Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64841 |
| ensemblid | ENSG00000100522.10 |
| hgncid | 19980 |
| symbol | GNPNAT1 |
| name | glucosamine-phosphate N-acetyltransferase 1 |
| refseq_nuc | NM_198066.4 |
| refseq_prot | NP_932332.1 |
| ensembl_nuc | ENST00000216410.8 |
| ensembl_prot | ENSP00000216410.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 52775193 |
| end | 52791607 |
| strand | - |
| ver | v1.2 |
| region | chr14:52775193-52791607 |
| region5000 | chr14:52770193-52796607 |
| regionname0 | GNPNAT1_chr14_52775193_52791607 |
| regionname5000 | GNPNAT1_chr14_52770193_52796607 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 184 | 389 | 80 | 78 | 182 | 12 | 35 | 140 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | MKPDE others(179): Show |
chr14 | 52770193 | 52796607 |
| a0002 | 0/0 | 184 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | MKPDE others(179): Show |
chr14 | 52770193 | 52796607 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 552 | 384 | 80 | 77 | 178 | 12 | 35 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | ATGAA others(547): Show |
chr14 | 52770193 | 52796607 | ||
| a0001c0002 | 0/0 | 552 | 4 | 0 | 0 | 4 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | ATGAA others(547): Show |
chr14 | 52770193 | 52796607 | ||
| a0001c0003 | 0/0 | 552 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | ATGAA others(547): Show |
chr14 | 52770193 | 52796607 | ||
| a0002c0004 | 0/0 | 552 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | ATGAA others(547): Show |
chr14 | 52770193 | 52796607 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3867 | 164 | 40 | 46 | 54 | 7 | 15 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0002 | 0/0 | 3867 | 108 | 19 | 17 | 55 | 4 | 13 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0003 | 0/0 | 3867 | 57 | 9 | 7 | 36 | 0 | 5 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0004 | 0/0 | 3867 | 16 | 0 | 0 | 16 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0005 | 0/0 | 3865 | 12 | 0 | 0 | 10 | 0 | 2 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3860): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0006 | 0/0 | 3872 | 5 | 5 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3867): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0007 | 0/0 | 3867 | 5 | 0 | 4 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0008 | 0/0 | 3867 | 4 | 0 | 0 | 4 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0009 | 0/0 | 3867 | 3 | 2 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0010 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0011 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0012 | 0/0 | 3872 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3867): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0013 | 0/0 | 3872 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3867): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0014 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0015 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0016 | 0/0 | 3877 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3872): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0017 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0018 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0001t0019 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0002t0002 | 0/0 | 3867 | 4 | 0 | 0 | 4 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0001c0003t0009 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| a0002c0004t0002 | 0/0 | 3867 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | AGAGG others(3862): Show |
chr14 | 52770193 | 52796607 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 61 | 3 | 22 | 23 | 2 | 10 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0004 | 0/0 | 20 | 0 | 8 | 11 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0009 | 1/0 | 8 | 6 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0002 | 0/0 | 28 | 4 | 1 | 11 | 3 | 9 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0005 | 0/0 | 18 | 1 | 1 | 15 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0011 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0012 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0003 | 0/0 | 20 | 4 | 6 | 7 | 0 | 3 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0006 | 0/0 | 17 | 0 | 0 | 17 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0008 | 0/0 | 8 | 5 | 1 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0005g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0007g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0008g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0012g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0014g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0016g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0018g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0001t0019g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0001c0003t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| a0002c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0024 | EUR | GBR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | GBR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | FIN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0100 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0024 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0024 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01175 | hp2 | a0001 | c0001 | t0014 | g0129 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0124 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01433 | hp2 | a0001 | c0003 | t0009 | g0057 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0092 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0111 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0090 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0070 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03486 | hp1 | a0001 | c0001 | t0017 | g0123 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0131 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03704 | hp2 | a0002 | c0004 | t0002 | g0072 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | BEB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | BEB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18941 | hp2 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18973 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18985 | hp2 | a0001 | c0001 | t0018 | g0112 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18997 | hp2 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19002 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | LWK | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19063 | hp2 | a0001 | c0001 | t0016 | g0068 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0099 | AFR | LWK | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | GNPNAT1_chr14_52770193_52796607 | GNPNAT1 | chr14 | 52770193 | 52796607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52778370 | T | C | 1 | a0002 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.496A>G | p.Lys166Glu | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 690/3867 | 496/555 | 166/184 | chr14 | 52778370 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52778446 | G | A | 1 | a0001c0002 | 4 | HG00438.hp2 HG00558.hp1 NA18947.hp2 others(1): Show |
synonymous_variant | LOW | c.420C>T | p.Thr140Thr | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 614/3867 | 420/555 | 140/184 | chr14 | 52778446 | |||
| chr14:52783427 | A | G | 1 | a0001c0003 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.213T>C | p.Phe71Phe | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/6 | 407/3867 | 213/555 | 71/184 | chr14 | 52783427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52775261 | G | A | 1 | a0001c0001t0017 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3050C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 3050 | chr14 | 52775261 | ||||||
| chr14:52775644 | G | A | 1 | a0001c0001t0003 | 57 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2667C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2667 | chr14 | 52775644 | ||||||
| chr14:52775834 | G | A | 2 | a0001c0001t0009 a0001c0003t0009 |
4 | HG01346.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2477C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2477 | chr14 | 52775834 | ||||||
| chr14:52775840 | A | G | 1 | a0001c0001t0011 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2471T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2471 | chr14 | 52775840 | ||||||
| chr14:52775860 | G | C | 1 | a0001c0001t0015 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2451C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2451 | chr14 | 52775860 | ||||||
| chr14:52775880 | C | A | 1 | a0001c0001t0007 | 5 | HG00140.hp1 HG00642.hp2 HG01099.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2431G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2431 | chr14 | 52775880 | ||||||
| chr14:52775905 | C | T | 1 | a0001c0001t0012 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2406G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2406 | chr14 | 52775905 | ||||||
| chr14:52775909 | G | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402C>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2402 | chr14 | 52775909 | ||||||
| chr14:52775959 | C | CAACAAAA others(3): Show |
1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2351_*2352insATTT others(6): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2351 | chr14 | 52775959 | ||||||
| chr14:52775962 | G | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2349C>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2349 | chr14 | 52775962 | ||||||
| chr14:52775964 | G | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2347C>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2347 | chr14 | 52775964 | ||||||
| chr14:52775977 | G | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2334C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2334 | chr14 | 52775977 | ||||||
| chr14:52775982 | C | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2329G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2329 | chr14 | 52775982 | ||||||
| chr14:52775983 | A | G | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2328 | chr14 | 52775983 | ||||||
| chr14:52775984 | G | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2327C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2327 | chr14 | 52775984 | ||||||
| chr14:52775987 | T | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2324A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2324 | chr14 | 52775987 | ||||||
| chr14:52775988 | G | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2323C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2323 | chr14 | 52775988 | ||||||
| chr14:52775989 | G | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2322C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2322 | chr14 | 52775989 | ||||||
| chr14:52775990 | G | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2321C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2321 | chr14 | 52775990 | ||||||
| chr14:52775994 | C | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2317G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2317 | chr14 | 52775994 | ||||||
| chr14:52775998 | G | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2313C>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2313 | chr14 | 52775998 | ||||||
| chr14:52776000 | C | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2311G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2311 | chr14 | 52776000 | ||||||
| chr14:52776003 | C | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2308G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2308 | chr14 | 52776003 | ||||||
| chr14:52776004 | A | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2307T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2307 | chr14 | 52776004 | ||||||
| chr14:52776006 | A | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2305 | chr14 | 52776006 | ||||||
| chr14:52776007 | C | A | 2 | a0001c0001t0016 a0001c0001t0018 |
2 | NA18985.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2304G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2304 | chr14 | 52776007 | ||||||
| chr14:52776008 | A | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2303 | chr14 | 52776008 | ||||||
| chr14:52776010 | A | T | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2301T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2301 | chr14 | 52776010 | ||||||
| chr14:52776011 | A | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2300T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2300 | chr14 | 52776011 | ||||||
| chr14:52776012 | A | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2299T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2299 | chr14 | 52776012 | ||||||
| chr14:52776013 | A | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2298T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2298 | chr14 | 52776013 | ||||||
| chr14:52776014 | T | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2297A>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2297 | chr14 | 52776014 | ||||||
| chr14:52776016 | T | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2295A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2295 | chr14 | 52776016 | ||||||
| chr14:52776018 | T | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2293A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2293 | chr14 | 52776018 | ||||||
| chr14:52776019 | T | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2292A>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2292 | chr14 | 52776019 | ||||||
| chr14:52776021 | A | C | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2290T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2290 | chr14 | 52776021 | ||||||
| chr14:52776024 | T | G | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2287A>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2287 | chr14 | 52776024 | ||||||
| chr14:52776033 | G | A | 1 | a0001c0001t0016 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2278C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2278 | chr14 | 52776033 | ||||||
| chr14:52776131 | C | T | 7 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(4): Show |
120 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2180G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2180 | chr14 | 52776131 | ||||||
| chr14:52776137 | G | A | 2 | a0001c0001t0009 a0001c0003t0009 |
4 | HG01346.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2174C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 2174 | chr14 | 52776137 | ||||||
| chr14:52776529 | C | T | 1 | a0001c0001t0005 | 12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1782G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1782 | chr14 | 52776529 | ||||||
| chr14:52776560 | T | G | 1 | a0001c0001t0008 | 4 | NA18941.hp2 NA18973.hp1 NA18992.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1751A>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1751 | chr14 | 52776560 | ||||||
| chr14:52776619 | G | C | 1 | a0001c0001t0013 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1692 | chr14 | 52776619 | ||||||
| chr14:52776714 | T | G | 1 | a0001c0001t0019 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1597A>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1597 | chr14 | 52776714 | ||||||
| chr14:52776991 | G | A | 2 | a0001c0001t0009 a0001c0003t0009 |
4 | HG01346.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1320C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1320 | chr14 | 52776991 | ||||||
| chr14:52777226 | A | C | 1 | a0001c0001t0014 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1085T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1085 | chr14 | 52777226 | ||||||
| chr14:52777263 | CAT | C | 1 | a0001c0001t0005 | 12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1046_*1047delAT | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 1046 | chr14 | 52777263 | ||||||
| chr14:52777396 | A | AAAAGT | 3 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0013 |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*914_*915insACTTT | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 914 | chr14 | 52777396 | ||||||
| chr14:52777919 | A | G | 2 | a0001c0001t0004 a0001c0001t0011 |
17 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*392T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 392 | chr14 | 52777919 | ||||||
| chr14:52778307 | A | T | 1 | a0001c0001t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 6/6 | 4 | chr14 | 52778307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:52778527 | A | G | 1 | a0001c0001t0009g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.408-69T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778527 | |||||||
| chr14:52778598 | T | C | 7 | a0001c0001t0006g0060 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.408-140A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778598 | |||||||
| chr14:52778765 | C | G | 1 | a0001c0001t0006g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.408-307G>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778765 | |||||||
| chr14:52778785 | A | G | 1 | a0001c0001t0003g0029 | 2 | NA18979.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.408-327T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778785 | |||||||
| chr14:52778796 | C | T | 1 | a0001c0001t0003g0027 | 2 | NA18990.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.408-338G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778796 | |||||||
| chr14:52778804 | C | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0047 a0001c0001t0005g0130 others(3): Show |
12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.408-346G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778804 | |||||||
| chr14:52778855 | A | C | 1 | a0001c0001t0002g0022 | 3 | HG02109.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.408-397T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778855 | |||||||
| chr14:52778977 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.408-519G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52778977 | |||||||
| chr14:52779366 | T | C | 1 | a0001c0001t0005g0131 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.408-908A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779366 | |||||||
| chr14:52779419 | A | T | 4 | a0001c0001t0002g0015 a0001c0001t0002g0073 a0001c0001t0002g0081 others(1): Show |
7 | HG01123.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.408-961T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779419 | |||||||
| chr14:52779435 | C | A | 1 | a0001c0001t0009g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.408-977G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779435 | |||||||
| chr14:52779544 | A | G | 7 | a0001c0001t0006g0060 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.408-1086T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779544 | |||||||
| chr14:52779585 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.407+1094G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779585 | |||||||
| chr14:52779662 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.407+1017T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779662 | |||||||
| chr14:52779706 | G | A | 1 | a0001c0001t0017g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.407+973C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779706 | |||||||
| chr14:52779724 | T | TA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0021 others(45): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.407+954dupT | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779724 | |||||||
| chr14:52779724 | T | TAA | 52 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0040 others(49): Show |
172 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.407+953_407+954dup others(2): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779724 | |||||||
| chr14:52779724 | T | TAAA | 16 | a0001c0001t0001g0074 a0001c0001t0001g0117 a0001c0001t0001g0127 others(13): Show |
32 | HG00733.hp1 HG01069.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.407+952_407+954dup others(3): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779724 | |||||||
| chr14:52779724 | T | TAAAA | 5 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0075 others(2): Show |
7 | HG00323.hp2 HG02109.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+951_407+954dup others(4): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779724 | |||||||
| chr14:52779724 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0001g0048 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.407+943_407+954del others(12): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779724 | |||||||
| chr14:52779762 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.407+917A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779762 | |||||||
| chr14:52779783 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.407+896C>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779783 | |||||||
| chr14:52779927 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.407+752G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52779927 | |||||||
| chr14:52780031 | G | C | 1 | a0001c0001t0001g0048 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.407+648C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52780031 | |||||||
| chr14:52780033 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG02165.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.407+646C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52780033 | |||||||
| chr14:52780038 | G | A | 1 | a0001c0001t0002g0022 | 3 | HG02109.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.407+641C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52780038 | |||||||
| chr14:52780195 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.407+484T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52780195 | |||||||
| chr14:52780273 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.407+406A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52780273 | |||||||
| chr14:52780277 | G | C | 5 | a0001c0001t0006g0060 a0001c0001t0006g0088 a0001c0001t0006g0089 others(2): Show |
5 | HG02280.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+402C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 5/5 | chr14 | 52780277 | |||||||
| chr14:52781087 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0103 others(6): Show |
11 | HG00323.hp1 HG01106.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.346-347C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 4/5 | chr14 | 52781087 | |||||||
| chr14:52781093 | G | A | 1 | a0001c0001t0009g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.346-353C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 4/5 | chr14 | 52781093 | |||||||
| chr14:52781162 | A | G | 1 | a0001c0001t0002g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.346-422T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 4/5 | chr14 | 52781162 | |||||||
| chr14:52781187 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0108 a0001c0001t0001g0125 |
5 | HG02027.hp1 NA18957.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.346-447T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 4/5 | chr14 | 52781187 | |||||||
| chr14:52782098 | A | G | 6 | a0001c0001t0005g0010 a0001c0001t0005g0047 a0001c0001t0005g0130 others(3): Show |
12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-187T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782098 | |||||||
| chr14:52782242 | AATAG | A | 6 | a0001c0001t0005g0010 a0001c0001t0005g0047 a0001c0001t0005g0130 others(3): Show |
12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-335_218-332del others(4): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782242 | |||||||
| chr14:52782547 | T | C | 1 | a0001c0001t0017g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.218-636A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782547 | |||||||
| chr14:52782684 | G | GAAAT | 75 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0071 others(72): Show |
200 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.217+735_217+738dup others(4): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782684 | |||||||
| chr14:52782754 | A | T | 6 | a0001c0001t0005g0010 a0001c0001t0005g0047 a0001c0001t0005g0130 others(3): Show |
12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+669T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782754 | |||||||
| chr14:52782916 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.217+507C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782916 | |||||||
| chr14:52782929 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.217+494G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782929 | |||||||
| chr14:52782935 | A | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0062 a0001c0001t0002g0064 |
4 | NA18956.hp2 NA18995.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+488T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52782935 | |||||||
| chr14:52783037 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0061 a0001c0001t0002g0063 |
4 | HG01934.hp1 HG01943.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+386G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 3/5 | chr14 | 52783037 | |||||||
| chr14:52783514 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.155-29G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52783514 | |||||||
| chr14:52783575 | G | C | 44 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0002g0002 others(41): Show |
122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.155-90C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52783575 | |||||||
| chr14:52783578 | A | T | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0093 others(17): Show |
67 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.155-93T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52783578 | |||||||
| chr14:52783637 | C | G | 1 | a0001c0001t0017g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.155-152G>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52783637 | |||||||
| chr14:52783653 | A | G | 1 | a0001c0001t0006g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.155-168T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52783653 | |||||||
| chr14:52783857 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.155-372T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52783857 | |||||||
| chr14:52784095 | G | A | 1 | a0001c0001t0015g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154+402C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52784095 | |||||||
| chr14:52784200 | A | G | 1 | a0001c0001t0005g0130 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.154+297T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52784200 | |||||||
| chr14:52784378 | C | CT | 2 | a0001c0001t0004g0041 a0001c0001t0004g0104 |
3 | HG00408.hp1 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.154+118dupA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52784378 | |||||||
| chr14:52784418 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.154+79T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 2/5 | chr14 | 52784418 | |||||||
| chr14:52784722 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-14-58C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52784722 | |||||||
| chr14:52784926 | C | CT | 14 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0103 others(11): Show |
23 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-14-263dupA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52784926 | |||||||
| chr14:52784926 | CT | C | 9 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0002g0005 others(6): Show |
33 | HG00673.hp1 HG01069.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-263delA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52784926 | |||||||
| chr14:52784945 | T | C | 4 | a0001c0001t0009g0056 a0001c0001t0009g0058 a0001c0001t0009g0059 others(1): Show |
4 | HG01346.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-281A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52784945 | |||||||
| chr14:52784956 | C | T | 1 | a0001c0001t0002g0018 | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-292G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52784956 | |||||||
| chr14:52785082 | C | A | 3 | a0001c0001t0006g0088 a0001c0001t0006g0089 a0001c0001t0013g0090 |
3 | HG02280.hp1 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-14-418G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785082 | |||||||
| chr14:52785111 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14-447T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785111 | |||||||
| chr14:52785155 | C | A | 1 | a0001c0001t0006g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-491G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785155 | |||||||
| chr14:52785155 | C | T | 13 | a0001c0001t0001g0038 a0001c0001t0003g0003 a0001c0001t0003g0006 others(10): Show |
59 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.-14-491G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785155 | |||||||
| chr14:52785166 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-14-502C>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785166 | |||||||
| chr14:52785229 | T | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0020 others(40): Show |
143 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-14-565A>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785229 | |||||||
| chr14:52785395 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-14-731A>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785395 | |||||||
| chr14:52785489 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-14-825C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785489 | |||||||
| chr14:52785513 | G | A | 7 | a0001c0001t0002g0085 a0001c0001t0005g0010 a0001c0001t0005g0047 others(4): Show |
13 | HG00544.hp2 HG02015.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-849C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785513 | |||||||
| chr14:52785561 | T | C | 1 | a0001c0001t0017g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-897A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785561 | |||||||
| chr14:52785693 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-1029G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785693 | |||||||
| chr14:52785724 | T | C | 4 | a0001c0001t0009g0056 a0001c0001t0009g0058 a0001c0001t0009g0059 others(1): Show |
4 | HG01346.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-1060A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785724 | |||||||
| chr14:52785748 | AGCCTTTT others(2606): Show |
A | 5 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
23 | HG00673.hp2 HG02132.hp2 NA18940.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15+3067_-14-1085d others(2): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785748 | |||||||
| chr14:52785751 | C | CT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0038 a0001c0001t0002g0018 others(8): Show |
40 | HG00639.hp1 HG01074.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-1088dupA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785751 | |||||||
| chr14:52785777 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-1113G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785777 | |||||||
| chr14:52785914 | G | A | 71 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0048 others(68): Show |
179 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.-14-1250C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785914 | |||||||
| chr14:52785948 | G | A | 1 | a0001c0001t0012g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-1284C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785948 | |||||||
| chr14:52785984 | C | T | 1 | a0001c0001t0010g0070 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-14-1320G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52785984 | |||||||
| chr14:52786059 | C | CT | 63 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0039 others(60): Show |
146 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.-14-1396dupA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786059 | |||||||
| chr14:52786059 | C | CTT | 16 | a0001c0001t0001g0038 a0001c0001t0002g0002 a0001c0001t0003g0003 others(13): Show |
45 | HG00639.hp1 HG01074.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-14-1397_-14-1396d others(4): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786059 | |||||||
| chr14:52786084 | A | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(4): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-1420T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786084 | |||||||
| chr14:52786171 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-14-1507A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786171 | |||||||
| chr14:52786278 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-14-1614C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786278 | |||||||
| chr14:52786379 | C | G | 1 | a0001c0001t0001g0007 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-14-1715G>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786379 | |||||||
| chr14:52786487 | A | G | 1 | a0001c0001t0003g0003 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-14-1823T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786487 | |||||||
| chr14:52786699 | T | C | 1 | a0001c0001t0015g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-14-2035A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786699 | |||||||
| chr14:52786857 | A | AT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(11): Show |
34 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-14-2194dupA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | A | ATT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(10): Show |
19 | HG00741.hp2 HG01074.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-14-2195_-14-2194d others(4): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | AT | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(13): Show |
40 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-2194delA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTT | A | 6 | a0001c0001t0001g0009 a0001c0001t0005g0010 a0001c0001t0005g0047 others(3): Show |
12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-2198_-14-2194d others(7): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-14-2203_-14-2194d others(12): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(4): Show |
A | 6 | a0001c0001t0002g0018 a0001c0001t0002g0078 a0001c0001t0003g0003 others(3): Show |
7 | HG01243.hp1 HG01496.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-2204_-14-2194d others(13): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(5): Show |
A | 29 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0071 others(26): Show |
57 | HG00639.hp1 HG01081.hp2 HG01433.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-2205_-14-2194d others(14): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(6): Show |
A | 43 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0011 others(40): Show |
107 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-14-2206_-14-2194d others(15): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(7): Show |
A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0032 others(2): Show |
6 | HG00323.hp2 HG01943.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-2207_-14-2194d others(16): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(8): Show |
A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0119 others(2): Show |
5 | HG01255.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-2208_-14-2194d others(17): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52786857 | ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0093 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-14-2209_-14-2194d others(18): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52786857 | |||||||
| chr14:52787298 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-14-2634A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787298 | |||||||
| chr14:52787454 | T | G | 1 | a0001c0001t0002g0022 | 3 | HG02109.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-2790A>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787454 | |||||||
| chr14:52787506 | G | A | 45 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0135 others(42): Show |
123 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-14-2842C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787506 | |||||||
| chr14:52787628 | A | AT | 1 | a0001c0001t0002g0022 | 3 | HG02109.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-2965dupA | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787628 | |||||||
| chr14:52787768 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-14-3104C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787768 | |||||||
| chr14:52787876 | A | G | 1 | a0001c0001t0009g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-14-3212T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787876 | |||||||
| chr14:52787908 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
5 | NA18952.hp1 NA18954.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-3244A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52787908 | |||||||
| chr14:52788007 | T | C | 1 | a0001c0001t0002g0082 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-14-3343A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788007 | |||||||
| chr14:52788180 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-15+3248C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788180 | |||||||
| chr14:52788229 | T | G | 1 | a0001c0001t0003g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-15+3199A>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788229 | |||||||
| chr14:52788232 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0020 others(5): Show |
20 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15+3196A>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788232 | |||||||
| chr14:52788271 | C | G | 7 | a0001c0001t0006g0060 a0001c0001t0006g0088 a0001c0001t0006g0089 others(4): Show |
7 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+3157G>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788271 | |||||||
| chr14:52788274 | C | T | 1 | a0001c0001t0017g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+3154G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788274 | |||||||
| chr14:52788494 | A | C | 1 | a0001c0001t0001g0048 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-15+2934T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788494 | |||||||
| chr14:52788876 | A | T | 52 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0071 others(49): Show |
132 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-15+2552T>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788876 | |||||||
| chr14:52788877 | T | A | 52 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0071 others(49): Show |
132 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-15+2551A>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788877 | |||||||
| chr14:52788938 | C | T | 1 | a0001c0001t0017g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+2490G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788938 | |||||||
| chr14:52788977 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-15+2451A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52788977 | |||||||
| chr14:52789019 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-15+2409C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789019 | |||||||
| chr14:52789090 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-15+2338T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789090 | |||||||
| chr14:52789182 | T | C | 3 | a0001c0001t0009g0058 a0001c0001t0009g0059 a0001c0003t0009g0057 |
3 | HG01433.hp2 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-15+2246A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789182 | |||||||
| chr14:52789265 | G | A | 1 | a0001c0001t0002g0018 | 4 | HG02559.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+2163C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789265 | |||||||
| chr14:52789279 | T | C | 1 | a0001c0001t0006g0091 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-15+2149A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789279 | |||||||
| chr14:52789287 | A | G | 43 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0002g0002 others(40): Show |
121 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-15+2141T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789287 | |||||||
| chr14:52789505 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-15+1923T>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789505 | |||||||
| chr14:52789578 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-15+1850C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789578 | |||||||
| chr14:52789986 | C | CA | 12 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
17 | HG01175.hp2 HG01243.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15+1441dupT | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789986 | |||||||
| chr14:52789986 | CA | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
9 | HG01255.hp2 HG01943.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+1441delT | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789986 | |||||||
| chr14:52789986 | CAAAAA | C | 8 | a0001c0001t0002g0022 a0001c0001t0002g0079 a0001c0001t0002g0080 others(5): Show |
10 | HG01981.hp2 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+1437_-15+1441d others(7): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789986 | |||||||
| chr14:52789986 | CAAAAAA | C | 39 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0087 others(36): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-15+1436_-15+1441d others(8): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789986 | |||||||
| chr14:52789986 | CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0001g0086 a0001c0001t0003g0003 a0001c0001t0003g0006 others(9): Show |
57 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.-15+1434_-15+1441d others(10): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789986 | |||||||
| chr14:52789986 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0004g0013 | 5 | HG00544.hp1 HG00558.hp2 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+1431_-15+1441d others(13): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52789986 | |||||||
| chr14:52790164 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0008 others(13): Show |
61 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.-15+1264A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790164 | |||||||
| chr14:52790289 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-15+1139C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790289 | |||||||
| chr14:52790320 | CCTT | C | 6 | a0001c0001t0005g0010 a0001c0001t0005g0047 a0001c0001t0005g0130 others(3): Show |
12 | HG00544.hp2 HG02015.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+1105_-15+1107d others(5): Show |
GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790320 | |||||||
| chr14:52790371 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0084 a0001c0001t0002g0085 |
6 | HG02074.hp2 NA18939.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+1057A>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790371 | |||||||
| chr14:52790503 | C | T | 44 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0002g0002 others(41): Show |
122 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-15+925G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790503 | |||||||
| chr14:52790504 | C | A | 1 | a0001c0001t0001g0048 | 2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-15+924G>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790504 | |||||||
| chr14:52790551 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15+877C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790551 | |||||||
| chr14:52790766 | A | G | 1 | a0001c0001t0006g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+662T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790766 | |||||||
| chr14:52790797 | C | T | 1 | a0001c0001t0015g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+631G>A | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790797 | |||||||
| chr14:52790897 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-15+531C>T | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52790897 | |||||||
| chr14:52791308 | A | AC | 17 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0008 others(14): Show |
62 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.-15+119dupG | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52791308 | |||||||
| chr14:52791374 | A | G | 1 | a0001c0001t0002g0022 | 3 | HG02109.hp1 HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-15+54T>C | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52791374 | |||||||
| chr14:52791415 | G | C | 1 | a0001c0001t0015g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+13C>G | GNPNAT1 | ENSG00000100522.10 | transcript | ENST00000216410.8 | protein_coding | 1/5 | chr14 | 52791415 |