Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 115024 |
| ensemblid | ENSG00000141698.17 |
| hgncid | 28300 |
| symbol | NT5C3B |
| name | 5'-nucleotidase, cytosolic IIIB |
| refseq_nuc | NM_052935.5 |
| refseq_prot | NP_443167.4 |
| ensembl_nuc | ENST00000435506.7 |
| ensembl_prot | ENSP00000389948.2 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 41825057 |
| end | 41836232 |
| strand | - |
| ver | v1.2 |
| region | chr17:41825057-41836232 |
| region5000 | chr17:41820057-41841232 |
| regionname0 | NT5C3B_chr17_41825057_41836232 |
| regionname5000 | NT5C3B_chr17_41820057_41841232 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 300 | 283 | 64 | 65 | 117 | 9 | 27 | 84 | NT5C3B_chr17_41820057_41841232 | NT5C3B | MAEEV others(295): Show |
chr17 | 41820057 | 41841232 |
| a0002 | 1/0 | 300 | 82 | 20 | 16 | 29 | 3 | 13 | 24 | NT5C3B_chr17_41820057_41841232 | NT5C3B | MAEEV others(295): Show |
chr17 | 41820057 | 41841232 |
| a0003 | 0/0 | 300 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | MAEEV others(295): Show |
chr17 | 41820057 | 41841232 |
| a0004 | 0/0 | 300 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | MAEEV others(295): Show |
chr17 | 41820057 | 41841232 |
| a0005 | 0/0 | 300 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | MAEEV others(295): Show |
chr17 | 41820057 | 41841232 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 900 | 258 | 42 | 64 | 115 | 9 | 27 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0001c0003 | 0/0 | 900 | 23 | 22 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0001c0005 | 0/0 | 900 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0002c0002 | 0/0 | 900 | 61 | 8 | 12 | 29 | 2 | 10 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0002c0004 | 1/0 | 900 | 21 | 12 | 4 | 0 | 1 | 3 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0003c0007 | 0/0 | 900 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0004c0006 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 | ||
| a0005c0008 | 0/0 | 900 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | ATGGC others(895): Show |
chr17 | 41820057 | 41841232 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1408 | 253 | 37 | 64 | 115 | 9 | 27 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0001c0001t0004 | 0/0 | 1408 | 4 | 4 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0001c0001t0005 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0001c0003t0001 | 0/0 | 1408 | 19 | 18 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0001c0003t0003 | 0/0 | 1408 | 4 | 4 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0001c0005t0001 | 0/0 | 1408 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0002c0002t0001 | 0/0 | 1408 | 31 | 8 | 7 | 12 | 1 | 3 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0002c0002t0002 | 0/0 | 1408 | 30 | 0 | 5 | 17 | 1 | 7 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0002c0004t0001 | 1/0 | 1408 | 21 | 12 | 4 | 0 | 1 | 3 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0003c0007t0001 | 0/0 | 1408 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0004c0006t0001 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| a0005c0008t0001 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | GTCGT others(1403): Show |
chr17 | 41820057 | 41841232 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 172 | 28 | 47 | 74 | 7 | 16 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0006 | 0/0 | 10 | 1 | 6 | 0 | 0 | 3 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0001g0082 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0004g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0001t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0003t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0001c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0003 | 0/0 | 18 | 3 | 5 | 7 | 0 | 3 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0002g0002 | 0/0 | 25 | 0 | 5 | 14 | 1 | 5 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0004t0001g0004 | 1/0 | 14 | 7 | 3 | 0 | 1 | 2 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0004t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0002c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0003c0007t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0004c0006t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| a0005c0008t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | FIN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01074 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01081 | hp1 | a0002 | c0004 | t0001 | g0004 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01243 | hp1 | a0003 | c0007 | t0001 | g0027 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | PUR | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01433 | hp2 | a0002 | c0004 | t0001 | g0004 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0031 | EUR | IBS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02004 | hp1 | a0002 | c0004 | t0001 | g0017 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02040 | hp1 | a0001 | c0005 | t0001 | g0021 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02135 | hp2 | a0001 | c0005 | t0001 | g0021 | EAS | KHV | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0018 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0004 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02723 | hp2 | a0002 | c0004 | t0001 | g0004 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02809 | hp2 | a0004 | c0006 | t0001 | g0026 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0017 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0004 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03453 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0030 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0081 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0044 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03579 | hp1 | a0005 | c0008 | t0001 | g0075 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03669 | hp1 | a0002 | c0004 | t0001 | g0028 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | STU | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG04184 | hp1 | a0002 | c0004 | t0001 | g0004 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG04184 | hp2 | a0002 | c0004 | t0001 | g0004 | SAS | BEB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | YRI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | YRI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0008 | AFR | LWK | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | ASW | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20752 | hp2 | a0002 | c0004 | t0001 | g0004 | EUR | TSI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02109 | hp1 | a0002 | c0004 | t0001 | g0004 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02559 | hp1 | a0002 | c0004 | t0001 | g0029 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0059 | AFR | ACB | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0010 | AFR | MSL | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | USA | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | USA | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0018 | AFR | LWK | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | LWK | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0082 | REF | REF | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0001 | g0004 | REF | REF | NT5C3B_chr17_41820057_41841232 | NT5C3B | chr17 | 41820057 | 41841232 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:41825647 | C | T | 1 | a0005 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.779G>A | p.Arg260Gln | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 9/9 | 818/1408 | 779/903 | 260/300 | chr17 | 41825647 | |||
| chr17:41827556 | G | C | 2 | a0001 a0005 |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
missense_variant | MODERATE | c.638C>G | p.Ser213Cys | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/9 | 677/1408 | 638/903 | 213/300 | chr17 | 41827556 | |||
| chr17:41827568 | G | A | 2 | a0001 a0005 |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
missense_variant | MODERATE | c.626C>T | p.Ala209Val | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/9 | 665/1408 | 626/903 | 209/300 | chr17 | 41827568 | |||
| chr17:41835933 | C | G | 1 | a0003 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.37G>C | p.Val13Leu | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/9 | 76/1408 | 37/903 | 13/300 | chr17 | 41835933 | |||
| chr17:41835947 | A | G | 1 | a0004 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.23T>C | p.Leu8Pro | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/9 | 62/1408 | 23/903 | 8/300 | chr17 | 41835947 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:41825580 | G | A | 1 | a0001c0005 | 2 | HG02040.hp1 HG02135.hp2 |
synonymous_variant | LOW | c.846C>T | p.Asn282Asn | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 9/9 | 885/1408 | 846/903 | 282/300 | chr17 | 41825580 | |||
| chr17:41827597 | G | C | 2 | a0001c0001 a0001c0005 |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(256): Show |
synonymous_variant | LOW | c.597C>G | p.Leu199Leu | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/9 | 636/1408 | 597/903 | 199/300 | chr17 | 41827597 | |||
| chr17:41830878 | T | C | 6 | a0001c0001 a0001c0003 a0001c0005 others(3): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
synonymous_variant | LOW | c.327A>G | p.Ala109Ala | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/9 | 366/1408 | 327/903 | 109/300 | chr17 | 41830878 | |||
| chr17:41832409 | T | C | 1 | a0004c0006 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.297A>G | p.Leu99Leu | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/9 | 336/1408 | 297/903 | 99/300 | chr17 | 41832409 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:41825137 | G | A | 1 | a0001c0001t0005 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*386C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 9/9 | 386 | chr17 | 41825137 | ||||||
| chr17:41825154 | C | G | 1 | a0002c0002t0002 | 30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*369G>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 9/9 | 369 | chr17 | 41825154 | ||||||
| chr17:41825443 | C | T | 1 | a0001c0003t0003 | 4 | HG02145.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*80G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 9/9 | 80 | chr17 | 41825443 | ||||||
| chr17:41825507 | G | A | 1 | a0001c0001t0004 | 4 | HG02486.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*16C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 9/9 | 16 | chr17 | 41825507 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:41825827 | C | T | 1 | a0001c0001t0001g0013 | 3 | HG02451.hp2 HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.769-170G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41825827 | |||||||
| chr17:41825828 | G | A | 1 | a0001c0003t0003g0010 | 4 | HG02145.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-171C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41825828 | |||||||
| chr17:41825899 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.769-242T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41825899 | |||||||
| chr17:41825933 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.769-276C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41825933 | |||||||
| chr17:41825948 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.769-291C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41825948 | |||||||
| chr17:41825982 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.769-325C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41825982 | |||||||
| chr17:41826012 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.769-355C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826012 | |||||||
| chr17:41826017 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.769-360A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826017 | |||||||
| chr17:41826109 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.769-452G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826109 | |||||||
| chr17:41826167 | A | AC | 4 | a0001c0001t0001g0064 a0001c0003t0001g0072 a0002c0002t0001g0037 others(1): Show |
4 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.769-511_769-510ins others(1): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826167 | |||||||
| chr17:41826167 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(66): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.769-510T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826167 | |||||||
| chr17:41826167 | A | T | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.769-510T>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826167 | |||||||
| chr17:41826168 | A | C | 1 | a0002c0002t0002g0045 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.769-511T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826168 | |||||||
| chr17:41826171 | A | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.769-514T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826171 | |||||||
| chr17:41826180 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.769-523T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826180 | |||||||
| chr17:41826211 | A | ATTTC | 5 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0074 others(2): Show |
8 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.769-558_769-555dup others(4): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826211 | |||||||
| chr17:41826211 | ATTTCTTT others(1): Show |
A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.769-562_769-555del others(8): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826211 | |||||||
| chr17:41826285 | A | G | 6 | a0002c0002t0002g0002 a0002c0002t0002g0041 a0002c0002t0002g0042 others(3): Show |
30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.769-628T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826285 | |||||||
| chr17:41826298 | A | G | 20 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(17): Show |
62 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.769-641T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826298 | |||||||
| chr17:41826383 | C | A | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.769-726G>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826383 | |||||||
| chr17:41826431 | C | G | 1 | a0001c0003t0001g0078 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.769-774G>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826431 | |||||||
| chr17:41826639 | T | C | 1 | a0002c0002t0001g0038 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.768+787A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826639 | |||||||
| chr17:41826738 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.768+688A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826738 | |||||||
| chr17:41826830 | G | A | 1 | a0001c0003t0001g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.768+596C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826830 | |||||||
| chr17:41826999 | CA | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.768+426delT | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41826999 | |||||||
| chr17:41827001 | A | T | 7 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(4): Show |
25 | HG01074.hp1 HG01109.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.768+425T>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827001 | |||||||
| chr17:41827002 | A | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0039 |
2 | HG01168.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.768+424T>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827002 | |||||||
| chr17:41827064 | T | C | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.768+362A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827064 | |||||||
| chr17:41827177 | G | A | 4 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0071 others(1): Show |
15 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.768+249C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827177 | |||||||
| chr17:41827292 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.768+134G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827292 | |||||||
| chr17:41827308 | T | A | 2 | a0001c0001t0001g0066 a0004c0006t0001g0026 |
2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.768+118A>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827308 | |||||||
| chr17:41827392 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.768+34T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 8/8 | chr17 | 41827392 | |||||||
| chr17:41827663 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.568-37G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41827663 | |||||||
| chr17:41827765 | G | A | 5 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(2): Show |
5 | HG01243.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-139C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41827765 | |||||||
| chr17:41827888 | G | C | 1 | a0001c0001t0001g0022 | 2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.568-262C>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41827888 | |||||||
| chr17:41827910 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.568-284A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41827910 | |||||||
| chr17:41828007 | C | G | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.568-381G>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828007 | |||||||
| chr17:41828073 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.568-447C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828073 | |||||||
| chr17:41828111 | C | A | 1 | a0001c0001t0001g0023 | 2 | HG01943.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.568-485G>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828111 | |||||||
| chr17:41828165 | C | A | 5 | a0001c0003t0001g0008 a0001c0003t0001g0009 a0001c0003t0001g0071 others(2): Show |
16 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.568-539G>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828165 | |||||||
| chr17:41828402 | A | C | 6 | a0002c0002t0002g0002 a0002c0002t0002g0041 a0002c0002t0002g0042 others(3): Show |
30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.567+388T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828402 | |||||||
| chr17:41828416 | C | G | 1 | a0001c0003t0001g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.567+374G>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828416 | |||||||
| chr17:41828494 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0011 |
13 | HG01099.hp2 HG01168.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.567+296C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828494 | |||||||
| chr17:41828509 | G | C | 1 | a0002c0002t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.567+281C>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828509 | |||||||
| chr17:41828561 | T | A | 1 | a0001c0001t0001g0015 | 3 | HG00280.hp2 HG01123.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.567+229A>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828561 | |||||||
| chr17:41828757 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.567+33C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 7/8 | chr17 | 41828757 | |||||||
| chr17:41829075 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.405-123C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829075 | |||||||
| chr17:41829078 | G | A | 20 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(17): Show |
62 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.405-126C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829078 | |||||||
| chr17:41829088 | C | T | 1 | a0002c0002t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.405-136G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829088 | |||||||
| chr17:41829101 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0040 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.405-149C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829101 | |||||||
| chr17:41829241 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.405-289A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829241 | |||||||
| chr17:41829308 | C | T | 1 | a0002c0004t0001g0028 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.405-356G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829308 | |||||||
| chr17:41829314 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.405-362G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829314 | |||||||
| chr17:41829334 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.405-382G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829334 | |||||||
| chr17:41829514 | C | T | 1 | a0001c0001t0001g0005 | 10 | HG01928.hp1 HG01928.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-562G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829514 | |||||||
| chr17:41829784 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.405-832G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41829784 | |||||||
| chr17:41830126 | G | A | 20 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(17): Show |
62 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.404+675C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830126 | |||||||
| chr17:41830232 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.404+569G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830232 | |||||||
| chr17:41830325 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.404+476A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830325 | |||||||
| chr17:41830365 | G | A | 1 | a0002c0004t0001g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.404+436C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830365 | |||||||
| chr17:41830377 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.404+424C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830377 | |||||||
| chr17:41830402 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.404+399C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830402 | |||||||
| chr17:41830465 | C | T | 1 | a0001c0003t0001g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.404+336G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830465 | |||||||
| chr17:41830502 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.404+299A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830502 | |||||||
| chr17:41830507 | TGAGAA | T | 3 | a0001c0003t0001g0072 a0001c0003t0001g0073 a0001c0003t0001g0078 |
3 | HG01884.hp1 HG02055.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.404+289_404+293del others(5): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830507 | |||||||
| chr17:41830677 | T | C | 1 | a0002c0004t0001g0017 | 2 | HG02004.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.404+124A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830677 | |||||||
| chr17:41830682 | C | T | 1 | a0002c0004t0001g0030 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.404+119G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 6/8 | chr17 | 41830682 | |||||||
| chr17:41831109 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.315-219C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831109 | |||||||
| chr17:41831175 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.315-285A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831175 | |||||||
| chr17:41831249 | G | A | 2 | a0002c0004t0001g0018 a0002c0004t0001g0030 |
3 | HG02257.hp2 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.315-359C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831249 | |||||||
| chr17:41831307 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0070 |
11 | HG02015.hp2 HG02155.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.315-417C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831307 | |||||||
| chr17:41831319 | C | CA | 9 | a0002c0002t0001g0019 a0002c0002t0001g0032 a0002c0002t0001g0033 others(6): Show |
10 | HG01243.hp1 HG02074.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-430dupT | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831319 | |||||||
| chr17:41831319 | C | CAA | 4 | a0002c0002t0002g0002 a0002c0002t0002g0041 a0002c0002t0002g0044 others(1): Show |
28 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.315-431_315-430dup others(2): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831319 | |||||||
| chr17:41831319 | CAA | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.315-431_315-430del others(2): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831319 | |||||||
| chr17:41831319 | CAAA | C | 9 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.315-432_315-430del others(3): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831319 | |||||||
| chr17:41831408 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.315-518A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831408 | |||||||
| chr17:41831509 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.315-619C>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831509 | |||||||
| chr17:41831513 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.315-623C>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831513 | |||||||
| chr17:41831681 | C | T | 1 | a0002c0002t0001g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.314+711G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831681 | |||||||
| chr17:41831919 | A | G | 1 | a0001c0003t0001g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314+473T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41831919 | |||||||
| chr17:41832018 | T | C | 6 | a0002c0002t0002g0002 a0002c0002t0002g0041 a0002c0002t0002g0042 others(3): Show |
30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.314+374A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41832018 | |||||||
| chr17:41832349 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(41): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.314+43G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 5/8 | chr17 | 41832349 | |||||||
| chr17:41832538 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.229-61G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41832538 | |||||||
| chr17:41832644 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0077 |
4 | HG00544.hp1 NA18995.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.229-167C>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41832644 | |||||||
| chr17:41832821 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(41): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.229-344G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41832821 | |||||||
| chr17:41832901 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.229-424T>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41832901 | |||||||
| chr17:41833007 | A | G | 5 | a0002c0002t0001g0032 a0002c0002t0001g0033 a0002c0002t0001g0034 others(2): Show |
5 | HG01243.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.229-530T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833007 | |||||||
| chr17:41833042 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.229-565C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833042 | |||||||
| chr17:41833076 | A | G | 1 | a0002c0002t0001g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.229-599T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833076 | |||||||
| chr17:41833077 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.229-600G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833077 | |||||||
| chr17:41833079 | C | G | 1 | a0002c0002t0001g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.229-602G>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833079 | |||||||
| chr17:41833189 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.229-712G>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833189 | |||||||
| chr17:41833321 | AT | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.229-845delA | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833321 | |||||||
| chr17:41833322 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.229-845A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833322 | |||||||
| chr17:41833340 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.229-864dupT | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833340 | |||||||
| chr17:41833355 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.229-878A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833355 | |||||||
| chr17:41833377 | C | A | 1 | a0001c0003t0001g0078 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.229-900G>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833377 | |||||||
| chr17:41833410 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.229-933C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833410 | |||||||
| chr17:41833482 | A | G | 20 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(17): Show |
62 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.229-1005T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833482 | |||||||
| chr17:41833514 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.229-1037A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833514 | |||||||
| chr17:41833552 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.229-1075T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833552 | |||||||
| chr17:41833767 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.229-1290T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833767 | |||||||
| chr17:41833826 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.228+1244A>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833826 | |||||||
| chr17:41833943 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.228+1127A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41833943 | |||||||
| chr17:41834105 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.228+965A>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834105 | |||||||
| chr17:41834170 | C | T | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228+900G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834170 | |||||||
| chr17:41834193 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG00609.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.228+877G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834193 | |||||||
| chr17:41834326 | G | A | 1 | a0001c0003t0001g0081 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.228+744C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834326 | |||||||
| chr17:41834393 | T | TACAC | 8 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0003t0001g0008 others(5): Show |
21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.228+673_228+676dup others(4): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | T | TACACAC | 30 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(27): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.228+671_228+676dup others(6): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | T | TACACACA others(1): Show |
15 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(12): Show |
57 | HG00673.hp2 HG00735.hp1 HG01515.hp2 others(54): Show |
intron_variant | MODIFIER | c.228+669_228+676dup others(8): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0001 a0001c0005t0001g0021 |
3 | HG02040.hp1 HG02135.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.228+667_228+676dup others(10): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | T | TACACACA others(5): Show |
1 | a0001c0003t0001g0072 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.228+665_228+676dup others(12): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | T | TACACACA others(7): Show |
1 | a0001c0001t0001g0001 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.228+663_228+676dup others(14): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | TACAC | T | 2 | a0002c0004t0001g0017 a0002c0004t0001g0030 |
3 | HG02004.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.228+673_228+676del others(4): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834393 | TACACAC | T | 22 | a0001c0001t0001g0064 a0001c0003t0001g0074 a0002c0002t0001g0003 others(19): Show |
64 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.228+671_228+676del others(6): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834393 | |||||||
| chr17:41834397 | C | T | 1 | a0002c0002t0002g0041 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.228+673G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834397 | |||||||
| chr17:41834617 | A | G | 1 | a0001c0001t0001g0046 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.228+453T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834617 | |||||||
| chr17:41834660 | G | T | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228+410C>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834660 | |||||||
| chr17:41834664 | A | G | 1 | a0002c0002t0001g0031 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.228+406T>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834664 | |||||||
| chr17:41834672 | C | T | 1 | a0004c0006t0001g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.228+398G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834672 | |||||||
| chr17:41834813 | C | T | 14 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(11): Show |
32 | HG01074.hp1 HG01109.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.228+257G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834813 | |||||||
| chr17:41834982 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.228+88G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 4/8 | chr17 | 41834982 | |||||||
| chr17:41835374 | G | C | 1 | a0001c0003t0001g0009 | 5 | HG01884.hp2 HG02280.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-102C>G | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/8 | chr17 | 41835374 | |||||||
| chr17:41835538 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.112-266G>A | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/8 | chr17 | 41835538 | |||||||
| chr17:41835549 | T | G | 20 | a0002c0002t0001g0003 a0002c0002t0001g0019 a0002c0002t0001g0031 others(17): Show |
62 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.112-277A>C | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/8 | chr17 | 41835549 | |||||||
| chr17:41835596 | CGCTG | C | 6 | a0002c0002t0002g0002 a0002c0002t0002g0041 a0002c0002t0002g0042 others(3): Show |
30 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.111+259_111+262del others(4): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/8 | chr17 | 41835596 | |||||||
| chr17:41835615 | A | ATATC | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.111+243_111+244ins others(4): Show |
NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/8 | chr17 | 41835615 | |||||||
| chr17:41835736 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.111+123C>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 2/8 | chr17 | 41835736 | |||||||
| chr17:41836107 | C | A | 1 | a0002c0002t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.12+75G>T | NT5C3B | ENSG00000141698.17 | transcript | ENST00000435506.7 | protein_coding | 1/8 | chr17 | 41836107 |