Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4820 |
| ensemblid | ENSG00000114857.19 |
| hgncid | 7833 |
| symbol | NKTR |
| name | natural killer cell triggering receptor |
| refseq_nuc | NM_005385.4 |
| refseq_prot | NP_005376.2 |
| ensembl_nuc | ENST00000232978.13 |
| ensembl_prot | ENSP00000232978.8 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 42600686 |
| end | 42648735 |
| strand | + |
| ver | v1.2 |
| region | chr3:42600686-42648735 |
| region5000 | chr3:42595686-42653735 |
| regionname0 | NKTR_chr3_42600686_42648735 |
| regionname5000 | NKTR_chr3_42595686_42653735 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1462 | 257 | 48 | 53 | 116 | 10 | 28 | 89 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0002 | 0/0 | 1462 | 37 | 6 | 3 | 25 | 1 | 2 | 21 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0003 | 0/0 | 1462 | 33 | 23 | 5 | 1 | 0 | 4 | 1 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0004 | 0/0 | 1462 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0005 | 0/0 | 1462 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0006 | 0/0 | 1462 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0007 | 0/0 | 1462 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0008 | 0/0 | 1462 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0009 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0010 | 0/0 | 1462 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0011 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0012 | 0/0 | 1462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0013 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0014 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0015 | 0/0 | 1462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| a0016 | 0/0 | 1462 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | MGAQD others(1457): Show |
chr3 | 42595686 | 42653735 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4386 | 249 | 47 | 52 | 111 | 9 | 28 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0001c0007 | 0/0 | 4386 | 3 | 1 | 1 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0001c0008 | 0/0 | 4386 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0001c0012 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0001c0013 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0002c0003 | 0/0 | 4386 | 25 | 1 | 1 | 22 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0002c0004 | 0/0 | 4386 | 12 | 5 | 2 | 3 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0003c0002 | 0/0 | 4386 | 31 | 22 | 4 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0003c0015 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0003c0019 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0004c0005 | 0/0 | 4386 | 6 | 6 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0005c0006 | 0/0 | 4386 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0006c0010 | 0/0 | 4386 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0007c0011 | 0/0 | 4386 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0008c0009 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0009c0020 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0010c0018 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0011c0016 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0012c0023 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0013c0017 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0014c0014 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0015c0022 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 | ||
| a0016c0021 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | ATGGG others(4381): Show |
chr3 | 42595686 | 42653735 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7265 | 83 | 20 | 12 | 41 | 3 | 7 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0002 | 1/1 | 7265 | 55 | 5 | 9 | 28 | 4 | 7 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0003 | 0/0 | 7267 | 58 | 4 | 14 | 35 | 0 | 5 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7262): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0005 | 0/0 | 7269 | 11 | 1 | 7 | 1 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7264): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0007 | 0/0 | 7271 | 8 | 0 | 3 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7266): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0010 | 0/0 | 7265 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0011 | 0/0 | 7265 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0012 | 0/0 | 7265 | 4 | 0 | 4 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0013 | 0/0 | 7259 | 3 | 1 | 1 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7254): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0014 | 0/0 | 7273 | 3 | 0 | 2 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7268): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0017 | 0/0 | 7265 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0018 | 0/0 | 7275 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7270): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0019 | 0/0 | 7265 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0020 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0021 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0023 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0024 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0025 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0026 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0027 | 0/0 | 7271 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7266): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0028 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7274): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0032 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0034 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0001t0036 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0007t0005 | 0/0 | 7269 | 2 | 1 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7264): Show |
chr3 | 42595686 | 42653735 |
| a0001c0007t0018 | 0/0 | 7275 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7270): Show |
chr3 | 42595686 | 42653735 |
| a0001c0008t0015 | 0/0 | 7265 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0012t0002 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0001c0013t0020 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0002c0003t0004 | 0/0 | 7265 | 21 | 1 | 1 | 18 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0002c0003t0029 | 0/0 | 7279 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7274): Show |
chr3 | 42595686 | 42653735 |
| a0002c0003t0030 | 0/0 | 7283 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7278): Show |
chr3 | 42595686 | 42653735 |
| a0002c0003t0033 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0002c0003t0035 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0002c0004t0004 | 0/0 | 7265 | 6 | 0 | 1 | 3 | 1 | 1 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0002c0004t0008 | 0/0 | 7265 | 6 | 5 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0003c0002t0004 | 0/0 | 7265 | 14 | 10 | 4 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0003c0002t0006 | 0/0 | 7265 | 12 | 7 | 0 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0003c0002t0009 | 0/0 | 7265 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0003c0015t0004 | 0/0 | 7265 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0003c0019t0006 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0004c0005t0001 | 0/0 | 7265 | 4 | 4 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0004c0005t0022 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0004c0005t0031 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0005c0006t0001 | 0/0 | 7265 | 5 | 5 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0006c0010t0002 | 0/0 | 7265 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0007c0011t0016 | 0/0 | 7252 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7247): Show |
chr3 | 42595686 | 42653735 |
| a0008c0009t0001 | 0/0 | 7265 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0009c0020t0005 | 0/0 | 7269 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7264): Show |
chr3 | 42595686 | 42653735 |
| a0010c0018t0006 | 0/0 | 7265 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0011c0016t0001 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0012c0023t0004 | 0/0 | 7265 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0013c0017t0001 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0014c0014t0004 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0015c0022t0001 | 0/0 | 7265 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| a0016c0021t0002 | 0/0 | 7265 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | GACGG others(7260): Show |
chr3 | 42595686 | 42653735 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 2 | 1 | 3 | 0 | 2 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0011g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0011g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0011g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0012g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0012g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0013g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0013g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0013g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0014g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0014g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0017g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0017g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0018g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0019g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0020g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0021g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0023g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0024g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0025g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0026g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0027g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0028g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0034g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0001t0036g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0007t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0007t0005g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0007t0018g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0008t0015g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0008t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0008t0015g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0012t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0001c0013t0020g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0029g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0030g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0033g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0003t0035g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0008g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0002c0004t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0006g0004 | 0/0 | 6 | 1 | 0 | 1 | 0 | 4 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0006g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0009g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0002t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0015t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0003c0019t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0004c0005t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0004c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0004c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0004c0005t0022g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0004c0005t0031g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0005c0006t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0005c0006t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0005c0006t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0006c0010t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0007c0011t0016g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0007c0011t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0008c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0008c0009t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0009c0020t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0010c0018t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0011c0016t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0012c0023t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0013c0017t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0014c0014t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0015c0022t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| a0016c0021t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00099 | hp2 | a0001 | c0007 | t0005 | g0167 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | GBR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00280 | hp1 | a0002 | c0004 | t0004 | g0069 | EUR | FIN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0037 | EUR | FIN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00423 | hp2 | a0001 | c0001 | t0028 | g0117 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00558 | hp1 | a0002 | c0003 | t0004 | g0023 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00597 | hp2 | a0002 | c0003 | t0004 | g0024 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00639 | hp2 | a0002 | c0004 | t0008 | g0066 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0213 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00673 | hp1 | a0002 | c0003 | t0030 | g0076 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0201 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG00741 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01081 | hp1 | a0009 | c0020 | t0005 | g0153 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01081 | hp2 | a0006 | c0010 | t0002 | g0039 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01106 | hp1 | a0002 | c0004 | t0004 | g0068 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01109 | hp2 | a0003 | c0015 | t0004 | g0061 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01167 | hp1 | a0003 | c0002 | t0004 | g0020 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01169 | hp1 | a0003 | c0002 | t0004 | g0020 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0187 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01192 | hp1 | a0003 | c0002 | t0004 | g0050 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01243 | hp2 | a0007 | c0011 | t0016 | g0257 | AMR | PUR | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01256 | hp1 | a0001 | c0001 | t0012 | g0031 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01256 | hp2 | a0001 | c0007 | t0018 | g0164 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01346 | hp1 | a0010 | c0018 | t0006 | g0004 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01358 | hp2 | a0001 | c0001 | t0012 | g0001 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0165 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0225 | EUR | IBS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | IBS | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01891 | hp2 | a0003 | c0002 | t0009 | g0021 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01934 | hp2 | a0003 | c0002 | t0004 | g0019 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01943 | hp1 | a0001 | c0001 | t0014 | g0002 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01943 | hp2 | a0001 | c0001 | t0012 | g0031 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01975 | hp1 | a0001 | c0001 | t0014 | g0002 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0241 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02027 | hp2 | a0002 | c0003 | t0004 | g0077 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02040 | hp2 | a0001 | c0013 | t0020 | g0118 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02056 | hp1 | a0011 | c0016 | t0001 | g0016 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02083 | hp2 | a0001 | c0001 | t0020 | g0259 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CDX | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02257 | hp1 | a0002 | c0003 | t0004 | g0073 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02257 | hp2 | a0001 | c0001 | t0013 | g0228 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02258 | hp1 | a0004 | c0005 | t0022 | g0015 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02293 | hp2 | a0006 | c0010 | t0002 | g0039 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02300 | hp1 | a0002 | c0003 | t0004 | g0006 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PEL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02451 | hp1 | a0003 | c0002 | t0006 | g0004 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0195 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02572 | hp2 | a0004 | c0005 | t0031 | g0143 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0229 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02622 | hp1 | a0005 | c0006 | t0001 | g0086 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02622 | hp2 | a0003 | c0002 | t0006 | g0010 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02630 | hp1 | a0003 | c0002 | t0006 | g0060 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0150 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02647 | hp2 | a0004 | c0005 | t0001 | g0015 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0208 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02723 | hp1 | a0003 | c0002 | t0009 | g0058 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02809 | hp1 | a0001 | c0001 | t0019 | g0145 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02818 | hp1 | a0003 | c0002 | t0006 | g0059 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02886 | hp1 | a0004 | c0005 | t0001 | g0131 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0146 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02895 | hp1 | a0005 | c0006 | t0001 | g0087 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02895 | hp2 | a0003 | c0002 | t0004 | g0049 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02896 | hp2 | a0003 | c0002 | t0004 | g0046 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02897 | hp1 | a0005 | c0006 | t0001 | g0012 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02897 | hp2 | a0001 | c0001 | t0027 | g0128 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02922 | hp1 | a0003 | c0002 | t0009 | g0021 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02922 | hp2 | a0005 | c0006 | t0001 | g0012 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02965 | hp2 | a0003 | c0002 | t0004 | g0048 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02976 | hp2 | a0005 | c0006 | t0001 | g0012 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0040 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03041 | hp1 | a0001 | c0001 | t0017 | g0207 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0015 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03130 | hp2 | a0003 | c0002 | t0004 | g0042 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03139 | hp1 | a0002 | c0004 | t0008 | g0063 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03139 | hp2 | a0003 | c0002 | t0004 | g0045 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03195 | hp1 | a0003 | c0002 | t0009 | g0044 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03209 | hp1 | a0001 | c0001 | t0036 | g0151 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0148 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03239 | hp1 | a0003 | c0002 | t0006 | g0004 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03239 | hp2 | a0001 | c0001 | t0014 | g0040 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03453 | hp1 | a0002 | c0004 | t0008 | g0065 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03453 | hp2 | a0003 | c0002 | t0006 | g0010 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03486 | hp1 | a0003 | c0002 | t0006 | g0010 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03490 | hp1 | a0003 | c0002 | t0006 | g0004 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03492 | hp1 | a0003 | c0002 | t0006 | g0004 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03516 | hp1 | a0002 | c0004 | t0008 | g0062 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03516 | hp2 | a0003 | c0002 | t0006 | g0056 | AFR | ESN | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0088 | AFR | GWD | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0089 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03654 | hp2 | a0002 | c0003 | t0004 | g0005 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03688 | hp1 | a0003 | c0002 | t0006 | g0004 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03704 | hp1 | a0002 | c0004 | t0004 | g0070 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03710 | hp1 | a0001 | c0001 | t0032 | g0001 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03710 | hp2 | a0001 | c0001 | t0026 | g0161 | SAS | PJL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG04199 | hp2 | a0001 | c0001 | t0018 | g0244 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0223 | SAS | STU | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18906 | hp1 | a0002 | c0004 | t0008 | g0064 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18906 | hp2 | a0001 | c0001 | t0019 | g0147 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18941 | hp1 | a0002 | c0004 | t0004 | g0022 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18949 | hp2 | a0001 | c0001 | t0023 | g0159 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18954 | hp1 | a0002 | c0004 | t0004 | g0022 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18960 | hp2 | a0002 | c0003 | t0004 | g0080 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18961 | hp2 | a0008 | c0009 | t0001 | g0003 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18963 | hp2 | a0002 | c0004 | t0004 | g0072 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18964 | hp1 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18964 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18965 | hp1 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18965 | hp2 | a0008 | c0009 | t0001 | g0096 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18966 | hp2 | a0002 | c0003 | t0004 | g0079 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18967 | hp2 | a0001 | c0001 | t0034 | g0246 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18969 | hp1 | a0001 | c0008 | t0015 | g0262 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18971 | hp1 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18978 | hp2 | a0002 | c0003 | t0004 | g0074 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18982 | hp2 | a0003 | c0002 | t0006 | g0004 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18983 | hp1 | a0002 | c0003 | t0004 | g0011 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18985 | hp2 | a0002 | c0003 | t0029 | g0078 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18994 | hp1 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18997 | hp1 | a0013 | c0017 | t0001 | g0016 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19011 | hp1 | a0002 | c0003 | t0004 | g0075 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19030 | hp1 | a0003 | c0002 | t0004 | g0051 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19030 | hp2 | a0002 | c0004 | t0008 | g0067 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19043 | hp1 | a0003 | c0002 | t0004 | g0055 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0002 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19057 | hp2 | a0002 | c0003 | t0004 | g0024 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19059 | hp1 | a0014 | c0014 | t0004 | g0071 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19059 | hp2 | a0001 | c0001 | t0021 | g0260 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19062 | hp1 | a0002 | c0003 | t0033 | g0006 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19072 | hp1 | a0002 | c0003 | t0004 | g0081 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19075 | hp1 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19076 | hp1 | a0001 | c0008 | t0015 | g0264 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19077 | hp2 | a0002 | c0003 | t0004 | g0023 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19079 | hp1 | a0002 | c0003 | t0035 | g0006 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19080 | hp1 | a0001 | c0008 | t0015 | g0263 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19080 | hp2 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19089 | hp2 | a0002 | c0003 | t0004 | g0006 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19090 | hp1 | a0002 | c0003 | t0004 | g0005 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19090 | hp2 | a0015 | c0022 | t0001 | g0103 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19240 | hp1 | a0003 | c0019 | t0006 | g0057 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0133 | AFR | YRI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20129 | hp1 | a0003 | c0002 | t0004 | g0019 | AFR | ASW | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20129 | hp2 | a0003 | c0002 | t0004 | g0047 | AFR | ASW | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20752 | hp1 | a0016 | c0021 | t0002 | g0181 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | TSI | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | GIH | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02109 | hp1 | a0001 | c0007 | t0005 | g0156 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0149 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03471 | hp1 | a0007 | c0011 | t0016 | g0258 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG03471 | hp2 | a0012 | c0023 | t0004 | g0054 | AFR | MSL | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA18955 | hp2 | a0001 | c0012 | t0002 | g0210 | EAS | JPT | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20300 | hp1 | a0003 | c0002 | t0009 | g0053 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA20300 | hp2 | a0001 | c0001 | t0025 | g0013 | AFR | USA | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| NA21309 | hp2 | a0003 | c0002 | t0004 | g0052 | AFR | LWK | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0211 | REF | REF | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0198 | REF | REF | NKTR_chr3_42595686_42653735 | NKTR | chr3 | 42595686 | 42653735 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42619708 | G | A | 1 | a0014 | 1 | NA19059.hp1 | missense_variant&splice_region_variant | MODERATE | c.286G>A | p.Asp96Asn | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/17 | 402/7265 | 286/4389 | 96/1462 | chr3 | 42619708 | |||
| chr3:42633618 | T | G | 1 | a0004 | 6 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
missense_variant | MODERATE | c.812T>G | p.Val271Gly | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/17 | 928/7265 | 812/4389 | 271/1462 | chr3 | 42633618 | |||
| chr3:42633713 | G | T | 1 | a0012 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.907G>T | p.Val303Phe | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/17 | 1023/7265 | 907/4389 | 303/1462 | chr3 | 42633713 | |||
| chr3:42634648 | A | G | 1 | a0015 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.965A>G | p.Gln322Arg | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/17 | 1081/7265 | 965/4389 | 322/1462 | chr3 | 42634648 | |||
| chr3:42637454 | C | T | 1 | a0005 | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.1750C>T | p.Pro584Ser | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 1866/7265 | 1750/4389 | 584/1462 | chr3 | 42637454 | |||
| chr3:42637658 | T | G | 1 | a0011 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.1954T>G | p.Leu652Val | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2070/7265 | 1954/4389 | 652/1462 | chr3 | 42637658 | |||
| chr3:42637686 | C | T | 1 | a0016 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1982C>T | p.Ser661Leu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2098/7265 | 1982/4389 | 661/1462 | chr3 | 42637686 | |||
| chr3:42637994 | A | G | 1 | a0009 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2290A>G | p.Lys764Glu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2406/7265 | 2290/4389 | 764/1462 | chr3 | 42637994 | |||
| chr3:42638006 | G | A | 1 | a0010 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2302G>A | p.Val768Ile | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2418/7265 | 2302/4389 | 768/1462 | chr3 | 42638006 | |||
| chr3:42638184 | A | C | 1 | a0013 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.2480A>C | p.Lys827Thr | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2596/7265 | 2480/4389 | 827/1462 | chr3 | 42638184 | |||
| chr3:42638185 | G | C | 1 | a0013 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.2481G>C | p.Lys827Asn | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2597/7265 | 2481/4389 | 827/1462 | chr3 | 42638185 | |||
| chr3:42638285 | T | G | 6 | a0002 a0003 a0007 others(3): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
missense_variant | MODERATE | c.2581T>G | p.Leu861Val | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2697/7265 | 2581/4389 | 861/1462 | chr3 | 42638285 | |||
| chr3:42638508 | C | T | 3 | a0002 a0006 a0014 |
40 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.2804C>T | p.Ser935Leu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2920/7265 | 2804/4389 | 935/1462 | chr3 | 42638508 | |||
| chr3:42638541 | G | C | 1 | a0007 | 2 | HG01243.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.2837G>C | p.Gly946Ala | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2953/7265 | 2837/4389 | 946/1462 | chr3 | 42638541 | |||
| chr3:42638979 | C | G | 1 | a0008 | 2 | NA18961.hp2 NA18965.hp2 |
missense_variant | MODERATE | c.3275C>G | p.Ser1092Cys | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 3391/7265 | 3275/4389 | 1092/1462 | chr3 | 42638979 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42617589 | G | A | 1 | a0001c0012 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.78G>A | p.Gln26Gln | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/17 | 194/7265 | 78/4389 | 26/1462 | chr3 | 42617589 | |||
| chr3:42617637 | G | A | 1 | a0001c0013 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.126G>A | p.Leu42Leu | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/17 | 242/7265 | 126/4389 | 42/1462 | chr3 | 42617637 | |||
| chr3:42619075 | G | A | 1 | a0001c0007 | 3 | HG00099.hp2 HG01256.hp2 HG02109.hp1 |
synonymous_variant | LOW | c.189G>A | p.Thr63Thr | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/17 | 305/7265 | 189/4389 | 63/1462 | chr3 | 42619075 | |||
| chr3:42632602 | T | C | 1 | a0003c0015 | 1 | HG01109.hp2 | splice_region_variant&synonymous_variant | LOW | c.552T>C | p.Val184Val | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/17 | 668/7265 | 552/4389 | 184/1462 | chr3 | 42632602 | |||
| chr3:42637918 | T | C | 1 | a0013c0017 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.2214T>C | p.Cys738Cys | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2330/7265 | 2214/4389 | 738/1462 | chr3 | 42637918 | |||
| chr3:42638005 | C | T | 10 | a0001c0008 a0002c0003 a0002c0004 others(7): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
synonymous_variant | LOW | c.2301C>T | p.Ser767Ser | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2417/7265 | 2301/4389 | 767/1462 | chr3 | 42638005 | |||
| chr3:42638053 | T | C | 1 | a0003c0019 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.2349T>C | p.Ser783Ser | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2465/7265 | 2349/4389 | 783/1462 | chr3 | 42638053 | |||
| chr3:42638201 | A | C | 1 | a0013c0017 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.2497A>C | p.Arg833Arg | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2613/7265 | 2497/4389 | 833/1462 | chr3 | 42638201 | |||
| chr3:42638356 | A | G | 2 | a0002c0003 a0014c0014 |
26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
synonymous_variant | LOW | c.2652A>G | p.Lys884Lys | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 2768/7265 | 2652/4389 | 884/1462 | chr3 | 42638356 | |||
| chr3:42639034 | C | T | 1 | a0001c0008 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.3330C>T | p.His1110His | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 3446/7265 | 3330/4389 | 1110/1462 | chr3 | 42639034 | |||
| chr3:42639610 | G | A | 1 | a0001c0008 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.3906G>A | p.Thr1302Thr | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/17 | 4022/7265 | 3906/4389 | 1302/1462 | chr3 | 42639610 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42600774 | G | C | 1 | a0001c0001t0021 | 1 | NA19059.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/17 | 233 | chr3 | 42600774 | ||||||
| chr3:42600775 | C | G | 2 | a0001c0001t0021 a0001c0001t0036 |
2 | HG03209.hp1 NA19059.hp2 |
5_prime_UTR_variant | MODIFIER | c.-27C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/17 | 232 | chr3 | 42600775 | ||||||
| chr3:42646131 | G | T | 1 | a0002c0003t0035 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 156 | chr3 | 42646131 | ||||||
| chr3:42646229 | C | T | 1 | a0001c0001t0012 | 4 | HG00741.hp2 HG01256.hp1 HG01358.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*254C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 254 | chr3 | 42646229 | ||||||
| chr3:42646368 | G | C | 1 | a0004c0005t0022 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 393 | chr3 | 42646368 | ||||||
| chr3:42646415 | T | C | 1 | a0001c0001t0023 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 440 | chr3 | 42646415 | ||||||
| chr3:42646449 | A | C | 1 | a0001c0001t0034 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 474 | chr3 | 42646449 | ||||||
| chr3:42646745 | C | T | 2 | a0001c0001t0020 a0001c0013t0020 |
2 | HG02040.hp2 HG02083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*770C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 770 | chr3 | 42646745 | ||||||
| chr3:42646830 | T | G | 1 | a0007c0011t0016 | 2 | HG01243.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*855T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 855 | chr3 | 42646830 | ||||||
| chr3:42647086 | C | G | 1 | a0003c0002t0009 | 5 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1111 | chr3 | 42647086 | ||||||
| chr3:42647241 | C | G | 1 | a0007c0011t0016 | 2 | HG01243.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1266C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1266 | chr3 | 42647241 | ||||||
| chr3:42647267 | A | AGT | 1 | a0001c0001t0003 | 58 | HG00544.hp2 HG00621.hp2 HG00639.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1326_*1327dupTG | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | |||||
| chr3:42647267 | A | AGTGT | 3 | a0001c0001t0005 a0001c0007t0005 a0009c0020t0005 |
14 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1324_*1327dupTGTG | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | |||||
| chr3:42647267 | A | AGTGTGT | 2 | a0001c0001t0007 a0001c0001t0027 |
9 | HG00642.hp1 HG01361.hp2 HG02300.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1322_*1327dupTGTG others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | |||||
| chr3:42647267 | A | AGTGTGTG others(1): Show |
1 | a0001c0001t0014 | 3 | HG01943.hp1 HG01975.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1320_*1327dupTGTG others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | |||||
| chr3:42647267 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0018 a0001c0007t0018 |
2 | HG01256.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1318_*1327dupTGTG others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | |||||
| chr3:42647267 | AGTGTGT | A | 1 | a0001c0001t0013 | 3 | HG00280.hp2 HG01169.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1322_*1327delTGTG others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1322 | INFO_REALIGN_3_PRIME | chr3 | 42647267 | |||||
| chr3:42647288 | GTGTGTGT others(6): Show |
G | 1 | a0007c0011t0016 | 2 | HG01243.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1314_*1326delTGTG others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1314 | chr3 | 42647288 | ||||||
| chr3:42647301 | T | TGTGTG | 2 | a0001c0001t0001 a0002c0003t0004 |
8 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(1): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG | 3 | a0001c0001t0001 a0003c0002t0004 a0003c0015t0004 |
10 | HG01109.hp2 HG02559.hp1 HG02723.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(2): Show |
8 | a0001c0001t0001 a0002c0003t0004 a0003c0002t0004 others(5): Show |
16 | HG00544.hp1 HG01192.hp1 HG01891.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(4): Show |
13 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(10): Show |
72 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(7): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(6): Show |
14 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0020 others(11): Show |
42 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(8): Show |
7 | a0001c0001t0001 a0002c0003t0004 a0002c0003t0033 others(4): Show |
15 | HG00741.hp1 HG01257.hp1 HG02300.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(10): Show |
5 | a0001c0001t0001 a0001c0001t0011 a0002c0003t0004 others(2): Show |
9 | HG01106.hp1 HG01123.hp1 HG02040.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(11): Show |
1 | a0002c0003t0004 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(12): Show |
2 | a0002c0003t0004 a0014c0014t0004 |
3 | NA18966.hp2 NA19059.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(14): Show |
2 | a0001c0001t0032 a0002c0003t0004 |
2 | HG00597.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647301 | T | TGTGTGTG others(18): Show |
1 | a0002c0003t0004 | 2 | NA18965.hp1 NA19011.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(21): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | INFO_REALIGN_3_PRIME | chr3 | 42647301 | |||||
| chr3:42647302 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0028 a0002c0003t0029 |
2 | HG00423.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | chr3 | 42647302 | ||||||
| chr3:42647302 | G | GTGTGTGT others(11): Show |
1 | a0002c0003t0030 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1327_*1328insTGTG others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | chr3 | 42647302 | ||||||
| chr3:42647303 | G | T | 34 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(31): Show |
192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1328 | chr3 | 42647303 | ||||||
| chr3:42647304 | T | G | 1 | a0001c0001t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1329T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1329 | chr3 | 42647304 | ||||||
| chr3:42647496 | C | T | 1 | a0001c0001t0026 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1521C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1521 | chr3 | 42647496 | ||||||
| chr3:42647617 | G | T | 15 | a0002c0003t0004 a0002c0003t0029 a0002c0003t0030 others(12): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1642G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1642 | chr3 | 42647617 | ||||||
| chr3:42647733 | T | C | 1 | a0001c0001t0011 | 4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1758T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1758 | chr3 | 42647733 | ||||||
| chr3:42647736 | A | C | 1 | a0001c0001t0010 | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1761A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1761 | chr3 | 42647736 | ||||||
| chr3:42647770 | T | C | 1 | a0001c0008t0015 | 3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1795T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1795 | chr3 | 42647770 | ||||||
| chr3:42647789 | C | T | 1 | a0001c0001t0019 | 2 | HG02809.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1814C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 1814 | chr3 | 42647789 | ||||||
| chr3:42648017 | T | C | 3 | a0003c0002t0006 a0003c0019t0006 a0010c0018t0006 |
14 | HG01346.hp1 HG02451.hp1 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2042T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2042 | chr3 | 42648017 | ||||||
| chr3:42648022 | T | A | 1 | a0001c0001t0019 | 2 | HG02809.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2047T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2047 | chr3 | 42648022 | ||||||
| chr3:42648084 | T | C | 1 | a0001c0001t0010 | 4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2109T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2109 | chr3 | 42648084 | ||||||
| chr3:42648212 | G | A | 2 | a0004c0005t0022 a0004c0005t0031 |
2 | HG02258.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2237G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2237 | chr3 | 42648212 | ||||||
| chr3:42648236 | T | C | 1 | a0001c0001t0017 | 2 | HG02451.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2261T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2261 | chr3 | 42648236 | ||||||
| chr3:42648285 | T | G | 37 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0011 others(34): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2310T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2310 | chr3 | 42648285 | ||||||
| chr3:42648289 | A | G | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2314A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2314 | chr3 | 42648289 | ||||||
| chr3:42648302 | A | G | 1 | a0002c0003t0033 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2327A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2327 | chr3 | 42648302 | ||||||
| chr3:42648460 | C | G | 1 | a0002c0004t0008 | 6 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2485C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 17/17 | 2485 | chr3 | 42648460 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:42600853 | G | A | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24+75G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/16 | chr3 | 42600853 | |||||||
| chr3:42600873 | G | C | 1 | a0001c0001t0002g0043 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-24+95G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 1/16 | chr3 | 42600873 | |||||||
| chr3:42601121 | G | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+57G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601121 | |||||||
| chr3:42601142 | T | TC | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+83dupC | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42601142 | ||||||
| chr3:42601228 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.58+164C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601228 | |||||||
| chr3:42601253 | C | G | 1 | a0001c0001t0021g0260 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.58+189C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601253 | |||||||
| chr3:42601254 | G | C | 1 | a0001c0001t0021g0260 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.58+190G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601254 | |||||||
| chr3:42601322 | C | T | 1 | a0001c0001t0020g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.58+258C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601322 | |||||||
| chr3:42601465 | C | A | 1 | a0001c0001t0021g0260 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.58+401C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601465 | |||||||
| chr3:42601485 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.58+421T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601485 | |||||||
| chr3:42601579 | A | G | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+515A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601579 | |||||||
| chr3:42601763 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+699C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601763 | |||||||
| chr3:42601892 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.58+828G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601892 | |||||||
| chr3:42601922 | G | A | 1 | a0003c0002t0009g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58+858G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601922 | |||||||
| chr3:42601933 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(141): Show |
191 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.58+869G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42601933 | |||||||
| chr3:42602108 | G | A | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+1044G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602108 | |||||||
| chr3:42602204 | G | A | 25 | a0003c0002t0004g0019 a0003c0002t0004g0020 a0003c0002t0004g0042 others(22): Show |
35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.58+1140G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602204 | |||||||
| chr3:42602239 | G | A | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1175G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602239 | |||||||
| chr3:42602246 | G | C | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+1182G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602246 | |||||||
| chr3:42602321 | G | C | 1 | a0001c0001t0002g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.58+1257G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602321 | |||||||
| chr3:42602338 | G | T | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.58+1274G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602338 | |||||||
| chr3:42602353 | C | A | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1289C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602353 | |||||||
| chr3:42602443 | G | A | 2 | a0003c0002t0006g0004 a0010c0018t0006g0004 |
7 | HG01346.hp1 HG02451.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1379G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602443 | |||||||
| chr3:42602524 | CAG | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(86): Show |
116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.58+1461_58+1462del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602524 | |||||||
| chr3:42602609 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0084 |
3 | HG01496.hp1 HG02145.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.58+1545G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602609 | |||||||
| chr3:42602628 | CTTT | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(92): Show |
122 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.58+1580_58+1582del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42602628 | ||||||
| chr3:42602628 | CTTTT | C | 52 | a0001c0001t0001g0085 a0002c0003t0004g0005 a0002c0003t0004g0006 others(49): Show |
72 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.58+1579_58+1582del others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42602628 | ||||||
| chr3:42602659 | C | T | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+1595C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602659 | |||||||
| chr3:42602755 | C | T | 1 | a0002c0003t0004g0079 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.58+1691C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602755 | |||||||
| chr3:42602786 | C | T | 1 | a0004c0005t0031g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.58+1722C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602786 | |||||||
| chr3:42602841 | AC | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0152 others(1): Show |
6 | HG01243.hp1 HG02486.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+1781delC | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42602841 | ||||||
| chr3:42602885 | C | T | 1 | a0001c0001t0003g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.58+1821C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602885 | |||||||
| chr3:42602903 | G | A | 8 | a0003c0002t0004g0019 a0003c0002t0004g0045 a0003c0002t0004g0046 others(5): Show |
9 | HG01192.hp1 HG01934.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+1839G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602903 | |||||||
| chr3:42602912 | G | A | 1 | a0003c0002t0004g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58+1848G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602912 | |||||||
| chr3:42602932 | T | C | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1868T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42602932 | |||||||
| chr3:42603025 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(83): Show |
112 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.58+1976dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603025 | ||||||
| chr3:42603195 | G | GTC | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+2133_58+2134dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603195 | ||||||
| chr3:42603224 | G | A | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58+2160G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603224 | |||||||
| chr3:42603289 | G | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(79): Show |
107 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.58+2225G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603289 | |||||||
| chr3:42603340 | A | G | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2276A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603340 | |||||||
| chr3:42603360 | T | TA | 29 | a0001c0001t0002g0166 a0001c0001t0002g0170 a0001c0001t0002g0174 others(26): Show |
36 | HG00099.hp2 HG00673.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.58+2321dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | ||||||
| chr3:42603360 | T | TAA | 6 | a0001c0001t0003g0034 a0001c0001t0003g0155 a0001c0001t0003g0157 others(3): Show |
7 | HG00639.hp1 HG02109.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+2320_58+2321dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | ||||||
| chr3:42603360 | TAAAAAAA others(1): Show |
T | 7 | a0001c0008t0015g0263 a0001c0008t0015g0264 a0002c0004t0008g0063 others(4): Show |
7 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+2314_58+2321del others(8): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | ||||||
| chr3:42603360 | TAAAAAAA others(2): Show |
T | 29 | a0002c0004t0004g0022 a0002c0004t0004g0068 a0002c0004t0004g0069 others(26): Show |
40 | HG00280.hp1 HG01106.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.58+2313_58+2321del others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | ||||||
| chr3:42603360 | TAAAAAAA others(3): Show |
T | 18 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(15): Show |
27 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.58+2312_58+2321del others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | ||||||
| chr3:42603360 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0003g0252 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58+2307_58+2321del others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603360 | ||||||
| chr3:42603373 | A | AC | 3 | a0001c0001t0001g0091 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02145.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+2309_58+2310ins others(1): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603373 | |||||||
| chr3:42603374 | A | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(74): Show |
101 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.58+2310A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603374 | |||||||
| chr3:42603457 | A | G | 4 | a0001c0001t0002g0041 a0001c0001t0002g0174 a0001c0001t0002g0250 others(1): Show |
5 | HG00423.hp1 NA18944.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2393A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603457 | |||||||
| chr3:42603651 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.58+2587G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603651 | |||||||
| chr3:42603732 | C | CT | 22 | a0001c0001t0002g0082 a0001c0001t0002g0242 a0001c0001t0002g0245 others(19): Show |
23 | HG00673.hp1 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.58+2689dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603732 | ||||||
| chr3:42603732 | CT | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(104): Show |
142 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.58+2689delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42603732 | ||||||
| chr3:42603804 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.58+2740C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603804 | |||||||
| chr3:42603881 | A | G | 1 | a0002c0003t0029g0078 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.58+2817A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603881 | |||||||
| chr3:42603976 | A | T | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2912A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603976 | |||||||
| chr3:42603980 | G | A | 25 | a0003c0002t0004g0019 a0003c0002t0004g0020 a0003c0002t0004g0042 others(22): Show |
35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.58+2916G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603980 | |||||||
| chr3:42603988 | C | T | 25 | a0003c0002t0004g0019 a0003c0002t0004g0020 a0003c0002t0004g0042 others(22): Show |
35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.58+2924C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42603988 | |||||||
| chr3:42604205 | C | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+3141C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604205 | |||||||
| chr3:42604379 | CT | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(57): Show |
80 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.58+3325delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604379 | ||||||
| chr3:42604386 | T | C | 3 | a0001c0001t0011g0026 a0001c0001t0011g0088 a0001c0001t0011g0089 |
4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3322T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604386 | |||||||
| chr3:42604446 | A | G | 1 | a0001c0001t0019g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.58+3382A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604446 | |||||||
| chr3:42604541 | G | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0152 |
3 | HG01243.hp1 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58+3477G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604541 | |||||||
| chr3:42604659 | C | CT | 26 | a0001c0001t0001g0255 a0001c0001t0002g0037 a0001c0001t0002g0041 others(23): Show |
31 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+3634dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTT | 19 | a0001c0001t0001g0256 a0001c0001t0002g0032 a0001c0001t0002g0170 others(16): Show |
20 | HG00140.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.58+3633_58+3634dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTT | 11 | a0001c0001t0001g0136 a0001c0001t0002g0227 a0001c0001t0002g0247 others(8): Show |
12 | HG00423.hp1 HG01981.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+3632_58+3634dup others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTT | 6 | a0001c0001t0001g0137 a0001c0001t0002g0230 a0001c0001t0002g0261 others(3): Show |
6 | HG03486.hp2 HG03540.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3631_58+3634dup others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT | 5 | a0001c0001t0002g0033 a0001c0001t0002g0232 a0001c0001t0002g0233 others(2): Show |
6 | HG03225.hp2 HG06807.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+3628_58+3634dup others(7): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58+3625_58+3634dup others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0003g0235 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.58+3624_58+3634dup others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.58+3623_58+3634dup others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0005g0236 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.58+3622_58+3634dup others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(7): Show |
1 | a0007c0011t0016g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58+3621_58+3634dup others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0237 a0001c0001t0011g0089 |
2 | HG03579.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.58+3620_58+3634dup others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0003g0249 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.58+3616_58+3634dup others(19): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(13): Show |
1 | a0007c0011t0016g0258 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58+3615_58+3634dup others(20): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0003g0238 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.58+3613_58+3634dup others(22): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CT | C | 9 | a0001c0001t0002g0144 a0001c0001t0002g0182 a0001c0001t0002g0183 others(6): Show |
9 | HG01099.hp2 HG01192.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3634delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTT | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0130 a0001c0001t0001g0132 others(3): Show |
8 | HG01074.hp2 HG01167.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3633_58+3634del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0129 a0001c0001t0019g0145 a0001c0001t0027g0128 others(3): Show |
6 | HG01109.hp2 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+3626_58+3634del others(9): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0127 a0002c0003t0004g0024 a0002c0003t0004g0074 others(17): Show |
30 | HG00597.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.58+3625_58+3634del others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(4): Show |
C | 22 | a0001c0001t0003g0155 a0001c0001t0003g0160 a0002c0003t0004g0005 others(19): Show |
31 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+3624_58+3634del others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(5): Show |
C | 14 | a0001c0001t0002g0179 a0002c0004t0004g0022 a0002c0004t0004g0072 others(11): Show |
17 | HG00639.hp2 HG02895.hp1 HG02897.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+3623_58+3634del others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(6): Show |
C | 1 | a0005c0006t0001g0086 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58+3622_58+3634del others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(7): Show |
C | 7 | a0001c0001t0001g0091 a0001c0001t0002g0178 a0001c0001t0010g0146 others(4): Show |
8 | HG02109.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+3621_58+3634del others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0125 a0001c0001t0025g0013 |
4 | HG01891.hp1 HG02976.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3619_58+3634del others(16): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
8 | HG01981.hp1 HG02015.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+3618_58+3634del others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(11): Show |
C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(51): Show |
73 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+3617_58+3634del others(18): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604659 | CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0005g0175 |
3 | HG02965.hp1 NA18612.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.58+3616_58+3634del others(19): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42604659 | ||||||
| chr3:42604941 | C | T | 1 | a0001c0001t0010g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.58+3877C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604941 | |||||||
| chr3:42604985 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58+3921C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42604985 | |||||||
| chr3:42605075 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0130 |
4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+4011T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605075 | |||||||
| chr3:42605115 | T | C | 2 | a0002c0003t0004g0073 a0002c0003t0004g0081 |
2 | HG02257.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.58+4051T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605115 | |||||||
| chr3:42605229 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.58+4165C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605229 | |||||||
| chr3:42605355 | G | C | 1 | a0003c0002t0004g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.58+4291G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605355 | |||||||
| chr3:42605419 | A | G | 1 | a0002c0004t0004g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+4355A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605419 | |||||||
| chr3:42605576 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.58+4512C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605576 | |||||||
| chr3:42605623 | T | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02145.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+4559T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605623 | |||||||
| chr3:42605660 | G | T | 1 | a0012c0023t0004g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.58+4596G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605660 | |||||||
| chr3:42605706 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.58+4642C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605706 | |||||||
| chr3:42605707 | C | T | 1 | a0001c0008t0015g0262 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.58+4643C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605707 | |||||||
| chr3:42605853 | A | G | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+4789A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605853 | |||||||
| chr3:42605895 | A | G | 2 | a0001c0001t0019g0145 a0001c0001t0019g0147 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58+4831A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42605895 | |||||||
| chr3:42606160 | G | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0134 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+5096G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606160 | |||||||
| chr3:42606179 | A | G | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+5115A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606179 | |||||||
| chr3:42606188 | A | G | 1 | a0002c0004t0008g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58+5124A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606188 | |||||||
| chr3:42606247 | T | TC | 6 | a0001c0001t0001g0120 a0001c0001t0002g0212 a0001c0001t0002g0232 others(3): Show |
11 | HG01346.hp1 HG02451.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+5190dupC | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42606247 | ||||||
| chr3:42606277 | T | C | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+5213T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606277 | |||||||
| chr3:42606286 | T | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0030 others(16): Show |
26 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.58+5222T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606286 | |||||||
| chr3:42606508 | A | G | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5444A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606508 | |||||||
| chr3:42606527 | G | A | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.58+5463G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606527 | |||||||
| chr3:42606867 | G | A | 1 | a0001c0001t0005g0243 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.58+5803G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606867 | |||||||
| chr3:42606868 | CT | C | 6 | a0001c0001t0001g0132 a0004c0005t0001g0015 a0004c0005t0001g0131 others(3): Show |
7 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+5813delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42606868 | ||||||
| chr3:42606886 | A | G | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+5822A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42606886 | |||||||
| chr3:42607051 | ATTAG | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(81): Show |
109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.58+5992_58+5995del others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607051 | ||||||
| chr3:42607109 | C | A | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+6045C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607109 | |||||||
| chr3:42607239 | G | A | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+6175G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607239 | |||||||
| chr3:42607270 | A | G | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.58+6206A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607270 | |||||||
| chr3:42607546 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58+6482G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607546 | |||||||
| chr3:42607658 | T | C | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+6594T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607658 | |||||||
| chr3:42607819 | A | T | 1 | a0001c0001t0002g0186 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.58+6755A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607819 | |||||||
| chr3:42607908 | G | A | 1 | a0002c0004t0004g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58+6844G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42607908 | |||||||
| chr3:42607967 | CTCTTTTT others(19): Show |
C | 2 | a0001c0001t0019g0145 a0001c0001t0019g0147 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58+6905_58+6930del others(26): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607967 | ||||||
| chr3:42607969 | C | CT | 12 | a0001c0001t0002g0186 a0001c0001t0002g0206 a0001c0001t0002g0221 others(9): Show |
12 | HG01069.hp1 HG02109.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.58+6948dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTT | 8 | a0001c0001t0002g0166 a0001c0001t0002g0199 a0001c0001t0002g0205 others(5): Show |
8 | HG01109.hp1 HG01981.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+6944_58+6948dup others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTTT | 13 | a0001c0001t0002g0082 a0001c0001t0002g0144 a0001c0001t0002g0182 others(10): Show |
13 | HG00423.hp1 HG00673.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.58+6943_58+6948dup others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTTTT | 8 | a0001c0001t0002g0204 a0001c0001t0002g0261 a0001c0001t0003g0002 others(5): Show |
8 | HG00621.hp2 HG00639.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+6942_58+6948dup others(7): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0017g0195 a0001c0001t0017g0207 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.58+6939_58+6948dup others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0238 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.58+6937_58+6948dup others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0008 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.58+6936_58+6948dup others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0196 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+6929_58+6948dup others(20): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CT | C | 25 | a0001c0001t0002g0018 a0001c0001t0002g0170 a0001c0001t0002g0180 others(22): Show |
26 | HG00140.hp2 HG01081.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.58+6948delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTT | C | 10 | a0001c0001t0002g0032 a0001c0001t0002g0037 a0001c0001t0002g0043 others(7): Show |
10 | HG00099.hp1 HG01361.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+6947_58+6948del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTT | C | 8 | a0001c0001t0002g0018 a0001c0001t0002g0032 a0001c0001t0002g0033 others(5): Show |
8 | HG00280.hp2 HG01243.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+6946_58+6948del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0007g0165 a0001c0001t0007g0213 a0001c0001t0013g0187 |
3 | HG00642.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.58+6939_58+6948del others(10): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0007g0040 a0001c0001t0014g0040 |
2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.58+6938_58+6948del others(11): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0003g0241 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.58+6937_58+6948del others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0010g0150 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+6936_58+6948del others(13): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0010g0146 a0001c0001t0010g0149 a0007c0011t0016g0257 others(2): Show |
5 | HG01243.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+6935_58+6948del others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(8): Show |
C | 13 | a0001c0001t0003g0173 a0001c0001t0003g0226 a0001c0001t0003g0235 others(10): Show |
17 | HG00558.hp1 HG00597.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.58+6934_58+6948del others(15): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(9): Show |
C | 50 | a0001c0001t0005g0009 a0001c0001t0007g0002 a0001c0001t0014g0002 others(47): Show |
64 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.58+6933_58+6948del others(16): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(10): Show |
C | 6 | a0001c0001t0003g0009 a0001c0001t0005g0236 a0001c0001t0014g0002 others(3): Show |
6 | HG01167.hp1 HG01433.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+6932_58+6948del others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0003g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.58+6931_58+6948del others(18): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(12): Show |
C | 4 | a0001c0001t0003g0176 a0001c0008t0015g0262 a0001c0008t0015g0263 others(1): Show |
4 | NA18969.hp1 NA19076.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+6930_58+6948del others(19): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0003g0007 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.58+6929_58+6948del others(20): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0002g0178 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.58+6927_58+6948del others(22): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0011g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.58+6926_58+6948del others(23): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(22): Show |
C | 2 | a0001c0001t0011g0088 a0001c0001t0011g0089 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58+6920_58+6948del others(29): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(23): Show |
C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0095 others(6): Show |
13 | HG00544.hp1 HG01123.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.58+6919_58+6948del others(30): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42607969 | CTTTTTTT others(24): Show |
C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(67): Show |
89 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.58+6918_58+6948del others(31): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42607969 | ||||||
| chr3:42608075 | C | T | 4 | a0003c0002t0009g0021 a0003c0002t0009g0044 a0003c0002t0009g0053 others(1): Show |
5 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+7011C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608075 | |||||||
| chr3:42608076 | G | A | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.58+7012G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608076 | |||||||
| chr3:42608082 | C | T | 1 | a0003c0002t0004g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58+7018C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608082 | |||||||
| chr3:42608107 | A | G | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.58+7043A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608107 | |||||||
| chr3:42608112 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.58+7048C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608112 | |||||||
| chr3:42608249 | C | T | 1 | a0001c0012t0002g0210 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.58+7185C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608249 | |||||||
| chr3:42608319 | A | G | 1 | a0001c0001t0005g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.58+7255A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608319 | |||||||
| chr3:42608439 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0011g0088 a0001c0001t0011g0089 |
4 | HG02572.hp1 HG02647.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+7375G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608439 | |||||||
| chr3:42608463 | G | A | 4 | a0001c0001t0005g0214 a0001c0001t0007g0165 a0001c0001t0007g0213 others(1): Show |
4 | HG00642.hp1 HG01169.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+7399G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608463 | |||||||
| chr3:42608557 | T | A | 1 | a0001c0001t0002g0250 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.58+7493T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608557 | |||||||
| chr3:42608610 | G | A | 1 | a0003c0002t0006g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+7546G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608610 | |||||||
| chr3:42608901 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(142): Show |
192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.58+7837A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42608901 | |||||||
| chr3:42609058 | G | A | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.58+7994G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609058 | |||||||
| chr3:42609128 | C | CA | 11 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0002g0032 others(8): Show |
14 | HG01243.hp1 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.58+8077dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609128 | ||||||
| chr3:42609139 | A | AAAG | 38 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(35): Show |
48 | HG00280.hp1 HG00639.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.58+8081_58+8083dup others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609139 | ||||||
| chr3:42609139 | A | AGAAG | 17 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(14): Show |
26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.58+8075_58+8076ins others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609139 | |||||||
| chr3:42609155 | A | C | 1 | a0001c0001t0003g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.58+8091A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609155 | |||||||
| chr3:42609208 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01257.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.58+8144A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609208 | |||||||
| chr3:42609234 | CAG | C | 16 | a0003c0002t0004g0020 a0003c0002t0004g0052 a0003c0002t0004g0055 others(13): Show |
25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+8173_58+8174del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609234 | ||||||
| chr3:42609365 | A | G | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-8205A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609365 | |||||||
| chr3:42609501 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.59-8069T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609501 | |||||||
| chr3:42609522 | G | C | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-8048G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609522 | |||||||
| chr3:42609629 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.59-7941A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609629 | |||||||
| chr3:42609646 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.59-7924G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609646 | |||||||
| chr3:42609717 | C | T | 15 | a0003c0002t0004g0020 a0003c0002t0004g0052 a0003c0002t0004g0055 others(12): Show |
24 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-7853C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609717 | |||||||
| chr3:42609802 | G | A | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.59-7768G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609802 | |||||||
| chr3:42609827 | G | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-7743G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609827 | |||||||
| chr3:42609850 | T | TAA | 16 | a0003c0002t0004g0020 a0003c0002t0004g0052 a0003c0002t0004g0055 others(13): Show |
25 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-7719_59-7718dup others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42609850 | ||||||
| chr3:42609973 | C | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-7597C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42609973 | |||||||
| chr3:42610011 | C | CT | 4 | a0001c0001t0001g0132 a0005c0006t0001g0012 a0005c0006t0001g0086 others(1): Show |
6 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-7550dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42610011 | ||||||
| chr3:42610033 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(81): Show |
109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.59-7537C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610033 | |||||||
| chr3:42610074 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.59-7496C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610074 | |||||||
| chr3:42610231 | C | T | 16 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(13): Show |
25 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.59-7339C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610231 | |||||||
| chr3:42610240 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-7330G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610240 | |||||||
| chr3:42610286 | G | A | 25 | a0003c0002t0004g0019 a0003c0002t0004g0020 a0003c0002t0004g0042 others(22): Show |
35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.59-7284G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610286 | |||||||
| chr3:42610500 | A | G | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.59-7070A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610500 | |||||||
| chr3:42610545 | T | A | 3 | a0003c0002t0004g0019 a0003c0002t0004g0046 a0003c0002t0004g0049 |
4 | HG01934.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-7025T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42610545 | |||||||
| chr3:42610594 | A | AT | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-6966dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42610594 | ||||||
| chr3:42611050 | A | G | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-6520A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611050 | |||||||
| chr3:42611128 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.59-6442C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611128 | |||||||
| chr3:42611182 | A | G | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-6388A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611182 | |||||||
| chr3:42611224 | G | A | 5 | a0002c0004t0004g0022 a0002c0004t0004g0068 a0002c0004t0004g0069 others(2): Show |
6 | HG00280.hp1 HG01106.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-6346G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611224 | |||||||
| chr3:42611354 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.59-6216A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611354 | |||||||
| chr3:42611377 | C | A | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-6193C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611377 | |||||||
| chr3:42611687 | C | G | 1 | a0001c0013t0020g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.59-5883C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611687 | |||||||
| chr3:42611732 | C | CA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(110): Show |
150 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.59-5821dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42611732 | ||||||
| chr3:42611750 | T | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59-5820T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611750 | |||||||
| chr3:42611890 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.59-5680A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611890 | |||||||
| chr3:42611916 | C | T | 1 | a0001c0001t0028g0117 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.59-5654C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611916 | |||||||
| chr3:42611978 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.59-5592A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42611978 | |||||||
| chr3:42612082 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59-5488C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612082 | |||||||
| chr3:42612086 | G | A | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-5484G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612086 | |||||||
| chr3:42612087 | C | T | 2 | a0002c0004t0008g0065 a0002c0004t0008g0066 |
2 | HG00639.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.59-5483C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612087 | |||||||
| chr3:42612164 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-5406G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612164 | |||||||
| chr3:42612230 | A | T | 17 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(14): Show |
26 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-5340A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612230 | |||||||
| chr3:42612233 | T | TTTGCTTG others(10): Show |
1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.59-5336_59-5320dup others(17): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42612233 | ||||||
| chr3:42612327 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-5243T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612327 | |||||||
| chr3:42612354 | C | T | 1 | a0001c0001t0007g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.59-5216C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612354 | |||||||
| chr3:42612366 | T | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-5204T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612366 | |||||||
| chr3:42612405 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.59-5165A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612405 | |||||||
| chr3:42612418 | A | G | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.59-5152A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612418 | |||||||
| chr3:42612460 | A | G | 1 | a0001c0012t0002g0210 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.59-5110A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612460 | |||||||
| chr3:42612640 | A | G | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.59-4930A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612640 | |||||||
| chr3:42612652 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.59-4918A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612652 | |||||||
| chr3:42612676 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.59-4894T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612676 | |||||||
| chr3:42612725 | A | G | 1 | a0001c0001t0017g0207 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-4845A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612725 | |||||||
| chr3:42612730 | A | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0093 others(4): Show |
9 | HG00423.hp2 HG00597.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-4840A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612730 | |||||||
| chr3:42612748 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-4822T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612748 | |||||||
| chr3:42612799 | G | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-4771G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612799 | |||||||
| chr3:42612853 | G | A | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-4717G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612853 | |||||||
| chr3:42612891 | G | A | 1 | a0002c0004t0008g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.59-4679G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612891 | |||||||
| chr3:42612909 | A | G | 1 | a0001c0001t0007g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.59-4661A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42612909 | |||||||
| chr3:42613044 | TAAC | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-4525_59-4523del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613044 | |||||||
| chr3:42613160 | C | T | 1 | a0001c0001t0011g0026 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.59-4410C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613160 | |||||||
| chr3:42613554 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.59-4016A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613554 | |||||||
| chr3:42613601 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.59-3969A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613601 | |||||||
| chr3:42613942 | T | C | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3628T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42613942 | |||||||
| chr3:42615082 | C | CT | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-2474dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42615082 | ||||||
| chr3:42615086 | T | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(85): Show |
115 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.59-2484T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615086 | |||||||
| chr3:42615266 | A | G | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-2304A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615266 | |||||||
| chr3:42615360 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.59-2210T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615360 | |||||||
| chr3:42615379 | G | A | 5 | a0001c0001t0002g0082 a0001c0001t0002g0182 a0001c0001t0002g0190 others(2): Show |
5 | HG01070.hp2 HG01123.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2191G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615379 | |||||||
| chr3:42615382 | A | AT | 7 | a0001c0001t0002g0179 a0001c0001t0034g0246 a0001c0008t0015g0262 others(4): Show |
7 | HG01109.hp2 NA18967.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-2171dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42615382 | ||||||
| chr3:42615618 | C | G | 1 | a0001c0001t0002g0240 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.59-1952C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615618 | |||||||
| chr3:42615732 | G | T | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-1838G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615732 | |||||||
| chr3:42615866 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(81): Show |
109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.59-1704T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615866 | |||||||
| chr3:42615905 | CCTGCTTG others(5): Show |
C | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-1662_59-1651del others(12): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr3 | 42615905 | ||||||
| chr3:42615961 | C | G | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.59-1609C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42615961 | |||||||
| chr3:42616176 | G | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-1394G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616176 | |||||||
| chr3:42616329 | G | A | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.59-1241G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616329 | |||||||
| chr3:42616349 | G | A | 7 | a0002c0003t0004g0006 a0002c0003t0004g0023 a0002c0003t0004g0075 others(4): Show |
9 | HG00558.hp1 HG02300.hp1 NA19011.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-1221G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616349 | |||||||
| chr3:42616463 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.59-1107T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616463 | |||||||
| chr3:42616692 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.59-878G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616692 | |||||||
| chr3:42616764 | A | G | 1 | a0001c0001t0002g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.59-806A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616764 | |||||||
| chr3:42616825 | T | C | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.59-745T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616825 | |||||||
| chr3:42616915 | C | T | 1 | a0003c0002t0004g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-655C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42616915 | |||||||
| chr3:42617080 | T | G | 3 | a0001c0001t0003g0163 a0001c0001t0003g0192 a0001c0001t0003g0218 |
3 | NA18950.hp2 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.59-490T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617080 | |||||||
| chr3:42617274 | A | G | 1 | a0001c0001t0005g0243 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.59-296A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617274 | |||||||
| chr3:42617282 | A | G | 2 | a0003c0002t0006g0056 a0003c0019t0006g0057 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.59-288A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617282 | |||||||
| chr3:42617391 | A | C | 2 | a0001c0001t0019g0145 a0001c0001t0019g0147 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.59-179A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 2/16 | chr3 | 42617391 | |||||||
| chr3:42617774 | T | TA | 28 | a0001c0001t0001g0137 a0003c0002t0004g0019 a0003c0002t0004g0020 others(25): Show |
38 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.133+131dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42617774 | ||||||
| chr3:42617856 | AAG | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0130 |
4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+217_133+218del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42617856 | ||||||
| chr3:42618207 | C | T | 3 | a0001c0001t0003g0035 a0001c0001t0003g0168 a0001c0001t0003g0172 |
4 | NA18961.hp1 NA18963.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+563C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618207 | |||||||
| chr3:42618282 | C | T | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.133+638C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618282 | |||||||
| chr3:42618307 | C | T | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.133+663C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618307 | |||||||
| chr3:42618349 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.134-671C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618349 | |||||||
| chr3:42618351 | C | CA | 30 | a0001c0001t0003g0169 a0001c0001t0003g0189 a0001c0001t0005g0236 others(27): Show |
40 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-650dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618351 | ||||||
| chr3:42618351 | CA | C | 16 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0002g0032 others(13): Show |
20 | HG01243.hp1 HG02109.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.134-650delA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618351 | ||||||
| chr3:42618371 | T | A | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.134-649T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618371 | |||||||
| chr3:42618411 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(81): Show |
109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.134-609A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618411 | |||||||
| chr3:42618462 | C | T | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.134-558C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618462 | |||||||
| chr3:42618696 | G | A | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.134-324G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618696 | |||||||
| chr3:42618736 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.134-284G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618736 | |||||||
| chr3:42618789 | T | C | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.134-231T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618789 | |||||||
| chr3:42618857 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.134-163C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42618857 | |||||||
| chr3:42618884 | T | TGTCATCT others(353): Show |
1 | a0001c0001t0001g0111 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.134-122_134-121ins others(360): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618884 | ||||||
| chr3:42618997 | C | CT | 13 | a0001c0001t0001g0025 a0001c0001t0001g0091 a0001c0001t0002g0178 others(10): Show |
15 | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.134-5dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618997 | ||||||
| chr3:42618997 | CT | C | 29 | a0001c0001t0001g0085 a0001c0001t0003g0193 a0003c0002t0004g0019 others(26): Show |
39 | HG01070.hp1 HG01109.hp2 HG01167.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.134-5delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618997 | ||||||
| chr3:42618997 | CTT | C | 27 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(24): Show |
37 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(34): Show |
splice_region_variant&intron_variant | LOW | c.134-6_134-5delTT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr3 | 42618997 | ||||||
| chr3:42619015 | T | C | 1 | a0003c0002t0009g0053 | 1 | NA20300.hp1 | splice_region_variant&intron_variant | LOW | c.134-5T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 3/16 | chr3 | 42619015 | |||||||
| chr3:42619164 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.241+37A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/16 | chr3 | 42619164 | |||||||
| chr3:42619370 | C | T | 11 | a0001c0001t0002g0179 a0001c0001t0003g0203 a0001c0001t0007g0040 others(8): Show |
11 | HG00099.hp2 HG00738.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+243C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/16 | chr3 | 42619370 | |||||||
| chr3:42619583 | G | A | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.242-81G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 4/16 | chr3 | 42619583 | |||||||
| chr3:42619820 | T | A | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+112T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619820 | |||||||
| chr3:42619867 | A | G | 1 | a0001c0001t0001g0028 | 2 | NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.286+159A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619867 | |||||||
| chr3:42619917 | A | T | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+209A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619917 | |||||||
| chr3:42619918 | T | A | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+210T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619918 | |||||||
| chr3:42619919 | G | T | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+211G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42619919 | |||||||
| chr3:42620088 | T | A | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+380T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620088 | |||||||
| chr3:42620090 | G | C | 1 | a0002c0004t0008g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286+382G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620090 | |||||||
| chr3:42620126 | A | T | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.286+418A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620126 | |||||||
| chr3:42620283 | A | G | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+575A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620283 | |||||||
| chr3:42620542 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0130 |
5 | HG01074.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+834T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620542 | |||||||
| chr3:42620584 | T | G | 1 | a0014c0014t0004g0071 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.287-845T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620584 | |||||||
| chr3:42620902 | G | A | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.287-527G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42620902 | |||||||
| chr3:42621001 | C | T | 25 | a0003c0002t0004g0019 a0003c0002t0004g0020 a0003c0002t0004g0042 others(22): Show |
35 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.287-428C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42621001 | |||||||
| chr3:42621079 | G | A | 1 | a0001c0001t0003g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.287-350G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 5/16 | chr3 | 42621079 | |||||||
| chr3:42621660 | T | C | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.374+144T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42621660 | |||||||
| chr3:42621758 | G | A | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.374+242G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42621758 | |||||||
| chr3:42622306 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.374+790A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622306 | |||||||
| chr3:42622410 | A | G | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.374+894A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622410 | |||||||
| chr3:42622451 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(86): Show |
116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.374+935T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622451 | |||||||
| chr3:42622616 | T | C | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.374+1100T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622616 | |||||||
| chr3:42622868 | C | T | 1 | a0002c0004t0004g0069 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.374+1352C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42622868 | |||||||
| chr3:42623047 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.374+1531C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623047 | |||||||
| chr3:42623248 | T | G | 1 | a0015c0022t0001g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.374+1732T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623248 | |||||||
| chr3:42623340 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.374+1824T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623340 | |||||||
| chr3:42623448 | T | G | 1 | a0001c0001t0005g0243 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.374+1932T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623448 | |||||||
| chr3:42623496 | T | G | 1 | a0001c0001t0007g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.374+1980T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623496 | |||||||
| chr3:42623753 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+2237C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623753 | |||||||
| chr3:42623786 | G | T | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.374+2270G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623786 | |||||||
| chr3:42623853 | A | T | 6 | a0001c0001t0001g0132 a0004c0005t0001g0015 a0004c0005t0001g0131 others(3): Show |
7 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.374+2337A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42623853 | |||||||
| chr3:42624105 | A | G | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.374+2589A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624105 | |||||||
| chr3:42624138 | G | A | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.374+2622G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624138 | |||||||
| chr3:42624326 | A | G | 1 | a0005c0006t0001g0086 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.374+2810A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624326 | |||||||
| chr3:42624463 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.374+2947A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624463 | |||||||
| chr3:42624571 | A | G | 1 | a0002c0004t0008g0067 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.374+3055A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624571 | |||||||
| chr3:42624666 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18975.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.374+3150A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624666 | |||||||
| chr3:42624836 | C | T | 1 | a0001c0001t0007g0223 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.374+3320C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624836 | |||||||
| chr3:42624987 | T | C | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+3471T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624987 | |||||||
| chr3:42624996 | A | G | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.374+3480A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42624996 | |||||||
| chr3:42625226 | C | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.374+3710C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625226 | |||||||
| chr3:42625278 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.374+3762C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625278 | |||||||
| chr3:42625425 | A | G | 1 | a0003c0002t0004g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.374+3909A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625425 | |||||||
| chr3:42625441 | T | TAAG | 58 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(55): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.374+3926_374+3928d others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42625441 | ||||||
| chr3:42625609 | G | A | 5 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0134 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.374+4093G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625609 | |||||||
| chr3:42625619 | T | A | 2 | a0001c0001t0019g0145 a0001c0001t0019g0147 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.374+4103T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625619 | |||||||
| chr3:42625714 | T | G | 6 | a0002c0004t0008g0062 a0002c0004t0008g0063 a0002c0004t0008g0064 others(3): Show |
6 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.374+4198T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42625714 | |||||||
| chr3:42626052 | C | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.375-4494C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626052 | |||||||
| chr3:42626123 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0141 |
2 | NA18985.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.375-4423T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626123 | |||||||
| chr3:42626167 | A | AT | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0126 others(22): Show |
30 | HG01074.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.375-4367dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42626167 | ||||||
| chr3:42626167 | A | ATT | 54 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(51): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.375-4368_375-4367d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42626167 | ||||||
| chr3:42626234 | TATTC | T | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.375-4309_375-4306d others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr3 | 42626234 | ||||||
| chr3:42626444 | A | G | 49 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0009 others(46): Show |
63 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.375-4102A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626444 | |||||||
| chr3:42626949 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(86): Show |
116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.375-3597A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42626949 | |||||||
| chr3:42627022 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.375-3524C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627022 | |||||||
| chr3:42627534 | G | T | 1 | a0003c0002t0004g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.375-3012G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627534 | |||||||
| chr3:42627608 | A | G | 1 | a0001c0001t0011g0088 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.375-2938A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627608 | |||||||
| chr3:42627630 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.375-2916A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627630 | |||||||
| chr3:42627901 | A | G | 58 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(55): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.375-2645A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627901 | |||||||
| chr3:42627968 | T | C | 58 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(55): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.375-2578T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42627968 | |||||||
| chr3:42628144 | A | T | 1 | a0001c0001t0002g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.375-2402A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628144 | |||||||
| chr3:42628176 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.375-2370T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628176 | |||||||
| chr3:42628198 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0130 |
4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.375-2348G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628198 | |||||||
| chr3:42628277 | C | T | 8 | a0003c0002t0004g0019 a0003c0002t0004g0045 a0003c0002t0004g0046 others(5): Show |
9 | HG01192.hp1 HG01934.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.375-2269C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628277 | |||||||
| chr3:42628280 | G | A | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.375-2266G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628280 | |||||||
| chr3:42628389 | C | T | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.375-2157C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628389 | |||||||
| chr3:42628573 | C | T | 1 | a0001c0008t0015g0262 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.375-1973C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628573 | |||||||
| chr3:42628727 | T | C | 58 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(55): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.375-1819T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628727 | |||||||
| chr3:42628737 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.375-1809C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628737 | |||||||
| chr3:42628786 | G | A | 1 | a0002c0004t0008g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.375-1760G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628786 | |||||||
| chr3:42628856 | G | A | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.375-1690G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628856 | |||||||
| chr3:42628957 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(144): Show |
194 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.375-1589A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42628957 | |||||||
| chr3:42629475 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.375-1071G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42629475 | |||||||
| chr3:42629567 | G | A | 1 | a0001c0012t0002g0210 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.375-979G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42629567 | |||||||
| chr3:42630122 | C | G | 1 | a0001c0001t0020g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.375-424C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630122 | |||||||
| chr3:42630170 | C | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.375-376C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630170 | |||||||
| chr3:42630176 | T | G | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.375-370T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630176 | |||||||
| chr3:42630362 | AGTAAGAT others(7): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.375-183_375-170del others(14): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 6/16 | chr3 | 42630362 | |||||||
| chr3:42630681 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404+106T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630681 | |||||||
| chr3:42630730 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0130 |
4 | HG01074.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+155T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630730 | |||||||
| chr3:42630761 | G | T | 1 | a0001c0001t0005g0201 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.404+186G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630761 | |||||||
| chr3:42630994 | G | A | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.405-177G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 7/16 | chr3 | 42630994 | |||||||
| chr3:42631490 | T | C | 58 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(55): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.550+174T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631490 | |||||||
| chr3:42631762 | A | G | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.550+446A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631762 | |||||||
| chr3:42631794 | T | C | 1 | a0001c0001t0003g0249 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.550+478T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631794 | |||||||
| chr3:42631987 | C | T | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.551-614C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42631987 | |||||||
| chr3:42632061 | C | CT | 22 | a0001c0001t0002g0008 a0001c0001t0002g0144 a0001c0001t0002g0174 others(19): Show |
24 | HG00544.hp2 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.551-515dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | ||||||
| chr3:42632061 | CT | C | 8 | a0001c0001t0001g0137 a0001c0001t0002g0190 a0001c0001t0005g0225 others(5): Show |
9 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.551-515delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | ||||||
| chr3:42632061 | CTT | C | 12 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0115 others(9): Show |
12 | HG02723.hp2 HG02809.hp2 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.551-516_551-515del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | ||||||
| chr3:42632061 | CTTT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(96): Show |
136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.551-517_551-515del others(3): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632061 | ||||||
| chr3:42632404 | G | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(84): Show |
114 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.551-197G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | chr3 | 42632404 | |||||||
| chr3:42632536 | A | AT | 27 | a0003c0002t0004g0019 a0003c0002t0004g0020 a0003c0002t0004g0042 others(24): Show |
37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.551-59dupT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr3 | 42632536 | ||||||
| chr3:42632836 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.773+13C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42632836 | |||||||
| chr3:42632967 | A | G | 11 | a0001c0001t0003g0038 a0001c0001t0003g0173 a0001c0001t0003g0189 others(8): Show |
12 | HG01358.hp1 HG01496.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.773+144A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42632967 | |||||||
| chr3:42633279 | C | T | 1 | a0002c0003t0004g0073 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.774-301C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42633279 | |||||||
| chr3:42633560 | G | A | 1 | a0001c0001t0003g0168 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.774-20G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 9/16 | chr3 | 42633560 | |||||||
| chr3:42633788 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.929+53G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42633788 | |||||||
| chr3:42633993 | T | C | 1 | a0001c0001t0013g0187 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.929+258T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42633993 | |||||||
| chr3:42634117 | T | C | 2 | a0001c0001t0011g0088 a0001c0001t0011g0089 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.929+382T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634117 | |||||||
| chr3:42634284 | T | G | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.930-329T>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634284 | |||||||
| chr3:42634357 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.930-256C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634357 | |||||||
| chr3:42634367 | T | A | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.930-246T>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 10/16 | chr3 | 42634367 | |||||||
| chr3:42634773 | G | T | 58 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(55): Show |
78 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1017+73G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | chr3 | 42634773 | |||||||
| chr3:42634933 | G | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1017+233G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | chr3 | 42634933 | |||||||
| chr3:42635054 | A | T | 2 | a0001c0001t0019g0145 a0001c0001t0019g0147 |
2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1018-167A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | chr3 | 42635054 | |||||||
| chr3:42635057 | TA | T | 6 | a0001c0001t0002g0174 a0001c0001t0002g0186 a0001c0001t0002g0240 others(3): Show |
6 | HG01516.hp1 HG03017.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-143delA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | ||||||
| chr3:42635057 | TAA | T | 58 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0010g0146 others(55): Show |
75 | HG00280.hp1 HG00597.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-144_1018-143d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | ||||||
| chr3:42635057 | TAAA | T | 8 | a0001c0001t0001g0090 a0002c0003t0004g0011 a0002c0003t0004g0023 others(5): Show |
11 | HG00558.hp1 HG00639.hp2 HG03453.hp1 others(8): Show |
intron_variant | MODIFIER | c.1018-145_1018-143d others(5): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | ||||||
| chr3:42635057 | TAAAA | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(76): Show |
106 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1018-146_1018-143d others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr3 | 42635057 | ||||||
| chr3:42635433 | C | A | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1163+67C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635433 | |||||||
| chr3:42635442 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1163+76A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635442 | |||||||
| chr3:42635561 | G | A | 1 | a0003c0002t0004g0019 | 2 | HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1163+195G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635561 | |||||||
| chr3:42635658 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(220): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1163+292G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635658 | |||||||
| chr3:42635695 | G | A | 1 | a0001c0007t0018g0164 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1163+329G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635695 | |||||||
| chr3:42635796 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1163+430A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635796 | |||||||
| chr3:42635862 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(57): Show |
80 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1163+496C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635862 | |||||||
| chr3:42635863 | G | A | 1 | a0001c0001t0003g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1163+497G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635863 | |||||||
| chr3:42635907 | C | CA | 8 | a0001c0001t0002g0182 a0001c0007t0005g0156 a0001c0007t0005g0167 others(5): Show |
8 | HG00099.hp2 HG01192.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163+556dupA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 42635907 | ||||||
| chr3:42635920 | A | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | NA18990.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1163+554A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42635920 | |||||||
| chr3:42636011 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01257.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1163+645C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636011 | |||||||
| chr3:42636090 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1163+724C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636090 | |||||||
| chr3:42636344 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(148): Show |
198 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.1164-524T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636344 | |||||||
| chr3:42636406 | C | T | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1164-462C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636406 | |||||||
| chr3:42636422 | A | G | 19 | a0003c0002t0004g0020 a0003c0002t0004g0042 a0003c0002t0004g0052 others(16): Show |
28 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.1164-446A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | chr3 | 42636422 | |||||||
| chr3:42636653 | TA | T | 6 | a0002c0004t0008g0062 a0002c0004t0008g0063 a0002c0004t0008g0064 others(3): Show |
6 | HG00639.hp2 HG03139.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1164-205delA | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | 42636653 | ||||||
| chr3:42639789 | GTC | G | 3 | a0005c0006t0001g0012 a0005c0006t0001g0086 a0005c0006t0001g0087 |
5 | HG02622.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4046+41_4046+42del others(2): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 42639789 | ||||||
| chr3:42639859 | G | A | 28 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(25): Show |
38 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.4046+109G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42639859 | |||||||
| chr3:42639895 | G | A | 55 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(52): Show |
75 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.4046+145G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42639895 | |||||||
| chr3:42639953 | A | ACT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(142): Show |
192 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.4046+204_4046+205d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 42639953 | ||||||
| chr3:42639960 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4046+210C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42639960 | |||||||
| chr3:42640158 | A | G | 2 | a0001c0001t0005g0036 a0001c0001t0005g0201 |
3 | HG00738.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.4046+408A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640158 | |||||||
| chr3:42640300 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4046+550C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640300 | |||||||
| chr3:42640301 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4046+551T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640301 | |||||||
| chr3:42640630 | A | G | 1 | a0002c0003t0004g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4046+880A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640630 | |||||||
| chr3:42640632 | C | T | 3 | a0001c0001t0002g0177 a0001c0001t0002g0199 a0001c0001t0002g0200 |
3 | NA18966.hp1 NA18991.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.4046+882C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640632 | |||||||
| chr3:42640696 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(57): Show |
80 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.4046+946C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640696 | |||||||
| chr3:42640755 | G | T | 1 | a0001c0008t0015g0264 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4046+1005G>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640755 | |||||||
| chr3:42640839 | C | G | 1 | a0001c0001t0002g0166 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4046+1089C>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640839 | |||||||
| chr3:42640843 | T | C | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4046+1093T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42640843 | |||||||
| chr3:42641052 | G | A | 53 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(50): Show |
73 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.4046+1302G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641052 | |||||||
| chr3:42641092 | C | T | 1 | a0001c0001t0018g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4046+1342C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641092 | |||||||
| chr3:42641197 | AG | A | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4047-1302delG | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr3 | 42641197 | ||||||
| chr3:42641403 | T | C | 1 | a0003c0002t0009g0021 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4047-1098T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641403 | |||||||
| chr3:42641618 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(270): Show |
343 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.4047-883A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641618 | |||||||
| chr3:42641627 | C | A | 52 | a0002c0003t0004g0005 a0002c0003t0004g0006 a0002c0003t0004g0011 others(49): Show |
72 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.4047-874C>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641627 | |||||||
| chr3:42641631 | G | A | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.4047-870G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641631 | |||||||
| chr3:42641646 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4047-855G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641646 | |||||||
| chr3:42641677 | A | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4047-824A>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641677 | |||||||
| chr3:42641735 | G | A | 1 | a0001c0001t0005g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4047-766G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641735 | |||||||
| chr3:42641750 | T | C | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4047-751T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641750 | |||||||
| chr3:42641890 | A | T | 2 | a0007c0011t0016g0257 a0007c0011t0016g0258 |
2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4047-611A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641890 | |||||||
| chr3:42641927 | T | C | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4047-574T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641927 | |||||||
| chr3:42641960 | C | T | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4047-541C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42641960 | |||||||
| chr3:42642059 | T | C | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4047-442T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42642059 | |||||||
| chr3:42642407 | G | C | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.4047-94G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 13/16 | chr3 | 42642407 | |||||||
| chr3:42642641 | A | G | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4142+45A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42642641 | |||||||
| chr3:42642770 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02083.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.4142+174C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42642770 | |||||||
| chr3:42643034 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4143-305C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42643034 | |||||||
| chr3:42643093 | C | T | 5 | a0003c0002t0006g0010 a0003c0002t0006g0056 a0003c0002t0006g0059 others(2): Show |
7 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.4143-246C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42643093 | |||||||
| chr3:42643295 | G | A | 56 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 others(53): Show |
76 | HG00280.hp1 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.4143-44G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 14/16 | chr3 | 42643295 | |||||||
| chr3:42643542 | C | T | 4 | a0001c0001t0010g0146 a0001c0001t0010g0148 a0001c0001t0010g0149 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.4199+147C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 15/16 | chr3 | 42643542 | |||||||
| chr3:42643874 | T | C | 1 | a0003c0002t0004g0042 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4200-28T>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 15/16 | chr3 | 42643874 | |||||||
| chr3:42644033 | C | T | 2 | a0003c0002t0004g0050 a0003c0002t0004g0051 |
2 | HG01192.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4301+30C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644033 | |||||||
| chr3:42644226 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0126 a0001c0001t0001g0130 |
5 | HG01074.hp2 HG02809.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.4301+223C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644226 | |||||||
| chr3:42644324 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(86): Show |
116 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.4301+321A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644324 | |||||||
| chr3:42644349 | AT | A | 6 | a0001c0001t0001g0132 a0004c0005t0001g0015 a0004c0005t0001g0131 others(3): Show |
7 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.4301+354delT | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 42644349 | ||||||
| chr3:42644419 | A | G | 66 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0003g0002 others(63): Show |
80 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.4301+416A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644419 | |||||||
| chr3:42644468 | A | G | 1 | a0001c0001t0002g0245 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4301+465A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644468 | |||||||
| chr3:42644509 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(81): Show |
109 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.4301+506C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644509 | |||||||
| chr3:42644658 | A | G | 3 | a0001c0008t0015g0262 a0001c0008t0015g0263 a0001c0008t0015g0264 |
3 | NA18969.hp1 NA19076.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.4301+655A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644658 | |||||||
| chr3:42644671 | G | C | 1 | a0001c0001t0002g0199 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4301+668G>C | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644671 | |||||||
| chr3:42644771 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4301+768A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42644771 | |||||||
| chr3:42644978 | T | TTG | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0014 others(76): Show |
102 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.4302-892_4302-891d others(4): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 42644978 | ||||||
| chr3:42644978 | T | TTGTG | 5 | a0001c0001t0001g0013 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
7 | HG01256.hp1 HG01891.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.4302-894_4302-891d others(6): Show |
NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr3 | 42644978 | ||||||
| chr3:42645208 | A | T | 2 | a0003c0002t0009g0044 a0003c0002t0009g0058 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4302-680A>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645208 | |||||||
| chr3:42645407 | G | A | 1 | a0001c0001t0007g0213 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4302-481G>A | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645407 | |||||||
| chr3:42645752 | A | G | 5 | a0001c0001t0002g0212 a0001c0001t0002g0224 a0001c0001t0002g0230 others(2): Show |
5 | NA18747.hp2 NA18970.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.4302-136A>G | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645752 | |||||||
| chr3:42645786 | C | T | 66 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0003g0002 others(63): Show |
80 | HG00099.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.4302-102C>T | NKTR | ENSG00000114857.19 | transcript | ENST00000232978.13 | protein_coding | 16/16 | chr3 | 42645786 |