253 | ||||||
| chr7:33036265
|
G | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0381 | 3 | HG00738.hp2 HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.139-9350C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036265 | ||||||
| chr7:33036300
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.139-9385A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036300 | ||||||
| chr7:33036448
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0238 | 2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.139-9533G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036448 | ||||||
| chr7:33036458
|
C | G | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.139-9543G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036458 | ||||||
| chr7:33036458
|
CT | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-9544delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036458 | ||||||
| chr7:33036467
|
T | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-9552A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036467 | ||||||
| chr7:33036571
|
T | C | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-9656A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036571 | ||||||
| chr7:33036604
|
C | T | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-9689G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036604 | ||||||
| chr7:33036676
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0301a0001c0001t0001g0322 | 3 | HG01070.hp2 HG02300.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.139-9761A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036676 | ||||||
| chr7:33036702
|
G | A | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-9787C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036702 | ||||||
| chr7:33036873
|
A | G | 277 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(274): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.139-9958T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036873 | ||||||
| chr7:33036979
|
T | G | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-10064A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33036979 | ||||||
| chr7:33037045
|
C | T | 63 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0174others(60): Show | 64 | HG00099.hp2 HG00544.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.139-10130G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037045 | ||||||
| chr7:33037105
|
C | T | 14 | a0001c0001t0001g0182a0001c0001t0001g0262a0001c0001t0001g0287others(11): Show | 14 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-10190G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037105 | ||||||
| chr7:33037144
|
G | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-10229C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037144 | ||||||
| chr7:33037374
|
TA | T | 101 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0161others(98): Show | 103 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.139-10460delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037374 | ||||||
| chr7:33037452
|
G | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-10537C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037452 | ||||||
| chr7:33037462
|
A | G | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.139-10547T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037462 | ||||||
| chr7:33037586
|
T | C | 1 | a0001c0002t0003g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-10671A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037586 | ||||||
| chr7:33037693
|
G | A | 1 | a0001c0002t0001g0037 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.139-10778C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037693 | ||||||
| chr7:33037925
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-11010A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037925 | ||||||
| chr7:33037942
|
T | C | 16 | a0001c0002t0003g0009a0001c0002t0003g0010a0001c0002t0003g0053others(13): Show | 18 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.139-11027A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037942 | ||||||
| chr7:33037993
|
CA | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-11079delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33037993 | ||||||
| chr7:33038001
|
A | G | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-11086T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038001 | ||||||
| chr7:33038004
|
T | C | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-11089A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038004 | ||||||
| chr7:33038030
|
T | C | 2 | a0001c0002t0003g0125a0001c0002t0003g0136 | 2 | NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.139-11115A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038030 | ||||||
| chr7:33038164
|
G | C | 34 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0183others(31): Show | 35 | HG00609.hp2 HG00738.hp2 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.139-11249C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038164 | ||||||
| chr7:33038203
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-11288G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038203 | ||||||
| chr7:33038212
|
C | T | 5 | a0001c0002t0003g0156a0001c0002t0003g0157a0001c0002t0003g0158others(2): Show | 5 | HG01361.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-11297G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038212 | ||||||
| chr7:33038456
|
A | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0360 | 2 | NA19056.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.139-11541T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038456 | ||||||
| chr7:33038477
|
T | C | 4 | a0001c0002t0003g0153a0001c0002t0003g0155a0001c0002t0003g0375others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-11562A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038477 | ||||||
| chr7:33038498
|
CT | C | 34 | a0001c0001t0001g0230a0001c0002t0001g0003a0001c0002t0001g0018others(31): Show | 35 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.139-11584delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038498 | ||||||
| chr7:33038961
|
C | A | 2 | a0001c0001t0001g0184a0002c0006t0001g0203 | 2 | NA18987.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.139-12046G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33038961 | ||||||
| chr7:33039049
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(227): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.139-12134A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039049 | ||||||
| chr7:33039086
|
T | G | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.139-12171A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039086 | ||||||
| chr7:33039097
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.139-12182T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039097 | ||||||
| chr7:33039248
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.139-12333G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039248 | ||||||
| chr7:33039351
|
G | A | 19 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0308others(16): Show | 20 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-12436C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039351 | ||||||
| chr7:33039402
|
G | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-12487C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039402 | ||||||
| chr7:33039555
|
G | GT | 8 | a0001c0002t0002g0073a0001c0002t0002g0077a0001c0002t0002g0089others(5): Show | 8 | HG02132.hp2 HG02293.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-12641dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTT | 4 | a0001c0001t0001g0266a0001c0002t0002g0097a0001c0002t0003g0010others(1): Show | 5 | HG02055.hp2 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-12642_139-1264 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTT | 6 | a0001c0002t0001g0025a0001c0002t0001g0027a0001c0002t0001g0036others(3): Show | 6 | HG00438.hp2 NA18951.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-12644_139-1264 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTT | 22 | a0001c0001t0001g0347a0001c0001t0001g0358a0001c0002t0001g0003others(19): Show | 23 | HG00423.hp1 HG00673.hp2 HG02293.hp1 others(20): Show |
intron_variant | MODIFIER | c.139-12645_139-1264 others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTTT | 20 | a0001c0001t0001g0167a0001c0001t0001g0169a0001c0001t0001g0225others(17): Show | 20 | HG01169.hp1 HG01943.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-12646_139-1264 others(10): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTTTT | 140 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(137): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.139-12641_139-1264 others(11): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTTTT others(1): Show |
52 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(49): Show | 53 | HG00099.hp1 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.139-12641_139-1264 others(12): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTTTT others(2): Show |
8 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0218others(5): Show | 8 | HG01123.hp1 HG01258.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-12641_139-1264 others(13): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0259 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139-12641_139-1264 others(16): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039555
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0001g0255 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.139-12641_139-1264 others(17): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039555 | ||||||
| chr7:33039561
|
TG | T | 15 | a0001c0002t0002g0096a0001c0002t0002g0115a0001c0002t0003g0053others(12): Show | 16 | HG01255.hp1 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-12647delC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039561 | ||||||
| chr7:33039562
|
G | T | 365 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(362): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.139-12647C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039562 | ||||||
| chr7:33039593
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0303a0001c0001t0001g0324 | 3 | HG02451.hp1 HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.139-12678C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039593 | ||||||
| chr7:33039613
|
A | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG03540.hp1 NA19240.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-12698T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039613 | ||||||
| chr7:33039702
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-12787C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039702 | ||||||
| chr7:33039737
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.139-12822T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039737 | ||||||
| chr7:33039869
|
C | A | 2 | a0001c0002t0004g0004a0001c0002t0004g0068 | 3 | HG02622.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.139-12954G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33039869 | ||||||
| chr7:33040023
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-13108A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040023 | ||||||
| chr7:33040077
|
T | C | 5 | a0001c0002t0005g0110a0001c0002t0005g0111a0001c0002t0005g0112others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-13162A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040077 | ||||||
| chr7:33040126
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-13211G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040126 | ||||||
| chr7:33040140
|
C | T | 1 | a0001c0001t0001g0377 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.139-13225G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040140 | ||||||
| chr7:33040236
|
A | C | 262 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(259): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.139-13321T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040236 | ||||||
| chr7:33040544
|
C | G | 1 | a0001c0002t0002g0060 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.139-13629G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040544 | ||||||
| chr7:33040626
|
G | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-13711C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040626 | ||||||
| chr7:33040860
|
G | A | 1 | a0001c0002t0003g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-13945C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040860 | ||||||
| chr7:33040888
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0195 | 2 | HG00609.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.139-13973G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33040888 | ||||||
| chr7:33041003
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.139-14088G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041003 | ||||||
| chr7:33041047
|
C | T | 7 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-14132G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041047 | ||||||
| chr7:33041406
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-14491A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041406 | ||||||
| chr7:33041623
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.139-14708G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041623 | ||||||
| chr7:33041642
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0234a0001c0001t0001g0262others(1): Show | 5 | HG02630.hp2 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-14727A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041642 | ||||||
| chr7:33041668
|
C | A | 1 | a0001c0001t0001g0333 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.139-14753G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041668 | ||||||
| chr7:33041682
|
G | T | 383 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(380): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.139-14767C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041682 | ||||||
| chr7:33041702
|
T | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-14787A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041702 | ||||||
| chr7:33041745
|
T | A | 1 | a0001c0002t0002g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.139-14830A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041745 | ||||||
| chr7:33041768
|
G | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-14853C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041768 | ||||||
| chr7:33041876
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-14961T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041876 | ||||||
| chr7:33041902
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0020others(90): Show | 95 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.139-14987T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041902 | ||||||
| chr7:33041921
|
C | G | 32 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(29): Show | 33 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-15006G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33041921 | ||||||
| chr7:33042006
|
T | C | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-15091A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042006 | ||||||
| chr7:33042145
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.139-15230A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042145 | ||||||
| chr7:33042174
|
C | T | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-15259G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042174 | ||||||
| chr7:33042267
|
T | C | 14 | a0001c0001t0001g0182a0001c0001t0001g0262a0001c0001t0001g0287others(11): Show | 14 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-15352A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042267 | ||||||
| chr7:33042328
|
C | CA | 7 | a0001c0002t0002g0056a0001c0002t0004g0004a0001c0002t0004g0052others(4): Show | 8 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-15414dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042328 | ||||||
| chr7:33042356
|
A | C | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-15441T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042356 | ||||||
| chr7:33042410
|
T | C | 49 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(46): Show | 52 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.139-15495A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042410 | ||||||
| chr7:33042763
|
A | G | 32 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.139-15848T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042763 | ||||||
| chr7:33042776
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0234a0001c0001t0001g0374 | 4 | HG02630.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-15861T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042776 | ||||||
| chr7:33042836
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-15921T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042836 | ||||||
| chr7:33042877
|
C | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.139-15962G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042877 | ||||||
| chr7:33042906
|
T | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-15991A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33042906 | ||||||
| chr7:33043013
|
C | G | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-16098G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043013 | ||||||
| chr7:33043048
|
A | G | 1 | a0001c0001t0001g0327 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.139-16133T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043048 | ||||||
| chr7:33043119
|
C | T | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.139-16204G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043119 | ||||||
| chr7:33043438
|
A | G | 1 | a0001c0002t0003g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-16523T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043438 | ||||||
| chr7:33043495
|
T | C | 132 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(129): Show | 135 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.139-16580A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043495 | ||||||
| chr7:33043566
|
A | C | 6 | a0001c0002t0003g0124a0001c0002t0003g0126a0001c0002t0003g0138others(3): Show | 6 | HG00673.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-16651T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043566 | ||||||
| chr7:33043608
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139-16693T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043608 | ||||||
| chr7:33043612
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.139-16697C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043612 | ||||||
| chr7:33043693
|
G | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(1): Show | 4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-16778C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043693 | ||||||
| chr7:33043702
|
G | C | 1 | a0001c0001t0001g0357 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-16787C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043702 | ||||||
| chr7:33043989
|
A | G | 1 | a0001c0002t0002g0057 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.139-17074T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33043989 | ||||||
| chr7:33044063
|
G | A | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-17148C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044063 | ||||||
| chr7:33044088
|
G | A | 1 | a0001c0002t0003g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.139-17173C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044088 | ||||||
| chr7:33044111
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.139-17196G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044111 | ||||||
| chr7:33044146
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-17231C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044146 | ||||||
| chr7:33044292
|
T | C | 19 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0308others(16): Show | 20 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-17377A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044292 | ||||||
| chr7:33044360
|
G | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.139-17445C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044360 | ||||||
| chr7:33044393
|
A | AT | 261 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.139-17479dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044393 | ||||||
| chr7:33044413
|
G | GA | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-17499dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044413 | ||||||
| chr7:33044481
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.139-17566T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044481 | ||||||
| chr7:33044552
|
C | T | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-17637G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044552 | ||||||
| chr7:33044625
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-17710C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044625 | ||||||
| chr7:33044854
|
A | G | 137 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(134): Show | 140 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.138+17714T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044854 | ||||||
| chr7:33044874
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.138+17694T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044874 | ||||||
| chr7:33044915
|
T | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.138+17653A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33044915 | ||||||
| chr7:33045059
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0206 | 2 | NA18991.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.138+17509G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045059 | ||||||
| chr7:33045150
|
A | G | 5 | a0001c0002t0005g0110a0001c0002t0005g0111a0001c0002t0005g0112others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+17418T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045150 | ||||||
| chr7:33045173
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0324 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138+17395A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045173 | ||||||
| chr7:33045380
|
C | T | 260 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(257): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.138+17188G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045380 | ||||||
| chr7:33045462
|
A | AT | 15 | a0001c0001t0001g0299a0001c0002t0002g0059a0001c0002t0003g0009others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+17105dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045462 | ||||||
| chr7:33045463
|
T | A | 1 | a0001c0003t0001g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.138+17105A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045463 | ||||||
| chr7:33045585
|
G | A | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+16983C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045585 | ||||||
| chr7:33045588
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.138+16980A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045588 | ||||||
| chr7:33045634
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.138+16934T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045634 | ||||||
| chr7:33045649
|
G | A | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+16919C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045649 | ||||||
| chr7:33045726
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0001g0320 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.138+16842C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045726 | ||||||
| chr7:33045752
|
C | T | 1 | a0001c0001t0001g0346 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.138+16816G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045752 | ||||||
| chr7:33045760
|
AT | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0020others(91): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.138+16807delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045760 | ||||||
| chr7:33045779
|
A | T | 11 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0308others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+16789T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045779 | ||||||
| chr7:33045780
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.138+16788A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045780 | ||||||
| chr7:33045907
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.138+16661C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33045907 | ||||||
| chr7:33046084
|
G | A | 1 | a0001c0002t0003g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138+16484C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046084 | ||||||
| chr7:33046227
|
T | C | 1 | a0001c0002t0002g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138+16341A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046227 | ||||||
| chr7:33046307
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | NA18948.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.138+16261A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046307 | ||||||
| chr7:33046315
|
T | C | 14 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(11): Show | 15 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+16253A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046315 | ||||||
| chr7:33046531
|
CA | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(316): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.138+16036delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046531 | ||||||
| chr7:33046770
|
C | T | 1 | a0001c0002t0004g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+15798G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046770 | ||||||
| chr7:33046779
|
G | A | 40 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.138+15789C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046779 | ||||||
| chr7:33046805
|
CT | C | 22 | a0001c0001t0001g0182a0001c0001t0001g0245a0001c0001t0001g0262others(19): Show | 22 | HG00733.hp1 HG01169.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.138+15762delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046805 | ||||||
| chr7:33046838
|
C | A | 3 | a0001c0002t0003g0125a0001c0002t0003g0135a0001c0002t0003g0136 | 3 | NA18939.hp1 NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.138+15730G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046838 | ||||||
| chr7:33046897
|
G | A | 4 | a0001c0002t0002g0082a0001c0002t0002g0085a0001c0002t0002g0097others(1): Show | 4 | HG02083.hp2 NA18953.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+15671C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046897 | ||||||
| chr7:33046935
|
T | C | 200 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(197): Show | 206 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.138+15633A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046935 | ||||||
| chr7:33046936
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+15632C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046936 | ||||||
| chr7:33046970
|
C | CT | 250 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.138+15597dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046970 | ||||||
| chr7:33046993
|
C | CG | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.138+15574dupC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33046993 | ||||||
| chr7:33047025
|
T | C | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+15543A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047025 | ||||||
| chr7:33047067
|
G | A | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+15501C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047067 | ||||||
| chr7:33047336
|
C | T | 1 | a0001c0002t0002g0088 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.138+15232G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047336 | ||||||
| chr7:33047538
|
C | A | 31 | a0001c0002t0001g0003a0001c0002t0001g0025a0001c0002t0001g0026others(28): Show | 32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+15030G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047538 | ||||||
| chr7:33047567
|
T | C | 14 | a0001c0002t0002g0099a0001c0002t0003g0009a0001c0002t0003g0151others(11): Show | 15 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+15001A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047567 | ||||||
| chr7:33047569
|
G | A | 15 | a0001c0002t0002g0099a0001c0002t0003g0009a0001c0002t0003g0151others(12): Show | 16 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+14999C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047569 | ||||||
| chr7:33047573
|
T | C | 4 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0281others(1): Show | 4 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+14995A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047573 | ||||||
| chr7:33047575
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.138+14993T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047575 | ||||||
| chr7:33047692
|
G | A | 2 | a0001c0002t0003g0137a0001c0002t0003g0145 | 2 | HG02056.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.138+14876C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047692 | ||||||
| chr7:33047777
|
C | T | 1 | a0001c0001t0014g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.138+14791G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047777 | ||||||
| chr7:33047799
|
G | T | 17 | a0001c0001t0001g0286a0001c0001t0001g0293a0001c0001t0001g0304others(14): Show | 17 | HG00621.hp1 HG02074.hp2 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+14769C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047799 | ||||||
| chr7:33047996
|
ATG | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0182others(113): Show | 119 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.138+14570_138+1457 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047996 | ||||||
| chr7:33047996
|
ATGTG | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0020others(76): Show | 81 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.138+14568_138+1457 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33047996 | ||||||
| chr7:33048037
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+14531T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048037 | ||||||
| chr7:33048046
|
A | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.138+14522T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048046 | ||||||
| chr7:33048176
|
T | TTG | 10 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0105others(7): Show | 12 | HG00639.hp2 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+14390_138+1439 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048176 | ||||||
| chr7:33048176
|
TTG | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.138+14390_138+1439 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048176 | ||||||
| chr7:33048176
|
TTGTG | T | 33 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0019others(30): Show | 34 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+14388_138+1439 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048176 | ||||||
| chr7:33048196
|
GT | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0299a0001c0001t0001g0306 | 3 | NA19000.hp1 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.138+14371delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048196 | ||||||
| chr7:33048199
|
G | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0299a0001c0001t0001g0306 | 3 | NA19000.hp1 NA19080.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.138+14369C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048199 | ||||||
| chr7:33048205
|
T | A | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+14363A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048205 | ||||||
| chr7:33048341
|
G | A | 3 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120 | 3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+14227C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048341 | ||||||
| chr7:33048625
|
A | C | 1 | a0001c0002t0002g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138+13943T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048625 | ||||||
| chr7:33048805
|
C | G | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+13763G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33048805 | ||||||
| chr7:33049017
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.138+13551A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049017 | ||||||
| chr7:33049031
|
C | T | 11 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0308others(8): Show | 11 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+13537G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049031 | ||||||
| chr7:33049180
|
ATTCT | A | 8 | a0001c0003t0001g0014a0001c0003t0001g0284a0001c0003t0001g0290others(5): Show | 9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+13384_138+1338 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049180 | ||||||
| chr7:33049268
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.138+13300G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049268 | ||||||
| chr7:33049314
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+13254C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049314 | ||||||
| chr7:33049327
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.138+13241A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049327 | ||||||
| chr7:33049518
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0169 | 2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+13050G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049518 | ||||||
| chr7:33049576
|
A | G | 8 | a0001c0003t0001g0014a0001c0003t0001g0284a0001c0003t0001g0290others(5): Show | 9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+12992T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049576 | ||||||
| chr7:33049661
|
A | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.138+12907T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049661 | ||||||
| chr7:33049693
|
G | T | 9 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(6): Show | 9 | HG00140.hp2 HG00639.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+12875C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049693 | ||||||
| chr7:33049735
|
C | T | 2 | a0001c0001t0001g0253a0001c0002t0004g0069 | 2 | HG03209.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.138+12833G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049735 | ||||||
| chr7:33049736
|
G | A | 1 | a0001c0002t0002g0106 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.138+12832C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049736 | ||||||
| chr7:33049774
|
C | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+12794G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049774 | ||||||
| chr7:33049830
|
C | T | 8 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+12738G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049830 | ||||||
| chr7:33049894
|
C | T | 2 | a0001c0002t0002g0074a0001c0002t0010g0086 | 2 | HG02523.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.138+12674G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049894 | ||||||
| chr7:33049966
|
T | C | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+12602A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049966 | ||||||
| chr7:33049969
|
C | CA | 72 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(69): Show | 75 | HG00280.hp2 HG00673.hp1 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.138+12598dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | ||||||
| chr7:33049969
|
C | CAA | 28 | a0001c0001t0001g0267a0001c0002t0001g0003a0001c0002t0001g0026others(25): Show | 29 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.138+12597_138+1259 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | ||||||
| chr7:33049969
|
C | CAAA | 8 | a0001c0001t0001g0268a0001c0002t0001g0018a0001c0002t0001g0042others(5): Show | 8 | HG02647.hp1 HG02886.hp1 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+12596_138+1259 others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | ||||||
| chr7:33049969
|
CA | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0182a0001c0001t0001g0212others(28): Show | 33 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.138+12598delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049969 | ||||||
| chr7:33049992
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.138+12576T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33049992 | ||||||
| chr7:33050151
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.138+12417G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050151 | ||||||
| chr7:33050169
|
A | G | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+12399T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050169 | ||||||
| chr7:33050186
|
T | G | 1 | a0001c0002t0003g0146 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.138+12382A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050186 | ||||||
| chr7:33050188
|
G | C | 6 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0067others(3): Show | 7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+12380C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050188 | ||||||
| chr7:33050205
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.138+12363C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050205 | ||||||
| chr7:33050748
|
A | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0381 | 3 | HG00738.hp2 HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.138+11820T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050748 | ||||||
| chr7:33050794
|
ACTTG | A | 6 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(3): Show | 6 | NA18953.hp1 NA18970.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+11770_138+1177 others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050794 | ||||||
| chr7:33050798
|
G | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.138+11770C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050798 | ||||||
| chr7:33050854
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+11714G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050854 | ||||||
| chr7:33050866
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+11702T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050866 | ||||||
| chr7:33050869
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+11699T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050869 | ||||||
| chr7:33050921
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.138+11647G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33050921 | ||||||
| chr7:33051166
|
T | C | 2 | a0001c0001t0001g0334a0001c0001t0001g0345 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.138+11402A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051166 | ||||||
| chr7:33051205
|
C | T | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+11363G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051205 | ||||||
| chr7:33051384
|
G | A | 6 | a0001c0002t0003g0151a0001c0002t0003g0156a0001c0002t0003g0157others(3): Show | 6 | HG01361.hp1 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+11184C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051384 | ||||||
| chr7:33051409
|
G | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.138+11159C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051409 | ||||||
| chr7:33051683
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+10885C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051683 | ||||||
| chr7:33051737
|
C | T | 280 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(277): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.138+10831G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051737 | ||||||
| chr7:33051952
|
G | A | 3 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120 | 3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+10616C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33051952 | ||||||
| chr7:33052058
|
TTTTTG | T | 15 | a0001c0001t0001g0324a0001c0002t0003g0009a0001c0002t0003g0010others(12): Show | 17 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.138+10505_138+1050 others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052058 | ||||||
| chr7:33052130
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+10438C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052130 | ||||||
| chr7:33052135
|
C | T | 1 | a0001c0002t0002g0087 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.138+10433G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052135 | ||||||
| chr7:33052236
|
C | T | 1 | a0001c0002t0003g0124 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.138+10332G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052236 | ||||||
| chr7:33052247
|
GC | G | 15 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(12): Show | 16 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.138+10320delG | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052247 | ||||||
| chr7:33052343
|
C | T | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+10225G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052343 | ||||||
| chr7:33052387
|
GCAC | G | 258 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.138+10178_138+1018 others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052387 | ||||||
| chr7:33052394
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+10174C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052394 | ||||||
| chr7:33052417
|
C | T | 1 | a0001c0002t0003g0140 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.138+10151G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052417 | ||||||
| chr7:33052479
|
C | T | 1 | a0001c0002t0002g0073 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.138+10089G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052479 | ||||||
| chr7:33052480
|
G | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.138+10088C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052480 | ||||||
| chr7:33052485
|
C | CA | 8 | a0001c0002t0002g0058a0001c0002t0002g0059a0001c0002t0002g0098others(5): Show | 8 | HG00544.hp1 HG00673.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+10082dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | ||||||
| chr7:33052485
|
C | CAA | 13 | a0001c0002t0003g0009a0001c0002t0003g0053a0001c0002t0003g0151others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.138+10081_138+1008 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | ||||||
| chr7:33052485
|
CA | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 9 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+10082delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | ||||||
| chr7:33052485
|
CAA | C | 10 | a0001c0001t0001g0177a0001c0001t0001g0202a0001c0001t0001g0206others(7): Show | 10 | HG00741.hp2 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+10081_138+1008 others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | ||||||
| chr7:33052485
|
CAAA | C | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(240): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.138+10080_138+1008 others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052485 | ||||||
| chr7:33052737
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+9831T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052737 | ||||||
| chr7:33052876
|
G | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+9692C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052876 | ||||||
| chr7:33052943
|
T | C | 1 | a0001c0002t0002g0107 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138+9625A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33052943 | ||||||
| chr7:33053025
|
C | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.138+9543G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053025 | ||||||
| chr7:33053064
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0169 | 2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+9504C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053064 | ||||||
| chr7:33053101
|
G | T | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+9467C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053101 | ||||||
| chr7:33053203
|
T | C | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+9365A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053203 | ||||||
| chr7:33053227
|
C | A | 1 | a0002c0006t0001g0203 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.138+9341G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053227 | ||||||
| chr7:33053254
|
T | C | 280 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(277): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.138+9314A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053254 | ||||||
| chr7:33053344
|
C | T | 1 | a0001c0002t0003g0152 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.138+9224G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053344 | ||||||
| chr7:33053346
|
C | T | 9 | a0001c0001t0001g0168a0001c0001t0001g0214a0001c0001t0001g0215others(6): Show | 9 | NA18960.hp1 NA18975.hp2 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+9222G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053346 | ||||||
| chr7:33053562
|
G | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0276 | 2 | HG02145.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.138+9006C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053562 | ||||||
| chr7:33053563
|
A | AG | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+9004dupC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053563 | ||||||
| chr7:33053647
|
T | C | 3 | a0001c0002t0001g0027a0001c0002t0001g0029a0001c0002t0001g0035 | 3 | HG00423.hp1 NA18941.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.138+8921A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053647 | ||||||
| chr7:33053683
|
T | TGAAA | 34 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0178others(31): Show | 35 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.138+8881_138+8884d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053683 | ||||||
| chr7:33053777
|
T | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+8791A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33053777 | ||||||
| chr7:33054011
|
G | T | 31 | a0001c0002t0001g0003a0001c0002t0001g0025a0001c0002t0001g0026others(28): Show | 32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+8557C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054011 | ||||||
| chr7:33054063
|
T | TAA | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+8504_138+8505i others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054063 | ||||||
| chr7:33054064
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+8504C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054064 | ||||||
| chr7:33054074
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+8494C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054074 | ||||||
| chr7:33054090
|
A | T | 383 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(380): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.138+8478T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054090 | ||||||
| chr7:33054094
|
G | A | 383 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(380): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.138+8474C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054094 | ||||||
| chr7:33054095
|
T | C | 383 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(380): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.138+8473A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054095 | ||||||
| chr7:33054098
|
G | A | 383 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(380): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.138+8470C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054098 | ||||||
| chr7:33054128
|
G | C | 2 | a0001c0002t0001g0018a0001c0002t0001g0019 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.138+8440C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054128 | ||||||
| chr7:33054241
|
C | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+8327G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054241 | ||||||
| chr7:33054286
|
C | T | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+8282G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054286 | ||||||
| chr7:33054353
|
CA | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(250): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.138+8214delT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054353 | ||||||
| chr7:33054525
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.138+8043C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054525 | ||||||
| chr7:33054650
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.138+7918A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054650 | ||||||
| chr7:33054663
|
C | T | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+7905G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054663 | ||||||
| chr7:33054675
|
G | T | 1 | a0001c0002t0003g0139 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.138+7893C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054675 | ||||||
| chr7:33054948
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+7620T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33054948 | ||||||
| chr7:33055011
|
A | G | 1 | a0001c0002t0005g0114 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.138+7557T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055011 | ||||||
| chr7:33055047
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.138+7521C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055047 | ||||||
| chr7:33055140
|
T | C | 1 | a0001c0002t0001g0036 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.138+7428A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055140 | ||||||
| chr7:33055370
|
C | T | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.138+7198G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055370 | ||||||
| chr7:33055485
|
C | T | 5 | a0001c0002t0005g0110a0001c0002t0005g0111a0001c0002t0005g0112others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+7083G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055485 | ||||||
| chr7:33055626
|
G | C | 1 | a0001c0002t0002g0100 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.138+6942C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055626 | ||||||
| chr7:33055710
|
C | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0207 | 2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.138+6858G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055710 | ||||||
| chr7:33055804
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+6764T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055804 | ||||||
| chr7:33055809
|
C | T | 6 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0067others(3): Show | 7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+6759G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055809 | ||||||
| chr7:33055831
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0251 | 2 | HG01258.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.138+6737C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055831 | ||||||
| chr7:33055872
|
AG | A | 31 | a0001c0002t0001g0003a0001c0002t0001g0025a0001c0002t0001g0026others(28): Show | 32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+6695delC | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055872 | ||||||
| chr7:33055908
|
T | G | 13 | a0001c0001t0001g0182a0001c0001t0001g0287a0001c0001t0001g0288others(10): Show | 13 | HG00733.hp1 HG01952.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+6660A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055908 | ||||||
| chr7:33055909
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138+6659C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055909 | ||||||
| chr7:33055993
|
C | G | 8 | a0001c0003t0001g0014a0001c0003t0001g0284a0001c0003t0001g0290others(5): Show | 9 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+6575G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33055993 | ||||||
| chr7:33056045
|
G | A | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+6523C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056045 | ||||||
| chr7:33056076
|
T | C | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.138+6492A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056076 | ||||||
| chr7:33056182
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.138+6386T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056182 | ||||||
| chr7:33056206
|
A | G | 1 | a0001c0001t0001g0326 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+6362T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056206 | ||||||
| chr7:33056227
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0169 | 2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+6341G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056227 | ||||||
| chr7:33056301
|
A | G | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+6267T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056301 | ||||||
| chr7:33056354
|
T | G | 133 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0017others(130): Show | 136 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.138+6214A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056354 | ||||||
| chr7:33056377
|
C | T | 6 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0067others(3): Show | 7 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+6191G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056377 | ||||||
| chr7:33056465
|
G | A | 1 | a0001c0002t0001g0029 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.138+6103C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056465 | ||||||
| chr7:33056473
|
C | CA | 16 | a0001c0002t0002g0006a0001c0002t0002g0059a0001c0002t0002g0087others(13): Show | 17 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+6094dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
C | CAA | 12 | a0001c0001t0001g0346a0001c0002t0002g0007a0001c0002t0002g0060others(9): Show | 13 | HG00621.hp2 HG01168.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+6093_138+6094d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
C | CAAAAA | 6 | a0001c0001t0001g0262a0001c0002t0002g0062a0001c0002t0002g0063others(3): Show | 6 | HG01433.hp2 NA18952.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+6090_138+6094d others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0002g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.138+6084_138+6094d others(13): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAA | C | 25 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0001g0178others(22): Show | 25 | HG00099.hp2 HG01981.hp2 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.138+6092_138+6094d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAA | C | 51 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0162others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.138+6091_138+6094d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAA | C | 48 | a0001c0001t0001g0011a0001c0001t0001g0164a0001c0001t0001g0172others(45): Show | 49 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.138+6090_138+6094d others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAA | C | 47 | a0001c0001t0001g0012a0001c0001t0001g0167a0001c0001t0001g0170others(44): Show | 48 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.138+6089_138+6094d others(8): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA | C | 49 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0001g0214others(46): Show | 50 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+6088_138+6094d others(9): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0002t0001g0027others(9): Show | 12 | HG02293.hp1 HG02965.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+6087_138+6094d others(10): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(2): Show |
C | 13 | a0001c0002t0001g0003a0001c0002t0001g0018a0001c0002t0001g0026others(10): Show | 14 | HG00423.hp1 HG02647.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+6086_138+6094d others(11): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0024a0001c0001t0001g0163a0001c0002t0001g0019others(2): Show | 5 | HG01167.hp2 HG02145.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+6085_138+6094d others(12): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 6 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+6084_138+6094d others(13): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0211a0001c0001t0001g0282a0001c0002t0002g0070 | 3 | HG01109.hp2 HG02922.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.138+6083_138+6094d others(14): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(6): Show |
C | 10 | a0001c0001t0001g0281a0001c0002t0003g0009a0001c0002t0003g0156others(7): Show | 11 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+6082_138+6094d others(15): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(7): Show |
C | 14 | a0001c0001t0001g0210a0001c0001t0001g0277a0001c0001t0001g0278others(11): Show | 15 | HG00741.hp2 HG01071.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.138+6081_138+6094d others(16): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0002t0003g0152others(1): Show | 4 | HG01070.hp1 HG01106.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+6080_138+6094d others(17): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG00140.hp2 HG00639.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+6079_138+6094d others(18): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0358 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.138+6078_138+6094d others(19): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0357a0001c0002t0003g0123 | 2 | NA18986.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.138+6077_138+6094d others(20): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0002t0001g0028 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.138+6075_138+6094d others(22): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(16): Show |
C | 5 | a0001c0002t0004g0004a0001c0002t0004g0052a0001c0002t0004g0068others(2): Show | 6 | HG02055.hp1 HG02622.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+6072_138+6094d others(25): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(17): Show |
C | 1 | a0001c0002t0004g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.138+6071_138+6094d others(26): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0001t0001g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.138+6070_138+6094d others(27): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(19): Show |
C | 3 | a0001c0001t0001g0161a0001c0001t0001g0169a0001c0001t0001g0267 | 3 | HG02258.hp2 HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+6069_138+6094d others(28): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056473
|
CAAAAAAA others(20): Show |
C | 1 | a0001c0001t0001g0361 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.138+6068_138+6094d others(29): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056473 | ||||||
| chr7:33056634
|
T | A | 1 | a0001c0004t0012g0015 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+5934A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056634 | ||||||
| chr7:33056655
|
G | A | 325 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(322): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.138+5913C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056655 | ||||||
| chr7:33056662
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.138+5906G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056662 | ||||||
| chr7:33056830
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.138+5738T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056830 | ||||||
| chr7:33056898
|
G | A | 1 | a0001c0002t0003g0149 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+5670C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33056898 | ||||||
| chr7:33057032
|
C | T | 72 | a0001c0001t0001g0012a0001c0001t0001g0163a0001c0001t0001g0164others(69): Show | 73 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.138+5536G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057032 | ||||||
| chr7:33057065
|
G | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+5503C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057065 | ||||||
| chr7:33057081
|
G | A | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+5487C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057081 | ||||||
| chr7:33057098
|
C | G | 1 | a0001c0002t0003g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.138+5470G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057098 | ||||||
| chr7:33057172
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.138+5396T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057172 | ||||||
| chr7:33057384
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.138+5184G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057384 | ||||||
| chr7:33057586
|
T | TA | 8 | a0001c0002t0004g0118a0001c0002t0004g0119a0001c0002t0004g0120others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+4981dupT | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33057586 | ||||||
| chr7:33058098
|
T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.138+4470A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058098 | ||||||
| chr7:33058297
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+4271C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058297 | ||||||
| chr7:33058340
|
T | A | 1 | a0001c0002t0003g0010 | 2 | HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+4228A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058340 | ||||||
| chr7:33058340
|
TTTTTA | T | 103 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0162others(100): Show | 105 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.138+4223_138+4227d others(7): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058340 | ||||||
| chr7:33058440
|
G | C | 31 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(28): Show | 32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+4128C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058440 | ||||||
| chr7:33058545
|
T | C | 1 | a0001c0002t0001g0049 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.138+4023A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058545 | ||||||
| chr7:33058587
|
A | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+3981T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058587 | ||||||
| chr7:33058688
|
C | T | 2 | a0001c0002t0003g0151a0001c0004t0012g0015 | 2 | HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.138+3880G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058688 | ||||||
| chr7:33058812
|
C | A | 2 | a0001c0001t0001g0367a0001c0001t0001g0368 | 2 | HG00733.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.138+3756G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058812 | ||||||
| chr7:33058826
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+3742G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058826 | ||||||
| chr7:33058906
|
T | C | 31 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(28): Show | 32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+3662A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058906 | ||||||
| chr7:33058912
|
T | C | 33 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0183others(30): Show | 34 | HG00609.hp2 HG00738.hp2 HG02155.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+3656A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058912 | ||||||
| chr7:33058919
|
G | C | 4 | a0001c0001t0001g0180a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00423.hp2 HG00558.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+3649C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33058919 | ||||||
| chr7:33059015
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.138+3553G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059015 | ||||||
| chr7:33059151
|
G | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.138+3417C>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059151 | ||||||
| chr7:33059168
|
A | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+3400T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059168 | ||||||
| chr7:33059188
|
T | G | 7 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0353others(4): Show | 7 | HG02451.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+3380A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059188 | ||||||
| chr7:33059193
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+3375G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059193 | ||||||
| chr7:33059196
|
C | G | 30 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0183others(27): Show | 31 | HG00609.hp2 HG00738.hp2 HG02155.hp2 others(28): Show |
intron_variant | MODIFIER | c.138+3372G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059196 | ||||||
| chr7:33059320
|
T | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0169 | 2 | HG02738.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.138+3248A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059320 | ||||||
| chr7:33059338
|
T | C | 1 | a0001c0001t0001g0356 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.138+3230A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059338 | ||||||
| chr7:33059528
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+3040T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059528 | ||||||
| chr7:33059768
|
G | A | 225 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.138+2800C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059768 | ||||||
| chr7:33059782
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+2786C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059782 | ||||||
| chr7:33059803
|
C | T | 4 | a0001c0002t0004g0004a0001c0002t0004g0067a0001c0002t0004g0068others(1): Show | 5 | HG02622.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+2765G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059803 | ||||||
| chr7:33059831
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.138+2737T>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33059831 | ||||||
| chr7:33060036
|
C | T | 1 | a0001c0001t0014g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.138+2532G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060036 | ||||||
| chr7:33060169
|
T | C | 2 | a0001c0001t0001g0357a0001c0001t0001g0358 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.138+2399A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060169 | ||||||
| chr7:33060344
|
T | C | 1 | a0001c0001t0001g0359 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.138+2224A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060344 | ||||||
| chr7:33060353
|
G | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+2215C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060353 | ||||||
| chr7:33060369
|
C | CT | 30 | a0001c0002t0002g0054a0001c0002t0002g0055a0001c0002t0002g0056others(27): Show | 32 | HG01070.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+2198dupA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | ||||||
| chr7:33060369
|
CT | C | 10 | a0001c0001t0001g0161a0001c0001t0001g0169a0001c0002t0001g0019others(7): Show | 10 | HG01516.hp2 HG02129.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+2198delA | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | ||||||
| chr7:33060369
|
CTT | C | 16 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(13): Show | 16 | HG01891.hp2 HG02976.hp2 HG03486.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+2197_138+2198d others(4): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | ||||||
| chr7:33060369
|
CTTT | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(228): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.138+2196_138+2198d others(5): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | ||||||
| chr7:33060369
|
CTTTT | C | 13 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(10): Show | 14 | HG00733.hp1 HG01167.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+2195_138+2198d others(6): Show |
NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060369 | ||||||
| chr7:33060432
|
T | G | 1 | a0001c0001t0001g0369 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.138+2136A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060432 | ||||||
| chr7:33060495
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.138+2073G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060495 | ||||||
| chr7:33060546
|
C | T | 13 | a0001c0002t0003g0009a0001c0002t0003g0151a0001c0002t0003g0152others(10): Show | 14 | HG01070.hp1 HG01071.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+2022G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060546 | ||||||
| chr7:33060741
|
G | A | 1 | a0001c0001t0001g0370 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.138+1827C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060741 | ||||||
| chr7:33060897
|
A | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+1671T>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33060897 | ||||||
| chr7:33061166
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.138+1402G>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061166 | ||||||
| chr7:33061252
|
G | A | 31 | a0001c0002t0003g0008a0001c0002t0003g0121a0001c0002t0003g0122others(28): Show | 32 | HG00280.hp2 HG00673.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+1316C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061252 | ||||||
| chr7:33061253
|
T | A | 265 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(262): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.138+1315A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061253 | ||||||
| chr7:33061292
|
A | G | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0165others(1): Show | 4 | HG00280.hp1 HG01167.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1276T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061292 | ||||||
| chr7:33061461
|
T | G | 1 | a0001c0001t0001g0371 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.138+1107A>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061461 | ||||||
| chr7:33061496
|
T | C | 279 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(276): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.138+1072A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061496 | ||||||
| chr7:33061539
|
A | G | 1 | a0001c0002t0004g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+1029T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061539 | ||||||
| chr7:33061603
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.138+965G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061603 | ||||||
| chr7:33061619
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+949A>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061619 | ||||||
| chr7:33061693
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.138+875T>C | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061693 | ||||||
| chr7:33061724
|
T | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+844A>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061724 | ||||||
| chr7:33061736
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 7 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.138+832C>G | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061736 | ||||||
| chr7:33061954
|
G | A | 31 | a0001c0002t0001g0003a0001c0002t0001g0025a0001c0002t0001g0026others(28): Show | 32 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+614C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33061954 | ||||||
| chr7:33062129
|
G | A | 2 | a0001c0001t0001g0372a0001c0001t0001g0373 | 2 | NA18946.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.138+439C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062129 | ||||||
| chr7:33062155
|
G | A | 1 | a0001c0001t0001g0374 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138+413C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062155 | ||||||
| chr7:33062175
|
G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.138+393C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062175 | ||||||
| chr7:33062214
|
C | A | 2 | a0001c0002t0003g0375a0001c0002t0003g0376 | 2 | HG03490.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.138+354G>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062214 | ||||||
| chr7:33062338
|
G | A | 3 | a0001c0001t0001g0377a0001c0001t0001g0378a0001c0001t0001g0379 | 3 | HG01167.hp1 HG01169.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.138+230C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062338 | ||||||
| chr7:33062355
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 41 | HG00423.hp1 HG00438.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.138+213G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062355 | ||||||
| chr7:33062378
|
G | A | 1 | a0001c0001t0001g0380 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+190C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062378 | ||||||
| chr7:33062459
|
G | A | 1 | a0001c0001t0001g0381 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.138+109C>T | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062459 | ||||||
| chr7:33062520
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+48G>A | NT5C3A | ENSG00000122643.23 | transcript | ENST00000610140.7 | protein_coding | 1/8 | chr7 | 33062520 |